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How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.

Assessed papers (1)

• Trem2 promotes anti-inflammatory responses in microglia and is suppressed under pro-inflammatory conditions.
  2020 L1 67/100

1 assessed by us (0 reproduced) · 1,199 not yet assessed — every PubMed paper on record, linked below.

• Early oligodendrocyte dysfunction signature in Alzheimer’s disease: Insights from DNA methylomics and transcriptomics ↗

  Molecular Psychiatry · 2026 · PMID 42315917
  not yet assessed
• Genetic drivers of progression in Alzheimer’s disease are distinct from disease risk ↗

  Alzheimer s Research & Therapy · 2026 · PMID 41332834
  not yet assessed
• Alzheimer's Disease: Treatment Challenges for the Future ↗

  Journal of Neurochemistry · 2025 · PMID 40739944
  not yet assessed
• Intracellular accumulation of amyloid-ß is a marker of selective neuronal vulnerability in Alzheimer’s disease ↗

  Nature Communications · 2025 · PMID 40467545
  not yet assessed
• Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer’s disease ↗

  Genome biology · 2025 · PMID 40676597
  not yet assessed
• The genetics of neurodegenerative diseases is the genetics of age-related damage clearance failure ↗

  Molecular Psychiatry · 2025 · PMID 39880902
  not yet assessed
• Machine learning in Alzheimer’s disease genetics ↗

  Nature Communications · 2025 · PMID 40691194
  not yet assessed
• Large-scale visualization of α-synuclein oligomers in Parkinson’s disease brain tissue ↗

  Nature Biomedical Engineering · 2025 · PMID 41034512
  not yet assessed
• Molnupiravir or nirmatrelvir–ritonavir plus usual care versus usual care alone in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial ↗

  The Lancet Infectious Diseases · 2025 · PMID 40383127
  not yet assessed
• Unravelling the plasma proteome: Pioneering biomarkers for differential dementia diagnosis ↗

  Alzheimer s & Dementia · 2025 · PMID 40613333
  not yet assessed
• Increased burden of rare risk variants across gene expression networks predisposes to sporadic Parkinson’s disease ↗

  Cell Reports · 2025 · PMID 40317721
  not yet assessed
• Milestone Review: The History of Molecular Genetics Analysis of Alzheimer's Disease ↗

  Journal of Neurochemistry · 2025 · PMID 40600356
  not yet assessed
• Mutations in PSEN1 predispose inflammation in an astrocyte model of familial Alzheimer’s disease through disrupted regulated intramembrane proteolysis ↗

  Molecular Neurodegeneration · 2025 · PMID 40542358
  not yet assessed
• Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores ↗

  npj Parkinson s Disease · 2025 · PMID 40610451
  not yet assessed
• TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations ↗

  npj Parkinson s Disease · 2025 · PMID 41331295
  not yet assessed
• Large-scale genetic characterization of Parkinson’s disease in the African and African admixed populations ↗

  Brain · 2025 · PMID 41058593
  not yet assessed
• The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population ↗

  npj Parkinson s Disease · 2025 · PMID 40133296
  not yet assessed
• Higher dose corticosteroids in hospitalised COVID-19 patients requiring ventilatory support (RECOVERY): a randomised, controlled, open-label, platform trial ↗

  EClinicalMedicine · 2025 · PMID 40036152
  not yet assessed
• Presenilin 1 hemizygosity has no overt deleterious phenotypic outcomes in sheep: Potential implications for therapeutic targets in Alzheimer's disease ↗

  Neurobiology of Aging · 2025 · PMID 40315540
  not yet assessed
• Evidence suggesting that microglia make amyloid from neuronally expressed APP: a hypothesis ↗

  Molecular Neurodegeneration · 2025 · PMID 40346674
  not yet assessed
• Increased frequency of repeat expansion mutations across different populations ↗

  Nature Medicine · 2024 · PMID 39354197
  not yet assessed
• Apolipoprotein E in Alzheimer’s disease trajectories and the next-generation clinical care pathway ↗

  Nature Neuroscience · 2024 · PMID 38898183
  not yet assessed
• Adaptive Long‐Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4 ↗

  Movement Disorders · 2024 · PMID 38197134
  not yet assessed
• Genome sequence analyses identify novel risk loci for multiple system atrophy ↗

  Neuron · 2024 · PMID 38701790
  not yet assessed
• Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes ↗

  Nature Communications · 2024 · PMID 39251599
  not yet assessed
• NeuroBooster Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations ↗

  Movement Disorders · 2024 · PMID 39283294
  not yet assessed
• Immunomodulatory therapy in children with paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS, MIS-C; RECOVERY): a randomised, controlled, open-label, platform trial ↗

  The Lancet Child & Adolescent Health · 2024 · PMID 38272046
  not yet assessed
• A blood‐based multi‐pathway biomarker assay for early detection and staging of Alzheimer's disease across ethnic groups ↗

  Alzheimer s & Dementia · 2024 · PMID 38183344
  not yet assessed
• Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease ↗

  Brain · 2024 · PMID 38193360
  not yet assessed
• The annotation of GBA1 has been concealed by its protein-coding pseudogene GBAP1 ↗

  Science Advances · 2024 · PMID 38924406
  not yet assessed
• Using blood transcriptome analysis for Alzheimer's disease diagnosis and patient stratification ↗

  Alzheimer s & Dementia · 2024 · PMID 38323937
  not yet assessed
• Profiling complex repeat expansions in RFC1 in Parkinson’s disease ↗

  npj Parkinson s Disease · 2024 · PMID 38789445
  not yet assessed
• Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia ↗

  The American Journal of Human Genetics · 2024 · PMID 38889728
  not yet assessed
• Amyloid-β predominant Alzheimer’s disease neuropathologic change ↗

  Brain · 2024 · PMID 39417691
  not yet assessed
• MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study ↗

  The Lancet Neurology · 2024 · PMID 38631765
  not yet assessed
• Large-scale proteomics analysis of five brain regions from Parkinson’s disease patients with a GBA1 mutation ↗

  npj Parkinson s Disease · 2024 · PMID 38331996
  not yet assessed
• Genome-wide determinants of mortality and motor progression in Parkinson’s disease ↗

  npj Parkinson s Disease · 2024 · PMID 38849413
  not yet assessed
• African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1 ↗

  Nature Structural & Molecular Biology · 2024 · PMID 39668204
  not yet assessed
• Towards cascading genetic risk in Alzheimer’s disease ↗

  Brain · 2024 · PMID 38820112
  not yet assessed
• Investigation of the genetic aetiology of Lewy body diseases with and without dementia ↗

  Brain Communications · 2024 · PMID 38978726
  not yet assessed
• Stratified analyses refine association between TLR7 rare variants and severe COVID-19 ↗

  Human Genetics and Genomics Advances · 2024 · PMID 38944683
  not yet assessed
• Amelioration of signaling deficits underlying metabolic shortfall in TREM2 R47H human iPSC ‐derived microglia ↗

  FEBS Journal · 2024 · PMID 39726135
  not yet assessed
• Human longevity and Alzheimer’s disease variants act via microglia and oligodendrocyte gene networks ↗

  Brain · 2024 · PMID 39778705
  not yet assessed
• Assessing clinical progression measures in Alzheimer's disease trials: A systematic review and meta‐analysis ↗

  Alzheimer s & Dementia · 2024 · PMID 39439251
  not yet assessed
• Transethnic analysis identifies SORL1 variants and haplotypes protective against Alzheimer's disease ↗

  Alzheimer s & Dementia · 2024 · PMID 39655505
  not yet assessed
• Chromosome X-wide association study in case control studies of pathologically confirmed Alzheimer’s disease in a European population ↗

  Translational Psychiatry · 2024 · PMID 39231932
  not yet assessed
• Elucidating the genomic basis of rare pediatric neurological diseases in Central Asia and Transcaucasia ↗

  Nature Genetics · 2024 · PMID 39578646
  not yet assessed
• Microglia contribute to the production of the amyloidogenic ABri peptide in familial British dementia ↗

  Acta Neuropathologica · 2024 · PMID 39546024
  not yet assessed
• The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder ↗

  Movement Disorders · 2024 · PMID 39635987
  not yet assessed
• Protection against Alzheimer’s Disease with APOE Christchurch Variant — How? ↗

  New England Journal of Medicine · 2024 · PMID 38899700
  not yet assessed
• Computing linkage disequilibrium aware genome embeddings using autoencoders ↗

  Bioinformatics · 2024 · PMID 38775680
  not yet assessed
• Development of a robust blood‐based multi‐pathway biomarker assay for early screening and classification of Alzheimer’s disease ↗

  Alzheimer s & Dementia · 2024
  not yet assessed
• A protocol for the study of environmental risk factors and candidate gene–environment interactions in neurodegenerative disorders in Nigeria (SERGEND): A cross-sectional descriptive study ↗

  Journal of Clinical Sciences · 2024
  not yet assessed
• Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease ↗

  Nature Genetics · 2023 · PMID 38155330
  not yet assessed
• GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19 ↗

  Nature · 2023 · PMID 37198478
  not yet assessed
• Microglia‐synapse engulfment via PtdSer‐TREM2 ameliorates neuronal hyperactivity in Alzheimer's disease models ↗

  The EMBO Journal · 2023 · PMID 37575021
  not yet assessed
• A second update on mapping the human genetic architecture of COVID-19 ↗

  Nature · 2023 · PMID 37674002
  not yet assessed
• Chronic effects of inflammation on tauopathies ↗

  The Lancet Neurology · 2023 · PMID 37059510
  not yet assessed
• Deep learning-based polygenic risk analysis for Alzheimer’s disease prediction ↗

  Communications Medicine · 2023 · PMID 37024668
  not yet assessed
• eQTL Catalogue 2023: New datasets, X chromosome QTLs, and improved detection and visualisation of transcript-level QTLs ↗

  PLoS Genetics · 2023 · PMID 37721944
  not yet assessed
• Associations of Sex, Race, and Apolipoprotein E Alleles With Multiple Domains of Cognition Among Older Adults ↗

  JAMA Neurology · 2023 · PMID 37459083
  not yet assessed
• Multiancestry analysis of the HLA locus in Alzheimer’s and Parkinson’s diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes ↗

  Proceedings of the National Academy of Sciences · 2023 · PMID 37643212
  not yet assessed
• An anti-amyloid therapy works for Alzheimer’s disease: why has it taken so long and what is next? ↗

  Brain · 2023 · PMID 36797987
  not yet assessed
• Large-scale rare variant burden testing in Parkinson's disease ↗

  Brain · 2023 · PMID 37348876
  not yet assessed
• What does heritability of Alzheimer’s disease represent? ↗

  PLoS ONE · 2023 · PMID 37115753
  not yet assessed
• Single-cell RNA sequencing analysis of human Alzheimer’s disease brain samples reveals neuronal and glial specific cells differential expression ↗

  PLoS ONE · 2023 · PMID 36827281
  not yet assessed
• Defining the Riddle in Order to Solve It: There Is More Than One “Parkinson's Disease” ↗

  Movement Disorders · 2023 · PMID 37156737
  not yet assessed
• The amyloid-β Pathway in Alzheimer’s Disease: A Plain Language Summary ↗

  Neurodegenerative Disease Management · 2023 · PMID 36994753
  not yet assessed
• Empagliflozin in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial ↗

  The Lancet Diabetes & Endocrinology · 2023 · PMID 37865101
  not yet assessed
• Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) ↗

  npj Parkinson s Disease · 2023 · PMID 37699923
  not yet assessed
• Genome‐Wide Analysis of Structural Variants in Parkinson Disease ↗

  Annals of Neurology · 2023 · PMID 36695634
  not yet assessed
• Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias ↗

  Cell Genomics · 2023 · PMID 37388914
  not yet assessed
• A dynamical systems approach for multiscale synthesis of Alzheimer’s pathogenesis ↗

  Neuron · 2023 · PMID 37172582
  not yet assessed
• Local genetic correlations exist among neurodegenerative and neuropsychiatric diseases ↗

  npj Parkinson s Disease · 2023 · PMID 37117178
  not yet assessed
• PINK1: From Parkinson’s disease to mitophagy and back again ↗

  PLoS Biology · 2023 · PMID 37384773
  not yet assessed
• Aβ efflux impairment and inflammation linked to cerebrovascular accumulation of amyloid-forming amylin secreted from pancreas ↗

  Communications Biology · 2023 · PMID 36596993
  not yet assessed
• Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia ↗

  Brain · 2023 · PMID 36624280
  not yet assessed
• New cases of dementia are rising in elderly populations in Wales, UK ↗

  Journal of the Neurological Sciences · 2023 · PMID 37385025
  not yet assessed
• LATE-NC risk alleles (in TMEM106B, GRN, and ABCC9 genes) among persons with African ancestry ↗

  Journal of Neuropathology & Experimental Neurology · 2023 · PMID 37528055
  not yet assessed
• Genetic meta-analysis of levodopa induced dyskinesia in Parkinson’s disease ↗

  npj Parkinson s Disease · 2023 · PMID 37652906
  not yet assessed
• Genome-wide Analysis of Motor Progression in Parkinson Disease ↗

  Neurology Genetics · 2023 · PMID 37560120
  not yet assessed
• Differential LRRK2 Signalling and Gene Expression in WT-LRRK2 and G2019S-LRRK2 Mouse Microglia Treated with Zymosan and MLi2 ↗

  Cells · 2023 · PMID 38201257
  not yet assessed
• Identifying Genetic Risk for Amyloid-Related Imaging Abnormalities ↗

  Neurology · 2023 · PMID 38165303
  not yet assessed
• The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases ↗

  Neurobiology of Disease · 2023 · PMID 36925053
  not yet assessed
• Association of cardiovascular disease management drugs with Lewy body dementia: a case–control study ↗

  Brain Communications · 2023 · PMID 38162907
  not yet assessed
• Isolation of biofluids from tissues using a vacuum-assisted filtration biomedical device ↗

  Analytical Methods · 2023 · PMID 37039091
  not yet assessed
• MAPT allele and haplotype frequencies in Nigerian Africans: Population distribution and association with Parkinson's disease risk and age at onset ↗

  Parkinsonism & Related Disorders · 2023 · PMID 37467655
  not yet assessed
• Anti-amyloid therapies work for Alzheimer’s disease ↗

  Brain Communications · 2023 · PMID 37492486
  not yet assessed
• Analysis of subcellular RNA fractions demonstrates significant genetic regulation of gene expression in human brain post-transcriptionally ↗

  Scientific Reports · 2023 · PMID 37620324
  not yet assessed
• New insights into the genetic etiology of Alzheimer’s disease and related dementias ↗

  Nature Genetics · 2022 · PMID 35379992
  not yet assessed
• Whole-genome sequencing reveals host factors underlying critical COVID-19 ↗

  Nature · 2022 · PMID 35255492
  not yet assessed
• Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease ↗

  Nature Genetics · 2022 · PMID 36411364
  not yet assessed
• Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer’s disease ↗

  Brain · 2022 · PMID 35383826
  not yet assessed
• Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study

  UCL Discovery (University College London) · 2022
  not yet assessed
• Genome-wide association studies for Alzheimer’s disease: bigger is not always better ↗

  Brain Communications · 2022 · PMID 35663382
  not yet assessed
• Plaque contact and unimpaired Trem2 is required for the microglial response to amyloid pathology ↗

  Cell Reports · 2022 · PMID 36417868
  not yet assessed
• Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson’s disease at 16q11.2 and MAPT H1 loci ↗

  Brain · 2022 · PMID 36074904
  not yet assessed
• Association between the LRP1B and APOE loci and the development of Parkinson’s disease dementia ↗

  Brain · 2022 · PMID 36348503
  not yet assessed
• Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood ↗

  Biological Psychiatry · 2022 · PMID 36759259
  not yet assessed
• An IL1RL1 genetic variant lowers soluble ST2 levels and the risk effects of APOE-ε4 in female patients with Alzheimer’s disease ↗

  Nature Aging · 2022 · PMID 37117777
  not yet assessed
• Whole genome analysis in APOE4 homozygotes identifies the DAB1-RELN pathway in Alzheimer's disease pathogenesis ↗

  Neurobiology of Aging · 2022 · PMID 35977442
  not yet assessed
• Exploring Links Between Psychosis and Frontotemporal Dementia Using Multimodal Machine Learning ↗

  JAMA Psychiatry · 2022 · PMID 35921104
  not yet assessed
• Combining biomarkers for prognostic modelling of Parkinson’s disease ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2022 · PMID 35577512
  not yet assessed
• Elevation of gangliosides in four brain regions from Parkinson’s disease patients with a GBA mutation ↗

  npj Parkinson s Disease · 2022 · PMID 35933559
  not yet assessed
• Prion-like α-synuclein pathology in the brain of infants with Krabbe disease ↗

  Brain · 2022 · PMID 34999780
  not yet assessed
• Multi‐Omics‐Based Autophagy‐Related Untypical Subtypes in Patients with Cerebral Amyloid Pathology ↗

  Advanced Science · 2022 · PMID 35694866
  not yet assessed
• Diabetes and Alzheimer's disease: shared genetic susceptibility? ↗

  The Lancet Neurology · 2022 · PMID 36270305
  not yet assessed
• Therapeutic anti‐amyloid β antibodies cause neuronal disturbances ↗

  Alzheimer s & Dementia · 2022 · PMID 36515320
  not yet assessed
• Dissecting the limited genetic overlap of Parkinson's and Alzheimer's disease ↗

  Annals of Clinical and Translational Neurology · 2022 · PMID 35684951
  not yet assessed
• Demographics and Medication Use of Patients with Late-Onset Alzheimer’s Disease in Hong Kong ↗

  Journal of Alzheimer s Disease · 2022 · PMID 35466936
  not yet assessed
• APOE E4 is associated with impaired self-declared cognition but not disease risk or age of onset in Nigerians with Parkinson’s disease ↗

  npj Parkinson s Disease · 2022 · PMID 36371506
  not yet assessed
• The PSEN1 E280G mutation leads to increased amyloid-β43 production in induced pluripotent stem cell neurons and deposition in brain tissue ↗

  Brain Communications · 2022 · PMID 36687397
  not yet assessed
• Human myeloid progenitor glucocorticoid receptor activation causes genomic instability, type 1 IFN ‐ response pathway activation and senescence in differentiated microglia; an early life stress model ↗

  Glia · 2022 · PMID 36571248
  not yet assessed
• PhenoExam: gene set analyses through integration of different phenotype databases ↗

  BMC Bioinformatics · 2022 · PMID 36587217
  not yet assessed
• Profiling the NOTCH2NLC GGC Repeat Expansion in Parkinson's Disease in the European Population ↗

  Movement Disorders · 2022 · PMID 35866887
  not yet assessed
• Seventy-Two-Hour LRRK2 Kinase Activity Inhibition Increases Lysosomal GBA Expression in H4, a Human Neuroglioma Cell Line ↗

  International Journal of Molecular Sciences · 2022 · PMID 35805938
  not yet assessed
• The Amyloid-β Pathway in Alzheimer’s Disease ↗

  Molecular Psychiatry · 2021 · PMID 34456336
  not yet assessed
• Mapping the human genetic architecture of COVID-19 ↗

  Nature · 2021 · PMID 34237774
  not yet assessed
• Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology ↗

  Nature Genetics · 2021 · PMID 34873335
  not yet assessed
• Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture ↗

  Nature Genetics · 2021 · PMID 33589841
  not yet assessed
• Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome ↗

  Nature Communications · 2021 · PMID 34930919
  not yet assessed
• Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets ↗

  JAMA Neurology · 2021 · PMID 33523105
  not yet assessed
• Large‐scale plasma proteomic profiling identifies a high‐performance biomarker panel for Alzheimer's disease screening and staging ↗

  Alzheimer s & Dementia · 2021 · PMID 34032364
  not yet assessed
• AD-linked R47H- TREM2 mutation induces disease-enhancing microglial states via AKT hyperactivation ↗

  Science Translational Medicine · 2021 · PMID 34851693
  not yet assessed
• Familial Alzheimer’s Disease Mutations in PSEN1 Lead to Premature Human Stem Cell Neurogenesis ↗

  Cell Reports · 2021 · PMID 33440141
  not yet assessed
• A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene ↗

  Brain · 2021 · PMID 34619763
  not yet assessed
• Measuring heritable contributions to Alzheimer’s disease: polygenic risk score analysis with twins ↗

  Brain Communications · 2021 · PMID 35169705
  not yet assessed
• SORL1 deficiency in human excitatory neurons causes APP-dependent defects in the endolysosome-autophagy network ↗

  Cell Reports · 2021 · PMID 34133918
  not yet assessed
• Identification of sixteen novel candidate genes for late onset Parkinson’s disease ↗

  Molecular Neurodegeneration · 2021 · PMID 34148545
  not yet assessed
• Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis ↗

  JAMA Neurology · 2021 · PMID 34459874
  not yet assessed
• Knock-in models related to Alzheimer’s disease: synaptic transmission, plaques and the role of microglia ↗

  Molecular Neurodegeneration · 2021 · PMID 34266459
  not yet assessed
• Cross-platform transcriptional profiling identifies common and distinct molecular pathologies in Lewy body diseases ↗

  Acta Neuropathologica · 2021 · PMID 34309761
  not yet assessed
• MIR-NATs repress MAPT translation and aid proteostasis in neurodegeneration ↗

  Nature · 2021 · PMID 34012113
  not yet assessed
• Heritability Enrichment Implicates Microglia in Parkinson's Disease Pathogenesis ↗

  Annals of Neurology · 2021 · PMID 33502028
  not yet assessed
• Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups ↗

  Brain · 2021 · PMID 35381062
  not yet assessed
• Aducanumab: a new phase in therapeutic development for Alzheimer’s disease? ↗

  EMBO Molecular Medicine · 2021 · PMID 34338436
  not yet assessed
• Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease ↗

  Annals of Neurology · 2021 · PMID 33901317
  not yet assessed
• Dissecting the Phenotype and Genotype of PLA2G6 ‐Related Parkinsonism ↗

  Movement Disorders · 2021 · PMID 34622992
  not yet assessed
• Microglial signalling pathway deficits associated with the patient derived R47H TREM2 variants linked to AD indicate inability to activate inflammasome ↗

  Scientific Reports · 2021 · PMID 34172778
  not yet assessed
• The influence of the R47H triggering receptor expressed on myeloid cells 2 variant on microglial exosome profiles ↗

  Brain Communications · 2021 · PMID 34704019
  not yet assessed
• RFC1 -related ataxia is a mimic of early multiple system atrophy ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2021 · PMID 33563805
  not yet assessed
• CoExp: A Web Tool for the Exploitation of Co-expression Networks ↗

  Frontiers in Genetics · 2021 · PMID 33719340
  not yet assessed
• Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity ↗

  Human Genetics · 2021 · PMID 34889978
  not yet assessed
• Polygenic risk scores for Alzheimer's disease are related to dementia risk in APOE ɛ4 negatives ↗

  Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · 2021 · PMID 33532541
  not yet assessed
• White matter abnormalities in active elite adult rugby players ↗

  Brain Communications · 2021 · PMID 34435188
  not yet assessed
• The association of circulating amylin with β‐amyloid in familial Alzheimer's disease ↗

  Alzheimer s & Dementia Translational Research & Clinical Interventions · 2021 · PMID 33521236
  not yet assessed
• Polygenic Risk Scoring is an Effective Approach to Predict Those Individuals Most Likely to Decline Cognitively Due to Alzheimer's Disease ↗

  The Journal of Prevention of Alzheimer s Disease · 2021 · PMID 33336228
  not yet assessed
• Genetic dissection of down syndrome-associated alterations in APP/amyloid-β biology using mouse models ↗

  Scientific Reports · 2021 · PMID 33707583
  not yet assessed
• Abrogation of LRRK2 dependent Rab10 phosphorylation with TLR4 activation and alterations in evoked cytokine release in immune cells ↗

  Neurochemistry International · 2021 · PMID 34004238
  not yet assessed
• Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage ↗

  Nature Communications · 2021 · PMID 33824317
  not yet assessed
• TREM2-mediated activation of microglia breaks link between amyloid and tau ↗

  The Lancet Neurology · 2021 · PMID 34022161
  not yet assessed
• Spastic paraplegia preceding PSEN1 ‐related familial Alzheimer's disease ↗

  Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · 2021 · PMID 33969176
  not yet assessed
• Differential Stimulation of Pluripotent Stem Cell-Derived Human Microglia Leads to Exosomal Proteomic Changes Affecting Neurons ↗

  Cells · 2021 · PMID 34831089
  not yet assessed
• Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes ↗

  Biological Psychiatry · 2021 · PMID 33637304
  not yet assessed
• Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer’s disease ↗

  Scientific Reports · 2021 · PMID 34615922
  not yet assessed
• SORL1 mutation in a Greek family with Parkinson's disease and dementia ↗

  Annals of Clinical and Translational Neurology · 2021 · PMID 34506082
  not yet assessed
• AmbiDots: An Ambient Interface to Mediate Casual Social Settings through Peripheral Interaction ↗

  2021
  not yet assessed
• A glimpse of the genetics of young‐onset Parkinson’s disease in Central Asia ↗

  Molecular Genetics & Genomic Medicine · 2021 · PMID 33818904
  not yet assessed
• TREM2 variants as a possible cause of frontotemporal dementia with distinct neuroimaging features ↗

  European Journal of Neurology · 2021 · PMID 33969597
  not yet assessed
• An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of α-synuclein ↗

  Cell Reports · 2021 · PMID 34107263
  not yet assessed
• The East Asian Parkinson Disease Genomics Consortium ↗

  The Lancet Neurology · 2021 · PMID 34800411
  not yet assessed
• Integrating protein networks and machine learning for disease stratification in the Hereditary Spastic Paraplegias ↗

  iScience · 2021 · PMID 34113825
  not yet assessed
• A high‐performance biomarker panel for Alzheimer’s disease screening and staging identified by large‐scale plasma proteomic profiling ↗

  Alzheimer s & Dementia · 2021
  not yet assessed
• The Amyloid-beta Pathway in Alzheimer's Disease

  UCL Discovery (University College London) · 2021
  not yet assessed
• Abelacimab. Anti-factor XI/XIa monoclonal antibody, Treatment of atrial fibrillation, Treatment of thrombotic disorders ↗

  Drugs of the Future · 2021
  not yet assessed
• Modeling multifunctionality of genes with secondary gene co-expression networks in human brain provides novel disease insights ↗

  Bioinformatics · 2021 · PMID 33734320
  not yet assessed
• Blood transcriptome analysis for Alzheimer' disease in Hong Kong Chinese population

  Rare & Special e-Zone (The Hong Kong University of Science and Technology) · 2021
  not yet assessed
• Exome sequencing identifies rare damaging variants in the ATB8B4 and ABCA1 genes as novel risk factors for Alzheimer's disease ↗

  EUR Research Repository (Erasmus University Rotterdam) · 2021
  not yet assessed
• The β-Secretase BACE1 in Alzheimer’s Disease ↗

  Biological Psychiatry · 2020 · PMID 32223911
  not yet assessed
• Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study ↗

  Nature Communications · 2020 · PMID 32015339
  not yet assessed
• Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel ↗

  JAMA Neurology · 2020 · PMID 33074286
  not yet assessed
• Trem2 promotes anti-inflammatory responses in microglia and is suppressed under pro-inflammatory conditions

  Human Molecular Genetics · 2020 · PMID 32959884
  L1 67/100
• Genome‐Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease ↗

  Movement Disorders · 2020 · PMID 33111402
  not yet assessed
• Parkinson’s disease determinants, prediction and gene–environment interactions in the UK Biobank ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2020 · PMID 32934108
  not yet assessed
• Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study ↗

  The Lancet Neurology · 2020 · PMID 33341150
  not yet assessed
• Incomplete annotation has a disproportionate impact on our understanding of Mendelian and complex neurogenetic disorders ↗

  Science Advances · 2020 · PMID 32917675
  not yet assessed
• Potential human transmission of amyloid β pathology: surveillance and risks ↗

  The Lancet Neurology · 2020 · PMID 32949547
  not yet assessed
• Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders ↗

  Brain · 2020 · PMID 32889528
  not yet assessed
• Neuronal intranuclear inclusion disease is genetically heterogeneous ↗

  Annals of Clinical and Translational Neurology · 2020 · PMID 32777174
  not yet assessed
• Plasma glial fibrillary acidic protein and neurofilament light chain, but not tau, are biomarkers of sports-related mild traumatic brain injury ↗

  Brain Communications · 2020 · PMID 33543129
  not yet assessed
• Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies ↗

  Acta Neuropathologica Communications · 2020 · PMID 31996268
  not yet assessed
• PINOT: an intuitive resource for integrating protein-protein interactions ↗

  Cell Communication and Signaling · 2020 · PMID 32527260
  not yet assessed
• Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information ↗

  Nature Communications · 2020 · PMID 32098967
  not yet assessed
• Annexin A5 prevents amyloid-β-induced toxicity in choroid plexus: implication for Alzheimer’s disease ↗

  Scientific Reports · 2020 · PMID 32523019
  not yet assessed
• A multi-level developmental approach to exploring individual differences in Down syndrome: genes, brain, behaviour, and environment ↗

  Research in Developmental Disabilities · 2020 · PMID 32653761
  not yet assessed
• Genetic and polygenic risk score analysis for Alzheimer's disease in the Chinese population ↗

  Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · 2020 · PMID 32775599
  not yet assessed
• Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease ↗

  Movement Disorders · 2020 · PMID 33107653
  not yet assessed
• Alzheimer‐like pathology in trisomy 21 cerebral organoids amenable to pharmacological inhibition reveals BACE2 as a gene‐dose‐sensitive AD‐suppressor in human brain ↗

  Alzheimer s & Dementia · 2020
  not yet assessed
• Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease ↗

  Neurobiology of Aging · 2020 · PMID 32873436
  not yet assessed
• Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates ↗

  Acta Neuropathologica · 2020 · PMID 31950334
  not yet assessed
• Genetic variants in glutamate-, Aβ−, and tau-related pathways determine polygenic risk for Alzheimer's disease ↗

  Neurobiology of Aging · 2020 · PMID 33303219
  not yet assessed
• Differential Associations of Apolipoprotein E ε4 Genotype With Attentional Abilities Across the Life Span of Individuals With Down Syndrome ↗

  JAMA Network Open · 2020 · PMID 32986108
  not yet assessed
• Exome sequencing identifies three novel AD‐associated genes ↗

  Alzheimer s & Dementia · 2020
  not yet assessed
• Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis ↗

  Scientific Reports · 2020 · PMID 32699404
  not yet assessed
• C9orf72 , age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts ↗

  Neurology · 2020 · PMID 32943482
  not yet assessed
• BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes ↗

  Neurobiology of Aging · 2020 · PMID 33189404
  not yet assessed
• Fibrillation and molecular characteristics are coherent with clinical and pathological features of 4-repeat tauopathy caused by MAPT variant G273R ↗

  Neurobiology of Disease · 2020 · PMID 32961270
  not yet assessed
• Deep geno- and phenotyping in two consanguineous families with CMT2 reveals HADHA as an unusual disease-causing gene and an intronic variant in GDAP1 as an unusual mutation ↗

  Journal of Neurology · 2020 · PMID 32897397
  not yet assessed
• Community‐based genetic study of Parkinson's disease in Estonia ↗

  Acta Neurologica Scandinavica · 2020 · PMID 32740907
  not yet assessed
• A novel Alzheimer disease locus located near the gene encoding tau protein ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2020
  not yet assessed
• Kohlschütter-Tönz Syndrome: Mutations in ROGDI and Evidence of Genetic Heterogeneity ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2020
  not yet assessed
• Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2020
  not yet assessed
• Premature neuronal differentiation in familial Alzheimer’s disease human stem cells in vitro and in postmortem brain tissue ↗

  Alzheimer s & Dementia · 2020
  not yet assessed
• Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing ↗

  Nature Genetics · 2019 · PMID 30820047
  not yet assessed
• Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies ↗

  The Lancet Neurology · 2019 · PMID 31701892
  not yet assessed
• Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk ↗

  Nature Genetics · 2019 · PMID 30617256
  not yet assessed
• Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms ↗

  Movement Disorders · 2019 · PMID 30957308
  not yet assessed
• Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia ↗

  Brain · 2019 · PMID 31755958
  not yet assessed
• Microtubules Deform the Nuclear Membrane and Disrupt Nucleocytoplasmic Transport in Tau-Mediated Frontotemporal Dementia ↗

  Cell Reports · 2019 · PMID 30650353
  not yet assessed
• Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset ↗

  npj Parkinson s Disease · 2019 · PMID 31123700
  not yet assessed
• Familial Alzheimer’s disease patient-derived neurons reveal distinct mutation-specific effects on amyloid beta ↗

  Molecular Psychiatry · 2019 · PMID 30980041
  not yet assessed
• A locked immunometabolic switch underlies TREM2 R47H loss of function in human iPSC‐derived microglia ↗

  The FASEB Journal · 2019 · PMID 31907987
  not yet assessed
• Non-coding variability at the APOE locus contributes to the Alzheimer’s risk ↗

  Nature Communications · 2019 · PMID 31346172
  not yet assessed
• Genetic risk for alzheimer disease is distinct from genetic risk for amyloid deposition ↗

  Annals of Neurology · 2019 · PMID 31199530
  not yet assessed
• Genetic variability in response to amyloid beta deposition influences Alzheimer’s disease risk ↗

  Brain Communications · 2019 · PMID 32274467
  not yet assessed
• Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability ↗

  npj Parkinson s Disease · 2019 · PMID 31016231
  not yet assessed
• Polygenic risk and hazard scores for Alzheimer's disease prediction ↗

  Annals of Clinical and Translational Neurology · 2019 · PMID 30911569
  not yet assessed
• Endo-lysosomal proteins and ubiquitin CSF concentrations in Alzheimer’s and Parkinson’s disease ↗

  Alzheimer s Research & Therapy · 2019 · PMID 31521194
  not yet assessed
• Alzheimer’s disease polygenic risk score as a predictor of conversion from mild-cognitive impairment ↗

  Translational Psychiatry · 2019 · PMID 31127079
  not yet assessed
• Plasma biomarkers for amyloid, tau, and cytokines in Down syndrome and sporadic Alzheimer’s disease ↗

  Alzheimer s Research & Therapy · 2019 · PMID 30902060
  not yet assessed
• Genetic analysis of Mendelian mutations in a large UK population-based Parkinson’s disease study ↗

  Brain · 2019 · PMID 31324919
  not yet assessed
• A comprehensive analysis of methods for assessing polygenic burden on Alzheimer’s disease pathology and risk beyond APOE ↗

  Brain Communications · 2019 · PMID 32226939
  not yet assessed
• The Parkinson's Disease Mendelian Randomization Research Portal ↗

  Movement Disorders · 2019 · PMID 31659794
  not yet assessed
• Polygenic Risk Score Analysis of Alzheimer's Disease in Cases without APOE4 or APOE2 Alleles ↗

  The Journal of Prevention of Alzheimer s Disease · 2019 · PMID 30569081
  not yet assessed
• De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes ↗

  European Journal of Human Genetics · 2019 · PMID 30886340
  not yet assessed
• Genetics and molecular mechanisms of frontotemporal lobar degeneration: an update and future avenues ↗

  Neurobiology of Aging · 2019 · PMID 30925302
  not yet assessed
• Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsy ↗

  Brain · 2019 · PMID 30932156
  not yet assessed
• Heritability and genetic variance of dementia with Lewy bodies ↗

  Neurobiology of Disease · 2019 · PMID 30953760
  not yet assessed
• L-dopa responsiveness in early Parkinson's disease is associated with the rate of motor progression ↗

  Parkinsonism & Related Disorders · 2019 · PMID 31105012
  not yet assessed
• Progress in the genetic analysis of Parkinson’s disease ↗

  Human Molecular Genetics · 2019 · PMID 31348493
  not yet assessed
• Progress in the genetic analysis of Parkinson’s disease ↗

  Human Molecular Genetics · 2019 · PMID 31518392
  not yet assessed
• An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids ↗

  Acta Neuropathologica Communications · 2019 · PMID 31775912
  not yet assessed
• Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer’s disease ↗

  PLoS ONE · 2019 · PMID 31283791
  not yet assessed
• Genes, pathways and risk prediction in Alzheimer’s disease ↗

  Human Molecular Genetics · 2019 · PMID 31332445
  not yet assessed
• Common BACE2 Polymorphisms are Associated with Altered Risk for Alzheimer’s Disease and CSF Amyloid Biomarkers in APOE ε4 Non-Carriers ↗

  Scientific Reports · 2019 · PMID 31270419
  not yet assessed
• Amyloid precursor protein processing in human neurons with an allelic series of the PSEN1 intron 4 deletion mutation and total presenilin-1 knockout ↗

  Brain Communications · 2019 · PMID 32395715
  not yet assessed
• Genetic analysis suggests high misassignment rates in clinical Alzheimer's cases and controls ↗

  Neurobiology of Aging · 2019 · PMID 30851568
  not yet assessed
• Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia ↗

  Scientific Reports · 2019 · PMID 31350420
  not yet assessed
• Do heterozygous mutations of Niemann–Pick type C predispose to late-onset neurodegeneration: a review of the literature ↗

  Journal of Neurology · 2019 · PMID 31701332
  not yet assessed
• Distinct proteomic profiles in monozygotic twins discordant for ischaemic stroke ↗

  Molecular and Cellular Biochemistry · 2019 · PMID 30694515
  not yet assessed
• Informing disease modelling with brain-relevant functional genomic annotations ↗

  Brain · 2019 · PMID 31603214
  not yet assessed
• Clinical Profile of Methotrexate-resistant Juvenile Localised Scleroderma ↗

  Acta Dermato Venereologica · 2019 · PMID 30810215
  not yet assessed
• Failures in Protein Clearance Partly Underlie Late Onset Neurodegenerative Diseases and Link Pathology to Genetic Risk ↗

  Frontiers in Neuroscience · 2019 · PMID 31866813
  not yet assessed
• Genome-wide Analyses Identify KIF5A as a Novel ALS Gene ↗

  Neuron · 2018 · PMID 29566793
  not yet assessed
• Selective vulnerability in neurodegenerative diseases ↗

  Nature Neuroscience · 2018 · PMID 30250262
  not yet assessed
• Functional Studies of Missense TREM2 Mutations in Human Stem Cell-Derived Microglia ↗

  Stem Cell Reports · 2018 · PMID 29606617
  not yet assessed
• Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies ↗

  PLoS Medicine · 2018 · PMID 29315334
  not yet assessed
• Association of Dementia With Mortality Among Adults With Down Syndrome Older Than 35 Years ↗

  JAMA Neurology · 2018 · PMID 30452522
  not yet assessed
• Human Induced Pluripotent Stem Cell-Derived Microglia-Like Cells Harboring TREM2 Missense Mutations Show Specific Deficits in Phagocytosis ↗

  Cell Reports · 2018 · PMID 30157425
  not yet assessed
• Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia ↗

  Nature Medicine · 2018 · PMID 30510257
  not yet assessed
• Features of GBA-associated Parkinson’s disease at presentation in the UK Tracking Parkinson’s study ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2018 · PMID 29378790
  not yet assessed
• Trisomy of human chromosome 21 enhances amyloid-β deposition independently of an extra copy of APP ↗

  Brain · 2018 · PMID 29945247
  not yet assessed
• Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study ↗

  The Lancet Neurology · 2018 · PMID 29724592
  not yet assessed
• The genetic landscape of Alzheimer disease ↗

  Handbook of clinical neurology · 2018 · PMID 29478590
  not yet assessed
• Alzheimer's disease in Down syndrome: An overlooked population for prevention trials ↗

  Alzheimer s & Dementia Translational Research & Clinical Interventions · 2018 · PMID 30581976
  not yet assessed
• Identification of genetic risk factors in the Chinese population implicates a role of immune system in Alzheimer’s disease pathogenesis ↗

  Proceedings of the National Academy of Sciences · 2018 · PMID 29432188
  not yet assessed
• Cognitive markers of preclinical and prodromal Alzheimer's disease in Down syndrome ↗

  Alzheimer s & Dementia · 2018 · PMID 30503169
  not yet assessed
• CXCR4 involvement in neurodegenerative diseases ↗

  Translational Psychiatry · 2018 · PMID 29636460
  not yet assessed
• Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum ↗

  JAMA Neurology · 2018 · PMID 29630712
  not yet assessed
• Aging related cognitive changes associated with Alzheimer's disease in Down syndrome ↗

  Annals of Clinical and Translational Neurology · 2018 · PMID 29928657
  not yet assessed
• A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease ↗

  Molecular Psychiatry · 2018 · PMID 29988083
  not yet assessed
• Neurofilament light as a blood biomarker for neurodegeneration in Down syndrome ↗

  Alzheimer s Research & Therapy · 2018 · PMID 29631614
  not yet assessed
• A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers ↗

  Brain · 2018 · PMID 30252044
  not yet assessed
• Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3 ↗

  Neurobiology of Aging · 2018 · PMID 29544907
  not yet assessed
• Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype ↗

  Annals of Neurology · 2018 · PMID 30066433
  not yet assessed
• The human brainome: network analysis identifies HSPA2 as a novel Alzheimer’s disease target ↗

  Brain · 2018 · PMID 30137212
  not yet assessed
• Stratification of candidate genes for Parkinson’s disease using weighted protein-protein interaction network analysis ↗

  BMC Genomics · 2018 · PMID 29898659
  not yet assessed
• Complexity of the Genetics and Clinical Presentation of Spinocerebellar Ataxia 17 ↗

  Frontiers in Cellular Neuroscience · 2018 · PMID 30532692
  not yet assessed
• A comprehensive screening of copy number variability in dementia with Lewy bodies ↗

  Neurobiology of Aging · 2018 · PMID 30448004
  not yet assessed
• LRP10 in α-synucleinopathies ↗

  The Lancet Neurology · 2018 · PMID 30507384
  not yet assessed
• LRP10 in α-synucleinopathies ↗

  The Lancet Neurology · 2018 · PMID 30507383
  not yet assessed
• An Aged Canid with Behavioral Deficits Exhibits Blood and Cerebrospinal Fluid Amyloid Beta Oligomers ↗

  Frontiers in Aging Neuroscience · 2018 · PMID 29441010
  not yet assessed
• Soluble Fibrinogen Triggers Non-cell Autonomous ER Stress-Mediated Microglial-Induced Neurotoxicity ↗

  Frontiers in Cellular Neuroscience · 2018 · PMID 30524237
  not yet assessed
• mTOR independent alteration in ULK1 Ser758 phosphorylation following chronic LRRK2 kinase inhibition ↗

  Bioscience Reports · 2018 · PMID 29563162
  not yet assessed
• Protein network analysis reveals selectively vulnerable regions and biological processes in FTD ↗

  Neurology Genetics · 2018 · PMID 30283816
  not yet assessed
• LRP10 in α-synucleinopathies ↗

  The Lancet Neurology · 2018 · PMID 30507385
  not yet assessed
• Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia ↗

  Journal of Alzheimer s Disease · 2018 · PMID 30475763
  not yet assessed
• Genetics of dementia in a Finnish cohort ↗

  European Journal of Human Genetics · 2018 · PMID 29476165
  not yet assessed
• Genotyping of the Alzheimer’s Disease Genome-Wide Association Study Index Single Nucleotide Polymorphisms in the Brains for Dementia Research Cohort ↗

  Journal of Alzheimer s Disease · 2018 · PMID 29914034
  not yet assessed
• Insights into the Influence of Specific Splicing Events on the Structural Organization of LRRK2 ↗

  International Journal of Molecular Sciences · 2018 · PMID 30223621
  not yet assessed
• Genetically elevated high‐density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease ↗

  Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · 2018 · PMID 30422133
  not yet assessed
• Loss of Function of TREM2 Results in Cytoskeletal Malfunction in Microglia ↗

  Journal of Neurology and Neurobiology · 2018
  not yet assessed
• Alzheimer's disease ↗

  European Journal of Neurology · 2017 · PMID 28872215
  not yet assessed
• Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease ↗

  Nature Genetics · 2017 · PMID 28714976
  not yet assessed
• APP mouse models for Alzheimer's disease preclinical studies ↗

  The EMBO Journal · 2017 · PMID 28768718
  not yet assessed
• Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease ↗

  Brain · 2017 · PMID 29140481
  not yet assessed
• Major Shifts in Glial Regional Identity Are a Transcriptional Hallmark of Human Brain Aging ↗

  Cell Reports · 2017 · PMID 28076797
  not yet assessed
• Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score ↗

  PLoS Medicine · 2017 · PMID 28323831
  not yet assessed
• Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases ↗

  JAMA Neurology · 2017 · PMID 28586827
  not yet assessed
• An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks ↗

  BMC Systems Biology · 2017 · PMID 28403906
  not yet assessed
• Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study ↗

  The Lancet Neurology · 2017 · PMID 29263008
  not yet assessed
• Mixed pathologies including chronic traumatic encephalopathy account for dementia in retired association football (soccer) players ↗

  Acta Neuropathologica · 2017 · PMID 28205009
  not yet assessed
• Hallmarks of Alzheimer’s Disease in Stem-Cell-Derived Human Neurons Transplanted into Mouse Brain ↗

  Neuron · 2017 · PMID 28238547
  not yet assessed
• Transethnic genome‐wide scan identifies novel Alzheimer's disease loci ↗

  Alzheimer s & Dementia · 2017 · PMID 28183528
  not yet assessed
• Polygenic risk score analysis of pathologically confirmed Alzheimer disease ↗

  Annals of Neurology · 2017 · PMID 28727176
  not yet assessed
• Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study ↗

  PLoS Medicine · 2017 · PMID 28609445
  not yet assessed
• NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases ↗

  Neurobiology of Aging · 2017 · PMID 28602509
  not yet assessed
• Genetic correlation between amyotrophic lateral sclerosis and schizophrenia ↗

  Nature Communications · 2017 · PMID 28322246
  not yet assessed
• The discovery of Alzheimer‐causing mutations in the APP gene and the formulation of the “amyloid cascade hypothesis” ↗

  FEBS Journal · 2017 · PMID 28054745
  not yet assessed
• Mitochondrial hyperpolarization in iPSC-derived neurons from patients of FTDP-17 with 10+16 MAPT mutation leads to oxidative stress and neurodegeneration ↗

  Redox Biology · 2017 · PMID 28319892
  not yet assessed
• Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia ↗

  Acta Neuropathologica · 2017 · PMID 28271184
  not yet assessed
• A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK ↗

  Brain · 2017 · PMID 28430856
  not yet assessed
• Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience ↗

  Genome Medicine · 2017 · PMID 29183403
  not yet assessed
• Pathogenic p62/SQSTM1 mutations impair energy metabolism through limitation of mitochondrial substrates ↗

  Scientific Reports · 2017 · PMID 28490746
  not yet assessed
• Peptidylarginine Deiminases—Roles in Cancer and Neurodegeneration and Possible Avenues for Therapeutic Intervention via Modulation of Exosome and Microvesicle (EMV) Release? ↗

  International Journal of Molecular Sciences · 2017 · PMID 28587234
  not yet assessed
• Study protocol: Insight 46 – a neuroscience sub-study of the MRC National Survey of Health and Development ↗

  BMC Neurology · 2017 · PMID 28420323
  not yet assessed
• PREDICT‐PD: An online approach to prospectively identify risk indicators of Parkinson's disease ↗

  Movement Disorders · 2017 · PMID 28090684
  not yet assessed
• Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson’s disease on chromosome 7p15.3 ↗

  Neurogenetics · 2017 · PMID 28391543
  not yet assessed
• Alzheimer’s disease: where next for anti-amyloid therapies? ↗

  Brain · 2017 · PMID 28375461
  not yet assessed
• Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia ↗

  Brain · 2017 · PMID 28387812
  not yet assessed
• GBA -Associated Parkinson’s Disease: Progression in a Deep Brain Stimulation Cohort ↗

  Journal of Parkinson s Disease · 2017 · PMID 28777757
  not yet assessed
• iPSC-derived neuronal models of PANK2-associated neurodegeneration reveal mitochondrial dysfunction contributing to early disease ↗

  PLoS ONE · 2017 · PMID 28863176
  not yet assessed
• Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease ↗

  Neurobiology of Aging · 2017 · PMID 29103623
  not yet assessed
• Whole‐exome sequencing of the BDR cohort: evidence to support the role of the PILRA gene in Alzheimer's disease ↗

  Neuropathology and Applied Neurobiology · 2017 · PMID 29181857
  not yet assessed
• Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS ↗

  Scientific Reports · 2017 · PMID 28827549
  not yet assessed
• Multi-infarct dementia of Swedish type is caused by a 3’UTR mutation of COL4A1 ↗

  Brain · 2017 · PMID 28369186
  not yet assessed
• Utility of the new Movement Disorder Society clinical diagnostic criteria for Parkinson's disease applied retrospectively in a large cohort study of recent onset cases ↗

  Parkinsonism & Related Disorders · 2017 · PMID 28431829
  not yet assessed
• A Clinicopathologic Entity

  2017
  not yet assessed
• Establishing the role of rare coding variants in known Parkinson's disease risk loci ↗

  Neurobiology of Aging · 2017 · PMID 28867149
  not yet assessed
• Membrane damage is at the core of Alzheimer's disease ↗

  The Lancet Neurology · 2017 · PMID 28414646
  not yet assessed
• Action Myoclonus and Seizure in Kufor‐Rakeb Syndrome ↗

  Movement Disorders Clinical Practice · 2017 · PMID 30868101
  not yet assessed
• Mutations in TYROBP are not a common cause of dementia in a Turkish cohort ↗

  Neurobiology of Aging · 2017 · PMID 28716534
  not yet assessed
• The Birth of the Modern Era of Parkinson's Disease Genetics

  UCL Discovery (University College London) · 2017
  not yet assessed
• Neurodegeneration: the first mechanistic therapy and other progress in 2017 ↗

  The Lancet Neurology · 2017 · PMID 29263004
  not yet assessed
• 10. Genetics of Alzheimer's disease ↗

  Princeton University Press eBooks · 2017
  not yet assessed
• Protein Deimination in Protein Misfolding Disorders: Modeled in Human Induced Pluripotent Stem Cells (iPSCs) ↗

  2017
  not yet assessed
• Antisense long non-coding RNA represses MAPT translation through an embedded MIR repeat

  UCL Discovery (University College London) · 2017
  not yet assessed
• [O2–03–02]: PROTEIN NETWORK ANALYSIS TO PRIORITIZE CANDIDATE GENES AND PATHWAYS FOR SPORADIC DISEASE: A COMPARISON BETWEEN FRONTOTEMPORAL DEMENTIA AND PARKINSON's DISEASE ↗

  Alzheimer s & Dementia · 2017
  not yet assessed
• The amyloid hypothesis of Alzheimer's disease at 25 years ↗

  EMBO Molecular Medicine · 2016 · PMID 27025652
  not yet assessed
• Genome, transcriptome and proteome: the rise of omics data and their integration in biomedical sciences ↗

  Briefings in Bioinformatics · 2016 · PMID 27881428
  not yet assessed
• Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis ↗

  Nature Genetics · 2016 · PMID 27455348
  not yet assessed
• Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy ↗

  The American Journal of Human Genetics · 2016 · PMID 26942284
  not yet assessed
• Increased cerebrospinal fluid soluble TREM2 concentration in Alzheimer’s disease ↗

  Molecular Neurodegeneration · 2016 · PMID 26754172
  not yet assessed
• Dementia in Down's syndrome ↗

  The Lancet Neurology · 2016 · PMID 27302127
  not yet assessed
• Novel genetic loci underlying human intracranial volume identified through genome-wide association ↗

  Nature Neuroscience · 2016 · PMID 27694991
  not yet assessed
• Assessment of the genetic variance of late-onset Alzheimer's disease ↗

  Neurobiology of Aging · 2016 · PMID 27036079
  not yet assessed
• Genetic and phenotypic characterization of complex hereditary spastic paraplegia ↗

  Brain · 2016 · PMID 27217339
  not yet assessed
• The importance of understanding individual differences in Down syndrome ↗

  F1000Research · 2016 · PMID 27019699
  not yet assessed
• Lithium Promotes Longevity through GSK3/NRF2-Dependent Hormesis ↗

  Cell Reports · 2016 · PMID 27068460
  not yet assessed
• Polygenic score prediction captures nearly all common genetic risk for Alzheimer's disease ↗

  Neurobiology of Aging · 2016 · PMID 27595457
  not yet assessed
• A genome-wide association study in multiple system atrophy ↗

  Neurology · 2016 · PMID 27629089
  not yet assessed
• ADrosophilaModel of Neuronopathic Gaucher Disease Demonstrates Lysosomal-Autophagic Defects and Altered mTOR Signalling and Is Functionally Rescued by Rapamycin ↗

  Journal of Neuroscience · 2016 · PMID 27852774
  not yet assessed
• Vascular disease and vascular risk factors in relation to motor features and cognition in early Parkinson's disease ↗

  Movement Disorders · 2016 · PMID 27324570
  not yet assessed
• Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology ↗

  Brain · 2016 · PMID 27797812
  not yet assessed
• Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease ↗

  Alzheimer s & Dementia · 2016 · PMID 26993346
  not yet assessed
• ATXN2 trinucleotide repeat length correlates with risk of ALS ↗

  Neurobiology of Aging · 2016 · PMID 28017481
  not yet assessed
• Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2016 · PMID 27899424
  not yet assessed
• De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions ↗

  The American Journal of Human Genetics · 2016 · PMID 27058447
  not yet assessed
• Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data ↗

  The Lancet Neurology · 2016 · PMID 27017469
  not yet assessed
• Genomics implicates adaptive and innate immunity in Alzheimer's and Parkinson's diseases ↗

  Annals of Clinical and Translational Neurology · 2016 · PMID 28097204
  not yet assessed
• The Evolution of Genetics: Alzheimer’s and Parkinson’s Diseases ↗

  Neuron · 2016 · PMID 27311081
  not yet assessed
• Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer’s Disease ↗

  PLoS ONE · 2016 · PMID 27249223
  not yet assessed
• mTOR independent regulation of macroautophagy by Leucine Rich Repeat Kinase 2 via Beclin-1 ↗

  Scientific Reports · 2016 · PMID 27731364
  not yet assessed
• Identification of Modifier Genes in a Mouse Model of Gaucher Disease ↗

  Cell Reports · 2016 · PMID 27568557
  not yet assessed
• Selective vulnerability in neurodegeneration: insights from clinical variants of Alzheimer's disease ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2016 · PMID 26746185
  not yet assessed
• Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies ↗

  Neurobiology of Disease · 2016 · PMID 27312774
  not yet assessed
• Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysis ↗

  Molecular Neurodegeneration · 2016 · PMID 26912063
  not yet assessed
• Additional rare variant analysis in Parkinson’s disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance ↗

  Human Molecular Genetics · 2016 · PMID 27798102
  not yet assessed
• Autonomic Dysfunction in Early Parkinson's Disease: Results from the United Kingdom Tracking Parkinson's Study ↗

  Movement Disorders Clinical Practice · 2016 · PMID 30363477
  not yet assessed
• ABCA7 p.G215S as potential protective factor for Alzheimer's disease ↗

  Neurobiology of Aging · 2016 · PMID 27289440
  not yet assessed
• Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array ↗

  Neurobiology of Aging · 2016 · PMID 27776828
  not yet assessed
• Intracerebral haemorrhage in Down syndrome: protected or predisposed? ↗

  F1000Research · 2016 · PMID 27239286
  not yet assessed
• Weighted Protein Interaction Network Analysis of Frontotemporal Dementia ↗

  Journal of Proteome Research · 2016 · PMID 28004582
  not yet assessed
• Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients ↗

  PLoS ONE · 2016 · PMID 27632209
  not yet assessed
• Pre- and postoperative complications of adult forearm fractures treated with plate fixation ↗

  Orthopaedics & Traumatology Surgery & Research · 2016 · PMID 27499115
  not yet assessed
• Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's disease ↗

  Neurobiology of Aging · 2016 · PMID 27640074
  not yet assessed
• 199 years of Parkinson disease – what have we learned and what is the path to the future? ↗

  Journal of Neurochemistry · 2016 · PMID 27581372
  not yet assessed
• Exome sequencing in a consanguineous family clinically diagnosed with early-onset Alzheimer's disease identifies a homozygous CTSF mutation ↗

  Neurobiology of Aging · 2016 · PMID 27524508
  not yet assessed
• Using the Gene Ontology to Annotate Key Players in Parkinson’s Disease ↗

  Neuroinformatics · 2016 · PMID 26825309
  not yet assessed
• Pseudohypoparathyroidism type I‐b with neurological involvement is associated with a homozygous PTH1R mutation ↗

  Genes Brain & Behavior · 2016 · PMID 27415614
  not yet assessed
• Perspective: Finding common ground ↗

  Nature · 2016 · PMID 27652785
  not yet assessed
• Catastrophic cliffs: a partial suggestion for selective vulnerability in neurodegenerative diseases ↗

  Biochemical Society Transactions · 2016 · PMID 27068985
  not yet assessed
• HLA-DRB*1501 associations with magnetic resonance imaging measures of grey matter pathology in multiple sclerosis ↗

  Multiple Sclerosis and Related Disorders · 2016 · PMID 27237756
  not yet assessed
• Review: Induced pluripotent stem cell models of frontotemporal dementia ↗

  Neuropathology and Applied Neurobiology · 2016 · PMID 27291591
  not yet assessed
• A blood-based gene expression and signaling pathway analysis to differentiate between high and low grade gliomas ↗

  Oncology Reports · 2016 · PMID 28004117
  not yet assessed
• Update on fluid biomarkers for concussion ↗

  Concussion · 2016 · PMID 30202555
  not yet assessed
• Pathways to Alzheimer's disease and other neurodegenerative diseases ↗

  Neurobiology of Aging · 2016
  not yet assessed
• Response to the commentary of Yates RL and DeLuca GC on the study: HLA-DRB1*1501 associations with magnetic resonance imaging measures of grey matter pathology in multiple sclerosis ↗

  Multiple Sclerosis and Related Disorders · 2016 · PMID 29409599
  not yet assessed
• Morphée pansclérotique d’évolution rapidement létale chez une jeune fille de 11ans ↗

  Annales de Dermatologie et de Vénéréologie · 2016 · PMID 27496274
  not yet assessed
• Complications pré- et postopératoires des fractures des deux os de l’avant-bras de l’adulte traitées par plaque ↗

  Revue de Chirurgie Orthopédique et Traumatologique · 2016
  not yet assessed
• P1‐003: Knockdown of Trem2 Expression in Microglia: Implications For Migration and Inflammation ↗

  Alzheimer s & Dementia · 2016
  not yet assessed
• Genetic influences on schizophrenia and subcortical brain volumes: Large-scale proof of concept ↗

  Maynooth University ePrints and eTheses Archive (Maynooth University) · 2016
  not yet assessed
• Common genetic variants influence human subcortical brain structures ↗

  Nature · 2015 · PMID 25607358
  not yet assessed
• The transcriptional landscape of age in human peripheral blood ↗

  Nature Communications · 2015 · PMID 26490707
  not yet assessed
• A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome ↗

  Nature reviews. Neuroscience · 2015 · PMID 26243569
  not yet assessed
• Common polygenic variation enhances risk prediction for Alzheimer’s disease ↗

  Brain · 2015 · PMID 26490334
  not yet assessed
• A Genome-wide Gene-Expression Analysis and Database in Transgenic Mice during Development of Amyloid or Tau Pathology ↗

  Cell Reports · 2015 · PMID 25620700
  not yet assessed
• A novel Alzheimer disease locus located near the gene encoding tau protein ↗

  Molecular Psychiatry · 2015 · PMID 25778476
  not yet assessed
• Microglial genes regulating neuroinflammation in the progression of Alzheimer's disease ↗

  Current Opinion in Neurobiology · 2015 · PMID 26517285
  not yet assessed
• C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis ↗

  The Lancet Neurology · 2015 · PMID 25638642
  not yet assessed
• Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study ↗

  The Lancet Neurology · 2015 · PMID 26271532
  not yet assessed
• Loss ofPLA2G6leads to elevated mitochondrial lipid peroxidation and mitochondrial dysfunction ↗

  Brain · 2015 · PMID 26001724
  not yet assessed
• Neurological consequences of traumatic brain injuries in sports ↗

  Molecular and Cellular Neuroscience · 2015 · PMID 25770439
  not yet assessed
• Neurobiology of Alzheimer’s Disease: Integrated Molecular, Physiological, Anatomical, Biomarker, and Cognitive Dimensions ↗

  Current Alzheimer Research · 2015 · PMID 26412218
  not yet assessed
• APP Metabolism Regulates Tau Proteostasis in Human Cerebral Cortex Neurons ↗

  Cell Reports · 2015 · PMID 25921538
  not yet assessed
• Recursive splicing in long vertebrate genes ↗

  Nature · 2015 · PMID 25970246
  not yet assessed
• Identification of novel CSF biomarkers for neurodegeneration and their validation by a high-throughput multiplexed targeted proteomic assay ↗

  Molecular Neurodegeneration · 2015 · PMID 26627638
  not yet assessed
• Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease ↗

  Circulation · 2015 · PMID 25862742
  not yet assessed
• Genetic overlap between Alzheimer’s disease and Parkinson’s disease at the MAPT locus ↗

  Molecular Psychiatry · 2015 · PMID 25687773
  not yet assessed
• Developmental regulation of tau splicing is disrupted in stem cell-derived neurons from frontotemporal dementia patients with the 10 + 16 splice-site mutation in MAPT ↗

  Human Molecular Genetics · 2015 · PMID 26136155
  not yet assessed
• A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia ↗

  The American Journal of Human Genetics · 2015 · PMID 25983243
  not yet assessed
• Polygenic risk of P arkinson disease is correlated with disease age at onset ↗

  Annals of Neurology · 2015 · PMID 25773351
  not yet assessed
• Mutations in PNKP Cause Recessive Ataxia with Oculomotor Apraxia Type 4 ↗

  The American Journal of Human Genetics · 2015 · PMID 25728773
  not yet assessed
• Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation ↗

  Molecular Neurodegeneration · 2015 · PMID 26306801
  not yet assessed
• Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke ↗

  Neurology · 2015 · PMID 26674333
  not yet assessed
• First effects of rising amyloid-β in transgenic mouse brain: synaptic transmission and gene expression ↗

  Brain · 2015 · PMID 25981962
  not yet assessed
• Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases ↗

  Neurobiology of Aging · 2015 · PMID 26643944
  not yet assessed
• Loss of GPR3 reduces the amyloid plaque burden and improves memory in Alzheimer’s disease mouse models ↗

  Science Translational Medicine · 2015 · PMID 26468326
  not yet assessed
• SnapShot: Genetics of Parkinson’s Disease ↗

  Cell · 2015 · PMID 25635463
  not yet assessed
• Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke ↗

  JAMA Neurology · 2015 · PMID 25961151
  not yet assessed
• Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease ↗

  Neurology Genetics · 2015 · PMID 27066548
  not yet assessed
• SnapShot: Genetics of ALS and FTD ↗

  Cell · 2015 · PMID 25679767
  not yet assessed
• Tracking Parkinson’s: Study Design and Baseline Patient Data ↗

  Journal of Parkinson s Disease · 2015 · PMID 26485428
  not yet assessed
• A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia ↗

  Neurobiology of Aging · 2015 · PMID 26154020
  not yet assessed
• StemBANCC: Governing Access to Material and Data in a Large Stem Cell Research Consortium ↗

  Stem Cell Reviews and Reports · 2015 · PMID 26024842
  not yet assessed
• CHCHD2 and Parkinson's disease ↗

  The Lancet Neurology · 2015 · PMID 26067110
  not yet assessed
• Global and local ancestry in African‐Americans: Implications for Alzheimer's disease risk ↗

  Alzheimer s & Dementia · 2015 · PMID 26092349
  not yet assessed
• Does the difference between PART and Alzheimer’s disease lie in the age-related changes in cerebral arteries that trigger the accumulation of Aβ and propagation of tau? ↗

  Acta Neuropathologica · 2015 · PMID 25814152
  not yet assessed
• Genome‐wide association study of neocortical Lewy‐related pathology ↗

  Annals of Clinical and Translational Neurology · 2015 · PMID 26401513
  not yet assessed
• Is the MC1R variant p.R160W associated with Parkinson's? ↗

  Annals of Neurology · 2015 · PMID 26389967
  not yet assessed
• TheCACNA1BR1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort ↗

  Human Molecular Genetics · 2015 · PMID 26157024
  not yet assessed
• Analysis of the genetic variability in Parkinson's disease from Southern Spain ↗

  Neurobiology of Aging · 2015 · PMID 26518746
  not yet assessed
• Gene co-expression networks shed light into diseases of brain iron accumulation ↗

  Neurobiology of Disease · 2015 · PMID 26707700
  not yet assessed
• DYT6 Dystonia: A Neuropathological Study ↗

  Neurodegenerative Diseases · 2015 · PMID 26610312
  not yet assessed
• Web‐based assessment of Parkinson's prodromal markers identifies GBA variants ↗

  Movement Disorders · 2015 · PMID 25970725
  not yet assessed
• Identical non-identical twins and non-identical identical twins ↗

  BMJ · 2015
  not yet assessed
• IsSIGMAR1a confirmed FTD/MND gene? ↗

  Brain · 2015 · PMID 26088964
  not yet assessed
• F2‐03‐04: Genetic risk factors for posterior cortical atrophy ↗

  Alzheimer s & Dementia · 2015
  not yet assessed
• Reducing β-Amyloid by Inhibition of BACE1: How Low Should You Go? ↗

  Biological Psychiatry · 2015 · PMID 25835287
  not yet assessed
• Elevated γ-Glutamyltransferase and Erythrocyte Sedimentation Rate in Ischemic Stroke in Discordant Monozygotic Twin Study ↗

  International Journal of Stroke · 2015 · PMID 25973705
  not yet assessed
• Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease ↗

  Nature Genetics · 2014 · PMID 25064009
  not yet assessed
• Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease ↗

  PLoS ONE · 2014 · PMID 24922517
  not yet assessed
• The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data ↗

  Brain Imaging and Behavior · 2014 · PMID 24399358
  not yet assessed
• TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis ↗

  Science Translational Medicine · 2014 · PMID 24990881
  not yet assessed
• Genetic variability in the regulation of gene expression in ten regions of the human brain ↗

  Nature Neuroscience · 2014 · PMID 25174004
  not yet assessed
• Time to redefine PD? Introductory statement of the MDS Task Force on the definition of Parkinson's disease ↗

  Movement Disorders · 2014 · PMID 24619848
  not yet assessed
• Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis ↗

  Nature Neuroscience · 2014 · PMID 24686783
  not yet assessed
• Frontotemporal dementia and its subtypes: a genome-wide association study ↗

  The Lancet Neurology · 2014 · PMID 24943344
  not yet assessed
• Apolipoprotein E in Alzheimer's Disease: An Update ↗

  Annual Review of Neuroscience · 2014 · PMID 24821312
  not yet assessed
• Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias ↗

  PLoS Genetics · 2014 · PMID 25188341
  not yet assessed
• Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease ↗

  Proceedings of the National Academy of Sciences · 2014 · PMID 24510904
  not yet assessed
• A critique of the drug discovery and phase 3 clinical programs targeting the amyloid hypothesis for Alzheimer disease ↗

  Annals of Neurology · 2014 · PMID 24853080
  not yet assessed
• Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies ↗

  Human Molecular Genetics · 2014 · PMID 24973356
  not yet assessed
• Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol ↗

  The American Journal of Human Genetics · 2014 · PMID 24507775
  not yet assessed
• Convergent genetic and expression data implicate immunity in Alzheimer's disease ↗

  Alzheimer s & Dementia · 2014 · PMID 25533204
  not yet assessed
• Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers ↗

  Brain · 2014 · PMID 24993959
  not yet assessed
• Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease ↗

  JAMA Neurology · 2014 · PMID 25199842
  not yet assessed
• Pathways to Alzheimer's disease ↗

  Journal of Internal Medicine · 2014 · PMID 24749173
  not yet assessed
• Genetics of Alzheimer's Disease ↗

  Neurotherapeutics · 2014 · PMID 25113539
  not yet assessed
• Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette’s Syndrome and OCD ↗

  American Journal of Psychiatry · 2014 · PMID 25158072
  not yet assessed
• Antiamyloid Therapy for Alzheimer's Disease — Are We on the Right Road? ↗

  New England Journal of Medicine · 2014 · PMID 24450897
  not yet assessed
• NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases ↗

  Neurobiology of Aging · 2014 · PMID 25444595
  not yet assessed
• Review: Prion‐like mechanisms of transactive response DNA binding protein of 43 kDa ( TDP ‐43) in amyotrophic lateral sclerosis ( ALS ) ↗

  Neuropathology and Applied Neurobiology · 2014 · PMID 25487060
  not yet assessed
• A 6.4 Mb Duplication of the α-Synuclein Locus Causing Frontotemporal Dementia and Parkinsonism ↗

  JAMA Neurology · 2014 · PMID 25003242
  not yet assessed
• Investigating the role of rare coding variability in Mendelian dementia genes ( APP , PSEN1 , PSEN2 , GRN , MAPT , and PRNP ) in late-onset Alzheimer's disease ↗

  Neurobiology of Aging · 2014 · PMID 25104557
  not yet assessed
• Insights From Cerebellar Transcriptomic Analysis Into the Pathogenesis of Ataxia ↗

  JAMA Neurology · 2014 · PMID 24862029
  not yet assessed
• H‐ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations? ↗

  Movement Disorders · 2014 · PMID 25545912
  not yet assessed
• Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations ↗

  Human Molecular Genetics · 2014 · PMID 24794858
  not yet assessed
• Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome ↗

  Neurobiology of Aging · 2014 · PMID 24462566
  not yet assessed
• Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy ↗

  Neurobiology of Aging · 2014 · PMID 24503276
  not yet assessed
• Novel CLN3 mutation causing autophagic vacuolar myopathy ↗

  Neurology · 2014 · PMID 24827497
  not yet assessed
• Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosis ↗

  Neurobiology of Aging · 2014 · PMID 25588603
  not yet assessed
• Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease ↗

  Neurobiology of Aging · 2014 · PMID 24880964
  not yet assessed
• A nonsense mutation in PRNP associated with clinical Alzheimer's disease ↗

  Neurobiology of Aging · 2014 · PMID 24958194
  not yet assessed
• Orchestrated increase of dopamine and PARK mRNAs but not miR-133b in dopamine neurons in Parkinson's disease ↗

  Neurobiology of Aging · 2014 · PMID 24742361
  not yet assessed
• Concomitant progressive supranuclear palsy and chronic traumatic encephalopathy in a boxer ↗

  Acta Neuropathologica Communications · 2014 · PMID 24559032
  not yet assessed
• Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusions ↗

  Acta Neuropathologica Communications · 2014 · PMID 25403864
  not yet assessed
• Scaffolding student engagement via online peer learning ↗

  European Journal of Physics · 2014
  not yet assessed
• A Phenotype of Atypical Apraxia of Speech in a Family Carrying SQSTM1 Mutation ↗

  Journal of Alzheimer s Disease · 2014 · PMID 25114083
  not yet assessed
• Atypical Parkinsonism‐Dystonia Syndrome Caused by a Novel DJ 1 Mutation ↗

  Movement Disorders Clinical Practice · 2014 · PMID 30363821
  not yet assessed
• Prurit brachioradial révélant un astrocytome médullaire cervical et traité par patchs de capsaïcine à 8 % ↗

  Annales de Dermatologie et de Vénéréologie · 2014 · PMID 24835651
  not yet assessed
• GNALMutations and Dystonia ↗

  JAMA Neurology · 2014 · PMID 25111208
  not yet assessed
• Stem cell reprogramming: Basic implications and future perspective for movement disorders ↗

  Movement Disorders · 2014 · PMID 25546831
  not yet assessed
• Novel single base-pair deletion in exon 1 of XK gene leading to McLeod syndrome with chorea, muscle wasting, peripheral neuropathy, acanthocytosis and haemolysis ↗

  Journal of the Neurological Sciences · 2014 · PMID 24529944
  not yet assessed
• Genetic Variants and Related Biomarkers in Sporadic Alzheimer’s Disease ↗

  Current Genetic Medicine Reports · 2014 · PMID 25664224
  not yet assessed
• White matter involvement may explain phenotypic pleiotropy amongst genes involved in episodic movement disorders

  UCL Discovery (University College London) · 2014
  not yet assessed
• Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease ↗

  Nature Genetics · 2013 · PMID 24162737
  not yet assessed
• Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease ↗

  Nature · 2013 · PMID 24336208
  not yet assessed
• α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson’s disease and multiple system atrophy? ↗

  Acta Neuropathologica · 2013 · PMID 23404372
  not yet assessed
• A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies ↗

  JAMA Neurology · 2013 · PMID 23588557
  not yet assessed
• Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement ↗

  JAMA Neurology · 2013 · PMID 23318515
  not yet assessed
• Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population ↗

  The American Journal of Human Genetics · 2013 · PMID 23434116
  not yet assessed
• The Parkinson's disease–linked proteins Fbxo7 and Parkin interact to mediate mitophagy ↗

  Nature Neuroscience · 2013 · PMID 23933751
  not yet assessed
• Widespread sex differences in gene expression and splicing in the adult human brain ↗

  Nature Communications · 2013 · PMID 24264146
  not yet assessed
• Molecular nexopathies: a new paradigm of neurodegenerative disease ↗

  Trends in Neurosciences · 2013 · PMID 23876425
  not yet assessed
• Beta-propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation ↗

  Brain · 2013 · PMID 23687123
  not yet assessed
• Insights into TREM2 biology by network analysis of human brain gene expression data ↗

  Neurobiology of Aging · 2013 · PMID 23855984
  not yet assessed
• Apolipoprotein E genotype, cardiovascular biomarkers and risk of stroke: Systematic review and meta-analysis of 14 015 stroke cases and pooled analysis of primary biomarker data from up to 60 883 individuals ↗

  International Journal of Epidemiology · 2013 · PMID 23569189
  not yet assessed
• Parkin Disease ↗

  JAMA Neurology · 2013 · PMID 23459986
  not yet assessed
• Pathogenic VCP Mutations Induce Mitochondrial Uncoupling and Reduced ATP Levels ↗

  Neuron · 2013 · PMID 23498975
  not yet assessed
• Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease ↗

  Neurology · 2013 · PMID 23645593
  not yet assessed
• Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA) ↗

  Current Neuropharmacology · 2013 · PMID 23814539
  not yet assessed
• Missense variant in TREML2 protects against Alzheimer's disease ↗

  Neurobiology of Aging · 2013 · PMID 24439484
  not yet assessed
• SnapShot: Genetics of Alzheimer’s Disease ↗

  Cell · 2013 · PMID 24209629
  not yet assessed
• Parkinson's Disease – the Debate on the Clinical Phenomenology, Aetiology, Pathology and Pathogenesis ↗

  Journal of Parkinson s Disease · 2013 · PMID 23938306
  not yet assessed
• Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies ↗

  Nucleic Acids Research · 2013 · PMID 23435227
  not yet assessed
• PREDICT-PD: Identifying risk of Parkinson's disease in the community: methods and baseline results ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2013 · PMID 23828833
  not yet assessed
• Blockage of CR1 prevents activation of rodent microglia ↗

  Neurobiology of Disease · 2013 · PMID 23454195
  not yet assessed
• Genotype and phenotype in Parkinson's disease: Lessons in heterogeneity from deep brain stimulation ↗

  Movement Disorders · 2013 · PMID 23818421
  not yet assessed
• Genetic Analysis of Inherited Leukodystrophies ↗

  JAMA Neurology · 2013 · PMID 23649896
  not yet assessed
• Pathogenic Parkinson’s disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvation ↗

  Biochemical and Biophysical Research Communications · 2013 · PMID 24211199
  not yet assessed
• Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not ↗

  Experimental Neurology · 2013 · PMID 24246281
  not yet assessed
• Genetic comorbidities in Parkinson's disease ↗

  Human Molecular Genetics · 2013 · PMID 24057672
  not yet assessed
• TDP-43 pathology in a patient carrying G2019S LRRK2 mutation and a novel p.Q124E MAPT ↗

  Neurobiology of Aging · 2013 · PMID 23664753
  not yet assessed
• Validation of next-generation sequencing technologies in genetic diagnosis of dementia ↗

  Neurobiology of Aging · 2013 · PMID 23998997
  not yet assessed
• Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel ↗

  Movement Disorders · 2013 · PMID 24227479
  not yet assessed
• Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosis ↗

  Multiple Sclerosis and Related Disorders · 2013 · PMID 25568836
  not yet assessed
• Fine-Mapping, Gene Expression and Splicing Analysis of the Disease Associated LRRK2 Locus ↗

  PLoS ONE · 2013 · PMID 23967090
  not yet assessed
• Initial Assessment of the Pathogenic Mechanisms of the Recently Identified Alzheimer Risk Loci ↗

  Annals of Human Genetics · 2013 · PMID 23360175
  not yet assessed
• α-Synuclein mutations cluster around a putative protein loop ↗

  Neuroscience Letters · 2013 · PMID 23669636
  not yet assessed
• Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2013 · PMID 24198383
  not yet assessed
• Genetic Influences on Atrophy Patterns in Familial Alzheimer's Disease: A Comparison of APP and PSEN1 Mutations ↗

  Journal of Alzheimer s Disease · 2013 · PMID 23380992
  not yet assessed
• The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2013 · PMID 23408064
  not yet assessed
• Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA) ↗

  Current Neuropharmacology · 2013
  not yet assessed
• Amyloid or tau: the chicken or the egg? ↗

  Acta Neuropathologica · 2013 · PMID 23925566
  not yet assessed
• Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease ↗

  Human Molecular Genetics · 2013
  not yet assessed
• Parkin disease and the Lewy body conundrum ↗

  Movement Disorders · 2013 · PMID 23653422
  not yet assessed
• CSF biomarkers for Alzheimer’s pathology and the effect size of APOE ɛ4 ↗

  Molecular Psychiatry · 2013 · PMID 23419830
  not yet assessed
• The pallidopyramidal syndromes ↗

  Current Opinion in Neurology · 2013 · PMID 23817214
  not yet assessed
• A novel A781V mutation in the CSF1R gene causes hereditary diffuse leucoencephalopathy with axonal spheroids ↗

  Journal of the Neurological Sciences · 2013 · PMID 23816250
  not yet assessed
• Assessment of Parkinson's disease risk loci in Greece ↗

  Neurobiology of Aging · 2013 · PMID 24080174
  not yet assessed
• RANTing about C9orf72 ↗

  Neuron · 2013 · PMID 23439112
  not yet assessed
• Profilin1 E117G is a moderate risk factor for amyotrophic lateral sclerosis ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2013 · PMID 24309268
  not yet assessed
• Ubi Displays: A Toolkit for the Rapid Creation of Interactive Projected Displays

  Lancaster EPrints (Lancaster University) · 2013
  not yet assessed
• A familial frontotemporal dementia associated with C9orf72 repeat expansion and dysplastic gangliocytoma ↗

  Neurobiology of Aging · 2013 · PMID 24080172
  not yet assessed
• Homozygosity analysis in amyotrophic lateral sclerosis ↗

  European Journal of Human Genetics · 2013 · PMID 23612577
  not yet assessed
• Genetic Analysis in Neurology ↗

  JAMA Neurology · 2013 · PMID 23571731
  not yet assessed
• Structural Study of the Microtubule-associated Protein Tau Locus of Alzheimer′s disease in Taiwan ↗

  Biomedical Journal · 2013 · PMID 24923570
  not yet assessed
• Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to l-DOPA treatment ↗

  Journal of Neurology · 2013 · PMID 23881105
  not yet assessed
• A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease ↗

  Human Molecular Genetics · 2013
  not yet assessed
• Putting less emphasis on classifying mental disorders and more on collaborative working ↗

  BMJ · 2013 · PMID 24108157
  not yet assessed
• Psychiatric Genetics ↗

  JAMA Psychiatry · 2013 · PMID 23571455
  not yet assessed
• The ignoble art ↗

  The New Scientist · 2013
  not yet assessed
• P1–061: CSF biomarkers for Alzheimer's pathology and the effect size of APOE‐ε4 ↗

  Alzheimer s & Dementia · 2013
  not yet assessed
• Synucleinopathy with a G51D a-synuclein mutation: a neuropathological and genetic study

  UCL Discovery (University College London) · 2013
  not yet assessed
• TREM2 Variants in Alzheimer's Disease ↗

  New England Journal of Medicine · 2012 · PMID 23150934
  not yet assessed
• Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study ↗

  The Lancet Neurology · 2012 · PMID 22406228
  not yet assessed
• The Neuropathology and Neurobiology of Traumatic Brain Injury ↗

  Neuron · 2012 · PMID 23217738
  not yet assessed
• Identification of common variants associated with human hippocampal and intracranial volumes ↗

  Nature Genetics · 2012 · PMID 22504417
  not yet assessed
• Glucocerebrosidase deficiency in substantia nigra of parkinson disease brains ↗

  Annals of Neurology · 2012 · PMID 23034917
  not yet assessed
• Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database ↗

  PLoS Genetics · 2012 · PMID 22438815
  not yet assessed
• Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features ↗

  Brain · 2012 · PMID 22366791
  not yet assessed
• Genome-wide association study of obsessive-compulsive disorder ↗

  Molecular Psychiatry · 2012 · PMID 22889921
  not yet assessed
• Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA ↗

  The American Journal of Human Genetics · 2012 · PMID 23176820
  not yet assessed
• Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72 ↗

  Brain · 2012 · PMID 22366792
  not yet assessed
• MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies ↗

  Human Molecular Genetics · 2012 · PMID 22723018
  not yet assessed
• Genome-wide association study of Tourette's syndrome ↗

  Molecular Psychiatry · 2012 · PMID 22889924
  not yet assessed
• Glucocerebrosidase inhibition causes mitochondrial dysfunction and free radical damage ↗

  Neurochemistry International · 2012 · PMID 23099359
  not yet assessed
• Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease ↗

  Human Molecular Genetics · 2012 · PMID 22892372
  not yet assessed
• Mutations in the autoregulatory domain of β‐tubulin 4a cause hereditary dystonia ↗

  Annals of Neurology · 2012 · PMID 23424103
  not yet assessed
• Repeat Expansion inC9ORF72in Alzheimer's Disease ↗

  New England Journal of Medicine · 2012 · PMID 22216764
  not yet assessed
• G2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarization ↗

  Human Molecular Genetics · 2012 · PMID 22736029
  not yet assessed
• The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease ↗

  Movement Disorders · 2012 · PMID 23225227
  not yet assessed
• Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain ↗

  Neurobiology of Disease · 2012 · PMID 22433082
  not yet assessed
• A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease ↗

  Human Molecular Genetics · 2012 · PMID 23223016
  not yet assessed
• Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research ↗

  PLoS ONE · 2012 · PMID 22952635
  not yet assessed
• Use of next-generation sequencing and other whole-genome strategies to dissect neurological disease ↗

  Nature reviews. Neuroscience · 2012 · PMID 22714018
  not yet assessed
• Hyposmia and cognitive impairment in Gaucher disease patients and carriers ↗

  Movement Disorders · 2012 · PMID 22344629
  not yet assessed
• A coding variant in CR1 interacts with APOE-ɛ4 to influence cognitive decline ↗

  Human Molecular Genetics · 2012 · PMID 22343410
  not yet assessed
• The Spread of Neurodegenerative Disease ↗

  New England Journal of Medicine · 2012 · PMID 22646635
  not yet assessed
• Analysis of Copy Number Variation in Alzheimer’s Disease in a Cohort of Clinically Characterized and Neuropathologically Verified Individuals ↗

  PLoS ONE · 2012 · PMID 23227193
  not yet assessed
• The MAPT p.A152T variant is a risk factor associated with tauopathies with atypical clinical and neuropathological features ↗

  Neurobiology of Aging · 2012 · PMID 22595371
  not yet assessed
• Screening for C9ORF72 repeat expansion in FTLD ↗

  Neurobiology of Aging · 2012 · PMID 22459598
  not yet assessed
• TREM2 Variants in Alz hei mer's Disease

  UCL Discovery (University College London) · 2012
  not yet assessed
• Microglia, Alzheimer's Disease, and Complement ↗

  International Journal of Alzheimer s Disease · 2012 · PMID 22957298
  not yet assessed
• Age-associated changes in gene expression in human brain and isolated neurons ↗

  Neurobiology of Aging · 2012 · PMID 23177596
  not yet assessed
• THAP1 mutations and dystonia phenotypes: Genotype phenotype correlations ↗

  Movement Disorders · 2012 · PMID 22903657
  not yet assessed
• Disintegrating Brain Networks: from Syndromes to Molecular Nexopathies ↗

  Neuron · 2012 · PMID 22445334
  not yet assessed
• The Role of Variation at AβPP, PSEN1, PSEN2, and MAPT in Late Onset Alzheimer's Disease ↗

  Journal of Alzheimer s Disease · 2012 · PMID 22027014
  not yet assessed
• Use of support vector machines for disease risk prediction in genome-wide association studies: Concerns and opportunities ↗

  Human Mutation · 2012 · PMID 22777693
  not yet assessed
• Pantothenate kinase‐associated neurodegeneration is not a synucleinopathy ↗

  Neuropathology and Applied Neurobiology · 2012 · PMID 22416811
  not yet assessed
• Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency ↗

  Neurology · 2012 · PMID 22815559
  not yet assessed
• No consistent evidence for association between mtDNA variants and Alzheimer disease ↗

  Neurology · 2012 · PMID 22442439
  not yet assessed
• Investigating the utility of human embryonic stem cell‐derived neurons to model ageing and neurodegenerative disease using whole‐genome gene expression and splicing analysis ↗

  Journal of Neurochemistry · 2012 · PMID 22681703
  not yet assessed
• Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases ↗

  Neurology · 2012 · PMID 22675081
  not yet assessed
• Ageing Increases Vulnerability to Aβ42 Toxicity in Drosophila ↗

  PLoS ONE · 2012 · PMID 22808195
  not yet assessed
• Study of the genetic variability in a Parkinson's Disease gene: EIF4G1 ↗

  Neuroscience Letters · 2012 · PMID 22561553
  not yet assessed
• Review: Genetics and neuropathology of primary pure dystonia ↗

  Neuropathology and Applied Neurobiology · 2012 · PMID 22897341
  not yet assessed
• Tau acts as an independent genetic risk factor in pathologically proven PD ↗

  Neurobiology of Aging · 2012 · PMID 22221882
  not yet assessed
• TOMM40 Association With Alzheimer Disease ↗

  Archives of Neurology · 2012 · PMID 22869030
  not yet assessed
• Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort ↗

  Neurobiology of Aging · 2012 · PMID 22221884
  not yet assessed
• Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion ↗

  Neurobiology of Aging · 2012 · PMID 22483864
  not yet assessed
• Genome Wide Assessment of Young Onset Parkinson’s Disease from Finland ↗

  PLoS ONE · 2012 · PMID 22911860
  not yet assessed
• Kohlschütter-Tönz Syndrome: Mutations inROGDIand Evidence of Genetic Heterogeneity ↗

  Human Mutation · 2012 · PMID 23086778
  not yet assessed
• Young‐onset parkinsonism due to homozygous duplication of α‐synuclein in a consanguineous family ↗

  Movement Disorders · 2012 · PMID 23283657
  not yet assessed
• Cooperative Genome-Wide Analysis Shows Increased Homozygosity in Early Onset Parkinson's Disease ↗

  PLoS ONE · 2012 · PMID 22427796
  not yet assessed
• Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease ↗

  Movement Disorders · 2012 · PMID 22488887
  not yet assessed
• Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohorts ↗

  Neuroscience Letters · 2012 · PMID 22743658
  not yet assessed
• Alzheimer's disease and related dementias ↗

  Neurogenetics · 2012
  not yet assessed
• Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement ↗

  JAMA Neurology · 2012
  not yet assessed
• Characterisation and Validation of Insertions and Deletions in 173 Patient Exomes ↗

  PLoS ONE · 2012 · PMID 23251486
  not yet assessed
• Identification of Stk25 as a Genetic Modifier of Tau Phosphorylation in Dab1-Mutant Mice ↗

  PLoS ONE · 2012 · PMID 22355340
  not yet assessed
• The genetic architecture of Alzheimer's disease: beyond APP, PSENs and APOE.

  UCL Discovery (University College London) · 2012
  not yet assessed
• THAP1 mutations in a Greek primary blepharospasm series ↗

  Parkinsonism & Related Disorders · 2012 · PMID 23036512
  not yet assessed
• Genetic analysis of inherited leukodystrophies: genotype phenotype correlations in the CSF1R gene

  UCL Discovery (University College London) · 2012
  not yet assessed
• Behavioral Variant Frontotemporal Lobar Degeneration with Amyotrophic Lateral Sclerosis with a Chromosome 9p21 Hexanucleotide Repeat ↗

  Frontiers in Neurology · 2012 · PMID 23060854
  not yet assessed
• Using genome-Wwide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

  Faculty of Health; Institute of Health and Biomedical Innovation · 2012
  not yet assessed
• Novel pathogenic mutations in the glucocerebrosidase locus ↗

  Molecular Genetics and Metabolism · 2012 · PMID 22658918
  not yet assessed
• Interesting clinical features associated with mutations in the SLC20A2 gene

  UCL Discovery (University College London) · 2012
  not yet assessed
• IC‐O2‐03: The neuroimaging phenotype of frontotemporal dementia with the C9ORF72 hexanucletoide repeat expansion ↗

  Alzheimer s & Dementia · 2012
  not yet assessed
• Is anything lying behind parkin heterozygous mutations?

  UCL Discovery (University College London) · 2012
  not yet assessed
• A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD ↗

  Neuron · 2011 · PMID 21944779
  not yet assessed
• Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease ↗

  Nature Genetics · 2011 · PMID 21460840
  not yet assessed
• Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease ↗

  Nature Genetics · 2011 · PMID 21460841
  not yet assessed
• Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy ↗

  Nature Genetics · 2011 · PMID 21685912
  not yet assessed
• Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus ↗

  Nature Communications · 2011 · PMID 21863007
  not yet assessed
• Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration ↗

  Brain · 2011 · PMID 21908872
  not yet assessed
• Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: a meta-analysis of genetic studies and randomised trials ↗

  The Lancet · 2011 · PMID 21803414
  not yet assessed
• Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies ↗

  Journal of Neurochemistry · 2011 · PMID 21848658
  not yet assessed
• Parkinson's disease and α‐synuclein expression ↗

  Movement Disorders · 2011 · PMID 21887711
  not yet assessed
• Syndromes of neurodegeneration with brain iron accumulation (NBIA): An update on clinical presentations, histological and genetic underpinnings, and treatment considerations ↗

  Movement Disorders · 2011 · PMID 22031173
  not yet assessed
• Milestones in PD genetics ↗

  Movement Disorders · 2011 · PMID 21626549
  not yet assessed
• Glucocerebrosidase mutations confer a greater risk of dementia during Parkinson's disease course ↗

  Movement Disorders · 2011 · PMID 22173904
  not yet assessed
• Twenty years of Alzheimer’s disease‐causing mutations ↗

  Journal of Neurochemistry · 2011 · PMID 22122678
  not yet assessed
• Complement receptor 1 (CR1) and Alzheimer's disease ↗

  Immunobiology · 2011 · PMID 21840620
  not yet assessed
• The chromosome 9 ALS and FTD locus is probably derived from a single founder ↗

  Neurobiology of Aging · 2011 · PMID 21925771
  not yet assessed
• Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis ↗

  Neurobiology of Aging · 2011 · PMID 21257233
  not yet assessed
• A generalizable hypothesis for the genetic architecture of disease: pleomorphic risk loci ↗

  Human Molecular Genetics · 2011 · PMID 21875901
  not yet assessed
• FUS and TDP43 genetic variability in FTD and CBS ↗

  Neurobiology of Aging · 2011 · PMID 21943958
  not yet assessed
• SCA15 Due to Large ITPR1 Deletions in a Cohort of 333 White Families With Dominant Ataxia ↗

  Archives of Neurology · 2011 · PMID 21555639
  not yet assessed
• Glucocerebrosidase mutations do not cause increased Lewy body pathology in Parkinson's disease ↗

  Molecular Genetics and Metabolism · 2011 · PMID 21621439
  not yet assessed
• Alzheimer's disease genetics: lessons to improve disease modelling ↗

  Biochemical Society Transactions · 2011 · PMID 21787322
  not yet assessed
• Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α‐synuclein triplication (Iowa kindred) ↗

  Movement Disorders · 2011 · PMID 21656851
  not yet assessed
• Siblings With Ischemic Stroke Study ↗

  Stroke · 2011 · PMID 21940970
  not yet assessed
• Pathogenic LRRK2 Mutations Do Not Alter Gene Expression in Cell Model Systems or Human Brain Tissue ↗

  PLoS ONE · 2011 · PMID 21799870
  not yet assessed
• Frontotemporal Dementia: From Mendelian Genetics Towards Genome Wide Association Studies ↗

  Journal of Molecular Neuroscience · 2011 · PMID 21898125
  not yet assessed
• Epigenetic mechanisms in Alzheimer's disease: progress but much to do ↗

  Neurobiology of Aging · 2011 · PMID 21669333
  not yet assessed
• Genomic Risk Profiling of Ischemic Stroke: Results of an International Genome-Wide Association Meta-Analysis ↗

  PLoS ONE · 2011 · PMID 21957438
  not yet assessed
• No evidence that extended tracts of homozygosity are associated with Alzheimer's disease ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2011 · PMID 21812096
  not yet assessed
• APOE and AβPP Gene Variation in Cortical and Cerebrovascular Amyloid-β Pathology and Alzheimer's Disease: A Population-Based Analysis ↗

  Journal of Alzheimer s Disease · 2011 · PMID 21654062
  not yet assessed
• Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies ↗

  Journal of Neurochemistry · 2011
  not yet assessed
• Parkinson's Disease and alpha-Synuclein Expression

  UCL Discovery (University College London) · 2011
  not yet assessed
• Genes and Environment in Psychiatry ↗

  Archives of General Psychiatry · 2011 · PMID 21536973
  not yet assessed
• A new way APP mismetabolism can lead to Alzheimer's disease ↗

  EMBO Molecular Medicine · 2011 · PMID 21523909
  not yet assessed
• Clusterin as an Alzheimer Biomarker ↗

  Archives of Neurology · 2011 · PMID 22084130
  not yet assessed
• Glycoprotein IIb/IIIa inhibitor associated severe thrombocytopenia in patients with coronary artery disease: Clinical course and outcomes ↗

  Platelets · 2011 · PMID 21913813
  not yet assessed
• O3‐01‐04: A candidate causal variant in the CR1 locus ↗

  Alzheimer s & Dementia · 2011
  not yet assessed
• The Genetics of Alzheimer's Disease and Other Tauopathies

  UCL Discovery (University College London) · 2011
  not yet assessed
• Digitally annexing desk space for software development.

  International Conference on Software Engineering · 2011
  not yet assessed
• Read all about it: Why we have an appetite for gossip ↗

  The New Scientist · 2011
  not yet assessed
• Biomarkers for Alzheimer's disease: academic, industry and regulatory perspectives ↗

  Nature Reviews Drug Discovery · 2010 · PMID 20592748
  not yet assessed
• Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions ↗

  Nature Genetics · 2010 · PMID 20154673
  not yet assessed
• Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease ↗

  PLoS ONE · 2010 · PMID 21085570
  not yet assessed
• The genetic architecture of Alzheimer's disease: beyond APP, PSENs and APOE ↗

  Neurobiology of Aging · 2010 · PMID 20594621
  not yet assessed
• Genetic Analysis of Pathways to Parkinson Disease ↗

  Neuron · 2010 · PMID 20955928
  not yet assessed
• Early‐onset L‐dopa‐responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations ↗

  Movement Disorders · 2010 · PMID 20669327
  not yet assessed
• Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals ↗

  Human Molecular Genetics · 2010 · PMID 20534741
  not yet assessed
• Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA) ↗

  Annals of Neurology · 2010 · PMID 20853438
  not yet assessed
• Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study ↗

  The Lancet Neurology · 2010 · PMID 20801717
  not yet assessed
• Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21 ↗

  Human Molecular Genetics · 2010 · PMID 21044948
  not yet assessed
• Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations ↗

  Neurobiology of Aging · 2010 · PMID 20619503
  not yet assessed
• ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation ↗

  Movement Disorders · 2010 · PMID 20310007
  not yet assessed
• Inhibition of GSK-3 Ameliorates Aβ Pathology in an Adult-Onset Drosophila Model of Alzheimer's Disease ↗

  PLoS Genetics · 2010 · PMID 20824130
  not yet assessed
• Cancer and Neurodegeneration: Between the Devil and the Deep Blue Sea ↗

  PLoS Genetics · 2010 · PMID 21203498
  not yet assessed
• CR1 is associated with amyloid plaque burden and age‐related cognitive decline ↗

  Annals of Neurology · 2010 · PMID 21391232
  not yet assessed
• Reelin and Stk25 Have Opposing Roles in Neuronal Polarization and Dendritic Golgi Deployment ↗

  Cell · 2010 · PMID 21111240
  not yet assessed
• Comparing Spatial Maps of Human Population-Genetic Variation Using Procrustes Analysis ↗

  Statistical Applications in Genetics and Molecular Biology · 2010 · PMID 20196748
  not yet assessed
• THAP1 mutations (DYT6) are an additional cause of early-onset dystonia ↗

  Neurology · 2010 · PMID 20211909
  not yet assessed
• Genetic variability at the PARK16 locus ↗

  European Journal of Human Genetics · 2010 · PMID 20683486
  not yet assessed
• Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series ↗

  Neurobiology of Aging · 2010 · PMID 21193246
  not yet assessed
• Towards a complete resolution of the genetic architecture of disease ↗

  Trends in Genetics · 2010 · PMID 20813421
  not yet assessed
• Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signaling ↗

  Trends in Neurosciences · 2010 · PMID 20226542
  not yet assessed
• Mendelian disorders and multifactorial traits: the big divide or one for all? ↗

  Nature Reviews Genetics · 2010 · PMID 20395971
  not yet assessed
• Advances and perspectives from genetic research: development of biological markers in Alzheimer’s disease ↗

  Expert Review of Molecular Diagnostics · 2010 · PMID 20629514
  not yet assessed
• Genetic Variability in CLU and Its Association with Alzheimer's Disease ↗

  PLoS ONE · 2010 · PMID 20209083
  not yet assessed
• Indian‐subcontinent NBIA: Unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms ↗

  Movement Disorders · 2010 · PMID 20629144
  not yet assessed
• Progranulin (GRN)in two siblings of a Latino family and in other patients with Schizophrenia ↗

  Neurocase · 2010 · PMID 20087814
  not yet assessed
• Familial early onset frontotemporal dementia caused by a novel S356T MAPT mutation, initially diagnosed as schizophrenia ↗

  Clinical Neurology and Neurosurgery · 2010 · PMID 20708332
  not yet assessed
• Disentangling the Role of the Tau Gene Locus in Sporadic Tauopathies ↗

  Current Alzheimer Research · 2010 · PMID 20704554
  not yet assessed
• Novel Missense Mutation in Charged Multivesicular Body Protein 2B in a Patient With Frontotemporal Dementia ↗

  Alzheimer Disease & Associated Disorders · 2010 · PMID 20592581
  not yet assessed
• Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series ↗

  Movement Disorders · 2010 · PMID 20437544
  not yet assessed
• Dissecting the familial risk of multiple sclerosis ↗

  Annals of Neurology · 2010 · PMID 21280071
  not yet assessed
• O2‐07‐05: Genetic evidence implicates the immune system and cholesterol metabolism in the etiology of Alzheimer's disease ↗

  Alzheimer s & Dementia · 2010
  not yet assessed
• Whole genome association analysis shows that ACE is a risk factor for Alzheimer's disease and fails to replicate most candidates from Meta-analysis. ↗

  PubMed · 2010 · PMID 21537449
  not yet assessed
• Low prevalence of PANK2 mutations in Brazilian patients with early onset generalised dystonia and basal ganglia abnormalities on MRI ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2010 · PMID 20551478
  not yet assessed
• Identification of Alzheimer Risk Factors Through Whole-Genome Analysis ↗

  Archives of Neurology · 2010 · PMID 20558384
  not yet assessed
• Functional Characterization of Three Single-Nucleotide Polymorphisms Present in the Human APOε Promoter Sequence: Differential Effects in Neuronal Cells and on DNA–Protein Interactions

  UCL Discovery (University College London) · 2010
  not yet assessed
• Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease ↗

  Nature Genetics · 2009 · PMID 19734902
  not yet assessed
• Genome-wide association study reveals genetic risk underlying Parkinson's disease ↗

  Nature Genetics · 2009 · PMID 19915575
  not yet assessed
• Parkinson's disease ↗

  The Lancet · 2009 · PMID 19524782
  not yet assessed
• Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria ↗

  The Lancet Neurology · 2009 · PMID 19909913
  not yet assessed
• The amyloid hypothesis for Alzheimer’s disease: a critical reappraisal ↗

  Journal of Neurochemistry · 2009 · PMID 19457065
  not yet assessed
• Genomewide Association Studies and Human Disease ↗

  New England Journal of Medicine · 2009 · PMID 19369657
  not yet assessed
• Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease ↗

  Brain · 2009 · PMID 19286695
  not yet assessed
• The heritability and genetics of frontotemporal lobar degeneration ↗

  Neurology · 2009 · PMID 19884572
  not yet assessed
• Genetic Control of Human Brain Transcript Expression in Alzheimer Disease ↗

  The American Journal of Human Genetics · 2009 · PMID 19361613
  not yet assessed
• SNCA variants are associated with increased risk for multiple system atrophy ↗

  Annals of Neurology · 2009 · PMID 19475667
  not yet assessed
• Genotype-Imputation Accuracy across Worldwide Human Populations ↗

  The American Journal of Human Genetics · 2009 · PMID 19215730
  not yet assessed
• A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease ↗

  The American Journal of Human Genetics · 2009 · PMID 19375058
  not yet assessed
• The genetics of Parkinson's syndromes: a critical review ↗

  Current Opinion in Genetics & Development · 2009 · PMID 19419854
  not yet assessed
• GLUT1 gene mutations cause sporadic paroxysmal exercise‐induced dyskinesias ↗

  Movement Disorders · 2009 · PMID 19630075
  not yet assessed
• A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis ↗

  Human Molecular Genetics · 2009 · PMID 19193627
  not yet assessed
• Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer’s disease ↗

  Neurogenetics · 2009 · PMID 19271249
  not yet assessed
• Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece ↗

  Neuroscience Letters · 2009 · PMID 19383421
  not yet assessed
• Measures of Autozygosity in Decline: Globalization, Urbanization, and Its Implications for Medical Genetics ↗

  PLoS Genetics · 2009 · PMID 19282984
  not yet assessed
• Complicated recessive dystonia parkinsonism syndromes ↗

  Movement Disorders · 2009 · PMID 19185014
  not yet assessed
• Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: Phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations ↗

  Movement Disorders · 2009 · PMID 19205068
  not yet assessed
• GLUCOCEREBROSIDASE MUTATIONS IN 108 NEUROPATHOLOGICALLY CONFIRMED CASES OF MULTIPLE SYSTEM ATROPHY ↗

  Neurology · 2009 · PMID 19332698
  not yet assessed
• The genetics of ischaemic stroke ↗

  Journal of Internal Medicine · 2009 · PMID 20175863
  not yet assessed
• Differential DJ-1 gene expression in Parkinson's disease ↗

  Neurobiology of Disease · 2009 · PMID 19716892
  not yet assessed
• Candidate Gene Polymorphisms for Ischemic Stroke ↗

  Stroke · 2009 · PMID 19729601
  not yet assessed
• Iron accumulation in syndromes of neurodegeneration with brain iron accumulation 1 and 2: causative or consequential? ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2009 · PMID 19147629
  not yet assessed
• Functional characterization of three single‐nucleotide polymorphisms present in the human APOE promoter sequence: Differential effects in neuronal cells and on DNA–protein interactions ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2009 · PMID 19504470
  not yet assessed
• Peritoneal Inclusion Cysts in Adolescent Females: A Clinicopathological Characterization of Four Cases ↗

  Journal of Pediatric and Adolescent Gynecology · 2009 · PMID 19232301
  not yet assessed
• A thorough assessment of benign genetic variability inGRNandMAPT ↗

  Human Mutation · 2009 · PMID 20020531
  not yet assessed
• Whole genome expression as a quantitative trait ↗

  Biochemical Society Transactions · 2009 · PMID 19909261
  not yet assessed
• Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs ↗

  BMC Medical Genetics · 2009 · PMID 19951422
  not yet assessed
• Genotypic analysis of gene expression in the dissection of the aetiology of complex neurological and psychiatric diseases ↗

  Briefings in Functional Genomics and Proteomics · 2009 · PMID 19734301
  not yet assessed
• CURRENT CONCEPTS Genomewide Association Studies and Human Disease

  UCL Discovery (University College London) · 2009
  not yet assessed
• A simple and efficient algorithm for genome‐wide homozygosity analysis in disease ↗

  Molecular Systems Biology · 2009 · PMID 19756043
  not yet assessed
• Genotype, haplotype and copy-number variation in worldwide human populations ↗

  Nature · 2008 · PMID 18288195
  not yet assessed
• Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation in alpha2‐macroglobulin and tau : A population‐based autopsy study ↗

  Annals of Medicine · 2008 · PMID 18382889
  not yet assessed
• Characterization of PLA2G6 as a locus for dystonia‐parkinsonism ↗

  Annals of Neurology · 2008 · PMID 18570303
  not yet assessed
• Evolutionary toggling of the MAPT 17q21.31 inversion region ↗

  Nature Genetics · 2008 · PMID 19165922
  not yet assessed
• DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA ↗

  The Lancet Neurology · 2008 · PMID 18243799
  not yet assessed
• Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP ↗

  Neurobiology of Aging · 2008 · PMID 18667258
  not yet assessed
• Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease ↗

  FEBS Journal · 2008 · PMID 19021754
  not yet assessed
• Whole Genome Analyses Suggest Ischemic Stroke and Heart Disease Share an Association With Polymorphisms on Chromosome 9p21 ↗

  Stroke · 2008 · PMID 18340101
  not yet assessed
• Genetic neuropathology of Parkinson's disease. ↗

  PubMed · 2008 · PMID 18784814
  not yet assessed
• Analysis of Nigerians with Apparently Sporadic Parkinson Disease for Mutations in LRRK2, PRKN and ATXN3 ↗

  PLoS ONE · 2008 · PMID 18927607
  not yet assessed
• TDP-43 Is Not a Common Cause of Sporadic Amyotrophic Lateral Sclerosis ↗

  PLoS ONE · 2008 · PMID 18545701
  not yet assessed
• Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2 ↗

  BMC Neurology · 2008 · PMID 18211709
  not yet assessed
• Parietal Lobe Deficits in Frontotemporal Lobar Degeneration Caused by a Mutation in the Progranulin Gene ↗

  Archives of Neurology · 2008 · PMID 18413474
  not yet assessed
• Structural genomic variation in ischemic stroke ↗

  Neurogenetics · 2008 · PMID 18288507
  not yet assessed
• Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases ↗

  Movement Disorders · 2008 · PMID 18464284
  not yet assessed
• Whole genome analysis in a consanguineous family with early onset Alzheimer's disease ↗

  Neurobiology of Aging · 2008 · PMID 18387709
  not yet assessed
• Gaucher and Parkinson diseases ↗

  Neurology · 2008 · PMID 18541881
  not yet assessed
• Neurofibrillary tau pathology modulated by genetic variation of α‐synuclein ↗

  Annals of Neurology · 2008 · PMID 18661559
  not yet assessed
• PINK1 in mitochondrial function ↗

  Proceedings of the National Academy of Sciences · 2008 · PMID 18687903
  not yet assessed
• Parkin‐related disease clinically diagnosed as a pallido‐pyramidal syndrome ↗

  Movement Disorders · 2008 · PMID 18942080
  not yet assessed
• The α2 chain of type 1 collagen does not map to mouse chromosome 16 but maps close to the Met proto-oncogene on mouse chromosome 6 ↗

  Cytogenetics and Cell Genetics · 2008 · PMID 2776477
  not yet assessed
• Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type? ↗

  American Journal of Medical Genetics Part A · 2008 · PMID 18680190
  not yet assessed
• The HapMap ↗

  Archives of Neurology · 2008 · PMID 18332243
  not yet assessed
• Race, genetics, and medicine at a crossroads ↗

  The Lancet · 2008
  not yet assessed
• P3‐213: Genetic screening in a large cohort of early‐onset Alzheimer's disease patients from Spain: Novel mutations in the amyloid precursor protein and presenilines ↗

  Alzheimer s & Dementia · 2008
  not yet assessed
• The relationship between nosology, etiology and pathogenesis in neurodegenerative diseases ↗

  Handbook of clinical neurology · 2008 · PMID 18631743
  not yet assessed
• P3‐279: A novel progranulin mutation in a large frontotemporal dementia calabrian kindred ↗

  Alzheimer s & Dementia · 2008
  not yet assessed
• A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder ↗

  Molecular Psychiatry · 2007 · PMID 17486107
  not yet assessed
• A High-Density Whole-Genome Association Study Reveals That APOE Is the Major Susceptibility Gene for Sporadic Late-Onset Alzheimer's Disease ↗

  The Journal of Clinical Psychiatry · 2007 · PMID 17474819
  not yet assessed
• DLB and PDD boundary issues ↗

  Neurology · 2007 · PMID 17353469
  not yet assessed
• A survey of genetic human cortical gene expression ↗

  Nature Genetics · 2007 · PMID 17982457
  not yet assessed
• GAB2 Alleles Modify Alzheimer's Risk in APOE ɛ4 Carriers ↗

  Neuron · 2007 · PMID 17553421
  not yet assessed
• Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans ↗

  PLoS Genetics · 2007 · PMID 17590087
  not yet assessed
• Common genetic variation within the Low-Density Lipoprotein Receptor-Related Protein 6 and late-onset Alzheimer's disease ↗

  Proceedings of the National Academy of Sciences · 2007 · PMID 17517621
  not yet assessed
• Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data ↗

  The Lancet Neurology · 2007 · PMID 17362836
  not yet assessed
• A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release ↗

  The Lancet Neurology · 2007 · PMID 17434096
  not yet assessed
• The Etiopathogenesis of Parkinson Disease and Suggestions for Future Research. Part I ↗

  Journal of Neuropathology & Experimental Neurology · 2007 · PMID 17413315
  not yet assessed
• Correlations Between Apolipoprotein E ε4 Gene Dose and Whole Brain Atrophy Rates ↗

  American Journal of Psychiatry · 2007 · PMID 17541051
  not yet assessed
• Sorl1 as an Alzheimer’s Disease Predisposition Gene? ↗

  Neurodegenerative Diseases · 2007 · PMID 17975299
  not yet assessed
• Clinical and pathological features of an Alzheimer's disease patient with the MAPT ΔK280 mutation ↗

  Neurobiology of Aging · 2007 · PMID 17723255
  not yet assessed
• Genomewide SNP assay reveals mutations underlying Parkinson disease ↗

  Human Mutation · 2007 · PMID 17994548
  not yet assessed
• A presenilin 1 mutation (L420R) in a family with early onset Alzheimer disease, seizures and cotton wool plaques, but not spastic paraparesis ↗

  Neuropathology · 2007 · PMID 17645236
  not yet assessed
• Heterogeneity within a large kindred with frontotemporal dementia ↗

  Neurology · 2007 · PMID 17620546
  not yet assessed
• Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease ↗

  Human Molecular Genetics · 2007 · PMID 17725986
  not yet assessed
• Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2007 · PMID 17492769
  not yet assessed
• The Etiopathogenesis of Parkinson Disease and Suggestions for Future Research. Part II ↗

  Journal of Neuropathology & Experimental Neurology · 2007
  not yet assessed
• IL1RN VNTR Polymorphism in Ischemic Stroke ↗

  Stroke · 2007 · PMID 17332449
  not yet assessed
• ABCA1 polymorphisms and Alzheimer's disease ↗

  Neuroscience Letters · 2007 · PMID 17324514
  not yet assessed
• Association of Integrin α2 Gene Variants with Ischemic Stroke ↗

  Journal of Cerebral Blood Flow & Metabolism · 2007 · PMID 17534386
  not yet assessed
• Psychiatric Disorder Criteria and their Application to Research in Different Racial Groups ↗

  BMC Psychiatry · 2007 · PMID 17214899
  not yet assessed
• What Is a Schizophrenic Mouse? ↗

  Neuron · 2007 · PMID 17481386
  not yet assessed
• Testing for Linkage and Association Across the Dihydrolipoyl Dehydrogenase Gene Region with Alzheimer’s Disease in Three Sample Populations ↗

  Neurochemical Research · 2007 · PMID 17342416
  not yet assessed
• Lack of aggregation of ischemic stroke subtypes within affected sibling pairs ↗

  Neurology · 2007 · PMID 17283317
  not yet assessed
• Amyotrophic Lateral Sclerosis: An Emerging Era of Collaborative Gene Discovery ↗

  PLoS ONE · 2007 · PMID 18060051
  not yet assessed
• Neurocirculatory and nigrostriatal abnormalities in Parkinson disease from LRRK2 mutation ↗

  Neurology · 2007 · PMID 17625107
  not yet assessed
• Association of phosphodiesterase 4D gene G0 haplotype and ischaemic stroke in a Greek population ↗

  European Journal of Neurology · 2007 · PMID 17594329
  not yet assessed
• Novel GCH1 mutation in a Brazilian family with dopa‐responsive dystonia ↗

  Movement Disorders · 2007 · PMID 18044725
  not yet assessed
• Whole genome association studies: Deciding when persistence becomes perseveration ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2007 · PMID 17541974
  not yet assessed
• Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13? ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2007 · PMID 18161859
  not yet assessed
• Putting presenilins centre stage ↗

  EMBO Reports · 2007 · PMID 17268503
  not yet assessed
• A Hundred Years of Alzheimer's Disease Research ↗

  Neuron · 2006 · PMID 17015223
  not yet assessed
• Alzheimer's disease: The amyloid cascade hypothesis: An update and reappraisal ↗

  Journal of Alzheimer s Disease · 2006 · PMID 16914853
  not yet assessed
• Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data ↗

  The Lancet Neurology · 2006 · PMID 17052657
  not yet assessed
• Genetics of Parkinson's disease and parkinsonism ↗

  Annals of Neurology · 2006 · PMID 17068789
  not yet assessed
• The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts ↗

  Neurobiology of Disease · 2006 · PMID 17174556
  not yet assessed
• Has the Amyloid Cascade Hypothesis for Alzheimers Disease been Proved? ↗

  Current Alzheimer Research · 2006 · PMID 16472206
  not yet assessed
• Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals ↗

  Human Molecular Genetics · 2006 · PMID 17116639
  not yet assessed
• Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome ↗

  Brain · 2006 · PMID 17030534
  not yet assessed
• Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2006 · PMID 17371905
  not yet assessed
• DAPK1 variants are associated with Alzheimer's disease and allele-specific expression ↗

  Human Molecular Genetics · 2006 · PMID 16847012
  not yet assessed
• Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort ↗

  BMC Neurology · 2006 · PMID 16824219
  not yet assessed
• A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan ↗

  BMC Neurology · 2006 · PMID 17187665
  not yet assessed
• The genetics of neurodegenerative diseases ↗

  Journal of Neurochemistry · 2006 · PMID 16805777
  not yet assessed
• Analysis of IFT74as a candidate gene for chromosome 9p-linked ALS-FTD ↗

  BMC Neurology · 2006 · PMID 17166276
  not yet assessed
• Characteristics of frontotemporal dementia patients with a Progranulin mutation ↗

  Annals of Neurology · 2006 · PMID 16983677
  not yet assessed
• Genetic Variability in CHMP2B and Frontotemporal Dementia ↗

  Neurodegenerative Diseases · 2006 · PMID 16954699
  not yet assessed
• A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia ↗

  Neurobiology of Disease · 2006 · PMID 16503405
  not yet assessed
• Amyloid at the blood vessel wall ↗

  Nature Medicine · 2006 · PMID 16829930
  not yet assessed
• Amyloid double trouble ↗

  Nature Genetics · 2006 · PMID 16380721
  not yet assessed
• Does Aβ 42 Have a Function Related to Blood Homeostasis? ↗

  Neurochemical Research · 2006 · PMID 17186373
  not yet assessed
• Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia ↗

  Journal of Medical Genetics · 2006 · PMID 16763011
  not yet assessed
• Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease ↗

  Movement Disorders · 2006 · PMID 16511860
  not yet assessed
• Association of Tau Haplotype-Tagging Polymorphisms with Parkinson’s Disease in Diverse Ethnic Parkinson’s Disease Cohorts ↗

  Neurodegenerative Diseases · 2006 · PMID 17192721
  not yet assessed
• Association of the Tau haplotype with Parkinson's disease in the Greek population ↗

  Movement Disorders · 2006 · PMID 16552760
  not yet assessed
• Conflicting Results Regarding the Semaphorin Gene (SEMA5A) and the Risk for Parkinson Disease ↗

  The American Journal of Human Genetics · 2006 · PMID 16685660
  not yet assessed
• Insulin-Degrading Enzyme Haplotypes Affect Insulin Levels but Not Dementia Risk ↗

  Neurodegenerative Diseases · 2006 · PMID 17192720
  not yet assessed
• A presenilin-1 mutation (T245P) in transmembrane domain 6 causes early onset Alzheimer's disease ↗

  Neuroscience Letters · 2006 · PMID 16469444
  not yet assessed
• Tangle Diseases and the Tau Haplotypes ↗

  Alzheimer Disease & Associated Disorders · 2006 · PMID 16493238
  not yet assessed
• Sequence analysis of all identified open reading frames on the frontal temporal dementia haplotype on chromosome 3 fails to identify unique coding variants except in CHMP2B ↗

  Neuroscience Letters · 2006 · PMID 17095158
  not yet assessed
• Frontal temporal dementia: dissecting the aetiology and pathogenesis ↗

  Brain · 2006 · PMID 16543401
  not yet assessed
• The Persistence of Memory ↗

  New England Journal of Medicine · 2006 · PMID 17182998
  not yet assessed
• Bad luck: An unappreciated limitation in the interpretation of twin studies ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2006 · PMID 16823802
  not yet assessed
• P1–349: Genetic analysis of Portuguese patients with Alzheimer's disease and frontotemporal dementia ↗

  Alzheimer s & Dementia · 2006
  not yet assessed
• P3–157: A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia ↗

  Alzheimer s & Dementia · 2006
  not yet assessed
• The genetics of frontotemporal dementia ↗

  2006
  not yet assessed
• Diagnosis and management of dementia with Lewy bodies ↗

  Neurology · 2005 · PMID 16237129
  not yet assessed
• Green Tea Epigallocatechin-3-Gallate (EGCG) Modulates Amyloid Precursor Protein Cleavage and Reduces Cerebral Amyloidosis in Alzheimer Transgenic Mice ↗

  Journal of Neuroscience · 2005 · PMID 16177050
  not yet assessed
• Aβ42 Is Essential for Parenchymal and Vascular Amyloid Deposition in Mice ↗

  Neuron · 2005 · PMID 16039562
  not yet assessed
• Correlations between apolipoprotein E ε4 gene dose and brain-imaging measurements of regional hypometabolism ↗

  Proceedings of the National Academy of Sciences · 2005 · PMID 15932949
  not yet assessed
• Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration ↗

  Journal of Medical Genetics · 2005 · PMID 15792962
  not yet assessed
• The H1c haplotype at the MAPT locus is associated with Alzheimer's disease ↗

  Human Molecular Genetics · 2005 · PMID 16000317
  not yet assessed
• Support for association between ADHD and two candidate genes: NET1 and DRD1 ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2005 · PMID 15717291
  not yet assessed
• Dense-Core Plaques in Tg2576 and PSAPP Mouse Models of Alzheimer's Disease Are Centered on Vessel Walls ↗

  American Journal Of Pathology · 2005 · PMID 16049337
  not yet assessed
• A Scan of Chromosome 10 Identifies a Novel Locus Showing Strong Association with Late-Onset Alzheimer Disease ↗

  The American Journal of Human Genetics · 2005 · PMID 16385451
  not yet assessed
• Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic stroke ↗

  Annals of Neurology · 2005 · PMID 16130105
  not yet assessed
• Expression of normal sequence pathogenic proteins for neurodegenerative disease contributes to disease risk: ‘permissive templating’ as a general mechanism underlying neurodegeneration ↗

  Biochemical Society Transactions · 2005 · PMID 16042548
  not yet assessed
• The dardarin G2019S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases ↗

  Neuroscience Letters · 2005 · PMID 16102903
  not yet assessed
• Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiens ↗

  Biochemical Society Transactions · 2005 · PMID 16042549
  not yet assessed
• Cholesterol 25-Hydroxylase on Chromosome 10q Is a Susceptibility Gene for Sporadic Alzheimer’s Disease ↗

  Neurodegenerative Diseases · 2005 · PMID 16909003
  not yet assessed
• Chromosome 21 BACE2 haplotype associates with Alzheimer's disease: A two-stage study ↗

  Journal of the Neurological Sciences · 2005 · PMID 16023140
  not yet assessed
• Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2005 · PMID 15924299
  not yet assessed
• G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort ↗

  Movement Disorders · 2005 · PMID 16149095
  not yet assessed
• Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2005 · PMID 15729734
  not yet assessed
• Gabapentin is Effective in the Treatment of Cancer-Related Neuropathic Pain: A Prospective, Open-Label Study a,b ↗

  Journal of Palliative Medicine · 2005 · PMID 16351524
  not yet assessed
• Torsin A haplotype predisposes to idiopathic dystonia ↗

  Annals of Neurology · 2005 · PMID 15852391
  not yet assessed
• Genetic variability at the LXR gene (NR1H2) may contribute to the risk of Alzheimer's disease ↗

  Neurobiology of Aging · 2005 · PMID 16207502
  not yet assessed
• An African American family with early-onset Alzheimer disease and an APP (T714I) mutation ↗

  Neurology · 2005 · PMID 15668448
  not yet assessed
• Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis ↗

  Neurobiology of Disease · 2005 · PMID 16084104
  not yet assessed
• Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease ↗

  Human Mutation · 2005 · PMID 15714520
  not yet assessed
• Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan ↗

  Neuroscience Letters · 2005 · PMID 16257123
  not yet assessed
• Load transmission through a healing tibial fracture ↗

  Clinical Biomechanics · 2005 · PMID 16226358
  not yet assessed
• Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2005 · PMID 15858813
  not yet assessed
• Ubiquilin 1 polymorphisms are not associated with late‐onset Alzheimer's disease ↗

  Annals of Neurology · 2005 · PMID 16278862
  not yet assessed
• The BDNF val66met polymorphism is not associated with late onset Alzheimer's disease in three case–control samples ↗

  Molecular Psychiatry · 2005 · PMID 15970929
  not yet assessed
• Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID) ↗

  Neurobiology of Aging · 2005 · PMID 16005115
  not yet assessed
• Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2005 · PMID 15635662
  not yet assessed
• Parkinson's disease: A broken nosology ↗

  Movement Disorders · 2005 · PMID 16092073
  not yet assessed
• Electrical and Dielectric Properties of ACu$_3$Ti$_4$O$_{12}$ Compounds

  Bulletin of the American Physical Society · 2005
  not yet assessed
• Prion genotypes in Central America suggest selection for the V129 allele ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2005 · PMID 16287045
  not yet assessed
• Taiwanese cases of SCA2 are derived from a single founder ↗

  Movement Disorders · 2005 · PMID 16078202
  not yet assessed
• Correlation of proband and sibling stroke latency: The SWISS Study ↗

  Neurology · 2005 · PMID 15781828
  not yet assessed
• Deletion at ITPR1 underlies ataxia in mice and humans (SCA15) ↗

  PLoS Genetics · 2005
  not yet assessed
• Mild cognitive impairment – beyond controversies, towards a consensus: report of the International Working Group on Mild Cognitive Impairment ↗

  Journal of Internal Medicine · 2004 · PMID 15324367
  not yet assessed
• The PARK8 Locus in Autosomal Dominant Parkinsonism: Confirmation of Linkage and Further Delineation of the Disease-Containing Interval ↗

  The American Journal of Human Genetics · 2004 · PMID 14691730
  not yet assessed
• Analysis of the PINK1 Gene in a Large Cohort of Cases With Parkinson Disease ↗

  Archives of Neurology · 2004 · PMID 15596610
  not yet assessed
• Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family ↗

  Proceedings of the National Academy of Sciences · 2004 · PMID 15507493
  not yet assessed
• Association between cardiac denervation and parkinsonism caused by α‐synuclein gene triplication ↗

  Brain · 2004 · PMID 14736756
  not yet assessed
• Profile of families with parkinsonism‐predominant spinocerebellar ataxia type 2 (SCA2) ↗

  Movement Disorders · 2004 · PMID 15197699
  not yet assessed
• The tau H2 haplotype is almost exclusively Caucasian in origin ↗

  Neuroscience Letters · 2004 · PMID 15464261
  not yet assessed
• Association of ABCA1 with late-onset Alzheimer’s disease is not observed in a case-control study ↗

  Neuroscience Letters · 2004 · PMID 15288432
  not yet assessed
• Analysis of an early‐onset Parkinson's disease cohort for DJ‐1 mutations ↗

  Movement Disorders · 2004 · PMID 15254937
  not yet assessed
• SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies ↗

  Neurology · 2004 · PMID 15304594
  not yet assessed
• Genetic testing in Parkinson's disease ↗

  Movement Disorders · 2004 · PMID 15503301
  not yet assessed
• Genome-Wide Analysis of the Parkinsonism-Dementia Complex of Guam ↗

  Archives of Neurology · 2004 · PMID 15596609
  not yet assessed
• Genome-wide scan linkage analysis for Parkinson’s disease: the European genetic study of Parkinson’s disease ↗

  Journal of Medical Genetics · 2004 · PMID 15591275
  not yet assessed
• Characterization of two APP gene promoter polymorphisms that appear to influence risk of late-onset Alzheimer's disease ↗

  Neurobiology of Aging · 2004 · PMID 16243604
  not yet assessed
• Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity features ↗

  Journal of Neurology · 2004 · PMID 15592737
  not yet assessed
• Smell testing is abnormal in ‘lubag’ or X-linked dystonia-parkinsonism: a pilot study ↗

  Parkinsonism & Related Disorders · 2004 · PMID 15465396
  not yet assessed
• Association of the dihydrolipoamide dehydrogenase gene with Alzheimer's disease in an Ashkenazi Jewish population ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2004 · PMID 15389771
  not yet assessed
• A new presenilin Alzheimer’s disease case confirms the helical alignment of pathogenic mutations in transmembrane domain 5 ↗

  Neuroscience Letters · 2004 · PMID 15196662
  not yet assessed
• Toward Alzheimer Therapies Based on Genetic Knowledge ↗

  Annual Review of Medicine · 2004 · PMID 14746507
  not yet assessed
• A consanguineous Turkish family with early‐onset Parkinson's disease and an exon 4 parkin deletion ↗

  Movement Disorders · 2004 · PMID 15254940
  not yet assessed
• An association study of the cholesteryl ester transfer protein TaqI B polymorphism with late onset Alzheimer's disease ↗

  Neuroscience Letters · 2004 · PMID 15036597
  not yet assessed
• Parkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with parkin mutations ↗

  Movement Disorders · 2004 · PMID 15197707
  not yet assessed
• The architecture of the tau haplotype block in different ethnicities ↗

  Neuroscience Letters · 2004 · PMID 15740841
  not yet assessed
• Dementia with Lewy bodies: no association of polymorphisms in the human synphilin gene ↗

  Neurogenetics · 2004 · PMID 15490287
  not yet assessed
• Problems and Solutions in the Genetic Analysis of Late-Onset Alzheimer’s Disease ↗

  Neurodegenerative Diseases · 2004 · PMID 16908992
  not yet assessed
• The uncertain anatomy of Alzheimer’s disease ↗

  Neurobiology of Aging · 2004 · PMID 15165693
  not yet assessed
• P4-094 Microarray profiling of Alzheimer's disease: findings based on segregation by APOE genotype ↗

  Neurobiology of Aging · 2004
  not yet assessed
• Vision therapy revealed: A guide to select vision therapy procedures

  CommonKnowledge Research Repository (Pacific University Oregon) · 2004
  not yet assessed
• α-Synuclein Locus Triplication Causes Parkinson's Disease ↗

  Science · 2003 · PMID 14593171
  not yet assessed
• Functional brain abnormalities in young adults at genetic risk for late-onset Alzheimer's dementia ↗

  Proceedings of the National Academy of Sciences · 2003 · PMID 14688411
  not yet assessed
• α‐Synuclein implicated in Parkinson's disease is present in extracellular biological fluids, including human plasma ↗

  The FASEB Journal · 2003 · PMID 14519670
  not yet assessed
• Biological markers for therapeutic trials in Alzheimer’s disease ↗

  Neurobiology of Aging · 2003 · PMID 12714109
  not yet assessed
• Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation ↗

  Annals of Neurology · 2003 · PMID 12891685
  not yet assessed
• Co‐ordinate transcriptional regulation of dopamine synthesis genes by α‐synuclein in human neuroblastoma cell lines ↗

  Journal of Neurochemistry · 2003 · PMID 12716427
  not yet assessed
• Genes and parkinsonism ↗

  The Lancet Neurology · 2003 · PMID 12849210
  not yet assessed
• Presenilin 1 Mutation in an African American Family Presenting With Atypical Alzheimer Dementia ↗

  Archives of Neurology · 2003 · PMID 12810495
  not yet assessed
• Parkin variants in North American Parkinson's disease: Cases and controls ↗

  Movement Disorders · 2003 · PMID 14639672
  not yet assessed
• The Relationship between Amyloid and Tau ↗

  Journal of Molecular Neuroscience · 2003 · PMID 12794314
  not yet assessed
• Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelic ↗

  Neurology · 2003 · PMID 14638969
  not yet assessed
• The Ischemic Stroke Genetics Study (ISGS) Protocol ↗

  BMC Neurology · 2003 · PMID 12848902
  not yet assessed
• α-Synuclein selectively increases manganese-induced viability loss in SK-N-MC neuroblastoma cells expressing the human dopamine transporter ↗

  Neuroscience Letters · 2003 · PMID 14698476
  not yet assessed
• Alzheimer's disease: Genetic evidence points to a single pathogenesis ↗

  Annals of Neurology · 2003 · PMID 12891664
  not yet assessed
• APH1, PEN2, and Nicastrin increase Aβ levels and γ-secretase activity ↗

  Biochemical and Biophysical Research Communications · 2003 · PMID 12763021
  not yet assessed
• Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease ↗

  Human Genetics · 2003 · PMID 12759818
  not yet assessed
• Polymorphism in the human DJ-1 gene is not associated with sporadic dementia with Lewy bodies or Parkinson's disease ↗

  Neuroscience Letters · 2003 · PMID 14625045
  not yet assessed
• Familial Clustering of Stroke According to Proband Age at Onset of Presenting Ischemic Stroke ↗

  Stroke · 2003 · PMID 12817106
  not yet assessed
• Assessment of a DJ-1 ( PARK7 ) polymorphism in Finnish PD ↗

  Neurology · 2003 · PMID 14557580
  not yet assessed
• Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation ↗

  Movement Disorders · 2003 · PMID 12815654
  not yet assessed
• Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2003 · PMID 14755449
  not yet assessed
• Ethnic Differences and Disease Phenotypes ↗

  Science · 2003 · PMID 12730580
  not yet assessed
• The Relationship between Lewy Body Disease, Parkinson's Disease, and Alzheimer's Disease ↗

  Annals of the New York Academy of Sciences · 2003 · PMID 12846985
  not yet assessed
• Mutation at the SCA17 locus is not a common cause of parkinsonism ↗

  Parkinsonism & Related Disorders · 2003 · PMID 12853230
  not yet assessed
• Microarray analysis reveals induction of heat shock proteins mRNAs by the torsion dystonia protein, TorsinA ↗

  Neuroscience Letters · 2003 · PMID 12749984
  not yet assessed
• Complex interactions in Parkinson's disease: A two‐phased approach ↗

  Movement Disorders · 2003 · PMID 12784265
  not yet assessed
• Variation in the urokinase‐plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2003 · PMID 14681909
  not yet assessed
• Parkin-proven disease ↗

  Neurology · 2003 · PMID 12771249
  not yet assessed
• Impact of genetic analysis on Parkinson's disease research ↗

  Movement Disorders · 2003 · PMID 14502662
  not yet assessed
• Expression of mBRI2 in mice ↗

  Neuroscience Letters · 2003 · PMID 12566161
  not yet assessed
• Case‐control study of the α‐synuclein interacting protein gene and Parkinson's disease ↗

  Movement Disorders · 2003 · PMID 14639662
  not yet assessed
• Inconsistent designs of association studies: a missed opportunity ↗

  Molecular Psychiatry · 2003 · PMID 12931204
  not yet assessed
• Addendum “APH1, PEN2, and Nicastrin increase Aβ levels and γ-secretase activity” [Biochem. Biophys. Res. Commun. 305 (2003) 502–509] ↗

  Biochemical and Biophysical Research Communications · 2003
  not yet assessed
• The Amyloid Hypothesis of Alzheimer's Disease: Progress and Problems on the Road to Therapeutics ↗

  Science · 2002 · PMID 12130773
  not yet assessed
• Toxic Proteins in Neurodegenerative Disease ↗

  Science · 2002 · PMID 12065827
  not yet assessed
• Parkin Protects against the Toxicity Associated with Mutant α-Synuclein ↗

  Neuron · 2002 · PMID 12495618
  not yet assessed
• Complex relationship between Parkin mutations and Parkinson disease ↗

  American Journal of Medical Genetics · 2002 · PMID 12116199
  not yet assessed
• Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene ↗

  Brain · 2002 · PMID 11912108
  not yet assessed
• Contribution of APOE promoter polymorphisms to Alzheimer’s disease risk ↗

  Neurology · 2002 · PMID 12105308
  not yet assessed
• SCA2 may present as levodopa‐responsive parkinsonism ↗

  Movement Disorders · 2002 · PMID 12671950
  not yet assessed
• Phenomenology of “Lubag” or X‐linked dystonia–parkinsonism ↗

  Movement Disorders · 2002 · PMID 12465067
  not yet assessed
• Testing times for the “amyloid cascade hypothesis” ↗

  Neurobiology of Aging · 2002 · PMID 12470803
  not yet assessed
• An Iranian family with Alzheimer’s disease caused by a novel APP mutation (Thr714Ala) ↗

  Neurology · 2002 · PMID 12034808
  not yet assessed
• Full genome screen for Alzheimer disease: Stage II analysis* ↗

  American Journal of Medical Genetics · 2002 · PMID 11857588
  not yet assessed
• A Presenilin 1 Mutation Associated with Familial Frontotemporal Dementia Inhibits γ-Secretase Cleavage of APP and Notch ↗

  Neurobiology of Disease · 2002 · PMID 11895378
  not yet assessed
• The Siblings With Ischemic Stroke Study (SWISS) Protocol ↗

  BMC Medical Genetics · 2002 · PMID 11882254
  not yet assessed
• Ethnic differences in the expression of neurodegenerative disease: Machado‐Joseph disease in Africans and Caucasians ↗

  Movement Disorders · 2002 · PMID 12360561
  not yet assessed
• Familial Frontotemporal Dementia Associated with a Novel Presenilin-1 Mutation ↗

  Dementia and Geriatric Cognitive Disorders · 2002 · PMID 12053127
  not yet assessed
• The Tau H1 Haplotype is associated with Parkinson's disease in the Norwegian population ↗

  Neuroscience Letters · 2002 · PMID 11958849
  not yet assessed
• Analysis of tau haplotypes in Pick’s disease ↗

  Neurology · 2002 · PMID 12177383
  not yet assessed
• An association study of a functional catalase gene polymorphism, −262C→T, and patients with Alzheimer's disease ↗

  Neuroscience Letters · 2002 · PMID 12231449
  not yet assessed
• Case‐Control study of dopamine transporter‐1, monoamine oxidase‐B, and catechol‐O‐methyl transferase polymorphisms in Parkinson's disease ↗

  Movement Disorders · 2002 · PMID 12465073
  not yet assessed
• Clinical, 18F‐dopa PET, and genetic analysis of an ethnic Chinese kindred with early‐onset parkinsonism and parkin gene mutations ↗

  Movement Disorders · 2002 · PMID 12210855
  not yet assessed
• Interleukin-1A polymorphism is not associated with late onset Alzheimer's disease ↗

  Neuroscience Letters · 2002 · PMID 11911995
  not yet assessed
• X‐linked dystonia (“Lubag”) presenting predominantly with parkinsonism: A more benign phenotype? ↗

  Movement Disorders · 2002 · PMID 11835466
  not yet assessed
• The tau locus is not significantly associated with pathologically confirmed sporadic Parkinson's disease ↗

  Neuroscience Letters · 2002 · PMID 12231446
  not yet assessed
• Apolipoprotein E4 and tau allele frequencies among Choctaw Indians ↗

  Neuroscience Letters · 2002 · PMID 11983299
  not yet assessed
• ApoE ϵ3‐haplotype modulates Alzheimer beta‐amyloid deposition in the brain ↗

  American Journal of Medical Genetics · 2002 · PMID 11920850
  not yet assessed
• The human sideroflexin 5 (SFXN5) gene: sequence, expression analysis and exclusion as a candidate for PARK3 ↗

  Gene · 2002 · PMID 12039050
  not yet assessed
• Clinical features and changing patterns of neurodegenerative disorders on Guam, 1997–2000 ↗

  Neurology · 2002 · PMID 12370488
  not yet assessed
• No association between the lipoprotein lipase S447X polymorphism and Alzheimer's disease ↗

  Neuroscience Letters · 2002 · PMID 11897170
  not yet assessed
• The real problem in association studies† ↗

  American Journal of Medical Genetics · 2002 · PMID 11857590
  not yet assessed
• Corticobasal Degeneration and Frontotemporal Dementia Presentations in a Kindred with Nonspecific Histopathology ↗

  Dementia and Geriatric Cognitive Disorders · 2002 · PMID 11844889
  not yet assessed
• A family with a tau P301L mutation presenting with parkinsonism ↗

  Parkinsonism & Related Disorders · 2002 · PMID 12473404
  not yet assessed
• Apolipoprotein E and Intellectual Achievement ↗

  Journal of the American Geriatrics Society · 2002 · PMID 12028246
  not yet assessed
• Possible association between genetic variability at the apolipoprotein(a) locus and Alzheimer's disease in apolipoprotein E2 carriers ↗

  Neuroscience Letters · 2002 · PMID 12359323
  not yet assessed
• Pathways to primary neurodegenerative disease. ↗

  PubMed · 2002 · PMID 12396967
  not yet assessed
• Biomedicine - Toxic proteins in neurodegenerative disease

  UCL Discovery (University College London) · 2002
  not yet assessed
• The search for an amyloid solution - Response

  UCL Discovery (University College London) · 2002
  not yet assessed
• Enhanced Neurofibrillary Degeneration in Transgenic Mice Expressing Mutant Tau and APP ↗

  Science · 2001 · PMID 11520987
  not yet assessed
• Lewy bodies and parkinsonism in families with parkin mutations ↗

  Annals of Neurology · 2001 · PMID 11558785
  not yet assessed
• Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype ↗

  Neurology · 2001 · PMID 11425937
  not yet assessed
• Prevalence of Alzheimer’s disease in very elderly people ↗

  Neurology · 2001 · PMID 11425935
  not yet assessed
• Lack of Nigral Pathology in Transgenic Mice Expressing Human α-Synuclein Driven by the Tyrosine Hydroxylase Promoter ↗

  Neurobiology of Disease · 2001 · PMID 11442360
  not yet assessed
• Spinocerebellar Ataxia Type 3 Phenotypically Resembling Parkinson Disease in a Black Family ↗

  Archives of Neurology · 2001 · PMID 11176969
  not yet assessed
• Variant Alzheimer Disease With Spastic paraparesis: Neuropathological phenotype ↗

  Journal of Neuropathology & Experimental Neurology · 2001 · PMID 11379823
  not yet assessed
• Cotton Wool Plaques in Non-Familial Late-Onset Alzheimer Disease ↗

  Journal of Neuropathology & Experimental Neurology · 2001 · PMID 11706935
  not yet assessed
• Number of A β Inoculations in APP+PS1 Transgenic Mice Influences Antibody Titers, Microglial Activation, and Congophilic Plaque Levels ↗

  DNA and Cell Biology · 2001 · PMID 11788051
  not yet assessed
• Transfected synphilin-1 forms cytoplasmic inclusions in HEK293 cells ↗

  Molecular Brain Research · 2001 · PMID 11744167
  not yet assessed
• Relationship of the extended tau haplotype to tau biochemistry and neuropathology in progressive supranuclear palsy ↗

  Annals of Neurology · 2001 · PMID 11601500
  not yet assessed
• Preclinical cognitive decline in late middle-aged asymptomatic apolipoprotein E-e4/4 homozygotes: a replication study ↗

  Journal of the Neurological Sciences · 2001 · PMID 11535238
  not yet assessed
• A novel presenilin mutation (M233V) causing very early onset Alzheimer's disease with Lewy bodies ↗

  Neuroscience Letters · 2001 · PMID 11684347
  not yet assessed
• Expression of BRI–amyloid β peptide fusion proteins: a novel method for specific high-level expression of amyloid β peptides ↗

  Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 2001 · PMID 11476963
  not yet assessed
• Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease ↗

  Human Genetics · 2001 · PMID 11810277
  not yet assessed
• A Pathogenic Presenilin-1 Deletion Causes Abberrant Aβ42 Production in the Absence of Congophilic Amyloid Plaques ↗

  Journal of Biological Chemistry · 2001 · PMID 11084029
  not yet assessed
• Co-association of parkin and α-synuclein ↗

  Neuroreport · 2001 · PMID 11588587
  not yet assessed
• Presenilin mutations line up along transmembrane α-helices ↗

  Neuroscience Letters · 2001 · PMID 11406330
  not yet assessed
• Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes ↗

  European Journal of Human Genetics · 2001 · PMID 11571553
  not yet assessed
• Association of lipoprotein base Ser447Ter polymorphism with brain infarction: a population-based neuropathological study ↗

  Annals of Medicine · 2001 · PMID 11680797
  not yet assessed
• Feasibility of an Affected Sibling Pair Study in Ischemic Stroke ↗

  Stroke · 2001 · PMID 11739999
  not yet assessed
• The genetic causes of neurodegenerative diseases ↗

  Journal of Alzheimer s Disease · 2001 · PMID 12214079
  not yet assessed
• Pathology of PD in monozygotic twins with a 20-year discordance interval ↗

  Neurology · 2001 · PMID 11294946
  not yet assessed
• Genetic dissection of primary neurodegenerative diseases ↗

  Biochemical Society Symposia · 2001 · PMID 11447839
  not yet assessed
• Case‐control study of the extended tau gene haplotype in Parkinson's disease ↗

  Annals of Neurology · 2001 · PMID 11706972
  not yet assessed
• Case‐control study of estrogen receptor gene polymorphisms in Parkinson's disease ↗

  Movement Disorders · 2001 · PMID 12112198
  not yet assessed
• Patients with pulmonary and cardiac disease show an elevated proportion of immature reticulocytes ↗

  Clinical & Laboratory Haematology · 2001 · PMID 11422227
  not yet assessed
• Genetic dissection of neurodegenerative disease ↗

  Clinical Neuroscience Research · 2001
  not yet assessed
• Identification and characterization of the human parkin gene promoter ↗

  Journal of Neurochemistry · 2001 · PMID 11553688
  not yet assessed
• Genetic Analysis of Synphilin-1 in Familial Parkinson's Disease ↗

  Neurobiology of Disease · 2001 · PMID 11300726
  not yet assessed
• Aβ peptide vaccination prevents memory loss in an animal model of Alzheimer's disease ↗

  Nature · 2000 · PMID 11140686
  not yet assessed
• Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein ↗

  Nature Genetics · 2000 · PMID 10932182
  not yet assessed
• The A53T alpha-synuclein mutation increases iron-dependent aggregation and toxicity. ↗

  PubMed · 2000 · PMID 10934254
  not yet assessed
• The A53T α-Synuclein Mutation Increases Iron-Dependent Aggregation and Toxicity ↗

  Journal of Neuroscience · 2000
  not yet assessed
• Variant Alzheimer’s disease with spastic paraparesis ↗

  Neurology · 2000 · PMID 10720282
  not yet assessed
• Susceptibility Locus for Alzheimer's Disease on Chromosome 10 ↗

  Science · 2000 · PMID 11125144
  not yet assessed
• Glycine 384 is required for presenilin-1 function and is conserved in bacterial polytopic aspartyl proteases ↗

  Nature Cell Biology · 2000 · PMID 11056541
  not yet assessed
• Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese ↗

  Neurology · 2000 · PMID 10993999
  not yet assessed
• Distinctive neuropathology revealed by α-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p ↗

  Acta Neuropathologica · 2000 · PMID 10867800
  not yet assessed
• Verifying the Stroke-Free Phenotype by Structured Telephone Interview ↗

  Stroke · 2000 · PMID 10797168
  not yet assessed
• Pick's disease is associated with mutations in thetau gene ↗

  Annals of Neurology · 2000 · PMID 11117542
  not yet assessed
• Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-? concentrations ↗

  Annals of Neurology · 2000 · PMID 11079548
  not yet assessed
• The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease ↗

  Human Molecular Genetics · 2000 · PMID 11001930
  not yet assessed
• Sensitization of Neuronal Cells to Oxidative Stress with Mutated Human α‐Synuclein ↗

  Journal of Neurochemistry · 2000 · PMID 11080208
  not yet assessed
• Cardiovascular risk factors and Alzheimer's disease: a genetic association study in a population aged 85 or over ↗

  Neuroscience Letters · 2000 · PMID 11018310
  not yet assessed
• Pathways to Primary Neurodegenerative Disease ↗

  Annals of the New York Academy of Sciences · 2000 · PMID 11193798
  not yet assessed
• Case-control study of debrisoquine 4-hydroxylase, n-acetyltransferase 2, and apolipoprotein e gene polymorphisms in Parkinson's disease ↗

  Movement Disorders · 2000 · PMID 10928584
  not yet assessed
• No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease ↗

  Neuroscience Letters · 2000 · PMID 10793248
  not yet assessed
• Linkage exclusion in French families with probable Parkinson's disease ↗

  Movement Disorders · 2000 · PMID 11104189
  not yet assessed
• A kindred with Parkinson’s disease not showing genetic linkage to established loci ↗

  Neurology · 2000 · PMID 10668726
  not yet assessed
• The Presenilin 1 C92S Mutation Increases Aβ 42 Production ↗

  Biochemical and Biophysical Research Communications · 2000 · PMID 11027672
  not yet assessed
• Pick's disease is associated with mutations in the tau gene ↗

  Annals of Neurology · 2000
  not yet assessed
• Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS‐1 mutations that lead to exceptionally high amyloid‐β concentrations ↗

  Annals of Neurology · 2000
  not yet assessed
• High A42 causing presenilin 1 mutations lead to the cotton wool plaques/spastic paraparesis variant of Alzheimer's disease ↗

  Neurobiology of Aging · 2000
  not yet assessed
• The Future of Genetic Analysis of Neurological Disorders ↗

  Neurobiology of Disease · 2000 · PMID 10783291
  not yet assessed
• Association of an Extended Haplotype in the Tau Gene with Progressive Supranuclear Palsy ↗

  Human Molecular Genetics · 1999 · PMID 10072441
  not yet assessed
• α-Synuclein Shares Physical and Functional Homology with 14-3-3 Proteins ↗

  Journal of Neuroscience · 1999 · PMID 10407019
  not yet assessed
• Widespread Alterations of α-Synuclein in Multiple System Atrophy ↗

  American Journal Of Pathology · 1999 · PMID 10514406
  not yet assessed
• Aberrant Splicing in the Presenilin-1 Intron 4 Mutation Causes Presenile Alzheimer's Disease by Increased A 42 Secretion ↗

  Human Molecular Genetics · 1999 · PMID 10401002
  not yet assessed
• A Loss of Function Mutation of Presenilin-2 Interferes with Amyloid β-Peptide Production and Notch Signaling ↗

  Journal of Biological Chemistry · 1999 · PMID 10497236
  not yet assessed
• Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson’s disease ↗

  Neurology · 1999 · PMID 10563640
  not yet assessed
• Low frequency of pathogenic mutations in the ubiquitin carboxyterminal hydrolase gene in familial Parkinsonʼs disease ↗

  Neuroreport · 1999 · PMID 10203348
  not yet assessed
• Genetic association of alpha2-macroglobulin with Alzheimer's disease in a Finnish elderly population. ↗

  PubMed · 1999 · PMID 10482269
  not yet assessed
• Genetic association of ?2-macroglobulin with Alzheimer's disease in a Finnish elderly population ↗

  Annals of Neurology · 1999
  not yet assessed
• Alzheimer disease PS-1 exon 9 deletion defined ↗

  Nature Medicine · 1999 · PMID 10502791
  not yet assessed
• Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's disease ↗

  Human Genetics · 1999 · PMID 10394937
  not yet assessed
• A novel mutation in the apolipoprotein E gene (APOE*4 Pittsburgh) is associated with the risk of late-onset Alzheimer's disease ↗

  Neuroscience Letters · 1999 · PMID 10213152
  not yet assessed
• Salvaging a stripped drive connection when removing screws ↗

  Injury · 1999 · PMID 10396464
  not yet assessed
• Antisense‐Induced Reduction of Presenilin 1 Expression Selectively Increases the Production of Amyloid β42 in Transfected Cells ↗

  Journal of Neurochemistry · 1999 · PMID 10582597
  not yet assessed
• Pathways to Primary Neurodegenerative Disease ↗

  Mayo Clinic Proceedings · 1999 · PMID 10473363
  not yet assessed
• Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimers disease by increased a beta 42 secretion

  Ghent University Academic Bibliography (Ghent University) · 1999
  not yet assessed
• In search of γ-secretase ↗

  Nature · 1999 · PMID 10206639
  not yet assessed
• Mutation in thetau exon 10 splice site region in familial frontotemporal dementia ↗

  Annals of Neurology · 1999 · PMID 9989634
  not yet assessed
• Genetic variability at the amyloid-β precursor protein locus may contribute to the risk of late-onset Alzheimer's disease ↗

  Neuroscience Letters · 1999 · PMID 10430506
  not yet assessed
• No pathogenic mutations in the β-synuclein gene in Parkinson's disease ↗

  Neuroscience Letters · 1999 · PMID 10430516
  not yet assessed
• α-2 macroglobulin gene and Alzheimer disease ↗

  Nature Genetics · 1999 · PMID 10319854
  not yet assessed
• The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease ↗

  Neuroscience Letters · 1999 · PMID 10454131
  not yet assessed
• No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease ↗

  Neuroscience Letters · 1999 · PMID 10203250
  not yet assessed
• Neurodegenerative diseases of Guam: Analysis of TAU ↗

  Neurology · 1999 · PMID 10430438
  not yet assessed
• Neurodegenerative disease: a different view of diagnosis ↗

  Molecular Medicine Today · 1999 · PMID 10562716
  not yet assessed
• Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations ↗

  Neuroscience Letters · 1999 · PMID 10076900
  not yet assessed
• L-dopa slows the progression of familial parkinsonism ↗

  The Lancet · 1999 · PMID 10359414
  not yet assessed
• Construction of a Detailed Physical and Transcript Map of the FTDP-17 Candidate Region on Chromosome 17q21 ↗

  Genomics · 1999 · PMID 10486204
  not yet assessed
• No pathogenic mutations in the persyn gene in Parkinson's disease ↗

  Neuroscience Letters · 1999 · PMID 10027558
  not yet assessed
• Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 ↗

  Nature · 1998 · PMID 9641683
  not yet assessed
• Accelerated Alzheimer-type phenotype in transgenic mice carrying both mutant amyloid precursor protein and presenilin 1 transgenes ↗

  Nature Medicine · 1998 · PMID 9427614
  not yet assessed
• Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease ↗

  Human Molecular Genetics · 1998 · PMID 9384602
  not yet assessed
• A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1 ↗

  Nature Medicine · 1998 · PMID 9546792
  not yet assessed
• Genetic dissection of Alzheimer's disease and related dementias: amyloid and its relationship to tau ↗

  Nature Neuroscience · 1998 · PMID 10196523
  not yet assessed
• Genetic Classification of Primary Neurodegenerative Disease ↗

  Science · 1998 · PMID 9804538
  not yet assessed
• Low frequency of α‐synuclein mutations in familial Parkinson's disease ↗

  Annals of Neurology · 1998 · PMID 9506559
  not yet assessed
• Genetics of Alzheimer's disease ↗

  Essays in Biochemistry · 1998 · PMID 10488446
  not yet assessed
• ApoE genotype is a risk factor in nonpresenilin early-onset alzheimer's disease families ↗

  American Journal of Medical Genetics · 1998 · PMID 9514597
  not yet assessed
• Increased Aβ42(43) from cell lines expressing presenilin 1 mutations ↗

  Annals of Neurology · 1998 · PMID 9485068
  not yet assessed
• Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucineright-arrowserine (L250S) substitution at codon 250 of the presenilin 1 gene ↗

  Journal of Neurology Neurosurgery & Psychiatry · 1998 · PMID 9436726
  not yet assessed
• The Effect of Desulphated Seawater Injection on Microbiological Hydrogen Sulphide Generation and Implication for Corrosion Control ↗

  1998
  not yet assessed
• Truncated presenilin 2 derived from differentially spliced mRNAs does not affect the ratio of amyloid β-peptide 1-42/1-40 ↗

  Neuroreport · 1998 · PMID 9831466
  not yet assessed
• Is the stability of a tibial fracture influenced by the type of unilateral external fixator? ↗

  Clinical Biomechanics · 1998 · PMID 11415839
  not yet assessed
• Amyloid, the presenilins and Alzheimer's disease ↗

  Trends in Neurosciences · 1997 · PMID 9106355
  not yet assessed
• A New Pathogenic Mutation in the APP Gene (I716V) Increases the Relative Proportion of A 42(43) ↗

  Human Molecular Genetics · 1997 · PMID 9328472
  not yet assessed
• The Alzheimer family of diseases: Many etiologies, one pathogenesis? ↗

  Proceedings of the National Academy of Sciences · 1997 · PMID 9122152
  not yet assessed
• Two novel (M233T and ρ278T) presenilin-1 mutations in early-onset Alzheimerʼs disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype ↗

  Neuroreport · 1997 · PMID 9172170
  not yet assessed
• Distortion of Allelic Expression of Apolipoprotein E in Alzheimer's Disease ↗

  Human Molecular Genetics · 1997 · PMID 9328480
  not yet assessed
• Dynamic Interfragmentary Motion in Fractures During Routine Patient Activity ↗

  Clinical Orthopaedics and Related Research · 1997 · PMID 9060508
  not yet assessed
• Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21–22 ↗

  Annals of Neurology · 1997 · PMID 9392579
  not yet assessed
• Early‐onset Alzheimer's disease with a presenilin‐1 mutation at the site corresponding to the volga German presenilin‐2 mutation ↗

  Annals of Neurology · 1997 · PMID 9225696
  not yet assessed
• Temporal changes in dynamic inter fragmentary motion and callus formation in fractures ↗

  Journal of Biomechanics · 1997 · PMID 9074998
  not yet assessed
• Association between the low density lipoprotein receptor-related protein (LRP) and Alzheimer's disease ↗

  Neuroscience Letters · 1997 · PMID 9178861
  not yet assessed
• Genetics of Parkinson's Disease ↗

  Science · 1997 · PMID 9411743
  not yet assessed
• Secreted amyloid β–protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease ↗

  Nature Medicine · 1996 · PMID 8705854
  not yet assessed
• Increased amyloid-β42(43) in brains of mice expressing mutant presenilin 1 ↗

  Nature · 1996 · PMID 8878479
  not yet assessed
• Endoproteolysis of Presenilin 1 and Accumulation of Processed Derivatives In Vivo ↗

  Neuron · 1996 · PMID 8755489
  not yet assessed
• Amyloid β protein (Aβ) deposition in chromosome 14–linked Alzheimer's disease: Predominance of Aβ42(43) ↗

  Annals of Neurology · 1996 · PMID 8773595
  not yet assessed
• Complete analysis of the presenilin 1 gene in early onset Alzheimerʼs disease ↗

  Neuroreport · 1996 · PMID 8733749
  not yet assessed
• New Insights into the Genetics of Alzheimer's Disease ↗

  Annals of Medicine · 1996 · PMID 8811169
  not yet assessed
• Structure and alternative splicing of the Presenilin-2 gene ↗

  Neuroreport · 1996 · PMID 8904781
  not yet assessed
• Low sulfate seawater mitigates barite scale

  Oil & gas journal/Oil and gas journal · 1996
  not yet assessed
• Polymorphism in AACT gene may lower age of onset of Alzheimerʼs disease ↗

  Neuroreport · 1996 · PMID 8730823
  not yet assessed
• A Further Presenilin 1 Mutation in the Exon 8 Cluster in Familial Alzheimer's Disease ↗

  Neurodegeneration · 1996 · PMID 8910898
  not yet assessed
• Presenilin–1 is Processed into Two Major Cleavage Products in Neuronal Cell Lines ↗

  Neurodegeneration · 1996 · PMID 9117540
  not yet assessed
• ApoE2 Allele, Down's Syndrome, and Dementiaa ↗

  Annals of the New York Academy of Sciences · 1996 · PMID 8624094
  not yet assessed
• Alteration in Brain Presenilin 1 mRNA Expression in Early Onset Familial Alzheimer's Disease ↗

  Neurodegeneration · 1996 · PMID 8910899
  not yet assessed
• Cytoskeletal and Alzheimer-type pathology in Lewy body disease ↗

  Cambridge University Press eBooks · 1996
  not yet assessed
• Study examines sulfate-reducing bacteria activity

  Oil & gas journal/Oil and gas journal · 1996
  not yet assessed
• The Genes Involved in Alzheimer’s Disease ↗

  1996
  not yet assessed
• The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families ↗

  Nature Genetics · 1995 · PMID 7550356
  not yet assessed
• A mutation in Alzheimerʼs disease destroying a splice acceptor site in the presenilin-1 gene ↗

  Neuroreport · 1995 · PMID 8742474
  not yet assessed
• Familial non-specific dementia maps to chromosome 3 ↗

  Human Molecular Genetics · 1995 · PMID 8541850
  not yet assessed
• Apolipoprotein E genotype and Lewy body disease ↗

  Neurology · 1995 · PMID 7824144
  not yet assessed
• Apolipoprotein E in the genetics and epidemiology of Alzheimer's disease ↗

  American Journal of Medical Genetics · 1995 · PMID 8546162
  not yet assessed
• Mouse model made ↗

  Nature · 1995 · PMID 7845455
  not yet assessed
• A mutation in Alzheimerʼs disease destroying a splice acceptor site in the presenilin-1 gene ↗

  Neuroreport · 1995
  not yet assessed
• Apolipoprotein E alleles but neither apolipoprotein B nor apolipoprotein AI/CIII alleles are associated with late onset, familial Alzheimer's disease ↗

  Neuroscience Letters · 1995 · PMID 7609909
  not yet assessed
• Single-day apolipoprotein E genotyping ↗

  Journal of Neuroscience Methods · 1994 · PMID 7823614
  not yet assessed
• Amyloid precursor protein mutation causes Alzheimer's disease in a Swedish family ↗

  Neuroscience Letters · 1994 · PMID 8028788
  not yet assessed
• Senile dementia of the Lewy body type has an apolipoprotein E ε4 allele frequency intermediate between controls and Alzheimer's disease ↗

  Neuroscience Letters · 1994 · PMID 7891871
  not yet assessed
• Apolipoprotein E ε2 allele promotes longevity and protects patients with Downʼs syndrome from dementia ↗

  Neuroreport · 1994 · PMID 7696609
  not yet assessed
• APOE genotype does not modulate age of onset in families with chromosome 14 encoded Alzheimer's disease ↗

  Neuroscience Letters · 1994 · PMID 8047278
  not yet assessed
• Chromosome 14–encoded Alzheimer's disease: Genetic and clinicopathological description ↗

  Annals of Neurology · 1994 · PMID 8080244
  not yet assessed
• ApoE, Amyloid, and Alzheimer's Disease ↗

  Science · 1994 · PMID 8290946
  not yet assessed
• Confirmation that familial clustering and age of onset in late onset Alzheimer's disease are determined at the apolipoprotein E locus ↗

  Neuroscience Letters · 1994 · PMID 7970184
  not yet assessed
• ApoE genotype and Down's syndrome ↗

  The Lancet · 1994 · PMID 7909036
  not yet assessed
• Insertion of a pathogenic mutation into a yeast artificial chromosome containing the human amyloid precursor protein gene. ↗

  PubMed · 1994 · PMID 7584064
  not yet assessed
• Lewy bodies in Alzheimer's disease in which the primary lesion is a mutation in the amyloid precursor protein ↗

  Neuroscience Letters · 1994 · PMID 7700596
  not yet assessed
• Familial Pick's disease and dementia in frontal lobe degeneration of non-Alzheimer type are not variants of prion disease. ↗

  Journal of Neurology Neurosurgery & Psychiatry · 1994 · PMID 8006666
  not yet assessed
• Parkinson's disease, but not Alzheimer's disease, Lewy body variant associated with mutant alleles at cytochrome P450 gene ↗

  The Lancet · 1994 · PMID 7916091
  not yet assessed
• Alzheimer's disease: the present situation and our tasks ↗

  Neurobiology of Aging · 1994 · PMID 7700432
  not yet assessed
• APOLIPOPROTEIN-E GENOTYPE AND ALZHEIMERS-DISEASE

  UCL Discovery (University College London) · 1993
  not yet assessed
• Clinical comparison of Alzheimer's disease in pedigrees with the codon 717 Val→Ile mutation in the amyloid precursor protein gene ↗

  Neurobiology of Aging · 1993 · PMID 8247223
  not yet assessed
• Familial Alzheimer's disease A pedigree with a mis-sense mutation in the amyloid precursor protein gene (amyloid precursor protein 717 valine → glycine) ↗

  Brain · 1993 · PMID 8461968
  not yet assessed
• Alzheimer's disease: Molecular genetics and transgenic animal models ↗

  Behavioural Brain Research · 1993 · PMID 8117426
  not yet assessed
• A novel silent variant at codon 711 and a variant at codon 708 of the APP sequence detected in Spanish Alzheimer and control cases ↗

  Neuroscience Letters · 1993 · PMID 8469399
  not yet assessed
• Exclusion Mapping in Familial Non-Specific Dementia ↗

  Dementia and Geriatric Cognitive Disorders · 1993 · PMID 8401786
  not yet assessed
• Genetic characterization of a familial non-specific dementia originating in Jutland, Denmark ↗

  Journal of the Neurological Sciences · 1993 · PMID 8445394
  not yet assessed
• Sequencing of exons 16 and 17 of the β-amyloid precursor protein gene reveals the β-amyloid sequence to be normal in cases of the parkinson dementia complex of guam ↗

  Journal of Neural Transmission - Parkinsons Disease and Dementia Section · 1993 · PMID 8439393
  not yet assessed
• "Prion dementia" ↗

  The Lancet · 1993
  not yet assessed
• Alzheimer's Disease: The Amyloid Cascade Hypothesis ↗

  Science · 1992 · PMID 1566067
  not yet assessed
• A locus for familial early–onset Alzhelmer's disease on the long arm of chromosome 14, proximal to the α1–antichymotrypsin gene ↗

  Nature Genetics · 1992 · PMID 1303291
  not yet assessed
• INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION: 2. CLINICAL AND PATHOLOGICAL FEATURES ↗

  Brain · 1992 · PMID 1352725
  not yet assessed
• INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION: 1. GENEALOGICAL AND MOLECULAR STUDIES ↗

  Brain · 1992 · PMID 1352724
  not yet assessed
• An ‘anatomical cascade hypothesis’ for Alzheimer's disease ↗

  Trends in Neurosciences · 1992 · PMID 1378661
  not yet assessed
• Framing β–amyloid ↗

  Nature Genetics · 1992 · PMID 1363811
  not yet assessed
• Screening for mutations in the open reading frame and promoter of the β-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val→lle ↗

  Human Molecular Genetics · 1992 · PMID 1303172
  not yet assessed
• Simulations of phase transitions in Rb2ZnCl4 ↗

  Physical review. B, Condensed matter · 1992 · PMID 10000568
  not yet assessed
• Pathological changes in the brain of a patient with familial Alzheimer's disease having a missense mutation at codon 717 in the amyloid precursor protein gene ↗

  Neuroscience Letters · 1992 · PMID 1584464
  not yet assessed
• In search of the soluble ↗

  Nature · 1992 · PMID 1406927
  not yet assessed
• A polymorphic dinucleotide repeat in intron 2 of the human cystatin-C gene ↗

  Human Molecular Genetics · 1992 · PMID 1301159
  not yet assessed
• Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease ↗

  Nature · 1991 · PMID 1671712
  not yet assessed
• Amyloid deposition as the central event in the aetiology of Alzheimer's disease ↗

  Trends in Pharmacological Sciences · 1991 · PMID 1763432
  not yet assessed
• Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene ↗

  Nature · 1991 · PMID 1944558
  not yet assessed
• Amyloid precursor protein gene mutation in early-onset Alzheimer's disease ↗

  The Lancet · 1991 · PMID 1678057
  not yet assessed
• Screening for the β-amyloid precursor protein mutation (APP717: Val → Ile) in extended pedigrees with early onset Alzheimer's disease ↗

  Neuroscience Letters · 1991 · PMID 1922963
  not yet assessed
• Insertions in the prion protein gene in atypical dementias ↗

  Experimental Neurology · 1991 · PMID 1674696
  not yet assessed
• Hereditary cerebral hemorrhage with amyloidosis — Dutch type: its importance for Alzheimer research ↗

  Trends in Neurosciences · 1991 · PMID 1716015
  not yet assessed
• Prion dimers: a deadly duo ↗

  Trends in Neurosciences · 1991 · PMID 1722358
  not yet assessed
• Sequencing of exons 16 and 17 of the β-amyloid precursor protein gene in 14 families with early onset Alzheimer's disease fails to reveal mutations in the β-amyloid sequence ↗

  Neuroscience Letters · 1991 · PMID 1791986
  not yet assessed
• Ex vivo release of GABA from tetanus toxin-induced chronic epileptic foci decreased during the active seizure phase ↗

  Neurochemistry International · 1991 · PMID 20504714
  not yet assessed
• Genetics of Alzheimer's disease ↗

  European Neuropsychopharmacology · 1991
  not yet assessed
• Genetic Characterization of a Novel Familial Dementia ↗

  Annals of the New York Academy of Sciences · 1991 · PMID 1776737
  not yet assessed
• Nicotine intake and Alzheimer's disease. ↗

  BMJ · 1991 · PMID 1912783
  not yet assessed
• Clinical and Pathologic Features of Chromosome 21‐Linked Familial Alzheimer's Disease ↗

  Annals of the New York Academy of Sciences · 1991 · PMID 1776736
  not yet assessed
• Evidence for Allelic Heterogeneity in Familial Early-Onset Alzheimer's Disease ↗

  The British Journal of Psychiatry · 1991 · PMID 2054561
  not yet assessed
• Amyloid β Protein Precursor Gene and Hereditary Cerebral Hemorrhage with Amyloidosis (Dutch) ↗

  Science · 1990 · PMID 1971458
  not yet assessed
• Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder ↗

  Nature · 1990 · PMID 2395471
  not yet assessed
• Prion dementia without characteristic pathology ↗

  The Lancet · 1990 · PMID 1973256
  not yet assessed
• Ventricular Cerebrospinal Fluid Monoamine Transmitter and Metabolite Concentrations Reflect Human Brain Neurochemistry in Autopsy Cases ↗

  Journal of Neurochemistry · 1990 · PMID 1968956
  not yet assessed
• Increased tau messenger RNA in Alzheimer's disease hippocampus. ↗

  PubMed · 1990 · PMID 2119143
  not yet assessed
• Links between passive smoking and disease: a best-evidence synthesis. A report of the Working Group on Passive Smoking. ↗

  PubMed · 1990 · PMID 2138069
  not yet assessed
• Antigens similar to major histocompatibility complex B-G are expressed in the intestinal epithelium in the chicken ↗

  Immunogenetics · 1990 · PMID 2373526
  not yet assessed
• Physical mapping around the Alzheimer disease locus on the proximal long arm of chromosome 21. ↗

  PubMed · 1990 · PMID 2301399
  not yet assessed
• Molecular Neurobiology ↗

  Trends in Neurosciences · 1990
  not yet assessed
• Glutamatergic neurotransmission in Alzheimer's disease ↗

  Biochemical Society Transactions · 1990 · PMID 2164981
  not yet assessed
• Genetics of Alzheimer's disease. ↗

  PubMed · 1990 · PMID 2403711
  not yet assessed
• Neurotransmitter Function in Post-Mortem Human Brain: An Overview ↗

  Neuropsychopharmacology · 1990
  not yet assessed
• PREDISPOSING LOCUS FOR ALZHEIMER'S DISEASE ON CHROMOSOME 21 ↗

  The Lancet · 1989 · PMID 2563508
  not yet assessed
• Uptake of γ-aminobutyric acid andl-glutamic acid by synaptosomes from postmortem human cerebral cortex: multiple sites, sodium dependence and effect of tissue preparation ↗

  Brain Research · 1989 · PMID 2569904
  not yet assessed
• Chapter 35 The role of nicotinic receptors in the pathophysiology ofAlzheimer's disease ↗

  Progress in brain research · 1989 · PMID 2685906
  not yet assessed
• Characterisation, Density, and Distribution of Kainate Receptors in Normal and Alzheimer's Diseased Human Brain ↗

  Journal of Neurochemistry · 1989 · PMID 2535708
  not yet assessed
• PRESENILE DEMENTIA ASSOCIATED WITH MOSAIC TRISOMY 21 IN A PATIENT WITH A DOWN SYNDROME CHILD ↗

  The Lancet · 1989 · PMID 2570989
  not yet assessed
• 1‐Methyl‐4‐Phenylpyridinium Uptake by Human and Rat Striatal Synaptosomes ↗

  Journal of Neurochemistry · 1989 · PMID 2783454
  not yet assessed
• Antibodies in Serum of Patients with Alzheimer's Disease Cause Immunolysis of Cholinergic Nerve Terminals from the Rat Cerebral Cortex ↗

  Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 1989 · PMID 2804815
  not yet assessed
• The Genetic Aetiology of Alzheimer's Disease ↗

  International Review of Psychiatry · 1989
  not yet assessed
• Amino acid neurotransmitter levels in gliomas and their relationship to the incidence of epilepsy ↗

  Neurological Research · 1988 · PMID 2902524
  not yet assessed
• Presynaptic and postsynaptic glutamatergic function in Alzheimer's disease ↗

  Neuroscience Letters · 1988 · PMID 2896322
  not yet assessed
• Regional distribution of pre- and postsynaptic glutamatergic function in Alzheimer's disease ↗

  Brain Research · 1988 · PMID 2900052
  not yet assessed
• Evidence for the presence of antibodies to cholinergic neurons in the serum of patients with Alzheimer's disease ↗

  Journal of Neurology · 1988 · PMID 3210051
  not yet assessed
• Blood brain barrier in ageing and Alzheimer's disease ↗

  Neurobiology of Aging · 1988 · PMID 3380253
  not yet assessed
• Change in nicotinic receptor subtypes in temporal cortex of Alzheimer brains ↗

  Neuroscience Letters · 1988 · PMID 3380323
  not yet assessed
• A Comparison of Methodologies for the Study of Functional Transmitter Neurochemistry in Human Brain ↗

  Journal of Neurochemistry · 1988 · PMID 2896227
  not yet assessed
• Characterisation of Na+‐Independent L‐[3H]Glutamate Binding Sites in Human Temporal Cortex ↗

  Journal of Neurochemistry · 1988 · PMID 2897429
  not yet assessed
• Dopamine and apomorphine do not modulate the uptake of [3H]D-aspartate in the rat striatum in-vitro ↗

  Journal of Pharmacy and Pharmacology · 1988 · PMID 2900322
  not yet assessed
• Alzheimer's disease. ↗

  PubMed · 1988 · PMID 3289659
  not yet assessed
• Autoimmunity to cholinergic‐specific antigens of the brain in senile dementia of the Alzheimer's type ↗

  Drug Development Research · 1988
  not yet assessed
• Region-specific loss of glutamate innervation in Alzheimer's disease ↗

  Neuroscience Letters · 1987 · PMID 2882446
  not yet assessed
• A disorder of cortical GABAergic innervation in Alzheimer's disease ↗

  Neuroscience Letters · 1987 · PMID 3822251
  not yet assessed
• Intra- and extra-dopamine-synaptosomal localization of monoamine oxidase in striatal homogenates from four species ↗

  Biochemical Pharmacology · 1987 · PMID 3632718
  not yet assessed
• Excitatory amino acid transmission ↗

  FEBS Letters · 1987
  not yet assessed
• Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families ↗

  Nature · 1987 · PMID 3306405
  not yet assessed
• Glutamate neurotoxicity and Alzheimer's disease ↗

  Trends in Neurosciences · 1987
  not yet assessed
• Oral administration of erythrocyte membrane antigen does not suppress anti-Rh(D) antibody responses in humans. ↗

  PubMed · 1987 · PMID 3113783
  not yet assessed
• Do tetrahydroaminoacridine (THA) and physostigmine restore acetylcholine release in Alzheimer brains via nicotinic receptors? ↗

  Journal of Neural Transmission · 1987 · PMID 3681290
  not yet assessed
• Advances in Gene Technology: Molecular biology of the endocrine system ↗

  FEBS Letters · 1987
  not yet assessed
• The regional distribution of dopamine and serotonin uptake and transmitter concentrations in the human brain ↗

  Neurochemistry International · 1987 · PMID 20501116
  not yet assessed
• LINKAGE STUDY BETWEEN THE AMYLOID GENE AND FAMILIAL ALZHEIMERS-DISEASE

  Cytogenetic and Genome Research · 1987
  not yet assessed
• An integrative hypothesis concerning the pathogenesis and progression of Alzheimer??s disease ↗

  Alzheimer Disease & Associated Disorders · 1987
  not yet assessed
• GLUTAMATE NEUROTOXICITY AND ALZHEIMERS-DISEASE

  UCL Discovery (University College London) · 1987
  not yet assessed
• An integrative hypothesis concerning the pathogenesis and progression of Alzheimer's disease ↗

  Neurobiology of Aging · 1986 · PMID 2882432
  not yet assessed
• Physostigmine restores3H-acetylcholine efflux from Alzheimer brain slices to normal level ↗

  Journal of Neural Transmission · 1986 · PMID 3806081
  not yet assessed
• Optimization of freezing, storage, and thawing conditions for the preparation of metabolically active synaptosomes from frozen rat and human brain ↗

  Neurochemical Pathology · 1986 · PMID 3561893
  not yet assessed
• Uptake of γ‐Aminobutyric Acid and Glycine by Synaptosomes from Postmortem Human Brain ↗

  Journal of Neurochemistry · 1986 · PMID 3734788
  not yet assessed
• Regional and Subcellular Distribution of Thy‐1 in Human Brain Assayed by a Solid‐Phase Radioimmunoassay ↗

  Journal of Neurochemistry · 1986 · PMID 2419494
  not yet assessed
• The patients dying after long terminal phase have acidotic brains; implications for biochemical measurements on autopsy tissue ↗

  Journal of Neural Transmission · 1985 · PMID 3989524
  not yet assessed
• Transmitter deficits in Alzheimer's disease ↗

  Neurochemistry International · 1985 · PMID 20492959
  not yet assessed
• The effects of hyperglycaemia on changes during reperfusion following focal cerebral ischaemia in the cat. ↗

  Journal of Neurology Neurosurgery & Psychiatry · 1985 · PMID 4031911
  not yet assessed
• Memory Function and Brain Biochemistry in Normal Aging and in Senile Dementia ↗

  Annals of the New York Academy of Sciences · 1985 · PMID 2861774
  not yet assessed
• Agonal status affects the metabolic activity of nerve endings isolated from postmortem human brain ↗

  Neurochemical Pathology · 1985 · PMID 4094727
  not yet assessed
• The uptake of serotonin and dopamine by homogenates of frozen rat and human brain tissue ↗

  Neurochemical Research · 1985 · PMID 4010874
  not yet assessed
• Catecholamine topochemistry in human basal ganglia. Comparison between normal and Alzheimer brains ↗

  Brain Research · 1985 · PMID 3995281
  not yet assessed
• The Corrosion of Mild Steel by Biogenic Sulfide Films Exposed to Air ↗

  CORROSION · 1984
  not yet assessed
• Serotonin concentrations in normal aging human brains: Relation to serotonin receptors ↗

  Neurobiology of Aging · 1984 · PMID 6083463
  not yet assessed
• Intralaminar Neurochemical Distributions in Human Midtemporal Cortex: Comparison Between Alzheimer's Disease and the Normal ↗

  Journal of Neurochemistry · 1984 · PMID 6142924
  not yet assessed
• Amino acid transport by synaptosomes isolated from post mortem human brain ↗

  Journal of Neural Transmission · 1984 · PMID 6148379
  not yet assessed
• Utilisation of Cathodic Hydrogen by Sulphate-Reducing Bacteria ↗

  British Corrosion Journal · 1983
  not yet assessed
• Metabolically Active Synaptosomes Can Be Prepared from Frozen Rat and Human Brain ↗

  Journal of Neurochemistry · 1983 · PMID 6827264
  not yet assessed
• Metabolic and functional studies on post-mortem human brain ↗

  Neurochemistry International · 1983 · PMID 20487948
  not yet assessed
• The Cortical Ischaemic Penumbra Associated with Occlusion of the Middle Cerebral Artery in the Cat: 2. Studies of Histopathology, Water Content, and in vitro Neurotransmitter Uptake ↗

  Journal of Cerebral Blood Flow & Metabolism · 1983 · PMID 6130100
  not yet assessed
• A radiorespirometric method for evaluating inhibitors of sulphate-reducing bacteria ↗

  Applied Microbiology and Biotechnology · 1983
  not yet assessed
• Pathway of inactivation of cholecystokinin octapeptide (CCK-8) by synaptosomal fractions ↗

  Neurochemistry International · 1983 · PMID 20487993
  not yet assessed
• Use of post-mortem human synaptosomes for studies of metabolism and transmitter amino acid release ↗

  Neuroscience Letters · 1982 · PMID 6131398
  not yet assessed
• A rapid method for preparing synaptosomes: Comparison, with alternative procedures ↗

  Brain Research · 1981 · PMID 7296283
  not yet assessed
• The oxygen tolerance of sulfate-reducing bacteria isolated from North Sea waters ↗

  Current Microbiology · 1981
  not yet assessed
• Synaptosomes prepared from fresh human cerebral cortex; morphology, respiration and release of transmitter amino acids ↗

  Brain Research · 1981 · PMID 6116530
  not yet assessed
• The Enumeration, Isolation and Characterization of Sulphate‐reducing Bacteria from North Sea Waters ↗

  Journal of Applied Bacteriology · 1981
  not yet assessed
• Degradation of luteinizing hormone-releasing hormone by serum and plasma in vitro ↗

  Regulatory Peptides · 1981 · PMID 6789408
  not yet assessed
• Rapid Preparation of Nerve Ending Particles (synaptosomes) From Rat-Brain - Comparison with 2 Standard Methods

  Journal of Anatomy · 1981
  not yet assessed
• The Determination and Distribution of 2‐Phenylethylamine in Sheep Brain ↗

  Journal of Neurochemistry · 1980 · PMID 7373300
  not yet assessed
• Metabolic and secretory processes in nerve-endings isolated from post-mortem brain ↗

  Neuroscience Letters · 1979 · PMID 431889
  not yet assessed
• Slit-scan flow system for automated cytopathology. ↗

  PubMed · 1975 · PMID 46661
  not yet assessed
• Semiology Of Tremors ↗

  Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 1975 · PMID 1097080
  not yet assessed
• X-linked cataract: two pedigrees. ↗

  PubMed · 1971 · PMID 4375503
  not yet assessed
• A Disorder of Tryptophan Metabolism in Chronic Granulomatous Disease ↗

  Archives of Disease in Childhood · 1970 · PMID 4248383
  not yet assessed