Andres Metspalu

The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.

Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.

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 (3)

• Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets.
  2023 L1 93/100
• Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome.
  2021 L1 100/100
• Cell Specific eQTL Analysis without Sorting Cells.
  2015 L1 90/100

3 assessed by us (3 reproduced) · 826 not yet assessed — every PubMed paper on record, linked below.

• Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. ↗

  Archive ouverte UNIGE (University of Geneva) · 2026
  not yet assessed
• Genetic influences on educational outcomes during and after the Soviet era: Revisiting evidence from Estonia ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2026
  not yet assessed
• Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction ↗

  Nature Genetics · 2026 · PMID 42009823
  not yet assessed
• An AI-Health Infrastructure for the Nordic Region: Technical Foundations, Data Assets, and a Roadmap for Deployment ↗

  SSRN Electronic Journal · 2026
  not yet assessed
• Psychiatric genetic liability is associated with the severity of COVID-19 and other acute respiratory infections: an observational study across five Northern European countries ↗

  Genome Medicine · 2026
  not yet assessed
• Publisher Correction: Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction ↗

  Nature Genetics · 2026 · PMID 42225866
  not yet assessed
• GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets ↗

  Nature Communications · 2025 · PMID 40021644
  not yet assessed
• The Estonian Biobank’s journey from biobanking to personalized medicine ↗

  Nature Communications · 2025 · PMID 40188112
  not yet assessed
• Polygenic prediction of body mass index and obesity through the life course and across ancestries ↗

  Nature Medicine · 2025 · PMID 40691366
  not yet assessed
• Atlas of genetic and phenotypic associations across 42 female reproductive health diagnoses ↗

  Nature Medicine · 2025 · PMID 40069456
  not yet assessed
• A hidden confounder for microbiome studies: medications used years before sample collection ↗

  mSystems · 2025 · PMID 40910778
  not yet assessed
• Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database ↗

  Nature Communications · 2025 · PMID 41173899
  not yet assessed
• A large-scale genome-wide association study on female genital tract polyps highlights role of DNA repair, cell proliferation, and cell growth ↗

  Human Reproduction · 2025 · PMID 39986329
  not yet assessed
• A scoping review of the assessment reports of genetic or genomic tests reveals inconsistent consideration of key dimensions of clinical utility ↗

  Journal of Clinical Epidemiology · 2025 · PMID 39986491
  not yet assessed
• Polygenic Risk Score Combined with Transcranial Sonography Refines Parkinson's Disease Risk Prediction ↗

  Movement Disorders Clinical Practice · 2025 · PMID 40019135
  not yet assessed
• Characterization of prevalent genetic variants in the Estonian Biobank body-mass index GWAS ↗

  Nature Communications · 2025 · PMID 41062462
  not yet assessed
• Genome-wide association study and polygenic risk prediction of hypothyroidism ↗

  Nature Genetics · 2025 · PMID 41238958
  not yet assessed
• Cohort Profiles: Personality Measurements at the Estonian Biobank of the Estonian Genome Center, University of Tartu ↗

  2025
  not yet assessed
• Genome-wide Association Study Identifies <i>SORCS3</i> as a Novel Susceptibility Locus for Panic Disorder in the FinnGen Study ↗

  medRxiv · 2025
  not yet assessed
• Cohort Profiles: Personality Measurements at the Estonian Biobank of the Estonian Genome Center, University of Tartu ↗

  2025
  not yet assessed
• Leveraging transdiagnostic genetic liability to psychiatric disorders to dissect clinical outcomes of anorexia nervosa ↗

  Molecular Psychiatry · 2025 · PMID 40983652
  not yet assessed
• Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. ↗

  UNC Libraries · 2025
  not yet assessed
• Genetic diversity fuels gene discovery for tobacco and alcohol use ↗

  UNC Libraries · 2025
  not yet assessed
• Genome-wide association study identifies ABCG1 as a susceptibility locus for tick-borne encephalitis ↗

  iScience · 2025 · PMID 41377660
  not yet assessed
• Genetic drivers of heterogeneity in type 2 diabetes pathophysiology ↗

  Nature · 2024 · PMID 38374256
  not yet assessed
• Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits ↗

  Nature Genetics · 2024 · PMID 38689001
  not yet assessed
• Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes ↗

  Nature Genetics · 2024 · PMID 38182742
  not yet assessed
• Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction ↗

  Nature Genetics · 2024 · PMID 38839884
  not yet assessed
• Rare copy-number variants as modulators of common disease susceptibility ↗

  Genome Medicine · 2024 · PMID 38185688
  not yet assessed
• Genetic drivers and cellular selection of female mosaic X chromosome loss ↗

  Nature · 2024 · PMID 38867047
  not yet assessed
• Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry ↗

  BMC Genomics · 2024 · PMID 38408933
  not yet assessed
• Cohort Profile Update: Mental Health Online Survey in the Estonian Biobank (EstBB MHoS) ↗

  International Journal of Epidemiology · 2024 · PMID 38381979
  not yet assessed
• Markers of imminent myocardial infarction ↗

  Nature Cardiovascular Research · 2024 · PMID 39196201
  not yet assessed
• Socio-demographic and genetic risk factors for drug adherence and persistence across 5 common medication classes ↗

  Nature Communications · 2024 · PMID 39443518
  not yet assessed
• Shared Genetic Architecture Between Schizophrenia and Anorexia Nervosa: A Cross-trait Genome-Wide Analysis ↗

  Schizophrenia Bulletin · 2024 · PMID 38848516
  not yet assessed
• Genetic architecture reconciles linkage and association studies of complex traits ↗

  Nature Genetics · 2024 · PMID 39375568
  not yet assessed
• The PROPHET project paves the way for personalized prevention in the future healthcare ↗

  European Journal of Cancer Prevention · 2024 · PMID 38598497
  not yet assessed
• Genetic determinants of plasma protein levels in the Estonian population ↗

  Scientific Reports · 2024 · PMID 38565889
  not yet assessed
• Comorbidities confound metabolomics studies of human disease ↗

  Scientific Reports · 2024 · PMID 39438584
  not yet assessed
• Metadata for Data dIscoverability aNd Study rEplicability in obseRVAtional Studies (MINERVA): Development and Pilot of a Metadata List and Catalogue in Europe ↗

  Pharmacoepidemiology and Drug Safety · 2024 · PMID 39145406
  not yet assessed
• Distinct Genetic Risk Profile in Aortic Stenosis Compared With Coronary Artery Disease ↗

  JAMA Cardiology · 2024 · PMID 39504041
  not yet assessed
• Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure ↗

  Kidney International Reports · 2024 · PMID 38899223
  not yet assessed
• Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression ↗

  UNC Libraries · 2024
  not yet assessed
• Metadata for Data dIscoverability aNd Study rEplicability in obseRVAtional Studies (MINERVA): Lessons Learnt From the MINERVA Project in Europe ↗

  Pharmacoepidemiology and Drug Safety · 2024 · PMID 39145403
  not yet assessed
• Author Correction: A genomic mutational constraint map using variation in 76,156 human genomes ↗

  Nature · 2024 · PMID 38225470
  not yet assessed
• Family-GWAS reveals effects of environment and mating on genetic associations ↗

  medRxiv · 2024 · PMID 41282763
  not yet assessed
• From Biobanking to Personalized Medicine: the journey of the Estonian Biobank ↗

  medRxiv · 2024
  not yet assessed
• Cohort Profiles: Personality Measurements at the Estonian Biobank of the Estonian Genome Center, University of Tartu ↗

  2024
  not yet assessed
• Cohort Profiles: Personality Measurements at the Estonian Biobank of the Estonian Genome Center, University of Tartu ↗

  2024
  not yet assessed
• Genome-wide association study and polygenic risk prediction of hypothyroidism ↗

  Research Square · 2024
  not yet assessed
• A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure ↗

  UNC Libraries · 2024
  not yet assessed
• Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration ↗

  UNC Libraries · 2024
  not yet assessed
• Roadmap for a precision-medicine initiative in the Nordic region ↗

  UNC Libraries · 2024
  not yet assessed
• Author Correction: Genetic drivers and cellular selection of female mosaic X chromosome loss ↗

  Nature · 2024 · PMID 39627447
  not yet assessed
• Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation ↗

  MDC Repository (Max-Delbrueck-Center for Molecular Medicine) · 2024
  not yet assessed
• FinnGen provides genetic insights from a well-phenotyped isolated population ↗

  Nature · 2023 · PMID 36653562
  not yet assessed
• A genomic mutational constraint map using variation in 76,156 human genomes ↗

  Nature · 2023 · PMID 38057664
  not yet assessed
• Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets

  Nature Immunology · 2023 · PMID 37563310
  L1 93/100
• European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation ↗

  Nature Communications · 2023 · PMID 37794016
  not yet assessed
• Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy ↗

  JAMA Cardiology · 2023 · PMID 37285119
  not yet assessed
• Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus ↗

  Nature Human Behaviour · 2023 · PMID 36864135
  not yet assessed
• Genome-wide association study of obstructive sleep apnoea in the Million Veteran Program uncovers genetic heterogeneity by sex ↗

  EBioMedicine · 2023 · PMID 36989840
  not yet assessed
• Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions ↗

  Cell Genomics · 2023 · PMID 37601975
  not yet assessed
• Nationwide health, socio-economic and genetic predictors of COVID-19 vaccination status in Finland ↗

  Nature Human Behaviour · 2023 · PMID 37081098
  not yet assessed
• Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris ↗

  European Journal of Human Genetics · 2023 · PMID 36922633
  not yet assessed
• Inferring compound heterozygosity from large-scale exome sequencing data ↗

  Nature Genetics · 2023 · PMID 38057443
  not yet assessed
• Dissecting the genetic heterogeneity of gastric cancer ↗

  EBioMedicine · 2023 · PMID 37209533
  not yet assessed
• HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases ↗

  Communications Biology · 2023 · PMID 37923823
  not yet assessed
• Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity ↗

  Stroke · 2023 · PMID 36655558
  not yet assessed
• Polygenic risk prediction: why and when out-of-sample prediction R2 can exceed SNP-based heritability ↗

  The American Journal of Human Genetics · 2023 · PMID 37379836
  not yet assessed
• Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH ↗

  Diabetologia · 2023 · PMID 37233759
  not yet assessed
• Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure ↗

  Nature Communications · 2023 · PMID 36653343
  not yet assessed
• Rare variant analyses across multiethnic cohorts identify novel genes for refractive error ↗

  Communications Biology · 2023 · PMID 36596879
  not yet assessed
• Transcriptome analysis reveals involvement of thiopurine S-methyltransferase in oxidation-reduction processes ↗

  European Journal of Pharmaceutical Sciences · 2023 · PMID 37865284
  not yet assessed
• 1725P Genetic counselling for cancer in EU member states: Review and foundation for consensus recommendations ↗

  Annals of Oncology · 2023
  not yet assessed
• Polygenic risk scores for cervical HPV infection, neoplasia and cancer show potential for personalised screening: comparison of two methods ↗

  Infectious Agents and Cancer · 2023 · PMID 38057845
  not yet assessed
• Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population ↗

  Nature · 2023 · PMID 36829046
  not yet assessed
• Author Correction: Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets ↗

  Nature Immunology · 2023 · PMID 37679551
  not yet assessed
• Multi-ancestry genome-wide study in &gt;2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications ↗

  medRxiv · 2023 · PMID 37034649
  not yet assessed
• Correction: Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris ↗

  European Journal of Human Genetics · 2023 · PMID 37076744
  not yet assessed
• HLA allele-calling using whole-exome sequencing identifies 129 novel associations in 11 autoimmune diseases: a multi-ancestry analysis in the UK Biobank ↗

  medRxiv · 2023
  not yet assessed
• Corrigendum to “Dissecting the genetic heterogeneity of gastric cancer” ↗

  EBioMedicine · 2023 · PMID 37480624
  not yet assessed
• Mechanistic endotyping of the ROS/cGMP disease cluster in the Estonian Biobank ↗

  2023
  not yet assessed
• Author response for "Genetic susceptibility to temporomandibular joint involvement in juvenile idiopathic arthritis" ↗

  2023
  not yet assessed
• Mapping genomic loci implicates genes and synaptic biology in schizophrenia ↗

  Nature · 2022 · PMID 35396580
  not yet assessed
• A saturated map of common genetic variants associated with human height ↗

  Nature · 2022 · PMID 36224396
  not yet assessed
• Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation ↗

  Nature Genetics · 2022 · PMID 35551307
  not yet assessed
• Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals ↗

  Nature Genetics · 2022 · PMID 35361970
  not yet assessed
• Genetic diversity fuels gene discovery for tobacco and alcohol use ↗

  Nature · 2022 · PMID 36477530
  not yet assessed
• A cross-disorder dosage sensitivity map of the human genome ↗

  Cell · 2022 · PMID 35917817
  not yet assessed
• Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention ↗

  Nature Genetics · 2022 · PMID 36071172
  not yet assessed
• Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia ↗

  JAMA Psychiatry · 2022 · PMID 35019943
  not yet assessed
• The individual and global impact of copy-number variants on complex human traits ↗

  The American Journal of Human Genetics · 2022 · PMID 35240056
  not yet assessed
• Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss ↗

  The American Journal of Human Genetics · 2022 · PMID 35580588
  not yet assessed
• Gut metagenome associations with extensive digital health data in a volunteer-based Estonian microbiome cohort ↗

  Nature Communications · 2022 · PMID 35169130
  not yet assessed
• Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study ↗

  Cell Reports Medicine · 2022 · PMID 36260985
  not yet assessed
• Effectiveness and feasibility of cardiovascular disease personalized prevention on high polygenic risk score subjects: a randomized controlled pilot study ↗

  European Heart Journal Open · 2022 · PMID 36600884
  not yet assessed
• Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals ↗

  Communications Biology · 2022 · PMID 35697829
  not yet assessed
• Elucidating the relationship between migraine risk and brain structure using genetic data ↗

  Brain · 2022 · PMID 35735024
  not yet assessed
• Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse ↗

  Nature Communications · 2022 · PMID 35739095
  not yet assessed
• Impact of the pre-examination phase on multicenter metabolomic studies ↗

  New Biotechnology · 2022 · PMID 35066155
  not yet assessed
• ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma ↗

  Communications Biology · 2022 · PMID 36192519
  not yet assessed
• Neandertal introgression partitions the genetic landscape of neuropsychiatric disorders and associated behavioral phenotypes ↗

  Translational Psychiatry · 2022 · PMID 36198681
  not yet assessed
• Prioritizing autoimmunity risk variants for functional analyses by fine-mapping mutations under natural selection ↗

  Nature Communications · 2022 · PMID 36400766
  not yet assessed
• Endometriosis and irritable bowel syndrome: similarities and differences in the spectrum of comorbidities ↗

  Human Reproduction · 2022 · PMID 35713579
  not yet assessed
• Genetic and modifiable risk factors combine multiplicatively in common disease ↗

  Clinical Research in Cardiology · 2022 · PMID 35987817
  not yet assessed
• Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome ↗

  Molecular Psychiatry · 2022 · PMID 35768638
  not yet assessed
• Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis ↗

  Communications Biology · 2022 · PMID 35978133
  not yet assessed
• Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank ↗

  European Journal of Human Genetics · 2022 · PMID 36192438
  not yet assessed
• Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical Setting ↗

  Frontiers in Genetics · 2022 · PMID 35938029
  not yet assessed
• Long-range regulatory effects of Neandertal DNA in modern humans ↗

  Genetics · 2022 · PMID 36560850
  not yet assessed
• Spectrum and frequency of CHEK2 variants in breast cancer affected and general population in the Baltic states region, initial results and literature review ↗

  European Journal of Medical Genetics · 2022 · PMID 35314380
  not yet assessed
• Do Biobank Recall Studies Matter? Long-Term Follow-Up of Research Participants With Familial Hypercholesterolemia ↗

  Frontiers in Genetics · 2022 · PMID 35928446
  not yet assessed
• Global priorities for large-scale biomarker-based prospective cohorts ↗

  Cell Genomics · 2022 · PMID 36778137
  not yet assessed
• FinnGen: Unique genetic insights from combining isolated population and national health register data ↗

  medRxiv · 2022
  not yet assessed
• A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2022
  not yet assessed
• Genome-wide analysis in over 1 million individuals reveals over 2,000 independent genetic signals for blood pressure ↗

  Research Square · 2022
  not yet assessed
• Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries ↗

  Nature · 2022 · PMID 36376532
  not yet assessed
• European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation ↗

  medRxiv · 2022
  not yet assessed
• GENOME-WIDE ANALYSIS IDENTIFIES SORCS3 AS A NOVEL SUSCEPTIBILITY LOCUS FOR PANIC DISORDER IN THE FINNGEN STUDY ↗

  European Neuropsychopharmacology · 2022
  not yet assessed
• Editorial: Can population health be personalized? Estonia and Finland as examples ↗

  Frontiers in Genetics · 2022 · PMID 36353106
  not yet assessed
• Genome-wide analysis identifies SORCS3 as a novel susceptibility locus for panic disorder in the FinnGen study ↗

  Neuroscience Applied · 2022
  not yet assessed
• Mapping the human genetic architecture of COVID-19 ↗

  Nature · 2021 · PMID 34237774
  not yet assessed
• The trans-ancestral genomic architecture of glycemic traits ↗

  Nature Genetics · 2021 · PMID 34059833
  not yet assessed
• Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation ↗

  Nature Genetics · 2021 · PMID 34493871
  not yet assessed
• Genetic insights into biological mechanisms governing human ovarian ageing ↗

  Nature · 2021 · PMID 34349265
  not yet assessed
• A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts ↗

  Biological Psychiatry · 2021 · PMID 34304866
  not yet assessed
• The Genetic Architecture of Depression in Individuals of East Asian Ancestry ↗

  JAMA Psychiatry · 2021 · PMID 34586374
  not yet assessed
• A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response ↗

  Nature Genetics · 2021 · PMID 34611364
  not yet assessed
• Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability ↗

  Nature Communications · 2021 · PMID 33402679
  not yet assessed
• Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour ↗

  Nature Human Behaviour · 2021 · PMID 34211149
  not yet assessed
• Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome

  Nature Communications · 2021 · PMID 34561431
  L1 100/100
• Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders ↗

  Biological Psychiatry · 2021 · PMID 34099189
  not yet assessed
• Identifying the Common Genetic Basis of Antidepressant Response ↗

  Biological Psychiatry Global Open Science · 2021 · PMID 35712048
  not yet assessed
• The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects ↗

  The American Journal of Human Genetics · 2021 · PMID 33740458
  not yet assessed
• Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans ↗

  Nature · 2021 · PMID 34373650
  not yet assessed
• SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues ↗

  Cell Reports · 2021 · PMID 34762851
  not yet assessed
• Genome-wide association study identifies five risk loci for pernicious anemia ↗

  Nature Communications · 2021 · PMID 34145262
  not yet assessed
• The blood metabolome of incident kidney cancer: A case–control study nested within the MetKid consortium ↗

  PLoS Medicine · 2021 · PMID 34543281
  not yet assessed
• Phantom epistasis between unlinked loci ↗

  Nature · 2021 · PMID 34381229
  not yet assessed
• <i>Cis</i>-epistasis at the <i>LPA</i> locus and risk of cardiovascular diseases ↗

  Cardiovascular Research · 2021 · PMID 33878186
  not yet assessed
• Stratification of Type 2 Diabetes by Age of Diagnosis in the UK Biobank Reveals Subgroup-Specific Genetic Associations and Causal Risk Profiles ↗

  Diabetes · 2021 · PMID 33972266
  not yet assessed
• Metabolomic Fingerprints in Large Population Cohorts: Impact of Preanalytical Heterogeneity ↗

  Clinical Chemistry · 2021 · PMID 34223627
  not yet assessed
• Mendelian Randomization Identifies the Potential Causal Impact of Dietary Patterns on Circulating Blood Metabolites ↗

  Frontiers in Genetics · 2021 · PMID 34790224
  not yet assessed
• Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure ↗

  Molecular Psychiatry · 2021 · PMID 33859359
  not yet assessed
• Advances in Genomic Discovery and Implications for Personalized Prevention and Medicine: Estonia as Example ↗

  Journal of Personalized Medicine · 2021 · PMID 33946982
  not yet assessed
• Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients ↗

  Clinical Rheumatology · 2021 · PMID 34101054
  not yet assessed
• Genetic insights into the biological mechanisms governing human ovarian ageing ↗

  medRxiv · 2021
  not yet assessed
• Genome-wide association study identifies new locus associated with OCD ↗

  medRxiv · 2021
  not yet assessed
• Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability ↗

  Nature Communications · 2021 · PMID 33558525
  not yet assessed
• Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response ↗

  Nature Genetics · 2021 · PMID 34728834
  not yet assessed
• Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes ↗

  Nature Communications · 2021 · PMID 33531481
  not yet assessed
• Retraction Note: Detection and replication of epistasis influencing transcription in humans ↗

  Nature · 2021 · PMID 34381240
  not yet assessed
• Physical activity and sedentary behavior; mechanistic insights and role in disease prevention ↗

  Research Square · 2021
  not yet assessed
• Author Correction: Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals ↗

  Nature Communications · 2021 · PMID 33531501
  not yet assessed
• The trans-ancestral genomic architecture of glycemic traits. ↗

  UCL Discovery (University College London) · 2021
  not yet assessed
• Publisher Correction: Identification of 371 genetic variants for age at first sex and birth linked to externalising behavior ↗

  Nature Human Behaviour · 2021 · PMID 34321615
  not yet assessed
• Metabolomic Fingerprints in Large Population Cohorts: Impact of Preanalytical Heterogeneity

  STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021
  not yet assessed
• Rare variant analyses across multiethnic cohorts identify novel genes for refractive error ↗

  Research Square · 2021
  not yet assessed
• Gut metagenome associations with extensive digital health data in a volunteer-based Estonian microbiome cohort ↗

  Research Square · 2021
  not yet assessed
• The mutational constraint spectrum quantified from variation in 141,456 humans ↗

  Nature · 2020 · PMID 32461654
  not yet assessed
• A structural variation reference for medical and population genetics ↗

  Nature · 2020 · PMID 32461652
  not yet assessed
• Personalized early detection and prevention of breast cancer: ENVISION consensus statement ↗

  Nature Reviews Clinical Oncology · 2020 · PMID 32555420
  not yet assessed
• Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease ↗

  Nature Genetics · 2020 · PMID 32341526
  not yet assessed
• Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank ↗

  Molecular Psychiatry · 2020 · PMID 31969693
  not yet assessed
• Transcript expression-aware annotation improves rare variant interpretation ↗

  Nature · 2020 · PMID 32461655
  not yet assessed
• Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals ↗

  Nature Communications · 2020 · PMID 32461616
  not yet assessed
• Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length ↗

  The American Journal of Human Genetics · 2020 · PMID 32109421
  not yet assessed
• Genome-wide association study identifies 48 common genetic variants associated with handedness ↗

  Nature Human Behaviour · 2020 · PMID 32989287
  not yet assessed
• Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes ↗

  Nature Communications · 2020 · PMID 32461613
  not yet assessed
• A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank ↗

  Nature Communications · 2020 · PMID 32385265
  not yet assessed
• The genetic architecture of sporadic and multiple consecutive miscarriage ↗

  Nature Communications · 2020 · PMID 33239672
  not yet assessed
• The effect of LRRK2 loss-of-function variants in humans ↗

  Nature Medicine · 2020 · PMID 32461697
  not yet assessed
• Identification of ALK in Thinness ↗

  Cell · 2020 · PMID 32442405
  not yet assessed
• Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache ↗

  International Journal of Epidemiology · 2020 · PMID 32306029
  not yet assessed
• Differences in local population history at the finest level: the case of the Estonian population ↗

  European Journal of Human Genetics · 2020 · PMID 32712624
  not yet assessed
• A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine ↗

  Nature Communications · 2020 · PMID 32632093
  not yet assessed
• Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies ↗

  Addiction Biology · 2020 · PMID 32064741
  not yet assessed
• Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy ↗

  The American Journal of Human Genetics · 2020 · PMID 32888428
  not yet assessed
• An epigenome-wide association study of metabolic syndrome and its components ↗

  Scientific Reports · 2020 · PMID 33239708
  not yet assessed
• Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants ↗

  European Journal of Human Genetics · 2020 · PMID 33230308
  not yet assessed
• Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error ↗

  Communications Biology · 2020 · PMID 32193507
  not yet assessed
• Development and validation of two SCORE-based cardiovascular risk prediction models for Eastern Europe: a multicohort study ↗

  European Heart Journal · 2020 · PMID 33011775
  not yet assessed
• Integrating untargeted metabolomics, genetically informed causal inference, and pathway enrichment to define the obesity metabolome ↗

  International Journal of Obesity · 2020 · PMID 32467615
  not yet assessed
• Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci ↗

  Molecular Psychiatry · 2020 · PMID 32372009
  not yet assessed
• Propelling Healthcare with Advanced Therapy Medicinal Products: A Policy Discussion ↗

  Biomedicine Hub · 2020 · PMID 33987187
  not yet assessed
• Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus ↗

  Circulation Genomic and Precision Medicine · 2020 · PMID 33321069
  not yet assessed
• A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape ↗

  UNC Libraries · 2020
  not yet assessed
• Genetic Predisposition to Coronary Artery Disease in Type 2 diabetes

  2020
  not yet assessed
• Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects ↗

  UNC Libraries · 2020
  not yet assessed
• Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent ↗

  UNC Libraries · 2020
  not yet assessed
• The genetic architecture of type 2 diabetes ↗

  UNC Libraries · 2020
  not yet assessed
• Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus ↗

  EUR Research Repository (Erasmus University Rotterdam) · 2020
  not yet assessed
• Genomic and phenomic insights from an atlas of genetic effects on DNA methylation ↗

  medRxiv · 2020
  not yet assessed
• Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation ↗

  medRxiv · 2020
  not yet assessed
• Publisher Correction: Personalized early detection and prevention of breast cancer: ENVISION consensus statement ↗

  Nature Reviews Clinical Oncology · 2020 · PMID 32601456
  not yet assessed
• A high-resolution HLA reference panel capturing global population diversity enables multi-ethnic fine-mapping in HIV host response ↗

  medRxiv · 2020
  not yet assessed
• The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2020
  not yet assessed
• The Trans-Ancestral Genomic Architecture of Glycaemic Traits ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2020
  not yet assessed
• Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome ↗

  medRxiv · 2020
  not yet assessed
• Genome-wide Screen of Otosclerosis in Population Biobanks: 18 Loci and Shared Heritability with Skeletal Structure ↗

  medRxiv · 2020
  not yet assessed
• Genome-wide study identifies association between HLA-B*55:01 and penicillin allergy ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2020
  not yet assessed
• Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2020
  not yet assessed
• Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank ↗

  Molecular Psychiatry · 2020 · PMID 32424234
  not yet assessed
• Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants ↗

  medRxiv · 2020
  not yet assessed
• Mendelian randomization identifies the potential causal impact of dietary patterns on circulating blood metabolites ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2020
  not yet assessed
• COVID-19 and Beyond: A Call for Action and Audacious Solidarity to All the Citizens and Nations, It Is Humanity’s Fight ↗

  SSRN Electronic Journal · 2020
  not yet assessed
• Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries ↗

  Nature Communications · 2020
  not yet assessed
• Post-GWAS analysis of six substance use traits improves the identification and functional interpretation of genetic risk loci

  2020
  not yet assessed
• Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length. ↗

  QUT ePrints (Queensland University of Technology) · 2020
  not yet assessed
• Abstract A06: Associations of prediagnostic metabolomic profiles with colorectal cancer risk—a collaborative reanalysis within the COnsortium of METabolomic Studies (COMETS) ↗

  Cancer Epidemiology Biomarkers & Prevention · 2020
  not yet assessed
• Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis ↗

  UNC Libraries · 2020
  not yet assessed
• The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals ↗

  UNC Libraries · 2020
  not yet assessed
• Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals ↗

  UNC Libraries · 2020
  not yet assessed
• Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits ↗

  UNC Libraries · 2020
  not yet assessed
• Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults ↗

  UNC Libraries · 2020
  not yet assessed
• Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases ↗

  UNC Libraries · 2020
  not yet assessed
• Ultra-rare disruptive and damaging mutations influence educational attainment in the general population ↗

  UNC Libraries · 2020
  not yet assessed
• An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans ↗

  UNC Libraries · 2020
  not yet assessed
• No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study ↗

  2020
  not yet assessed
• Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits ↗

  Digital Commons@Becker (Washington University School of Medicine) · 2020
  not yet assessed
• Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ↗

  UNC Libraries · 2020
  not yet assessed
• Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity ↗

  UNC Libraries · 2020
  not yet assessed
• Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk ↗

  UNC Libraries · 2020
  not yet assessed
• Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions ↗

  UNC Libraries · 2020
  not yet assessed
• Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept ↗

  UNC Libraries · 2020
  not yet assessed
• An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype ↗

  UNC Libraries · 2020
  not yet assessed
• Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use ↗

  Nature Genetics · 2019 · PMID 30643251
  not yet assessed
• Genome-wide association study identifies 30 loci associated with bipolar disorder ↗

  Nature Genetics · 2019 · PMID 31043756
  not yet assessed
• Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders ↗

  Cell · 2019 · PMID 31835028
  not yet assessed
• Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa ↗

  Nature Genetics · 2019 · PMID 31308545
  not yet assessed
• A catalog of genetic loci associated with kidney function from analyses of a million individuals ↗

  Nature Genetics · 2019 · PMID 31152163
  not yet assessed
• Improved polygenic prediction by Bayesian multiple regression on summary statistics ↗

  Nature Communications · 2019 · PMID 31704910
  not yet assessed
• Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels ↗

  Nature Genetics · 2019 · PMID 31578528
  not yet assessed
• A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individuals ↗

  Nature Communications · 2019 · PMID 31431621
  not yet assessed
• Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances ↗

  eLife · 2019 · PMID 30642433
  not yet assessed
• Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection ↗

  Journal of the American College of Cardiology · 2019 · PMID 30621952
  not yet assessed
• Associations of autozygosity with a broad range of human phenotypes ↗

  Nature Communications · 2019 · PMID 31673082
  not yet assessed
• Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids ↗

  Nature Genetics · 2019 · PMID 30926973
  not yet assessed
• Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression ↗

  Molecular Psychiatry · 2019 · PMID 31712720
  not yet assessed
• Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns ↗

  Nature Communications · 2019 · PMID 31186427
  not yet assessed
• Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci ↗

  Molecular Psychiatry · 2019 · PMID 30617275
  not yet assessed
• Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions ↗

  American Journal of Epidemiology · 2019 · PMID 30698716
  not yet assessed
• Leveraging European infrastructures to access 1 million human genomes by 2022 ↗

  Nature Reviews Genetics · 2019 · PMID 31455890
  not yet assessed
• Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration ↗

  Nature Communications · 2019 · PMID 31719535
  not yet assessed
• The effect of X-linked dosage compensation on complex trait variation ↗

  Nature Communications · 2019 · PMID 31285442
  not yet assessed
• Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches ↗

  Biological Psychiatry · 2019 · PMID 31301758
  not yet assessed
• Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification ↗

  BMC Cancer · 2019 · PMID 31182048
  not yet assessed
• A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure ↗

  Human Molecular Genetics · 2019 · PMID 31127295
  not yet assessed
• Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders ↗

  Molecular Psychiatry · 2019 · PMID 31712721
  not yet assessed
• Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression ↗

  Biological Psychiatry · 2019 · PMID 31570195
  not yet assessed
• Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation ↗

  Genetics · 2019 · PMID 31123039
  not yet assessed
• Manhattan Harvester and Cropper: a system for GWAS peak detection ↗

  BMC Bioinformatics · 2019 · PMID 30634901
  not yet assessed
• Manifesto for an international digital mental health network ↗

  Digital Psychiatry · 2019
  not yet assessed
• Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events ↗

  Circulation Genomic and Precision Medicine · 2019 · PMID 30897348
  not yet assessed
• Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics ↗

  Endocrinology · 2019 · PMID 31125048
  not yet assessed
• Roadmap for a precision-medicine initiative in the Nordic region ↗

  Nature Genetics · 2019 · PMID 30988515
  not yet assessed
• Subsequent Event Risk in Individuals With Established Coronary Heart Disease ↗

  Circulation Genomic and Precision Medicine · 2019 · PMID 30896328
  not yet assessed
• PAIRUP-MS: Pathway analysis and imputation to relate unknowns in profiles from mass spectrometry-based metabolite data ↗

  PLoS Computational Biology · 2019 · PMID 30640898
  not yet assessed
• Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium ↗

  Scientific Reports · 2019 · PMID 31406173
  not yet assessed
• Genome-Wide Association Scan of Serum Urea in European Populations Identifies Two Novel Loci ↗

  American Journal of Nephrology · 2019 · PMID 30808845
  not yet assessed
• Estimating the performance of three cardiovascular disease risk scores: the Estonian Biobank cohort study ↗

  Journal of Epidemiology & Community Health · 2019 · PMID 30635435
  not yet assessed
• Improved polygenic prediction by Bayesian multiple regression on summary statistics ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Genome-wide association study identifies 48 common genetic variants associated with handedness ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Advantages of genotype imputation with ethnically matched reference panel for rare variant association analyses ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Characterising the loss-of-function impact of 5’ untranslated region variants in whole genome sequence data from 15,708 individuals ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Search for early pancreatic cancer blood biomarkers in five European prospective population biobanks using metabolomics ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• The genetic architecture of sporadic and recurrent miscarriage ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Integrating untargeted metabolomics, genetically informed causal inference, and pathway enrichment to define the obesity metabolome ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. ↗

  Archive ouverte UNIGE (University of Geneva) · 2019
  not yet assessed
• Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies (vol 14, pg 707, 2018)

  WOS · 2019
  not yet assessed
• Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant

  STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019
  not yet assessed
• Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. ↗

  Open Research Online - ORO (The Open University) · 2019
  not yet assessed
• A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individuals

  Data Archiving and Networked Services (DANS) · 2019
  not yet assessed
• Insights from the largest genetic study of sporadic and recurrent miscarriage

  Queensland's institutional digital repository (The University of Queensland) · 2019
  not yet assessed
• Application of non-HDL cholesterol for population-based cardiovascular risk stratification: results from the Multinational Cardiovascular Risk Consortium

  Research Portal (Queen's University Belfast) · 2019
  not yet assessed
• Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

  QUT ePrints (Queensland University of Technology) · 2019
  not yet assessed
• Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics

  Data Archiving and Networked Services (DANS) · 2019
  not yet assessed
• Supplementary Material for: Genome-Wide Association Scan of Serum Urea in European Populations Identifies Two Novel Loci ↗

  University of Groningen research database (University of Groningen / Centre for Information Technology) · 2019
  not yet assessed
• Additional file 1: of Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification ↗

  Figshare · 2019
  not yet assessed
• Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression ↗

  Nature Genetics · 2018 · PMID 29700475
  not yet assessed
• Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals ↗

  Nature Genetics · 2018 · PMID 30038396
  not yet assessed
• Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps ↗

  Nature Genetics · 2018 · PMID 30297969
  not yet assessed
• Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries ↗

  PLoS ONE · 2018 · PMID 29912962
  not yet assessed
• Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes ↗

  Nature Communications · 2018 · PMID 30054458
  not yet assessed
• Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes ↗

  Cell · 2018 · PMID 29906448
  not yet assessed
• Signatures of negative selection in the genetic architecture of human complex traits ↗

  Nature Genetics · 2018 · PMID 29662166
  not yet assessed
• Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood ↗

  Nature Communications · 2018 · PMID 29891976
  not yet assessed
• Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ↗

  Nature Genetics · 2018 · PMID 29632382
  not yet assessed
• Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error ↗

  Nature Genetics · 2018 · PMID 29808027
  not yet assessed
• Association of branched‐chain amino acids and other circulating metabolites with risk of incident dementia and Alzheimer's disease: A prospective study in eight cohorts ↗

  Alzheimer s & Dementia · 2018 · PMID 29519576
  not yet assessed
• Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies ↗

  Alzheimer s & Dementia · 2018 · PMID 29316447
  not yet assessed
• Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood ↗

  The American Journal of Human Genetics · 2018 · PMID 29754766
  not yet assessed
• A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure ↗

  The American Journal of Human Genetics · 2018 · PMID 29455858
  not yet assessed
• Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Genome biology · 2018 · PMID 30241495
  not yet assessed
• Interethnic analyses of blood pressure loci in populations of East Asian and European descent ↗

  Nature Communications · 2018 · PMID 30487518
  not yet assessed
• Genetic influence on social outcomes during and after the Soviet era in Estonia ↗

  Nature Human Behaviour · 2018 · PMID 29881783
  not yet assessed
• Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries ↗

  Nature Communications · 2018 · PMID 29973585
  not yet assessed
• Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use ↗

  Biological Psychiatry · 2018 · PMID 30679032
  not yet assessed
• Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland ↗

  The American Journal of Human Genetics · 2018 · PMID 29706349
  not yet assessed
• Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia ↗

  Genetics in Medicine · 2018 · PMID 30270359
  not yet assessed
• Circulating metabolic biomarkers of renal function in diabetic and non-diabetic populations ↗

  Scientific Reports · 2018 · PMID 30323304
  not yet assessed
• Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records ↗

  European Journal of Human Genetics · 2018 · PMID 30420678
  not yet assessed
• Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank ↗

  Biological Psychiatry Cognitive Neuroscience and Neuroimaging · 2018 · PMID 30197049
  not yet assessed
• Age at first birth in women is genetically associated with increased risk of schizophrenia ↗

  Scientific Reports · 2018 · PMID 29977057
  not yet assessed
• Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder ↗

  Communications Biology · 2018 · PMID 30320231
  not yet assessed
• Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant ↗

  European Journal of Medical Genetics · 2018 · PMID 30031151
  not yet assessed
• ePerMed - Rise of scientific excellence and collaboration for implementing personalised medicine in Estonia - H2020 ↗

  Impact · 2018
  not yet assessed
• Genome-Wide Analysis of Nuclear Magnetic Resonance Metabolites Revealed Parent-of-Origin Effect on Triglycerides in Medium Very Low-Density Lipoprotein in <i>PTPRD</i> Gene ↗

  Biomarkers in Medicine · 2018 · PMID 29536759
  not yet assessed
• Associations of autozygosity with a broad range of human phenotypes ↗

  Apollo (University of Cambridge) · 2018
  not yet assessed
• Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• GENETIC ANALYSIS OF OVER ONE MILLION PEOPLE IDENTIFIES 535 NOVEL LOCI ASSOCIATED WITH BLOOD PRESSURE AND RISK OF CARDIOVASCULAR DISEASE ↗

  Journal of Hypertension · 2018
  not yet assessed
• Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits : (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x)

  Nature Genetics · 2018
  not yet assessed
• The effect of X-linked dosage compensation on complex trait variation ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls ↗

  Scientific Data · 2018
  not yet assessed
• Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (vol 9, 2606, 2018)

  STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018
  not yet assessed
• Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries ↗

  Nature Communications · 2018 · PMID 30140049
  not yet assessed
• Author response: Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances ↗

  2018
  not yet assessed
• Polygenic prediction of breast cancer: comparison of genetic predictors and implications for screening ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies

  Kölner Universitäts PublikationsServer (Universität zu Köln) · 2018
  not yet assessed
• Association of branched-chain amino acids and other circulating metabolites with risk of incident dementia and Alzheimer's disease: A prospective study in eight cohorts

  Tampere University Institutional Repository (Tampere University) · 2018
  not yet assessed
• Nordic Exome Variant Catalogue a Web Resource for Genomic Data Browsing ↗

  2018
  not yet assessed
• Signatures of negative selection in the genetic architecture of human complex traits

  Queensland's institutional digital repository (The University of Queensland) · 2018
  not yet assessed
• Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland

  STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018
  not yet assessed
• Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci ↗

  Apollo (University of Cambridge) · 2018
  not yet assessed
• Genome-wide analysis of nuclear magnetic resonance metabolites revealed parent-of-origin effect on triglycerides in medium very low-density lipoprotein in PTPRD gene

  STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018
  not yet assessed
• Large population cohorts reveal unrecognized adult traits of the 16p11.2 CNV syndromes

  European Journal of Human Genetics · 2018
  not yet assessed
• Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K i

  PLoS ONE · 2018
  not yet assessed
• Genetic determinants of healthy ageing

  STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018
  not yet assessed
• Additional file 9: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 8: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 17: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 14: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 11: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 7: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 15: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 6: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 10: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 16: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 1: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 13: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 4: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• Additional file 5: of Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations ↗

  Figshare · 2018
  not yet assessed
• An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans ↗

  Diabetes · 2017 · PMID 28566273
  not yet assessed
• Association analyses based on false discovery rate implicate new loci for coronary artery disease ↗

  Nature Genetics · 2017 · PMID 28714975
  not yet assessed
• Rare and low-frequency coding variants alter human adult height ↗

  Nature · 2017 · PMID 28146470
  not yet assessed
• Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk ↗

  Nature Genetics · 2017 · PMID 28436984
  not yet assessed
• Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa ↗

  American Journal of Psychiatry · 2017 · PMID 28494655
  not yet assessed
• Exome-wide association study of plasma lipids in &gt;300,000 individuals ↗

  Nature Genetics · 2017 · PMID 29083408
  not yet assessed
• Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants ↗

  Nature Communications · 2017 · PMID 28537254
  not yet assessed
• Genetic evidence of assortative mating in humans ↗

  Nature Human Behaviour · 2017
  not yet assessed
• Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults ↗

  PLoS Genetics · 2017 · PMID 28448500
  not yet assessed
• The Genetic Architecture of Gene Expression in Peripheral Blood ↗

  The American Journal of Human Genetics · 2017 · PMID 28065468
  not yet assessed
• Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel ↗

  European Journal of Human Genetics · 2017 · PMID 28401899
  not yet assessed
• Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease ↗

  Journal of the American College of Cardiology · 2017 · PMID 28209224
  not yet assessed
• Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis ↗

  The Lancet Neurology · 2017 · PMID 29029846
  not yet assessed
• Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits ↗

  Nature Communications · 2017 · PMID 28443625
  not yet assessed
• Hidden heritability due to heterogeneity across seven populations ↗

  Nature Human Behaviour · 2017 · PMID 29051922
  not yet assessed
• Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity ↗

  Nature Communications · 2017 · PMID 29030599
  not yet assessed
• Genotype–covariate interaction effects and the heritability of adult body mass index ↗

  Nature Genetics · 2017 · PMID 28692066
  not yet assessed
• Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney ↗

  Hypertension · 2017 · PMID 28739976
  not yet assessed
• Genetic correlation between amyotrophic lateral sclerosis and schizophrenia ↗

  Nature Communications · 2017 · PMID 28322246
  not yet assessed
• Rare and low-frequency coding variants alter human adult height ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2017
  not yet assessed
• Pathogenic implications for autoimmune mechanisms derived by comparative eQTL analysis of CD4+ versus CD8+ T cells ↗

  PLoS Genetics · 2017 · PMID 28248954
  not yet assessed
• Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium ↗

  Biological Psychiatry · 2017 · PMID 29129318
  not yet assessed
• Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. ↗

  Lancaster EPrints (Lancaster University) · 2017
  not yet assessed
• 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function ↗

  Scientific Reports · 2017 · PMID 28452372
  not yet assessed
• CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits ↗

  Nature Communications · 2017 · PMID 28963451
  not yet assessed
• An epigenome-wide association study meta-analysis of educational attainment ↗

  Molecular Psychiatry · 2017 · PMID 29086770
  not yet assessed
• Exome-wide association study of plasma lipids in > 300,000 individuals

  Figshare · 2017
  not yet assessed
• An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗

  Genome biology · 2017 · PMID 28764798
  not yet assessed
• The Genetic Architecture of Gene Expression in Peripheral Blood ↗

  The American Journal of Human Genetics · 2017
  not yet assessed
• Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes ↗

  Scientific Reports · 2017 · PMID 29127340
  not yet assessed
• Genetic risk scores and family history as predictors of schizophrenia in Nordic registers ↗

  Psychological Medicine · 2017 · PMID 28942743
  not yet assessed
• A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk ↗

  Diabetes · 2017 · PMID 28341696
  not yet assessed
• DNA breaks and chromatin structural changes enhance the transcription of autoimmune regulator target genes ↗

  Journal of Biological Chemistry · 2017 · PMID 28242760
  not yet assessed
• A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling ↗

  Scientific Reports · 2017 · PMID 28630421
  not yet assessed
• Genome‐wide association study and meta‐analysis in Northern European populations replicate multiple colorectal cancer risk loci ↗

  International Journal of Cancer · 2017 · PMID 28960316
  not yet assessed
• Constraints on eQTL Fine Mapping in the Presence of Multisite Local Regulation of Gene Expression ↗

  G3 Genes Genomes Genetics · 2017 · PMID 28600440
  not yet assessed
• Demographic associations for autoantibodies in disease-free individuals of a European population ↗

  Scientific Reports · 2017 · PMID 28349935
  not yet assessed
• Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood ↗

  Nature Communications · 2017 · PMID 28883458
  not yet assessed
• Human basonuclin 2 up-regulates a cascade set of interferon-stimulated genes with anti-cancerous properties in a lung cancer model ↗

  Cancer Cell International · 2017 · PMID 28184177
  not yet assessed
• Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts ↗

  PLoS ONE · 2017 · PMID 29236708
  not yet assessed
• A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk ↗

  University of Southern Denmark Research Portal (University of Southern Denmark) · 2017
  not yet assessed
• Identifying pathways modulating sleep duration: from genomics to transcriptomics ↗

  Scientific Reports · 2017 · PMID 28676676
  not yet assessed
• MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies ↗

  PLoS ONE · 2017 · PMID 28107396
  not yet assessed
• Exome analysis in an Estonian multiplex family with neural tube defects—a case report ↗

  Child s Nervous System · 2017 · PMID 28721594
  not yet assessed
• Viva Europa, a Land of Excellence in Research and Innovation for Health and Wellbeing ↗

  Progress in Preventive Medicine · 2017
  not yet assessed
• Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits ↗

  Tampere University Institutional Repository (Tampere University) · 2017
  not yet assessed
• Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

  Archive ouverte UNIGE (University of Geneva) · 2017
  not yet assessed
• Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. ↗

  Duo Research Archive (University of Oslo) · 2017
  not yet assessed
• Rare and low-frequency coding variants alter human adult height ↗

  Apollo (University of Cambridge) · 2017
  not yet assessed
• Sequence data and association statistics from 12,940 type 2 diabetes cases and controls ↗

  Scientific Data · 2017 · PMID 29257133
  not yet assessed
• Widespread signatures of negative selection in the genetic architecture of human complex traits ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• Genetic analysis of over one million people identifies 535 novel loci for blood pressure ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• Erratum: Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer ↗

  Nature Genetics · 2017 · PMID 28358128
  not yet assessed
• Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults ↗

  PLoS Genetics · 2017 · PMID 28832619
  not yet assessed
• Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• Haplotype sharing provides insights into fine-scale population history and disease in Finland ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• Correction: Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function ↗

  Scientific Reports · 2017 · PMID 28548086
  not yet assessed
• Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• An epigenome-wide association study of educational attainment ( <i>n</i> = 10,767) ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• PAIRUP-MS: Pathway Analysis and Imputation to Relate Unknowns in Profiles from Mass Spectrometry-based metabolite data ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• Correction: Methylation Markers of Early-Stage Non-Small Cell Lung Cancer ↗

  PLoS ONE · 2017 · PMID 28107536
  not yet assessed
• Probe-level differences between CD4&lt;sup&gt;+&lt;/sup&gt; and CD8&lt;sup&gt;+&lt;/sup&gt; T cells in the &lt;i&gt;CTLA4&lt;/i&gt; gene. ↗

  Figshare · 2017
  not yet assessed
• 52 Genetic Loci Influencing Myocardial Mass

  Utrecht University Repository (Utrecht University) · 2017
  not yet assessed
• Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. ↗

  eScholarship@McGill (McGill) · 2017
  not yet assessed
• Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci

  UCL Discovery (University College London) · 2017
  not yet assessed
• Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk ↗

  White Rose Research Online (University of Leeds, The University of Sheffield, University of York) · 2017
  not yet assessed
• Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease (vol 374, pg 1134, 2016)

  Data Archiving and Networked Services (DANS) · 2017
  not yet assessed
• Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. ↗

  Apollo (University of Cambridge) · 2017
  not yet assessed
• An epigenome-wide association study meta-analysis of educational attainment

  Max Planck Digital Library · 2017
  not yet assessed
• Genome-wide association meta-analysis of fish and EPA plus DHA consumption in 17 US and European cohorts

  Data Archiving and Networked Services (DANS) · 2017
  not yet assessed
• An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2017
  not yet assessed
• Additional file 7: Table S6. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗

  Figshare · 2017
  not yet assessed
• Additional file 8: Table S7. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗

  Figshare · 2017
  not yet assessed
• Additional file 5: Table S4. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗

  Figshare · 2017
  not yet assessed
• Additional file 11: Table S10. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗

  Figshare · 2017
  not yet assessed
• Additional file 10: Table S9. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗

  Figshare · 2017
  not yet assessed
• Additional file 1: Table S1. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗

  Figshare · 2017
  not yet assessed
• Additional file 6: Table S5. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗

  Figshare · 2017
  not yet assessed
• Additional file 2: Table S2. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗

  Figshare · 2017
  not yet assessed
• Additional file 9: Table S8. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗

  Figshare · 2017
  not yet assessed
• Additional file 3: Table S3. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗

  Figshare · 2017
  not yet assessed
• Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects ↗

  Nature Genetics · 2016 · PMID 27869829
  not yet assessed
• The genetic architecture of type 2 diabetes ↗

  Nature · 2016 · PMID 27398621
  not yet assessed
• Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA ↗

  Nature Communications · 2016 · PMID 27005778
  not yet assessed
• Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci ↗

  Nature Genetics · 2016 · PMID 26974007
  not yet assessed
• Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine ↗

  Nature Genetics · 2016 · PMID 27322543
  not yet assessed
• Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease ↗

  Science · 2016 · PMID 26965621
  not yet assessed
• Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function ↗

  Nature Communications · 2016 · PMID 26831199
  not yet assessed
• Genomic analyses inform on migration events during the peopling of Eurasia ↗

  Nature · 2016 · PMID 27654910
  not yet assessed
• Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci ↗

  PLoS Genetics · 2016 · PMID 27494321
  not yet assessed
• Genome-wide analysis identifies 12 loci influencing human reproductive behavior ↗

  Nature Genetics · 2016 · PMID 27798627
  not yet assessed
• Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ↗

  Nature Genetics · 2016 · PMID 27618447
  not yet assessed
• Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium ↗

  Translational Psychiatry · 2016 · PMID 27023175
  not yet assessed
• Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores ↗

  Genetics in Medicine · 2016 · PMID 27513194
  not yet assessed
• Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error ↗

  Nature Communications · 2016 · PMID 27020472
  not yet assessed
• Genetic variants linked to education predict longevity ↗

  Proceedings of the National Academy of Sciences · 2016 · PMID 27799538
  not yet assessed
• 52 Genetic Loci Influencing Myocardial Mass ↗

  Journal of the American College of Cardiology · 2016 · PMID 27659466
  not yet assessed
• Ultra-rare disruptive and damaging mutations influence educational attainment in the general population ↗

  Nature Neuroscience · 2016 · PMID 27694993
  not yet assessed
• Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium ↗

  Scientific Reports · 2016 · PMID 27174397
  not yet assessed
• Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals ↗

  The American Journal of Human Genetics · 2016 · PMID 27346686
  not yet assessed
• A Whole-Blood Transcriptome Meta-Analysis Identifies Gene Expression Signatures of Cigarette Smoking ↗

  Human Molecular Genetics · 2016 · PMID 28158590
  not yet assessed
• Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits ↗

  The American Journal of Human Genetics · 2016 · PMID 27346685
  not yet assessed
• An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype ↗

  Biological Psychiatry · 2016 · PMID 28049566
  not yet assessed
• Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index ↗

  Molecular Psychiatry · 2016 · PMID 27184124
  not yet assessed
• Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms ↗

  Proceedings of the National Academy of Sciences · 2016 · PMID 28031487
  not yet assessed
• Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women ↗

  JAMA Psychiatry · 2016 · PMID 27007234
  not yet assessed
• Sequence variation in nuclear ribosomal small subunit, internal transcribed spacer and large subunit regions of <i>Rhizophagus irregularis</i> and <i>Gigaspora margarita</i> is high and isolate‐dependent ↗

  Molecular Ecology · 2016 · PMID 27092961
  not yet assessed
• A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape ↗

  Nature Communications · 2016 · PMID 27876822
  not yet assessed
• Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases ↗

  The American Journal of Human Genetics · 2016 · PMID 27346689
  not yet assessed
• Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis ↗

  The American Journal of Human Genetics · 2016 · PMID 27486782
  not yet assessed
• Imprinted Genes and Imprinting Control Regions Show Predominant Intermediate Methylation in Adult Somatic Tissues ↗

  Epigenomics · 2016 · PMID 27004446
  not yet assessed
• Polymorphic Variation in <i>TPMT</i> Is the Principal Determinant of TPMT Phenotype: A Meta‐Analysis of Three Genome‐Wide Association Studies ↗

  Clinical Pharmacology & Therapeutics · 2016 · PMID 27770449
  not yet assessed
• SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function ↗

  Journal of the American Society of Nephrology · 2016 · PMID 27920155
  not yet assessed
• Ageing with elegans: a research proposal to map healthspan pathways ↗

  Biogerontology · 2016 · PMID 27040825
  not yet assessed
• Genetic variants in RBFOX3 are associated with sleep latency ↗

  European Journal of Human Genetics · 2016 · PMID 27142678
  not yet assessed
• Metabolites of milk intake: a metabolomic approach in UK twins with findings replicated in two European cohorts ↗

  European Journal of Nutrition · 2016 · PMID 27469612
  not yet assessed
• No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis ↗

  Scientific Reports · 2016 · PMID 27731410
  not yet assessed
• Quality Matters: 2016 Annual Conference of the National Infrastructures for Biobanking ↗

  Biopreservation and Biobanking · 2016 · PMID 27992240
  not yet assessed
• The Role of the Five–factor Personality Traits in General Self–rated Health ↗

  European Journal of Personality · 2016
  not yet assessed
• Whole-genome expression analysis reveals genes associated with treatment response to escitalopram in major depression ↗

  European Neuropsychopharmacology · 2016 · PMID 27461515
  not yet assessed
• Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis ↗

  The American Journal of Human Genetics · 2016
  not yet assessed
• Autosomal genetic control of human gene expression does not differ across the sexes ↗

  Genome biology · 2016 · PMID 27908293
  not yet assessed
• Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participants ↗

  Personalized Medicine · 2016 · PMID 29749813
  not yet assessed
• From Biobanking to Precision Medicine ↗

  Elsevier eBooks · 2016
  not yet assessed
• Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal hernia ↗

  Hernia · 2016 · PMID 27115767
  not yet assessed
• Ancient Haplotypes at the 15q24.2 Microdeletion Region Are Linked to Brain Expression of MAN2C1 and Children's Intelligence ↗

  PLoS ONE · 2016 · PMID 27355585
  not yet assessed
• Genetic influence on educational attainment and occupational status during and after the Soviet era in Estonia

  Queensland's institutional digital repository (The University of Queensland) · 2016
  not yet assessed
• Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease ↗

  Apollo (University of Cambridge) · 2016
  not yet assessed
• Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses ↗

  Nature Genetics · 2016
  not yet assessed
• Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine ↗

  Nature Genetics · 2016 · PMID 27681292
  not yet assessed
• Personalized Risk Prediction for Type 2 Diabetes: the Potential of Genetic Risk Scores ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2016
  not yet assessed
• A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2016
  not yet assessed
• Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses ↗

  Nature Genetics · 2016 · PMID 27463399
  not yet assessed
• Ultra-rare disruptive and damaging mutations influence educational attainment in the general population ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2016
  not yet assessed
• Genome-wide association analyses in &gt; 119,000 individuals identifies thirteen morningness and two sleep duration loci ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2016
  not yet assessed
• Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2016
  not yet assessed
• Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (Nature Genetics, (2016), 10.1038/ng.3598)

  Nature Genetics · 2016
  not yet assessed
• Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2016
  not yet assessed
• Constraints on eQTL fine mapping in the presence of multi-site local regulation of gene expression ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2016
  not yet assessed
• Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci

  QUT ePrints (Queensland University of Technology) · 2016
  not yet assessed
• Abstract 19854: Whole Genome Sequences and Plasma Lipids in 2,255 Participants

  Circulation · 2016
  not yet assessed
• No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis

  Tampere University Institutional Repository (Tampere University) · 2016
  not yet assessed
• Improved Imputation Accuracy of Rare and Low-Frequency Genetic Variants Using Population-Specific High-Coverage Whole-Genome Sequencing Data Based Imputation Reference Panel

  2016
  not yet assessed
• Discovery and validation of 107 blood pressure loci from UK Biobank offers novel biological insights into cardiovascular risk

  2016
  not yet assessed
• Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2016
  not yet assessed
• Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects ↗

  Arrow@dit (Dublin Institute of Technology) · 2016
  not yet assessed
• The genetic architecture of type 2 diabetes. ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2016
  not yet assessed
• The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals ↗

  Zurich Open Repository and Archive (University of Zurich) · 2016
  not yet assessed
• Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (vol 48, pg 856, 2016)

  Data Archiving and Networked Services (DANS) · 2016
  not yet assessed
• Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease (vol 374, pg 1134, 2016, Correction)

  STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2016
  not yet assessed
• Ultra-rare disruptive and damaging mutations influence educational attainment in the general population ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2016
  not yet assessed
• List of Contributors ↗

  Elsevier eBooks · 2016
  not yet assessed
• Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans ↗

  PLoS ONE · 2015 · PMID 25811787
  not yet assessed
• The transcriptional landscape of age in human peripheral blood ↗

  Nature Communications · 2015 · PMID 26490707
  not yet assessed
• The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study ↗

  PLoS Genetics · 2015 · PMID 26426971
  not yet assessed
• A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease

  EUR Research Repository (Erasmus University Rotterdam) · 2015
  not yet assessed
• Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair ↗

  Nature Genetics · 2015 · PMID 26414677
  not yet assessed
• Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci ↗

  Nature Genetics · 2015 · PMID 26551672
  not yet assessed
• The impact of low-frequency and rare variants on lipid levels ↗

  Nature Genetics · 2015 · PMID 25961943
  not yet assessed
• Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation ↗

  Nature Genetics · 2015 · PMID 26390057
  not yet assessed
• Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder ↗

  JAMA Psychiatry · 2015 · PMID 25993607
  not yet assessed
• Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities ↗

  JAMA Psychiatry · 2015 · PMID 26629640
  not yet assessed
• Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium ↗

  Behavior Genetics · 2015 · PMID 26362575
  not yet assessed
• Copy Number Variations and Cognitive Phenotypes in Unselected Populations ↗

  JAMA · 2015 · PMID 26010633
  not yet assessed
• Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels ↗

  Nature Communications · 2015 · PMID 26068415
  not yet assessed
• Age-related profiling of DNA methylation in CD8+ T cells reveals changes in immune response and transcriptional regulator genes ↗

  Scientific Reports · 2015 · PMID 26286994
  not yet assessed
• Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci ↗

  Nature Communications · 2015 · PMID 25939698
  not yet assessed
• Cell Specific eQTL Analysis without Sorting Cells

  PLoS Genetics · 2015 · PMID 25955312
  L1 90/100
• Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity ↗

  Nature Genetics · 2015 · PMID 26098870
  not yet assessed
• Adiposity as a cause of cardiovascular disease: a Mendelian randomization study ↗

  International Journal of Epidemiology · 2015 · PMID 26016847
  not yet assessed
• Effects of Metformin on Metabolite Profiles and LDL Cholesterol in Patients With Type 2 Diabetes ↗

  Diabetes Care · 2015 · PMID 26251408
  not yet assessed
• A Meta-analysis of Gene Expression Signatures of Blood Pressure and Hypertension ↗

  PLoS Genetics · 2015 · PMID 25785607
  not yet assessed
• Epigenetic profiling in CD4+ and CD8+ T cells from Graves' disease patients reveals changes in genes associated with T cell receptor signaling ↗

  Journal of Autoimmunity · 2015 · PMID 26459776
  not yet assessed
• The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition ↗

  Biological Psychiatry · 2015 · PMID 26742926
  not yet assessed
• Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation ↗

  PLoS Genetics · 2015 · PMID 26132169
  not yet assessed
• Linking a Population Biobank with National Health Registries—The Estonian Experience ↗

  Journal of Personalized Medicine · 2015 · PMID 25894366
  not yet assessed
• The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects ↗

  Molecular Psychiatry · 2015 · PMID 25917368
  not yet assessed
• Age- and Sex-Specific Causal Effects of Adiposity on Cardiovascular Risk Factors ↗

  Diabetes · 2015 · PMID 25712996
  not yet assessed
• Within-Trait Heterogeneity in Age Group Differences in Personality Domains and Facets: Implications for the Development and Coherence of Personality Traits ↗

  PLoS ONE · 2015 · PMID 25751273
  not yet assessed
• Rare coding variants and X-linked loci associated with age at menarche ↗

  Nature Communications · 2015 · PMID 26239645
  not yet assessed
• 16p11.2 Locus modulates response to satiety before the onset of obesity ↗

  International Journal of Obesity · 2015 · PMID 26620891
  not yet assessed
• Harmonising and linking biomedical and clinical data across disparate data archives to enable integrative cross-biobank research ↗

  European Journal of Human Genetics · 2015 · PMID 26306643
  not yet assessed
• Extensive alterations of the whole-blood transcriptome are associated with body mass index: results of an mRNA profiling study involving two large population-based cohorts ↗

  BMC Medical Genomics · 2015 · PMID 26470795
  not yet assessed
• Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia ↗

  Carcinogenesis · 2015 · PMID 26363033
  not yet assessed
• The relationship between the Five‐Factor Model personality traits and peptic ulcer disease in a large population‐based adult sample ↗

  Scandinavian Journal of Psychology · 2015 · PMID 26437682
  not yet assessed
• Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair ↗

  Obstetrical & Gynecological Survey · 2015
  not yet assessed
• Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta ↗

  Human Genomics · 2015 · PMID 25958000
  not yet assessed
• Is the adiposity‐associated <scp><i>FTO</i></scp> gene variant related to all‐cause mortality independent of adiposity? Meta‐analysis of data from 169,551 <scp>C</scp>aucasian adults ↗

  Obesity Reviews · 2015 · PMID 25752329
  not yet assessed
• Haplotype Phasing and Inheritance of Copy Number Variants in Nuclear Families ↗

  PLoS ONE · 2015 · PMID 25853576
  not yet assessed
• De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion ↗

  Neuromuscular Disorders · 2015 · PMID 26782017
  not yet assessed
• Cumulative Small Effect Genetic Markers and the Risk of Colorectal Cancer in Poland, Estonia, Lithuania, and Latvia ↗

  Gastroenterology Research and Practice · 2015 · PMID 26101521
  not yet assessed
• Rare coding variants and X-linked loci associated with age at menarche

  LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · 2015
  not yet assessed
• A recent bottleneck of Y chromosome diversity coincides with a global change in culture ↗

  Genome Research · 2015 · PMID 25770088
  not yet assessed
• Correction: Corrigendum: Rare coding variants and X-linked loci associated with age at menarche ↗

  Nature Communications · 2015 · PMID 26674845
  not yet assessed
• The effect of maternal sleep on epigenome of newborn

  STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2015
  not yet assessed
• Scatter plot of age versus biomarker summary score for men and women from the Estonian Biobank cohort. ↗

  Figshare · 2015
  not yet assessed
• Directional dominance on stature and cognition in diverse human populations ↗

  Archive ouverte UNIGE (University of Geneva) · 2015
  not yet assessed
• Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2015
  not yet assessed
• The impact of low-frequency and rare variants on lipid levels

  Data Archiving and Networked Services (DANS) · 2015
  not yet assessed
• Discovery and Refinement Supplementary

  2015
  not yet assessed
• The association between lower educational attainment and depression owing to shared genetic effects? Results in ∼25 000 subjects

  QUT ePrints (Queensland University of Technology) · 2015
  not yet assessed
• Nature Genetics | Article

  2015
  not yet assessed
• Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2015
  not yet assessed
• Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu

  STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2015
  not yet assessed
• Cell Specific eQTL Analysis without Sorting Cells

  Northumbria Research Link (Northumbria University) · 2015
  not yet assessed
• P202 – 2912: Methylenetetrahydrofolate reductase (MTHFR) polymorphisms A1298C and C677T as genetic risk factors for perinatal and childhood arterial ischemic stroke? ↗

  European Journal of Paediatric Neurology · 2015
  not yet assessed
• Additional file 4: of Extensive alterations of the whole-blood transcriptome are associated with body mass index: results of an mRNA profiling study involving two large population-based cohorts ↗

  Figshare · 2015
  not yet assessed
• Additional file 2: Table S1. of Extensive alterations of the whole-blood transcriptome are associated with body mass index: results of an mRNA profiling study involving two large population-based cohorts ↗

  Figshare · 2015
  not yet assessed
• Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta ↗

  Figshare · 2015
  not yet assessed
• Additional file 3: of Extensive alterations of the whole-blood transcriptome are associated with body mass index: results of an mRNA profiling study involving two large population-based cohorts ↗

  Figshare · 2015
  not yet assessed
• Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility ↗

  Nature Genetics · 2014 · PMID 24509480
  not yet assessed
• Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche ↗

  Nature · 2014 · PMID 25231870
  not yet assessed
• Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases ↗

  The American Journal of Human Genetics · 2014 · PMID 25439723
  not yet assessed
• The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: A collaborative analysis of ten large cohort studies

  Duo Research Archive (University of Oslo) · 2014
  not yet assessed
• Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu ↗

  International Journal of Epidemiology · 2014 · PMID 24518929
  not yet assessed
• Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer ↗

  Nature Genetics · 2014 · PMID 24880342
  not yet assessed
• Biomarker Profiling by Nuclear Magnetic Resonance Spectroscopy for the Prediction of All-Cause Mortality: An Observational Study of 17,345 Persons ↗

  PLoS Medicine · 2014 · PMID 24586121
  not yet assessed
• A genome-wide association study of anorexia nervosa ↗

  Molecular Psychiatry · 2014 · PMID 24514567
  not yet assessed
• Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption ↗

  Molecular Psychiatry · 2014 · PMID 25288136
  not yet assessed
• Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age ↗

  Human Molecular Genetics · 2014 · PMID 24688116
  not yet assessed
• A metabolic view on menopause and ageing ↗

  Nature Communications · 2014 · PMID 25144627
  not yet assessed
• RETRACTED ARTICLE: Detection and replication of epistasis influencing transcription in humans ↗

  Nature · 2014 · PMID 24572353
  not yet assessed
• Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. ↗

  White Rose Research Online (University of Leeds, The University of Sheffield, University of York) · 2014
  not yet assessed
• Chronotype and sleep duration: The influence of season of assessment ↗

  Chronobiology International · 2014 · PMID 24679223
  not yet assessed
• Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of Item Response Theory ↗

  Behavior Genetics · 2014 · PMID 24828478
  not yet assessed
• Oral health, dental care and mouthwash associated with upper aerodigestive tract cancer risk in Europe: The ARCAGE study ↗

  Oral Oncology · 2014 · PMID 24680035
  not yet assessed
• BBMRI-ERIC as a resource for pharmaceutical and life science industries: the development of biobank-based Expert Centres ↗

  European Journal of Human Genetics · 2014 · PMID 25407005
  not yet assessed
• Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index ↗

  PLoS Genetics · 2014 · PMID 25078964
  not yet assessed
• A genome-wide association study of anorexia nervosa

  Research Portal (Queen's University Belfast) · 2014
  not yet assessed
• A Common 16p11.2 Inversion Underlies the Joint Susceptibility to Asthma and Obesity ↗

  The American Journal of Human Genetics · 2014 · PMID 24560518
  not yet assessed
• The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studies ↗

  BMC Endocrine Disorders · 2014 · PMID 24484869
  not yet assessed
• Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta ↗

  Epigenetics · 2014 · PMID 25437054
  not yet assessed
• Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population ↗

  PLoS Genetics · 2014 · PMID 25078778
  not yet assessed
• Copper Metabolism Domain-Containing 1 Represses Genes That Promote Inflammation and Protects Mice From Colitis and Colitis-Associated Cancer ↗

  Gastroenterology · 2014 · PMID 24727021
  not yet assessed
• Comprehensive Meta-analysis of MicroRNA Expression Using a Robust Rank Aggregation Approach ↗

  Methods in molecular biology · 2014 · PMID 25055923
  not yet assessed
• CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing ↗

  Immunity & Ageing · 2014 · PMID 24405718
  not yet assessed
• Coffin–Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene ↗

  European Journal of Human Genetics · 2014 · PMID 24569609
  not yet assessed
• An epidemiological perspective of personalized medicine: the <scp>E</scp>stonian experience ↗

  Journal of Internal Medicine · 2014 · PMID 25339628
  not yet assessed
• Population distribution and ancestry of the cancer protective MDM2 SNP285 (rs117039649) ↗

  Oncotarget · 2014 · PMID 25327560
  not yet assessed
• Mapping the Genetic Architecture of Gene Regulation in Whole Blood ↗

  PLoS ONE · 2014 · PMID 24740359
  not yet assessed
• Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis ↗

  Nature Communications · 2014 · PMID 25352340
  not yet assessed
• Hemani et al. reply ↗

  Nature · 2014 · PMID 25279929
  not yet assessed
• Genetic variants of inducible costimulator are associated with allergic asthma susceptibility ↗

  Journal of Allergy and Clinical Immunology · 2014 · PMID 25109803
  not yet assessed
• Another Explanation for Apparent Epistasis ↗

  PubMed Central · 2014
  not yet assessed
• Cell specific eQTL analysis without sorting cells ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2014
  not yet assessed
• Another explanation for apparent epistasis: reply ↗

  University of Groningen research database (University of Groningen / Centre for Information Technology) · 2014
  not yet assessed
• Abundance and distribution of hydroxymethylcytosine (5hmC) in human liver ↗

  F1000Research · 2014
  not yet assessed
• Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of Item Response Theory

  Tampere University Institutional Repository (Tampere University) · 2014
  not yet assessed
• P460: Electroencephalography and clinical findings in a SCN8A epileptic encephalopathy: a case report ↗

  Clinical Neurophysiology · 2014
  not yet assessed
• Loote reesusstaatuse mitteinvasiivne diagnostika – prenataalse diagnostika uus võimalus Eestis ↗

  Ajakirjad. Journals by UT · 2014
  not yet assessed
• Hereditaarset spastilist parapleegiat süsteemselt käsitlenud uuring Eestis tõi esile uusi andmeid ↗

  Ajakirjad. Journals by UT · 2014
  not yet assessed
• Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

  UWA Profiles and Research Repository (University of Western Australia) · 2014
  not yet assessed
• Imprinting landscape of human placenta as discovered by whole transcriptome RNA-sequencing and exome variant data analysis

  Murdoch Research Repository (Murdoch University) · 2014
  not yet assessed
• A metabolic view on menopause and ageing

  RePEc: Research Papers in Economics · 2014
  not yet assessed
• Implementation of Individualized Medicine: Education, Prediction and Treatment ↗

  2014
  not yet assessed
• Faculty Opinions recommendation of Epigenome-wide association studies without the need for cell-type composition. ↗

  Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · 2014
  not yet assessed
• Implementation of Individualized Medicine: Education, Prediction and Treatment (IndiMedDep) ↗

  2014
  not yet assessed
• Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta ↗

  Figshare · 2014
  not yet assessed
• Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta ↗

  Figshare · 2014
  not yet assessed
• Genetics of rheumatoid arthritis contributes to biology and drug discovery ↗

  Nature · 2013 · PMID 24390342
  not yet assessed
• Systematic identification of trans eQTLs as putative drivers of known disease associations ↗

  Nature Genetics · 2013 · PMID 24013639
  not yet assessed
• Identification of seven loci affecting mean telomere length and their association with disease ↗

  Nature Genetics · 2013 · PMID 23535734
  not yet assessed
• GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment ↗

  Science · 2013 · PMID 23722424
  not yet assessed
• Common variants associated with plasma triglycerides and risk for coronary artery disease ↗

  Nature Genetics · 2013 · PMID 24097064
  not yet assessed
• Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia ↗

  Nature Genetics · 2013 · PMID 23396134
  not yet assessed
• Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders ↗

  Nature Genetics · 2013 · PMID 23583979
  not yet assessed
• Human Disease-Associated Genetic Variation Impacts Large Intergenic Non-Coding RNA Expression ↗

  PLoS Genetics · 2013 · PMID 23341781
  not yet assessed
• The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis ↗

  PLoS Medicine · 2013 · PMID 23824655
  not yet assessed
• Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error ↗

  The American Journal of Human Genetics · 2013 · PMID 24144296
  not yet assessed
• Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course ↗

  Human Molecular Genetics · 2013 · PMID 23669352
  not yet assessed
• A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip ↗

  Annals of the Rheumatic Diseases · 2013 · PMID 23989986
  not yet assessed
• A Genome-Wide Analysis of Populations from European Russia Reveals a New Pole of Genetic Diversity in Northern Europe ↗

  PLoS ONE · 2013 · PMID 23505534
  not yet assessed
• Ontogeny, distribution and potential roles of 5-hydroxymethylcytosine in human liver function ↗

  Genome biology · 2013 · PMID 23958281
  not yet assessed
• Sex- and age-interacting eQTLs in human complex diseases ↗

  Human Molecular Genetics · 2013 · PMID 24242183
  not yet assessed
• DNA mismatch repair gene MSH6 implicated in determining age at natural menopause ↗

  Human Molecular Genetics · 2013 · PMID 24357391
  not yet assessed
• <i>De Novo</i> <i>SCN8A</i> Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy, Multiple Congenital Anomalies, and Movement Disorders ↗

  Journal of Child Neurology · 2013 · PMID 24352161
  not yet assessed
• Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent ↗

  American Journal of Epidemiology · 2013 · PMID 23558354
  not yet assessed
• A Missense Mutation in <i>DUSP6</i> is Associated with Class III Malocclusion ↗

  Journal of Dental Research · 2013 · PMID 23965468
  not yet assessed
• In-solution hybrid capture of bisulfite-converted DNA for targeted bisulfite sequencing of 174 ADME genes ↗

  Nucleic Acids Research · 2013 · PMID 23325842
  not yet assessed
• Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity ↗

  PLoS ONE · 2013 · PMID 23554873
  not yet assessed
• Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function ↗

  Journal of the American Society of Nephrology · 2013 · PMID 24029420
  not yet assessed
• Non-syndromic Tooth Agenesis Associated with a Nonsense Mutation in Ectodysplasin-A <i>(EDA)</i> ↗

  Journal of Dental Research · 2013 · PMID 23603338
  not yet assessed
• Whole-exome sequencing identifies a polymorphism in the BMP5 gene associated with SSRI treatment response in major depression ↗

  Journal of Psychopharmacology · 2013 · PMID 23926243
  not yet assessed
• Lynch syndrome mutations shared by the Baltic States and Poland ↗

  Clinical Genetics · 2013 · PMID 24032978
  not yet assessed
• Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

  UCL Discovery (University College London) · 2013
  not yet assessed
• Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits ↗

  Tampere University Institutional Repository (Tampere University) · 2013
  not yet assessed
• Erratum: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia ↗

  Nature Genetics · 2013
  not yet assessed
• Supplementary Material 15

  2013
  not yet assessed
• The genetic basis of cross-phenotype correlation with bone fracture risk: the GEFOS consortium

  Data Archiving and Networked Services (DANS) · 2013
  not yet assessed
• Identification of seven loci affecting mean telomere length and their association with disease ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2013
  not yet assessed
• Functional characterization of GWAS loci associated with fracture risk

  Data Archiving and Networked Services (DANS) · 2013
  not yet assessed
• Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes ↗

  Nature Genetics · 2012 · PMID 22885922
  not yet assessed
• Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity ↗

  Nature Genetics · 2012 · PMID 23143594
  not yet assessed
• Genome-wide association analyses identify 18 new loci associated with serum urate concentrations ↗

  Nature Genetics · 2012 · PMID 23263486
  not yet assessed
• FTO genotype is associated with phenotypic variability of body mass index ↗

  Nature · 2012 · PMID 22982992
  not yet assessed
• Combined Analysis of Genome-wide Association Studies for Crohn Disease and Psoriasis Identifies Seven Shared Susceptibility Loci ↗

  The American Journal of Human Genetics · 2012 · PMID 22482804
  not yet assessed
• Seventy-five genetic loci influencing the human red blood cell ↗

  Nature · 2012 · PMID 23222517
  not yet assessed
• Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls ↗

  Human Molecular Genetics · 2012 · PMID 22899653
  not yet assessed
• Meta‐analysis of microRNA expression in lung cancer ↗

  International Journal of Cancer · 2012 · PMID 23225545
  not yet assessed
• Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function ↗

  PLoS Genetics · 2012 · PMID 22479191
  not yet assessed
• Toward a roadmap in global biobanking for health ↗

  European Journal of Human Genetics · 2012 · PMID 22713808
  not yet assessed
• Reconstructing the Population History of European Romani from Genome-wide Data ↗

  Current Biology · 2012 · PMID 23219723
  not yet assessed
• Personality traits and eating habits in a large sample of Estonians. ↗

  Health Psychology · 2012 · PMID 22268715
  not yet assessed
• Evidence of Inbreeding Depression on Human Height ↗

  PLoS Genetics · 2012 · PMID 22829771
  not yet assessed
• Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium ↗

  Human Genetics · 2012 · PMID 22665138
  not yet assessed
• Replication and meta-analysis of TMEM132D gene variants in panic disorder ↗

  Translational Psychiatry · 2012 · PMID 22948381
  not yet assessed
• Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways ↗

  QUT ePrints (Queensland University of Technology) · 2012
  not yet assessed
• Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity ↗

  European Journal of Human Genetics · 2012 · PMID 23249956
  not yet assessed
• Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function ↗

  Human Molecular Genetics · 2012 · PMID 22962313
  not yet assessed
• Methylation Markers of Early-Stage Non-Small Cell Lung Cancer ↗

  PLoS ONE · 2012 · PMID 22768131
  not yet assessed
• Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium ↗

  Carcinogenesis · 2012 · PMID 22382497
  not yet assessed
• Genome-wide meta-analysis of common variant differences between men and women ↗

  Human Molecular Genetics · 2012 · PMID 22843499
  not yet assessed
• Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions ↗

  European Journal of Human Genetics · 2012 · PMID 23211697
  not yet assessed
• Self-Other Agreement in Happiness and Life-Satisfaction: The Role of Personality Traits ↗

  Social Indicators Research · 2012
  not yet assessed
• Post-translational stabilization of thiopurine S-methyltransferase by S-adenosyl-l-methionine reveals regulation of TPMT*1 and *3C allozymes ↗

  Biochemical Pharmacology · 2012 · PMID 22274639
  not yet assessed
• Direct-to-consumer genetic testing for health-related purposes in the European Union

  2012
  not yet assessed
• History of the Diagnosis of a Sexually Transmitted Disease is Linked to Normal Variation in Personality Traits ↗

  The Journal of Sexual Medicine · 2012 · PMID 22905653
  not yet assessed
• Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2012
  not yet assessed
• Genome-wide meta-analysis of common variant differences between men and women ↗

  University of Regensburg Publication Server (University of Regensburg) · 2012
  not yet assessed
• Seventy-five genetic loci influencing the human red blood cell

  Maynooth University ePrints and eTheses Archive (Maynooth University) · 2012
  not yet assessed
• FTO genotype is associated with phenotypic variability of body mass index

  University of Regensburg Publication Server (University of Regensburg) · 2012
  not yet assessed
• Survey of Estonian Primary Care Physicians ↗

  PsycTESTS Dataset · 2012
  not yet assessed
• A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma ↗

  The American Journal of Human Genetics · 2011 · PMID 28472664
  not yet assessed
• Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus ↗

  Nature · 2011 · PMID 21881559
  not yet assessed
• Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure ↗

  Nature Genetics · 2011 · PMID 21909110
  not yet assessed
• New gene functions in megakaryopoiesis and platelet formation ↗

  Nature · 2011 · PMID 22139419
  not yet assessed
• Design of a peptide-based vector, PepFect6, for efficient delivery of siRNA in cell culture and systemically in vivo ↗

  Nucleic Acids Research · 2011 · PMID 21245043
  not yet assessed
• Genome-wide association and genetic functional studies identify <i>autism susceptibility candidate 2</i> gene ( <i>AUTS2</i> ) in the regulation of alcohol consumption ↗

  Proceedings of the National Academy of Sciences · 2011 · PMID 21471458
  not yet assessed
• Systems medicine and integrated care to combat chronic noncommunicable diseases ↗

  Genome Medicine · 2011 · PMID 21745417
  not yet assessed
• A KATP channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila ↗

  Molecular Psychiatry · 2011 · PMID 22105623
  not yet assessed
• Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking ↗

  Translational Psychiatry · 2011 · PMID 22833195
  not yet assessed
• Genome-Wide Meta-Analysis of Psoriatic Arthritis Identifies Susceptibility Locus at REL ↗

  Journal of Investigative Dermatology · 2011 · PMID 22170493
  not yet assessed
• Identification of miR‐374a as a prognostic marker for survival in patients with early‐stage nonsmall cell lung cancer ↗

  Genes Chromosomes and Cancer · 2011 · PMID 21748820
  not yet assessed
• The role of COX-2 and Nrf2/ARE in anti-inflammation and antioxidative stress: Aging and anti-aging ↗

  Medical Hypotheses · 2011 · PMID 21530094
  not yet assessed
• The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data ↗

  Translational Psychiatry · 2011 · PMID 22833196
  not yet assessed
• Feasibility of innovative dietary assessment in epidemiological studies using the approach of combining different assessment instruments ↗

  Public Health Nutrition · 2011 · PMID 21385523
  not yet assessed
• Variation in FGF1, FOXE1, and TIMP2genes is associated with nonsyndromic cleft lip with or without cleft palate ↗

  Birth Defects Research Part A Clinical and Molecular Teratology · 2011 · PMID 21462296
  not yet assessed
• A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol ↗

  PLoS Genetics · 2011 · PMID 22028671
  not yet assessed
• Sequence Variants and the Risk of Head and Neck Cancer: Pooled Analysis in the INHANCE Consortium ↗

  Frontiers in Oncology · 2011 · PMID 22655231
  not yet assessed
• Metagenes Associated with Survival in Non-Small Cell Lung Cancer ↗

  Cancer Informatics · 2011 · PMID 21695068
  not yet assessed
• Longevity candidate genes and their association with personality traits in the elderly ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2011 · PMID 22213687
  not yet assessed
• Giving and Withholding of Information following Genomic Screening: Challenges Identified in a Study of Primary Care Physicians in Estonia ↗

  Journal of Genetic Counseling · 2011 · PMID 22160497
  not yet assessed
• Investigating gene expression profile of non-small cell lung cancer ↗

  Open Medicine · 2011
  not yet assessed
• Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

  Data Archiving and Networked Services (DANS) · 2011
  not yet assessed
• Comprehensive catalog of European biobanks ↗

  Nature Biotechnology · 2011 · PMID 21904320
  not yet assessed
• Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution ↗

  Nature Genetics · 2011
  not yet assessed
• Bio-resources for sharing: which communities and what specific needs ↗

  Nature Precedings · 2011
  not yet assessed
• The number of commercial SNPs necessary to describe all SNPs in different populations ↗

  Figshare · 2011
  not yet assessed
• A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol

  Tampere University Institutional Repository (Tampere University) · 2011
  not yet assessed
• Systems medicine and integrated care to combat chronic noncommunicable diseases ↗

  Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona) · 2011
  not yet assessed
• Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with Excitement-Seeking

  Queensland's institutional digital repository (The University of Queensland) · 2011
  not yet assessed
• Erratum ↗

  Oncology · 2011
  not yet assessed
• Supplementary Material for: Gene Expression Profiles of Non-Small Cell Lung Cancer: Survival Prediction and New Biomarkers ↗

  Figshare · 2011
  not yet assessed
• Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index ↗

  Nature Genetics · 2010 · PMID 20935630
  not yet assessed
• Hundreds of variants clustered in genomic loci and biological pathways affect human height ↗

  Nature · 2010 · PMID 20881960
  not yet assessed
• Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution ↗

  Nature Genetics · 2010
  not yet assessed
• Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2010
  not yet assessed
• Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior ↗

  Nature Genetics · 2010 · PMID 20418888
  not yet assessed
• A new highly penetrant form of obesity due to deletions on chromosome 16p11.2 ↗

  Nature · 2010 · PMID 20130649
  not yet assessed
• Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies ↗

  Nature Genetics · 2010 · PMID 21102462
  not yet assessed
• Common variants in KCNN3 are associated with lone atrial fibrillation ↗

  Nature Genetics · 2010 · PMID 20173747
  not yet assessed
• Meta-analysis of genome-wide association studies for personality ↗

  Molecular Psychiatry · 2010 · PMID 21173776
  not yet assessed
• Human microRNAs miR-22, miR-138-2, miR-148a, and miR-488 Are Associated with Panic Disorder and Regulate Several Anxiety Candidate Genes and Related Pathways ↗

  Biological Psychiatry · 2010 · PMID 21168126
  not yet assessed
• Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies ↗

  International Journal of Epidemiology · 2010 · PMID 20813861
  not yet assessed
• Gene Expression Profiles of Non-Small Cell Lung Cancer: Survival Prediction and New Biomarkers ↗

  Oncology · 2010 · PMID 21412013
  not yet assessed
• Polymorphisms in<i>ESR1</i>,<i>ESR2</i>and<i>HSD17B1</i>genes are associated with fertility status in endometriosis ↗

  Gynecological Endocrinology · 2010 · PMID 20586553
  not yet assessed
• <i>MTHFR</i>and<i>MSX1</i>contribute to the risk of nonsyndromic cleft lip/palate ↗

  European Journal Of Oral Sciences · 2010 · PMID 20572854
  not yet assessed
• Genetic variants in <i>COL2A1</i>, <i>COL11A2</i>, and <i>IRF6</i> contribute risk to nonsyndromic cleft palate ↗

  Birth Defects Research Part A Clinical and Molecular Teratology · 2010 · PMID 20672350
  not yet assessed
• Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. ↗

  PubMed · 2010 · PMID 20935629
  not yet assessed
• Polymorphisms in MMP-2 and MMP-9 promoter regions are associated with endometriosis ↗

  Fertility and Sterility · 2010 · PMID 20100617
  not yet assessed
• Variance determines self-observer agreement on the Big Five personality traits ↗

  Journal of Research in Personality · 2010
  not yet assessed
• BRCA1 mutations in women with familial or early-onset breast cancer and BRCA2 mutations in familial cancer in Estonia ↗

  Hereditary Cancer in Clinical Practice · 2010 · PMID 20380699
  not yet assessed
• Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study ↗

  BMC Medical Genetics · 2010 · PMID 20167083
  not yet assessed
• Genetic variations in vascular endothelial growth factor but not in angiotensin I-converting enzyme genes are associated with endometriosis in Estonian women ↗

  European Journal of Obstetrics & Gynecology and Reproductive Biology · 2010 · PMID 20685027
  not yet assessed
• Susceptibility locus for non‐syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients ↗

  European Journal Of Oral Sciences · 2010 · PMID 20572868
  not yet assessed
• A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia ↗

  European Journal of Medical Genetics · 2010 · PMID 21112420
  not yet assessed
• Unique spectrum of SPAST variants in Estonian HSP patients: presence of benign missense changes but lack of exonic rearrangements ↗

  BMC Neurology · 2010 · PMID 20214791
  not yet assessed
• Molecular diagnosis of Down syndrome using quantitative APEX‐2 microarrays ↗

  Prenatal Diagnosis · 2010 · PMID 20949644
  not yet assessed
• Arrayed Primer Extension Microarrays for Molecular Diagnostics ↗

  Elsevier eBooks · 2010
  not yet assessed
• Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2010
  not yet assessed
• Correction: Genetic Structure of Europeans: A View from the North–East ↗

  PLoS ONE · 2010
  not yet assessed
• Gene Expression-Based Approaches in Differentiation of Metastases and Second Primary Tumour ↗

  Case Reports in Oncology · 2010 · PMID 20740207
  not yet assessed
• MS471 FIBRINOGEN BETA VARIANTS CONFER PROTECTION AGAINST CORONARY ARTERY DISEASE IN A GREEK CASE–CONTROL STUDY ↗

  Atherosclerosis Supplements · 2010
  not yet assessed
• Gene-nutrition interactions that modify the risk of upper aero-digestive tract cancer. Screening results of a European multi-center case-control study ↗

  Das Gesundheitswesen · 2010
  not yet assessed
• HGV2009 meeting: bigger and better studies provide more answers and more questions ↗

  Human Mutation · 2010 · PMID 20506253
  not yet assessed
• early-onset breast cancer and BRCA2 mutations in familial cancer in Estonia

  2010
  not yet assessed
• Hundreds of variants clustered in genomic loci and biological pathways affect human height

  UWA Profiles and Research Repository (University of Western Australia) · 2010
  not yet assessed
• Contributors ↗

  Elsevier eBooks · 2010
  not yet assessed
• Genetic Structure of Europeans: A View from the North–East ↗

  PLoS ONE · 2009 · PMID 19424496
  not yet assessed
• Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals ↗

  International Journal of Epidemiology · 2009 · PMID 19776245
  not yet assessed
• Genetic Associations of 115 Polymorphisms with Cancers of the Upper Aerodigestive Tract across 10 European Countries: The ARCAGE Project ↗

  Cancer Research · 2009 · PMID 19339270
  not yet assessed
• Serotonin transporter promoter region polymorphisms do not influence treatment response to escitalopram in patients with major depression ↗

  European Neuropsychopharmacology · 2009 · PMID 19272758
  not yet assessed
• Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients ↗

  American Journal of Medical Genetics Part A · 2009 · PMID 19839039
  not yet assessed
• Evaluation of the 124-plex SNP typing microarray for forensic testing ↗

  Forensic Science International Genetics · 2009 · PMID 19948333
  not yet assessed
• Aromatase gene (CYP19A1) variants, female infertility and ovarian stimulation outcome: a preliminary report ↗

  Reproductive BioMedicine Online · 2009 · PMID 19549443
  not yet assessed
• Comparison of DNA extraction methods for multiplex polymerase chain reaction ↗

  Analytical Biochemistry · 2009 · PMID 19932073
  not yet assessed
• ROS1 Asp2213Asn polymorphism is not associated with coronary artery disease in a Greek case-control study ↗

  Clinical Chemistry and Laboratory Medicine (CCLM) · 2009 · PMID 19863298
  not yet assessed
• Analysis of Allele and Haplotype Diversity Across 25 Genomic Regions in Three Eastern European Populations ↗

  Human Heredity · 2009 · PMID 19339784
  not yet assessed
• Meta-analysis of genome-wide association results in > 10.000 individuals for the big five personality traits

  2009
  not yet assessed
• Abstract: P868 A PROSTACYCLIN SYNTHASE (PTGIS) GENE POLYMORPHISM INCREASES RISK OF CORONARY ARTERY DISEASE (CAD) ↗

  Atherosclerosis Supplements · 2009
  not yet assessed
• Supplementary Material for: Analysis of Allele and Haplotype Diversity Across 25 Genomic Regions in Three Eastern European Populations ↗

  Figshare · 2009
  not yet assessed
• Alcohol-related cancers and genetic susceptibility in Europe: the ARCAGE project: study samples and data collection ↗

  European Journal of Cancer Prevention · 2008 · PMID 18830131
  not yet assessed
• Development of a single tube 640-plex genotyping method for detection of nucleic acid variations on microarrays ↗

  Nucleic Acids Research · 2008 · PMID 18539607
  not yet assessed
• Thiopurine S-methyltransferase (TPMT) pharmacogenetics: three new mutations and haplotype analysis in the Estonian population ↗

  Clinical Chemistry and Laboratory Medicine (CCLM) · 2008 · PMID 18605963
  not yet assessed
• Arrayed Primer Extension Reaction for Genotyping on Oligonucleotide Microarray ↗

  Methods in molecular biology · 2008 · PMID 18425479
  not yet assessed
• Peripheral gene expression profiling of CCK‐4‐induced panic in healthy subjects ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2008 · PMID 19051287
  not yet assessed
• Arrayed primer extension on in situ synthesized 5′ → 3′ oligonucleotides in microchannels ↗

  New Biotechnology · 2008 · PMID 18786662
  not yet assessed
• P.2.c.012 Serotonin transporter promoter polymorphism does not influence treatment response to escitalopram in depression ↗

  European Neuropsychopharmacology · 2008
  not yet assessed
• Molecular diagnostics of Down syndrome using quantitative apex microarrays ↗

  Reproductive BioMedicine Online · 2008
  not yet assessed
• Investigation of the role of alcohol- metabolizing genes and DNA repair genes in the increase of levels of N2-ethylidenedeoxyguanosine

  Cancer Research · 2008
  not yet assessed
• Allelic estrogen receptor 1 (ESR1) gene variants predict the outcome of ovarian stimulation in in vitro fertilization ↗

  Molecular Human Reproduction · 2007 · PMID 17540666
  not yet assessed
• Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation ↗

  BMC Genomics · 2007 · PMID 17562002
  not yet assessed
• Optimization of candidate-gene SNP-genotyping by flexible oligonucleotide microarrays; analyzing variations in immune regulator genes of hay-fever samples ↗

  BMC Genomics · 2007 · PMID 17705862
  not yet assessed
• P2-030: NSCLC gene expression study in Estonia ↗

  Journal of Thoracic Oncology · 2007
  not yet assessed
• Microarray analysis of gene expression in scrapie-infected neuroblastoma cells: Implication of oxidative stress

  2007
  not yet assessed
• An Evaluation of the Performance of Tag SNPs Derived from HapMap in a Caucasian Population ↗

  PLoS Genetics · 2006 · PMID 16532062
  not yet assessed
• Simultaneous Multigene Mutation Detection in Patients With Sensorineural Hearing Loss Through a Novel Diagnostic Microarray: A New Approach for Newborn Screening Follow-up ↗

  PEDIATRICS · 2006 · PMID 16950989
  not yet assessed
• Association study of sporadic Parkinson's disease genetic risk factors in patients from Russia by APEX technology ↗

  Neuroscience Letters · 2006 · PMID 16876316
  not yet assessed
• Microarrays and Single Nucleotide Polymorphism (SNP) Genotyping ↗

  Encyclopedia of Life Sciences · 2006
  not yet assessed
• Association study of 90 candidate gene polymorphisms in panic disorder ↗

  Psychiatric Genetics · 2005 · PMID 15722953
  not yet assessed
• Analysis of SNP profiles in patients with major depressive disorder ↗

  The International Journal of Neuropsychopharmacology · 2005 · PMID 15927089
  not yet assessed
• Linkage Disequilibrium Patterns and tagSNP Transferability among European Populations ↗

  The American Journal of Human Genetics · 2005 · PMID 15637659
  not yet assessed
• Polymorphisms in wolframin (WFS1) gene are possibly related to increased risk for mood disorders ↗

  The International Journal of Neuropsychopharmacology · 2005 · PMID 15473915
  not yet assessed
• Genotyping Microarray for the Detection of More Than 200 CFTR Mutations in Ethnically Diverse Populations ↗

  Journal of Molecular Diagnostics · 2005 · PMID 16049310
  not yet assessed
• Arrayed Primer Extension Resequencing of Mutations in the TP53 Tumor Suppressor Gene: Comparison with Denaturing HPLC and Direct Sequencing ↗

  Clinical Chemistry · 2005 · PMID 15976115
  not yet assessed
• An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population ↗

  PLoS Genetics · 2005
  not yet assessed
• P.3.05 Association and haplotype analaysis of90 single-nucleotide polymorphisms in mood disorders ↗

  European Neuropsychopharmacology · 2005
  not yet assessed
• P.3.05 Association and haplotype analaysis of 90 single-nucleotide polymorphisms in mood disorders

  Murdoch Research Repository (Murdoch University) · 2005
  not yet assessed
• The Estonian Genome Project ↗

  Drug Development Research · 2004
  not yet assessed
• Das estnische Genomprojekt im Kontext der europäischen Genomforschung ↗

  DMW - Deutsche Medizinische Wochenschrift · 2004 · PMID 15133739
  not yet assessed
• Severe CF manifestation with anaemia and failure to thrive in a 394delTT homozygous patient ↗

  Journal of Cystic Fibrosis · 2004 · PMID 15463888
  not yet assessed
• Elevated incidence of chromosomally chaotic embryos among frozen-thawed preimplantation embryos ↗

  European Journal of Obstetrics & Gynecology and Reproductive Biology · 2004 · PMID 15099872
  not yet assessed
• P.3.031 Association study of 90 candidategenetic polymorphisms in panic disorder: Positive findings with SNPs in serotonin, cholecystokinin and dopamine related genes ↗

  European Neuropsychopharmacology · 2004
  not yet assessed
• P.3.031 Association study of 90 candidate genetic polymorphisms in panic disorder: Positive findings with SNPs in serotonin, cholecystokinin and dopamine related genes

  Murdoch Research Repository (Murdoch University) · 2004
  not yet assessed
• Analysis of single nucleotide polymorphisms in patients with mood disorders

  Murdoch Research Repository (Murdoch University) · 2003
  not yet assessed
• A first-generation linkage disequilibrium map of human chromosome 22 ↗

  Nature · 2002 · PMID 12110843
  not yet assessed
• Evaluating the arrayed primer extension resequencing assay of TP53 tumor suppressor gene ↗

  Proceedings of the National Academy of Sciences · 2002 · PMID 11960007
  not yet assessed
• Reliable detection of beta-thalassemia and G6PD mutations by a DNA microarray. ↗

  PubMed · 2002 · PMID 12406995
  not yet assessed
• Locations of several novel 2'-O-methylated nucleotides in human 28S rRNA ↗

  BMC Molecular Biology · 2002 · PMID 11897011
  not yet assessed
• Reliable Detection of β-Thalassemia and G6PD Mutations by a DNA Microarray ↗

  Clinical Chemistry · 2002
  not yet assessed
• A bovine papillomavirus-1 based vector restores the function of the low-density lipoprotein receptor in the receptor-deficient CHO-ldlA7 cell line ↗

  BMC Molecular Biology · 2002 · PMID 11967145
  not yet assessed
• Estonian Genome Project—before the take-off andtake-off ↗

  Bioinformatics · 2002 · PMID 12385997
  not yet assessed
• High-density genotyping and linkage disequilibrium in the human genome using chromosome 22 as a model ↗

  Current Opinion in Chemical Biology · 2002 · PMID 11827819
  not yet assessed
• Genes, technology and public dialogue in Tartu, Estonia ↗

  Trends in biotechnology · 2002 · PMID 11814590
  not yet assessed
• Erratum to: A bovine papillomavirus-1 based vector restores the function of the low-density lipoprotein receptor in the receptor-deficient CHO-ldlA7 cell line ↗

  BMC Molecular Biology · 2002
  not yet assessed
• Possible association of serotonin 1B receptor and cholecystolkinin 1 receptor gene polymorphisms in bipolar and unipolar affective disorder cases in Estonia

  Murdoch Research Repository (Murdoch University) · 2002
  not yet assessed
• Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chain ↗

  Journal of Inherited Metabolic Disease · 2001 · PMID 11286378
  not yet assessed
• Arrayed Primer Extension: Solid-Phase Four-Color DNA Resequencing and Mutation Detection Technology ↗

  Genetic Testing · 2000 · PMID 10794354
  not yet assessed
• Unravelling Genetic Data by Arrayed Primer Extension ↗

  Clinical Chemistry and Laboratory Medicine (CCLM) · 2000 · PMID 10834405
  not yet assessed
• Human N-benzoyl-l-tyrosyl-p-aminobenzoic acid hydrolase (human meprin): genomic structure of the α and β subunits ↗

  Biochemical Journal · 2000 · PMID 10657243
  not yet assessed
• Mutation 985A&gt;G in the MCAD gene shows low incidence in Estonian population ↗

  Human Mutation · 2000 · PMID 10679947
  not yet assessed
• DNA arrays: methods and applications: report on HUGO Meeting, Tartu, Estonia, 23–26 May, 1999 ↗

  European Journal of Human Genetics · 2000 · PMID 10780791
  not yet assessed
• Immobilisation of arrayed oligonucleotides for mutation detection by primer extension ↗

  Biochemical Society Transactions · 2000
  not yet assessed
• Universal and flexible DNA microarray approach: arrayed primer extension ↗

  Nature Genetics · 1999
  not yet assessed
• U82, a novel snoRNA identified from the fifth intron of human and mouse nucleolin gene ↗

  Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · 1999 · PMID 10524220
  not yet assessed
• Genomic organization of the human complex I 13-kDa subunit gene NDUFA5 ↗

  Cytogenetic and Genome Research · 1999 · PMID 10343126
  not yet assessed
• DNA resequencing, mutation detection and gene expression analysis by oligonucleotide microchips ↗

  Birkhäuser Basel eBooks · 1999
  not yet assessed
• Oligonucleotide Array for Mutation Analysis in Familial Breast Cancer ↗

  Disease Markers · 1999
  not yet assessed
• Nuclear Import and Nucleolar Accumulation of the Human Ribosomal Protein S7 Depends on both a Minimal Nuclear Localization Sequence and an Adjacent Basic Region ↗

  Biochemical and Biophysical Research Communications · 1998 · PMID 9731210
  not yet assessed
• A novel snoRNA (U73) is encoded within the introns of the human and mouse ribosomal protein S3a genes ↗

  Gene · 1998 · PMID 9573378
  not yet assessed
• Neonatal screening for the cystic fibrosis main mutation ΔF508 in Estonia ↗

  Journal of Medical Screening · 1998 · PMID 9575453
  not yet assessed
• Minisequencing: A Specific Tool for DNA Analysis and Diagnostics on Oligonucleotide Arrays ↗

  Genome Research · 1997 · PMID 9199933
  not yet assessed
• A human cDNA encoding the homologue of NADH:ubiquinone oxidoreductase subunit B13 ↗

  Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · 1997 · PMID 9048877
  not yet assessed
• A specific tool for DNA analysis and diagnostics on oligonucleotide arrays

  STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 1997
  not yet assessed
• Mutation detection by solid phase primer extension ↗

  Human Mutation · 1996 · PMID 8723685
  not yet assessed
• Mutation detection by solid phase primer extension ↗

  Human Mutation · 1996
  not yet assessed
• Phenylalanine Hydroxylase GeneMutation R408W Is Present on84% of Estonian PhenylketonuriaChromosomes ↗

  European Journal of Human Genetics · 1996 · PMID 8946176
  not yet assessed
• The incidence and characterization of phenylketonuric patients in Estonia ↗

  Journal of Inherited Metabolic Disease · 1996 · PMID 8803791
  not yet assessed
• The human ribosomal protein S7-encoding gene: isolation, structure and localization in 2p25 ↗

  Gene · 1995 · PMID 8522193
  not yet assessed
• Detecting Lesch-Nyhan syndrome by solid phase primer extension ↗

  The American Journal of Human Genetics · 1994
  not yet assessed
• A dinucleotide repeat polymorphism at the ribosomal protein S6 (RPS6) gene ↗

  Human Molecular Genetics · 1993 · PMID 8268945
  not yet assessed
• Human ribosomal protein S3a: cloning of the cDNA and primary structure of the protein ↗

  Gene · 1992 · PMID 1398113
  not yet assessed
• The human ribosomal protein S6 gene: isolation, primary structure and location in chromosome 9 ↗

  Gene · 1992 · PMID 1446836
  not yet assessed
• A 5S rRNA/L5 complex is a precursor to ribosome assembly in mammalian cells. ↗

  The Journal of Cell Biology · 1988 · PMID 3279045
  not yet assessed
• Structure and expression of the genes coding for human alpha 1‐acid glycoprotein. ↗

  The EMBO Journal · 1987 · PMID 2822385
  not yet assessed
• Location of single-stranded and double-stranded regions in rat liver ribosomal 5S RNA and 5.8S RNA ↗

  Nucleic Acids Research · 1981 · PMID 6272219
  not yet assessed
• 5 S RNA and 5.8 S RNA build up eukaryotic subribosomal domains active in tRNA binding ↗

  FEBS Letters · 1981 · PMID 7327261
  not yet assessed
• FUNCTIONAL ACTIVITIES OF 5S RNA- AND 5.8S RNA-PROTEIN COMPLEXES IN EUKARYOTIC TRANSLATION ↗

  Biochemical Society Transactions · 1981
  not yet assessed
• The ternary complex consisting of rat liver ribosomal 5 S RNA, 5.8 S RNA and protein L5 ↗

  FEBS Letters · 1980 · PMID 7428930
  not yet assessed
• Immobilized eukaryotic 5.8 S RNA binds <i>escherichia coli</i> and rat liver ribosomal proteins ↗

  FEBS Letters · 1979 · PMID 383507
  not yet assessed
• New aspects of the eukaryotic ribosomal subunit interaction ↗

  FEBS Letters · 1979 · PMID 499560
  not yet assessed
• Interaction of 5-S RNA, 5.8-S RNA and tRNA with Rat-Liver Ribosomal Proteins ↗

  European Journal of Biochemistry · 1978 · PMID 720348
  not yet assessed