Alexander Teumer

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.

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

Assessed papers (2)

• Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities.
  2022 L1 No data access
• Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome.
  2021 L1 100/100

2 assessed by us (1 reproduced) · 647 not yet assessed — every PubMed paper on record, linked below.

• Genetic basis of the circle of Willis characteristics in the healthy and intracranial aneurysm population ↗

  European Journal of Human Genetics · 2026 · PMID 41826712
  not yet assessed
• 46. Epigenomic Embedding of Childhood Adversity Links to Disease Risk and Chronic Inflammation ↗

  Biological Psychiatry · 2026
  not yet assessed
• The impact of glucose and metabolic disturbances on white matter hyperintensity volume in apparently healthy adults ↗

  Frontiers in Endocrinology · 2026 · PMID 41928882
  not yet assessed
• Thyroid hormones are associated with pituitary and thyroid volume in a population-based study ↗

  Journal of the Endocrine Society · 2026 · PMID 42005304
  not yet assessed
• Thyroid function and risk of sepsis: a population-based prospective cohort study with traditional and genetic epidemiological analyses ↗

  Frontiers in Endocrinology · 2026 · PMID 42445872
  not yet assessed
• DNA methylation signatures associated with bipolar disorder in peripheral blood improve prediction models ↗

  JuSER Publikationsportal · 2026
  not yet assessed
• Multi-ancestry genome-wide association analyses provide insights into the genetic basis of Hashimoto’s thyroiditis ↗

  Nature Genetics · 2026 · PMID 42527560
  not yet assessed
• Genome-wide meta-analysis of quantitatively measured generalized anxiety symptoms in individuals of European ancestry ↗

  Nature Human Behaviour · 2026 · PMID 42265330
  not yet assessed
• Genome-wide association study meta-analysis identifies susceptibility loci informing Ewing sarcoma etiology and potential mechanisms of risk ↗

  medRxiv · 2026 · PMID 41728338
  not yet assessed
• Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling ↗

  JuSER Publikationsportal · 2026
  not yet assessed
• Combined periodontitis GWAS identifies <i>LINC01541</i> as a regulator of innate immunity in the oral mucosa ↗

  Human Molecular Genetics · 2026 · PMID 42224457
  not yet assessed
• Distinct and shared genetics of kidney filtration function versus albuminuria revealed by multi-trait GWAS ↗

  medRxiv · 2026
  not yet assessed
• Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes ↗

  Nature Genetics · 2025 · PMID 40038546
  not yet assessed
• Associations between common genetic variants and income provide insights about the socio-economic health gradient ↗

  Nature Human Behaviour · 2025 · PMID 39875632
  not yet assessed
• A methylome-wide association study of major depression with out-of-sample case–control classification and trans-ancestry comparison ↗

  Nature Mental Health · 2025 · PMID 41069367
  not yet assessed
• Insights from a methylome-wide association study of antidepressant exposure ↗

  Nature Communications · 2025 · PMID 39994233
  not yet assessed
• DNA Methylation Signatures of Cardiovascular Health Provide Insights Into Diseases ↗

  Circulation · 2025 · PMID 40654086
  not yet assessed
• Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration ↗

  Nature Communications · 2025 · PMID 40075072
  not yet assessed
• DNA methylation of genes involved in lipid metabolism drives adiponectin levels and metabolic disease ↗

  Diabetologia · 2025 · PMID 41057690
  not yet assessed
• Strength of Genetic Associations with Thyrotropin Values Differs Between Populations with Similarity to African and European Reference Populations ↗

  Thyroid · 2025 · PMID 39869013
  not yet assessed
• Genetics of Thyroid Function: Relevance for Biology and Disease Management ↗

  The Journal of Clinical Endocrinology & Metabolism · 2025 · PMID 41252260
  not yet assessed
• Cross-sectional and longitudinal association of seven DNAm-based predictors with metabolic syndrome and type 2 diabetes ↗

  Clinical Epigenetics · 2025 · PMID 40200378
  not yet assessed
• Genomic and molecular evidence that the LncRNA DSP-AS1 modulates desmoplakin expression ↗

  Human Genetics · 2025 · PMID 40736537
  not yet assessed
• Removing array-specific batch effects in GWAS mega-analyses by applying a two-step imputation workflow ↗

  Bioinformatics Advances · 2025 · PMID 41808772
  not yet assessed
• Genomics of diffusion-imaging integrating GWAS, exome data and single-cell sequencing unravels lifespan determinants of cerebral small vessel disease ↗

  Research Square · 2025
  not yet assessed
• Genomic and molecular evidence that the lncRNA <i>DSP-AS1</i> modulates Desmoplakin expression ↗

  medRxiv · 2025 · PMID 40236443
  not yet assessed
• Time to change the electrocardiography (ECG) indices of left ventricular hypertrophy: the Bialystok PLUS and SHIP-TREND population-based studies ↗

  European Journal of Preventive Cardiology · 2025
  not yet assessed
• Novel and Known Genetic Players in Hypertension: From Gene Expression to Striking Insights ↗

  medRxiv · 2025
  not yet assessed
• Using Two-Sample Mendelian Randomization to Identify Potential Drug Targets: The Case of Desmoplakin ↗

  Epidemiology Biostatistics and Public Health · 2025
  not yet assessed
• T43. CAUSALITY BETWEEN DEPRESSION AND THYROID FUNCTION: A BI-DIRECTIONAL MENDELIAN RANDOMIZATION STUDY ↗

  European Neuropsychopharmacology · 2025
  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
• Abstract 4359763: Genetic determinants of left ventricular diastolic function ↗

  Circulation · 2025
  not yet assessed
• Epigenome-Wide Association Study in Asian Cohort Identifies Novel DNA Methylation Markers for Carotid Intima-Media Thickness ↗

  medRxiv · 2025 · PMID 41334702
  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
• Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications ↗

  Nature Communications · 2024 · PMID 38291025
  not yet assessed
• Thyroid Function, Diabetes, and Common Age-Related Eye Diseases: A Mendelian Randomization Study ↗

  Thyroid · 2024 · PMID 39283829
  not yet assessed
• X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements ↗

  Nature Communications · 2024 · PMID 38233393
  not yet assessed
• Methylation Patterns of the FKBP5 Gene in Association with Childhood Maltreatment and Depressive Disorders ↗

  International Journal of Molecular Sciences · 2024 · PMID 38338761
  not yet assessed
• Towards Personalized TSH Reference Ranges: A Genetic and Population-Based Approach in Three Independent Cohorts ↗

  Thyroid · 2024 · PMID 38919119
  not yet assessed
• Genetic variants for head size share genes and pathways with cancer ↗

  Cell Reports Medicine · 2024 · PMID 38703765
  not yet assessed
• Distinct genetic liability profiles define clinically relevant patient strata across common diseases ↗

  Nature Communications · 2024 · PMID 38951512
  not yet assessed
• A meta-analysis of genome-wide studies of resilience in the German population ↗

  Molecular Psychiatry · 2024 · PMID 39112778
  not yet assessed
• Cortical similarities in psychiatric and mood disorders identified in federated VBM analysis via COINSTAC ↗

  Patterns · 2024 · PMID 39081570
  not yet assessed
• New insights into the hypothalamic–pituitary–thyroid axis: a transcriptome- and proteome-wide association study ↗

  European Thyroid Journal · 2024 · PMID 38805593
  not yet assessed
• Integrating multiple kidney function markers to predict all-cause and cardiovascular disease mortality: prospective analysis of 366 758 UK Biobank participants ↗

  Clinical Kidney Journal · 2024 · PMID 39135936
  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
• Cardiovascular risk and preclinical atherosclerosis are associated with white matter hyperintensities in apparently healthy adults: the population-based cross-sectional study BIALYSTOK PLUS ↗

  Polskie Archiwum Medycyny Wewnętrznej · 2024 · PMID 39140449
  not yet assessed
• Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance ↗

  Alzheimer s Research & Therapy · 2024 · PMID 38245754
  not yet assessed
• Association analysis between an epigenetic alcohol risk score and blood pressure ↗

  Clinical Epigenetics · 2024 · PMID 39468603
  not yet assessed
• Epigenetic associations with kidney disease in individuals of African ancestry with <i>APOL1</i> high-risk genotypes and HIV ↗

  Nephrology Dialysis Transplantation · 2024 · PMID 39448372
  not yet assessed
• The role of thyroid function in borderline personality disorder and schizophrenia: a Mendelian Randomisation study ↗

  Borderline Personality Disorder and Emotion Dysregulation · 2024 · PMID 38355654
  not yet assessed
• Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling ↗

  medRxiv · 2024 · PMID 39006447
  not yet assessed
• Associations between common genetic variants and income provide insights about the socioeconomic health gradient ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2024
  not yet assessed
• Antidepressant Exposure and DNA Methylation: Insights from a Methylome-Wide Association Study ↗

  medRxiv · 2024 · PMID 38746357
  not yet assessed
• Associations between common genetic variants and income provide insights about the socioeconomic health gradient ↗

  Research Square · 2024
  not yet assessed
• Associations between common genetic variants and income provide insights about the socio-economic health gradient ↗

  2024
  not yet assessed
• DNA Methylation Signatures of Cardiovascular Health Provide Insights into Diseases ↗

  medRxiv · 2024 · PMID 39606375
  not yet assessed
• Association analysis between an epigenetic alcohol risk score and blood pressure ↗

  medRxiv · 2024 · PMID 38464320
  not yet assessed
• Association analysis between an epigenetic alcohol risk score and blood pressure ↗

  Research Square · 2024 · PMID 38699335
  not yet assessed
• GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes ↗

  UNC Libraries · 2024
  not yet assessed
• Association of Forced Vital Capacity with the Developmental Gene NCOR2 ↗

  Tampere University Institutional Repository (Tampere University) · 2024
  not yet assessed
• NFAT5 and SLC4A10 loci associate with plasma osmolality ↗

  UNC Libraries · 2024
  not yet assessed
• Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women ↗

  UNC Libraries · 2024
  not yet assessed
• Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data ↗

  UNC Libraries · 2024
  not yet assessed
• Towards personalized TSH reference ranges: a genetic and population-based approach in three independent cohorts ↗

  Endocrine Abstracts · 2024
  not yet assessed
• Unraveling the genetic landscape of hypothyroidism: insights from a multi-ancestry GWAS meta-analysis ↗

  Endocrine Abstracts · 2024
  not yet assessed
• Towards Personalized TSH Reference Ranges: A Genetic and Population-Based Approach in Three Independent Cohorts ↗

  VideoEndocrinology · 2024
  not yet assessed
• Genetic variants for head size share genes and pathways with cancer ↗

  UNC Libraries · 2024
  not yet assessed
• Removing array-specific batch effects in GWAS mega-analyses by applying a two-step imputation workflow reveals new associations for thyroid volume and goiter ↗

  medRxiv · 2024
  not yet assessed
• X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements ↗

  UNC Libraries · 2024
  not yet assessed
• Integrative cross-omics analysis identifies DNA methylation signatures associated with bilateral hippocampal volume, asymmetry and atrophy rate in the general population ↗

  medRxiv · 2024
  not yet assessed
• Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease ↗

  Nature Medicine · 2023 · PMID 37069360
  not yet assessed
• A second update on mapping the human genetic architecture of COVID-19 ↗

  Nature · 2023 · PMID 37674002
  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
• OTTERS: a powerful TWAS framework leveraging summary-level reference data ↗

  Nature Communications · 2023 · PMID 36882394
  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
• Imputation-powered whole-exome analysis identifies genes associated with kidney function and disease in the UK Biobank ↗

  Nature Communications · 2023 · PMID 36890159
  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
• DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood ↗

  Journal of Thrombosis and Haemostasis · 2023 · PMID 36716967
  not yet assessed
• Height, Autoimmune Thyroid Disease, and Thyroid Cancer: A Mendelian Randomization Study ↗

  Thyroid · 2023 · PMID 37772697
  not yet assessed
• Alpha-1 Antitrypsin Augmentation and the Liver Phenotype of Adults With Alpha-1 Antitrypsin Deficiency (Genotype Pi∗ZZ) ↗

  Clinical Gastroenterology and Hepatology · 2023 · PMID 37716616
  not yet assessed
• Novel (sulfated) thyroid hormone transporters in the solute carrier 22 family ↗

  European Thyroid Journal · 2023 · PMID 37074673
  not yet assessed
• Epigenome-Wide Association Study Reveals CpG Sites Associated with Thyroid Function and Regulatory Effects on <i>KLF9</i> ↗

  Thyroid · 2023 · PMID 36719767
  not yet assessed
• High Thyroid-Stimulating Hormone and Low Free Triiodothyronine Levels Are Associated with Chronic Kidney Disease in Three Population-Based Studies from Germany ↗

  Journal of Clinical Medicine · 2023 · PMID 37685830
  not yet assessed
• Allometric body shape indices, <scp>type 2 diabetes</scp> and kidney function: A two‐sample Mendelian randomization study ↗

  Diabetes Obesity and Metabolism · 2023 · PMID 36855799
  not yet assessed
• Mendelian randomization indicates causal effects of estradiol levels on kidney function in males ↗

  Frontiers in Endocrinology · 2023 · PMID 38169598
  not yet assessed
• Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers ↗

  Biological Psychiatry · 2023 · PMID 37661008
  not yet assessed
• A Step Toward Disentangling the Complex Relationship Between Vitamin D and Kidney Function ↗

  The Journal of Clinical Endocrinology & Metabolism · 2023 · PMID 36715302
  not yet assessed
• Genetic Variants in WNT16 and PKD2L1 Locus Affect Heel Ultrasound Bone Stiffness: Analyses from the General Population and Patients Evaluated for Osteoporosis ↗

  Calcified Tissue International · 2023 · PMID 37831088
  not yet assessed
• Multi-Trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications ↗

  Endocrine Abstracts · 2023
  not yet assessed
• Mapping the aetiological foundations of the heart failure spectrum using human genetics ↗

  medRxiv · 2023
  not yet assessed
• A methylome-wide association study of major depression with out-of-sample case-control classification and trans-ancestry comparison ↗

  medRxiv · 2023
  not yet assessed
• Distinct genetic liability profiles define clinically relevant patient strata across common diseases ↗

  medRxiv · 2023 · PMID 37214898
  not yet assessed
• The Genetic Basis of Resilience: A Genome-Wide Association Study Meta-Analysis in the German Population ↗

  Research Square · 2023
  not yet assessed
• Author response for "Allometric body shape indices, &lt;scp&gt;T2D&lt;/scp&gt; and kidney function: A two‐sample Mendelian randomization study" ↗

  2023
  not yet assessed
• Author response for "Allometric body shape indices, &lt;scp&gt;T2D&lt;/scp&gt; and kidney function: A two‐sample Mendelian randomization study" ↗

  2023
  not yet assessed
• Data from Physical Activity Does Not Lower the Risk of Lung Cancer ↗

  2023
  not yet assessed
• Data from Physical Activity Does Not Lower the Risk of Lung Cancer ↗

  2023
  not yet assessed
• Supplementary Tables from Physical Activity Does Not Lower the Risk of Lung Cancer ↗

  2023
  not yet assessed
• Supplementary Tables from Physical Activity Does Not Lower the Risk of Lung Cancer ↗

  2023
  not yet assessed
• Supplementary Note from Physical Activity Does Not Lower the Risk of Lung Cancer ↗

  2023
  not yet assessed
• Supplementary Note from Physical Activity Does Not Lower the Risk of Lung Cancer ↗

  2023
  not yet assessed
• 418-P: Allometric Body Shape Indices, T2D, and Kidney Function—A Two-Sample Mendelian Randomization Study ↗

  Diabetes · 2023
  not yet assessed
• Epigenome-wide association study reveals cpg sites associated with thyroid function and regulatory effects on KLF9 ↗

  Endocrine Abstracts · 2023
  not yet assessed
• The effects of common genetic variation in 96 genes involved in thyroid hormone regulation on TSH and FT4 concentrations ↗

  Yearbook of pediatric endocrinology · 2023
  not yet assessed
• Correction: Analysis of epidemiological association patterns of serum thyrotropin by combining random forests and Bayesian networks ↗

  PLoS ONE · 2023 · PMID 37948441
  not yet assessed
• New insights into the genetic etiology of Alzheimer’s disease and related dementias ↗

  Nature Genetics · 2022 · PMID 35379992
  not yet assessed
• A saturated map of common genetic variants associated with human height ↗

  Nature · 2022 · PMID 36224396
  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
• Stroke genetics informs drug discovery and risk prediction across ancestries ↗

  Nature · 2022 · PMID 36180795
  not yet assessed
• Genetic variants associated with longitudinal changes in brain structure across the lifespan ↗

  Nature Neuroscience · 2022 · PMID 35383335
  not yet assessed
• Association of Telomere Length With Risk of Disease and Mortality ↗

  JAMA Internal Medicine · 2022 · PMID 35040871
  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
• Cohort Profile Update: The Study of Health in Pomerania (SHIP) ↗

  International Journal of Epidemiology · 2022 · PMID 35348705
  not yet assessed
• DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases ↗

  Nature Communications · 2022 · PMID 35504910
  not yet assessed
• Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities

  Nature Communications · 2022 · PMID 35922433
  L1 No data access
• Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies ↗

  Kidney International · 2022 · PMID 35716955
  not yet assessed
• Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI ↗

  Brain · 2022 · PMID 35943854
  not yet assessed
• Virtual Ontogeny of Cortical Growth Preceding Mental Illness ↗

  Biological Psychiatry · 2022 · PMID 35489875
  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
• Thyroid function, pernicious anemia and erythropoiesis: a two-sample Mendelian randomization study ↗

  Human Molecular Genetics · 2022 · PMID 35225327
  not yet assessed
• Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning ↗

  Molecular Psychiatry · 2022 · PMID 35974141
  not yet assessed
• Limited evidence for blood eQTLs in human sexual dimorphism ↗

  Genome Medicine · 2022 · PMID 35953856
  not yet assessed
• Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort ↗

  Metabolites · 2022 · PMID 35888728
  not yet assessed
• Insulin-Like Growth Factor, Inflammation, and MRI Markers of Alzheimer’s Disease in Predominantly Middle-Aged Adults ↗

  Journal of Alzheimer s Disease · 2022 · PMID 35599493
  not yet assessed
• Longitudinal association of Apolipoprotein E polymorphism with lipid profile, type 2 diabetes and metabolic syndrome: Results from a 15 year follow-up study ↗

  Diabetes Research and Clinical Practice · 2022 · PMID 35167921
  not yet assessed
• Effects of Apolipoprotein E polymorphism on carotid intima-media thickness, incident myocardial infarction and incident stroke ↗

  Scientific Reports · 2022 · PMID 35332187
  not yet assessed
• The Effects of Common Genetic Variation in 96 Genes Involved in Thyroid Hormone Regulation on TSH and FT4 Concentrations ↗

  The Journal of Clinical Endocrinology & Metabolism · 2022 · PMID 35262175
  not yet assessed
• Association of Alpha-1 Antitrypsin Pi*Z Allele Frequency and Progressive Liver Fibrosis in Two Chronic Hepatitis C Cohorts ↗

  Journal of Clinical Medicine · 2022 · PMID 36615054
  not yet assessed
• TREML2 Gene Expression and Its Missense Variant rs3747742 Associate with White Matter Hyperintensity Volume and Alzheimer’s Disease-Related Brain Atrophy in the General Population ↗

  International Journal of Molecular Sciences · 2022 · PMID 36430248
  not yet assessed
• Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease ↗

  Alzheimer s & Dementia · 2022
  not yet assessed
• Discovery of novel eGFR-associated multiple independent signals using a quasi-adaptive method ↗

  Frontiers in Genetics · 2022 · PMID 36386835
  not yet assessed
• Analysis of epidemiological association patterns of serum thyrotropin by combining random forests and Bayesian networks ↗

  PLoS ONE · 2022 · PMID 35862421
  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
• OTTERS: A powerful TWAS framework leveraging summary-level reference data ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2022
  not yet assessed
• Alpha-1 antitrypsin (AAT) augmentation therapy and liver phenotype in individuals with homozygous Pi*Z AAT mutation (Pi*ZZ genotype) ↗

  Journal of Hepatology · 2022
  not yet assessed
• Imputation-powered whole-exome analysis identifies rare coding variants and genes associated with kidney function and disease in the UK Biobank ↗

  Research Square · 2022
  not yet assessed
• Fifteen Genetic Loci Associated with the Electrocardiographic P Wave ↗

  UNC Libraries · 2022
  not yet assessed
• Additional file 2 of Limited evidence for blood eQTLs in human sexual dimorphism ↗

  Open MIND · 2022
  not yet assessed
• Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression ↗

  Nature Genetics · 2021 · PMID 34475573
  not yet assessed
• Mapping the human genetic architecture of COVID-19 ↗

  Nature · 2021 · PMID 34237774
  not yet assessed
• Genetic insights into biological mechanisms governing human ovarian ageing ↗

  Nature · 2021 · PMID 34349265
  not yet assessed
• Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ↗

  Biological Psychiatry · 2021 · PMID 34861974
  not yet assessed
• Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women ↗

  Nature Communications · 2021 · PMID 33510174
  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
• 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
• Identifying the Common Genetic Basis of Antidepressant Response ↗

  Biological Psychiatry Global Open Science · 2021 · PMID 35712048
  not yet assessed
• Obesity and Kidney Function: A Two-Sample Mendelian Randomization Study ↗

  Clinical Chemistry · 2021 · PMID 34922334
  not yet assessed
• Physical activity, sedentary behavior and risk of coronary artery disease, myocardial infarction and ischemic stroke: a two-sample Mendelian randomization study ↗

  Clinical Research in Cardiology · 2021 · PMID 33774696
  not yet assessed
• Thyroid function, sex hormones and sexual function: a Mendelian randomization study ↗

  European Journal of Epidemiology · 2021 · PMID 33548002
  not yet assessed
• Meta-analyses identify DNA methylation associated with kidney function and damage ↗

  Nature Communications · 2021 · PMID 34887417
  not yet assessed
• Thyroid Function and Mood Disorders: A Mendelian Randomization Study ↗

  Thyroid · 2021 · PMID 33899528
  not yet assessed
• Genome-wide association study of circulating interleukin 6 levels identifies novel loci ↗

  Human Molecular Genetics · 2021 · PMID 33517400
  not yet assessed
• Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease ↗

  Neurology · 2021 · PMID 34845052
  not yet assessed
• Genome-wide interaction study with major depression identifies novel variants associated with cognitive function ↗

  Molecular Psychiatry · 2021 · PMID 34782712
  not yet assessed
• Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate ↗

  Brain · 2021 · PMID 35511193
  not yet assessed
• Plasma Proteomics of Renal Function: A Transethnic Meta-Analysis and Mendelian Randomization Study ↗

  Journal of the American Society of Nephrology · 2021 · PMID 34135082
  not yet assessed
• 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans ↗

  Translational Psychiatry · 2021 · PMID 33753722
  not yet assessed
• Thyroid Function and the Risk of Alzheimer's Disease: A Mendelian Randomization Study ↗

  Thyroid · 2021 · PMID 34847795
  not yet assessed
• Effects of Thyroid Function on Hemostasis, Coagulation, and Fibrinolysis: A Mendelian Randomization Study ↗

  Thyroid · 2021 · PMID 34210154
  not yet assessed
• Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus ↗

  Nature Communications · 2021 · PMID 34887389
  not yet assessed
• Meta-analysis of epigenome-wide association studies of carotid intima-media thickness ↗

  European Journal of Epidemiology · 2021 · PMID 34091768
  not yet assessed
• Validating biomarkers and models for epigenetic inference of alcohol consumption from blood ↗

  Clinical Epigenetics · 2021 · PMID 34702360
  not yet assessed
• SHIP-MR and Radiology: 12 Years of Whole-Body Magnetic Resonance Imaging in a Single Center ↗

  Healthcare · 2021 · PMID 35052197
  not yet assessed
• The Genomics of Heart Failure: Design and Rationale of the HERMES Consortium ↗

  ESC Heart Failure · 2021 · PMID 34480422
  not yet assessed
• Associations and interactions of the serotonin receptor genes 5-HT1A, 5-HT2A, and childhood trauma with alexithymia in two independent general-population samples ↗

  Psychiatry Research · 2021 · PMID 33567384
  not yet assessed
• Genetic factors influencing a neurobiological substrate for psychiatric disorders ↗

  Translational Psychiatry · 2021 · PMID 33782385
  not yet assessed
• Sex effects for the interaction of dopamine related genetic variants for COMT and BDNF on declarative memory performance ↗

  Genes Brain & Behavior · 2021 · PMID 33876571
  not yet assessed
• Assessment of significance of conditionally independent GWAS signals ↗

  Bioinformatics · 2021 · PMID 33978749
  not yet assessed
• A Deeper Understanding of the Causal Relationships Between Thyroid Function and Atrial Fibrillation ↗

  The Journal of Clinical Endocrinology & Metabolism · 2021 · PMID 34279034
  not yet assessed
• Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

  Figshare · 2021
  not yet assessed
• Genetic insights into the biological mechanisms governing human ovarian ageing ↗

  medRxiv · 2021
  not yet assessed
• DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases ↗

  Research Square · 2021
  not yet assessed
• Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease ↗

  Research Square · 2021
  not yet assessed
• Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer ↗

  Nature Communications · 2021 · PMID 34916535
  not yet assessed
• 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans ↗

  2021
  not yet assessed
• Thyroid function and the risk of Alzheimer’s disease: A Mendelian Randomisation study ↗

  medRxiv · 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
• Einfluss der Augmentationstherapie mit Alpha1-Antitrypsin auf den Leberphänotyp von Individuen mit klassischem Alpha1-Antitrypsin-Mangel (Genotyp Pi*ZZ) ↗

  Zeitschrift für Gastroenterologie · 2021
  not yet assessed
• Investigating the genetic and environmental basis of head micromovements during MRI ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2021
  not yet assessed
• Additional file 3 of Validating biomarkers and models for epigenetic inference of alcohol consumption from blood ↗

  Open MIND · 2021
  not yet assessed
• Additional file 2 of Validating biomarkers and models for epigenetic inference of alcohol consumption from blood ↗

  Figshare · 2021
  not yet assessed
• Additional file 7 of Validating biomarkers and models for epigenetic inference of alcohol consumption from blood ↗

  Figshare · 2021
  not yet assessed
• Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders ↗

  Biological Psychiatry · 2021 · PMID 34099189
  not yet assessed
• Investigation of the Interplay between Circulating Lipids and IGF-I and Relevance to Breast Cancer Risk: An Observational and Mendelian Randomization Study ↗

  Cancer Epidemiology Biomarkers & Prevention · 2021 · PMID 34583967
  not yet assessed
• Obesity and Kidney Function: A Two-Sample Mendelian Randomization Study. ↗

  Apollo (University of Cambridge) · 2021
  not yet assessed
• Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure ↗

  Nature Communications · 2020 · PMID 31919418
  not yet assessed
• The genetic architecture of the human cerebral cortex ↗

  Science · 2020 · PMID 32193296
  not yet assessed
• ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries ↗

  Translational Psychiatry · 2020 · PMID 32198361
  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
• Cerebral small vessel disease genomics and its implications across the lifespan ↗

  Nature Communications · 2020 · PMID 33293549
  not yet assessed
• White Blood Cells and Blood Pressure ↗

  Circulation · 2020 · PMID 32148083
  not yet assessed
• A bidirectional Mendelian randomization study supports causal effects of kidney function on blood pressure ↗

  Kidney International · 2020 · PMID 32454124
  not yet assessed
• GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer ↗

  Nature Communications · 2020 · PMID 32769997
  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
• Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults ↗

  Nature Communications · 2020 · PMID 32963231
  not yet assessed
• Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline ↗

  Kidney International · 2020 · PMID 33137338
  not yet assessed
• Liver Phenotypes of European Adults Heterozygous or Homozygous for Pi∗Z Variant of AAT (Pi∗MZ vs Pi∗ZZ genotype) and Noncarriers ↗

  Gastroenterology · 2020 · PMID 32376409
  not yet assessed
• The Genetic Makeup of the Electrocardiogram ↗

  Cell Systems · 2020 · PMID 32916098
  not yet assessed
• Association of polygenic score for major depression with response to lithium in patients with bipolar disorder ↗

  Molecular Psychiatry · 2020 · PMID 32203155
  not yet assessed
• Epigenetic Link Between Statin Therapy and Type 2 Diabetes ↗

  Diabetes Care · 2020 · PMID 32033992
  not yet assessed
• Thyroid Function Affects the Risk of Stroke via Atrial Fibrillation: A Mendelian Randomization Study ↗

  The Journal of Clinical Endocrinology & Metabolism · 2020 · PMID 32374820
  not yet assessed
• Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity ↗

  Diabetes · 2020 · PMID 32917775
  not yet assessed
• Physical activity and risk of Alzheimer disease ↗

  Neurology · 2020 · PMID 32680943
  not yet assessed
• Variation in Normal Range Thyroid Function Affects Serum Cholesterol Levels, Blood Pressure, and Type 2 Diabetes Risk: A Mendelian Randomization Study ↗

  Thyroid · 2020 · PMID 32746749
  not yet assessed
• The Genetic Basis of Thyroid Function: Novel Findings and New Approaches ↗

  The Journal of Clinical Endocrinology & Metabolism · 2020 · PMID 32271924
  not yet assessed
• Integration of GWAS Summary Statistics and Gene Expression Reveals Target Cell Types Underlying Kidney Function Traits ↗

  Journal of the American Society of Nephrology · 2020 · PMID 32764137
  not yet assessed
• Effects of Thyroid Status on Regional Brain Volumes: A Diagnostic and Genetic Imaging Study in UK Biobank ↗

  The Journal of Clinical Endocrinology & Metabolism · 2020 · PMID 33274371
  not yet assessed
• Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation ↗

  Circulation Genomic and Precision Medicine · 2020 · PMID 32822252
  not yet assessed
• The genetics of circulating BDNF: towards understanding the role of BDNF in brain structure and function in middle and old ages ↗

  Brain Communications · 2020 · PMID 33345186
  not yet assessed
• Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies ↗

  Biological Psychiatry · 2020 · PMID 32684367
  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
• Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study ↗

  UNC Libraries · 2020
  not yet assessed
• Polygenic Architecture of Human Neuroanatomical Diversity ↗

  Cerebral Cortex · 2020 · PMID 32109272
  not yet assessed
• Physical Activity Does Not Lower the Risk of Lung Cancer ↗

  Cancer Research · 2020 · PMID 32646967
  not yet assessed
• Physical activity and Parkinson’s disease: a two-sample Mendelian randomisation study ↗

  Journal of Neurology Neurosurgery & Psychiatry · 2020 · PMID 33093192
  not yet assessed
• Mendelian randomization provides evidence for a causal effect of higher serum IGF-1 concentration on risk of hip and knee osteoarthritis ↗

  Lara D. Veeken · 2020 · PMID 33027520
  not yet assessed
• Dynamics of Brain Structure and its Genetic Architecture over the Lifespan ↗

  Zenodo (CERN European Organization for Nuclear Research) · 2020
  not yet assessed
• Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels ↗

  UNC Libraries · 2020
  not yet assessed
• Functional polymorphisms of the mineralocorticoid receptor gene <i>NR3C2</i> are associated with diminished memory decline: Results from a longitudinal general‐population study ↗

  Molecular Genetics & Genomic Medicine · 2020 · PMID 32558353
  not yet assessed
• A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape ↗

  UNC Libraries · 2020
  not yet assessed
• Genome-wide association and functional studies identify a role for IGFBP3 in hip osteoarthritis ↗

  UNC Libraries · 2020
  not yet assessed
• Large-scale genomic analyses link reproductive ageing to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair ↗

  PMC · 2020
  not yet assessed
• Distinct Loci in the CHRNA5 / CHRNA3 / CHRNB4 Gene Cluster Are Associated With Onset of Regular Smoking ↗

  UNC Libraries · 2020
  not yet assessed
• Genetic loci associated with heart rate variability and their effects on cardiac disease risk ↗

  Digital Commons@Becker (Washington University School of Medicine) · 2020
  not yet assessed
• Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2020
  not yet assessed
• Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women ↗

  medRxiv · 2020
  not yet assessed
• Age-dependent genetic variants associated with longitudinal changes in brain structure across the lifespan ↗

  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
• Genetic variants for head size share genes and pathways with cancer ↗

  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
• Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity ↗

  2020
  not yet assessed
• New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk ↗

  Research at the University of Copenhagen (University of Copenhagen) · 2020
  not yet assessed
• Thyroid Genetics and the Cardiovascular System ↗

  2020
  not yet assessed
• Corrigendum: Polygenic Architecture of Human Neuroanatomical Diversity ↗

  Cerebral Cortex · 2020 · PMID 32249901
  not yet assessed
• Estimating the effect of lipids on IGF axis and subsequent breast cancer risk ↗

  medRxiv · 2020
  not yet assessed
• Higher serum IGF-1 concentration is causally related to increased risk of hip and knee osteoarthritis: a Mendelian Randomization study

  Lara D. Veeken · 2020
  not yet assessed
• Physical activity and risk of Alzheimer disease

  University of Regensburg Publication Server (University of Regensburg) · 2020
  not yet assessed
• Genome wide association study of circulating interleukin 6 levels identifies novel loci

  Murdoch Research Repository (Murdoch University) · 2020
  not yet assessed
• Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity ↗

  2020
  not yet assessed
• Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity ↗

  2020
  not yet assessed
• Clinical, histological, and biochemical liver phenotype of European adults with heterozygous alpha-1 antitrypsin deficiency (Pi*MZ genotype) ↗

  Journal of Hepatology · 2020
  not yet assessed
• Multiethnic Exome-Wide Association Study of Subclinical AtherosclerosisCLINICAL PERSPECTIVE ↗

  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
• Genome-wide association analysis identifies six new loci associated with forced vital capacity ↗

  UNC Libraries · 2020
  not yet assessed
• Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium ↗

  UNC Libraries · 2020
  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 ↗

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

  UNC Libraries · 2020
  not yet assessed
• Multi-Ethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI ↗

  Maynooth University ePrints and eTheses Archive (Maynooth University) · 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
• Genetic diversity is a predictor of mortality in humans ↗

  UNC Libraries · 2020
  not yet assessed
• A reference panel of 64,976 haplotypes for genotype imputation ↗

  UNC Libraries · 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
• Genome-wide association study identifies eight loci associated with blood pressure ↗

  UNC Libraries · 2020
  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 ↗

  UNC Libraries · 2020
  not yet assessed
• Novel genetic loci underlying human intracranial volume identified through genome-wide association ↗

  UNC Libraries · 2020
  not yet assessed
• Novel genetic loci associated with hippocampal volume ↗

  UNC Libraries · 2020
  not yet assessed
• Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium ↗

  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
• Rare coding variants and X-linked loci associated with age at menarche ↗

  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
• Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche ↗

  UNC Libraries · 2020
  not yet assessed
• Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies ↗

  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
• Increased Genetic Vulnerability to Smoking at CHRNA5 in Early-Onset Smokers ↗

  UNC Libraries · 2020
  not yet assessed
• Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 2011; 478: 103-109 ↗

  UNC Libraries · 2020
  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
• Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels ↗

  Nature Genetics · 2019 · PMID 31578528
  not yet assessed
• Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data ↗

  Nature Communications · 2019 · PMID 31235808
  not yet assessed
• Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ↗

  Nature Communications · 2019 · PMID 31341166
  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
• Genetic architecture of subcortical brain structures in 38,851 individuals ↗

  Nature Genetics · 2019 · PMID 31636452
  not yet assessed
• Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria ↗

  Nature Communications · 2019 · PMID 31511532
  not yet assessed
• The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls ↗

  Biological Psychiatry · 2019 · PMID 31926635
  not yet assessed
• Associations of autozygosity with a broad range of human phenotypes ↗

  Nature Communications · 2019 · PMID 31673082
  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
• Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution ↗

  Nature Genetics · 2019 · PMID 30778226
  not yet assessed
• New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders ↗

  Nature Human Behaviour · 2019 · PMID 31358974
  not yet assessed
• Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition ↗

  JAMA Psychiatry · 2019 · PMID 31665216
  not yet assessed
• Serum magnesium and calcium levels in relation to ischemic stroke ↗

  Neurology · 2019 · PMID 30804065
  not yet assessed
• Methylation of the FKBP5 gene in association with FKBP5 genotypes, childhood maltreatment and depression ↗

  Neuropsychopharmacology · 2019 · PMID 30700816
  not yet assessed
• Validated inference of smoking habits from blood with a finite DNA methylation marker set ↗

  European Journal of Epidemiology · 2019 · PMID 31494793
  not yet assessed
• Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting ↗

  Neurology · 2019 · PMID 30651383
  not yet assessed
• Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 ↗

  BMC Cardiovascular Disorders · 2019 · PMID 31664920
  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
• Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity ↗

  Current Biology · 2019
  not yet assessed
• Pathway-Specific Genetic Risk for Alzheimer’s Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults ↗

  Cerebral Cortex · 2019 · PMID 31402375
  not yet assessed
• KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern ↗

  JCI Insight · 2019 · PMID 31600170
  not yet assessed
• Interaction of childhood trauma with rs1360780 of the FKBP5 gene on trait resilience in a general population sample ↗

  Journal of Psychiatric Research · 2019 · PMID 31226578
  not yet assessed
• The importance of high-quality mendelian randomisation studies for clinical thyroidology ↗

  The Lancet Diabetes & Endocrinology · 2019 · PMID 31076377
  not yet assessed
• Lipidomics, Atrial Conduction, and Body Mass Index ↗

  Circulation Genomic and Precision Medicine · 2019 · PMID 31306056
  not yet assessed
• Evaluation of a rare glucose‐dependent insulinotropic polypeptide receptor variant in a patient with diabetes ↗

  Diabetes Obesity and Metabolism · 2019 · PMID 30784161
  not yet assessed
• Common Genetic Variation in Relation to Brachial Vascular Dimensions and Flow-Mediated Vasodilation ↗

  Circulation Genomic and Precision Medicine · 2019 · PMID 30779634
  not yet assessed
• Full exploitation of high dimensionality in brain imaging: The JPND working group statement and findings ↗

  Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · 2019 · PMID 30976649
  not yet assessed
• Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

  Kölner Universitäts PublikationsServer (Universität zu Köln) · 2019
  not yet assessed
• Full exploitation of high dimensionality in brain imaging: The JPND working group statement and findings

  Queensland's institutional digital repository (The University of Queensland) · 2019
  not yet assessed
• GENETIC FACTORS INFLUENCING THE COMMON NEUROBIOLOGICAL SUBSTRATE FOR MENTAL DISORDERS ↗

  European Neuropsychopharmacology · 2019
  not yet assessed
• Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation ↗

  Yearbook of pediatric endocrinology · 2019
  not yet assessed
• ENIGMA and Global Neuroscience: A Decade of Large-Scale Studies of the Brain in Health and Disease across more than 40 Countries ↗

  2019
  not yet assessed
• Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗

  Nature Genetics · 2019
  not yet assessed
• Polygenic architecture of human neuroanatomical diversity ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• The genetic makeup of the electrocardiogram ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia ↗

  Molecular Psychiatry · 2019 · PMID 30705424
  not yet assessed
• Genetic factors influencing a neurobiological substrate for psychiatric disorders ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Abstract WP216: Epigenome-Wide Association Study of Cerebral White Matter Hyperintensities ↗

  Stroke · 2019
  not yet assessed
• <i>KCND3</i> is a novel susceptibility locus for early repolarization ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Physical activity and risk of breast and endometrial cancers: a Mendelian randomization study ↗

  medRxiv · 2019
  not yet assessed
• Physical activity and risk of Alzheimer’s disease: a two-sample Mendelian randomization study ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Kidney Function and Blood Pressure: A Bi-directional Mendelian Randomisation Study ↗

  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
• Mendelian Randomization analyses reveal a causal effect of thyroid function on stroke via atrial fibrillation ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

  Data Archiving and Networked Services (DANS) · 2019
  not yet assessed
• Physical activity and risk of lung cancer: a two-sample Mendelian randomization study ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 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
• Coding Variant In&amp;nbsp; &lt;i&gt;LEP&lt;/i&gt;&amp;nbsp;Associated with Lower Leptin Concentrations Implicates Leptin in the Regulation of Early Adiposity ↗

  SSRN Electronic Journal · 2019
  not yet assessed
• Additional file 1: of Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 ↗

  Figshare · 2019
  not yet assessed
• Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure ↗

  Apollo (University of Cambridge) · 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
• Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes ↗

  Nature Genetics · 2018 · PMID 29531354
  not yet assessed
• Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits ↗

  Nature Genetics · 2018 · PMID 30224653
  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
• Multi-ethnic genome-wide association study for atrial fibrillation ↗

  Nature Genetics · 2018 · PMID 29892015
  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
• Genome Analyses of &gt;200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders ↗

  The American Journal of Human Genetics · 2018 · PMID 30388399
  not yet assessed
• Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation ↗

  Nature Communications · 2018 · PMID 30367059
  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
• GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes ↗

  Nature Communications · 2018 · PMID 30510157
  not yet assessed
• Common Methods for Performing Mendelian Randomization ↗

  Frontiers in Cardiovascular Medicine · 2018 · PMID 29892602
  not yet assessed
• Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits ↗

  The American Journal of Human Genetics · 2018 · PMID 30595373
  not yet assessed
• Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity ↗

  Current Biology · 2018 · PMID 30554901
  not yet assessed
• PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity ↗

  Nature Communications · 2018 · PMID 30046033
  not yet assessed
• Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci ↗

  European Journal of Human Genetics · 2018 · PMID 30218097
  not yet assessed
• Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia ↗

  Molecular Psychiatry · 2018 · PMID 30283035
  not yet assessed
• Genetic Determinants of Circulating Estrogen Levels and Evidence of a Causal Effect of Estradiol on Bone Density in Men ↗

  The Journal of Clinical Endocrinology & Metabolism · 2018 · PMID 29325096
  not yet assessed
• Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels ↗

  Nature Communications · 2018 · PMID 30315176
  not yet assessed
• Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume ↗

  Nature Communications · 2018 · PMID 30258056
  not yet assessed
• Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus ↗

  Scientific Reports · 2018 · PMID 30209331
  not yet assessed
• Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males ↗

  Pain · 2018 · PMID 30431558
  not yet assessed
• Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults ↗

  EBioMedicine · 2018 · PMID 30442561
  not yet assessed
• Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. ↗

  Open Access CRIS of the University of Bern · 2018
  not yet assessed
• Exome Chip Analysis Identifies Low-Frequency and Rare Variants in <i>MRPL38</i> for White Matter Hyperintensities on Brain Magnetic Resonance Imaging ↗

  Stroke · 2018 · PMID 30002152
  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
• Meta-analysis of exome array data identifies six novel genetic loci for lung function ↗

  Wellcome Open Research · 2018 · PMID 30175238
  not yet assessed
• Negative effect of vitamin D on kidney function: a Mendelian randomization study ↗

  Nephrology Dialysis Transplantation · 2018 · PMID 29718335
  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
• A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis ↗

  Human Molecular Genetics · 2018
  not yet assessed
• Meta-analysis of exome array data identifies six novel genetic loci for lung function ↗

  Wellcome Open Research · 2018
  not yet assessed
• Reassessing the Association between Circulating Vitamin D and IGFBP-3: Observational and Mendelian Randomization Estimates from Independent Sources ↗

  Cancer Epidemiology Biomarkers & Prevention · 2018 · PMID 30072546
  not yet assessed
• An InDel in Phospholipase-C-B-1 Is Linked with Euthyroid Multinodular Goiter ↗

  Thyroid · 2018 · PMID 29897006
  not yet assessed
• Meta-analysis of exome array data identifies six novel genetic loci for lung function ↗

  Wellcome Open Research · 2018
  not yet assessed
• Associations of autozygosity with a broad range of human phenotypes ↗

  Apollo (University of Cambridge) · 2018
  not yet assessed
• Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• The genetic architecture of the human cerebral cortex ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits ↗

  Nature Genetics · 2018 · PMID 30429575
  not yet assessed
• Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• Protein-Coding Variants Implicate Novel Genes Related to Lipid Homeostasis Contributing to Body Fat Distribution ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗

  Nature Genetics · 2018 · PMID 29549329
  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
• Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗

  Nature Genetics · 2018 · PMID 29549330
  not yet assessed
• Discovering patterns of pleiotropy in genome-wide association studies ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in <i>PCSK9</i> ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• Planar cell polarity pathway and development of the human visual cortex ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  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
• Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. ↗

  Kölner Universitäts PublikationsServer (Universität zu Köln) · 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
• P1‐004: GENOME‐WIDE ASSOCIATION STUDY OF 11,785 INDIVIDUALS IDENTIFIES SEVEN LOCI ASSOCIATED WITH BRAIN‐DERIVED NEUROTROPHIC FACTOR ↗

  Alzheimer s & Dementia · 2018
  not yet assessed
• O3‐03‐03: EPIGENOME‐WIDE ASSOCIATION STUDIES IMPLICATE GENES INVOLVED IN GLIAL CELL FUNCTION AND VIRAL RESPONSE IN CEREBRAL WHITE MATTER HYPERINTENSITIES ↗

  Alzheimer s & Dementia · 2018
  not yet assessed
• IC‐P‐107: IGF‐1 AND IGFBP‐3 ASSOCIATIONS WITH BRAIN MRI: META‐ANALYSIS IN MIDDLE‐AGED ADULTS FROM THE FRAMINGHAM HEART STUDY AND STUDY OF HEALTH IN POMERANIA ↗

  Alzheimer s & Dementia · 2018
  not yet assessed
• Neanderthal introgression sheds light on modern human brain globularity

  MPG.PuRe (Max Planck Society) · 2018
  not yet assessed
• Meta-Analysis of Maternal Prenatal Smoking GFI1-Locus and Cardio-Metabolic Phenotypes in Adults ↗

  SSRN Electronic Journal · 2018
  not yet assessed
• P3‐237: IGF‐1 AND IGFBP‐3 ASSOCIATIONS WITH BRAIN MRI: META‐ANALYSIS IN MIDDLE‐AGED ADULTS FROM THE FRAMINGHAM HEART STUDY AND STUDY OF HEALTH IN POMERANIA ↗

  Alzheimer s & Dementia · 2018
  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
• Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗

  Nature Genetics · 2017 · PMID 29273807
  not yet assessed
• Genetic evidence of assortative mating in humans ↗

  Nature Human Behaviour · 2017
  not yet assessed
• Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation ↗

  Nature Genetics · 2017 · PMID 28416818
  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
• Novel genetic loci associated with hippocampal volume ↗

  Nature Communications · 2017 · PMID 28098162
  not yet assessed
• Genetic Association of Major Depression With Atypical Features and Obesity-Related Immunometabolic Dysregulations ↗

  JAMA Psychiatry · 2017 · PMID 29049554
  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
• 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 loci associated with heart rate variability and their effects on cardiac disease risk ↗

  Nature Communications · 2017 · PMID 28613276
  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
• Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function ↗

  Journal of Clinical Investigation · 2017 · PMID 28394258
  not yet assessed
• Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease ↗

  Journal of the American Heart Association · 2017 · PMID 28550093
  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
• A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis ↗

  Human Molecular Genetics · 2017 · PMID 28449029
  not yet assessed
• 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function ↗

  Scientific Reports · 2017 · PMID 28452372
  not yet assessed
• Multiethnic Meta-Analysis Identifies <i>RAI1</i> as a Possible Obstructive Sleep Apnea–related Quantitative Trait Locus in Men ↗

  American Journal of Respiratory Cell and Molecular Biology · 2017 · PMID 29077507
  not yet assessed
• Genome‐wide gene‐environment interaction in depression: A systematic evaluation of candidate genes ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2017 · PMID 29159863
  not yet assessed
• Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study ↗

  PLoS ONE · 2017 · PMID 28107422
  not yet assessed
• Genetic effects influencing risk for major depressive disorder in China and Europe ↗

  Translational Psychiatry · 2017 · PMID 28350396
  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
• Fifteen Genetic Loci Associated With the Electrocardiographic P Wave ↗

  Circulation Cardiovascular Genetics · 2017 · PMID 28794112
  not yet assessed
• Transcriptome-Wide Analysis Identifies Novel Associations With Blood Pressure ↗

  Hypertension · 2017 · PMID 28784648
  not yet assessed
• Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism ↗

  Scientific Reports · 2017 · PMID 28588231
  not yet assessed
• GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos ↗

  Journal of Dental Research · 2017 · PMID 28081371
  not yet assessed
• Bivariate Genome-Wide Association Study of Depressive Symptoms With Type 2 Diabetes and Quantitative Glycemic Traits ↗

  Psychosomatic Medicine · 2017 · PMID 29280852
  not yet assessed
• Investigation of Naturally Occurring Single-Nucleotide Variants in Human TAAR1 ↗

  Frontiers in Pharmacology · 2017 · PMID 29225575
  not yet assessed
• NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality ↗

  Journal of the American Society of Nephrology · 2017 · PMID 28360221
  not yet assessed
• Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium ↗

  Scientific Reports · 2017 · PMID 28900195
  not yet assessed
• Two statistical criteria to choose the method for dilution correction in metabolomic urine measurements ↗

  Metabolomics · 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
• Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depressive disorder ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide ↗

  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
• Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults ↗

  PLoS Genetics · 2017 · PMID 28832619
  not yet assessed
• Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk ↗

  Nature Communications · 2017
  not yet assessed
• Meta-analysis of exome array data identifies six novel genetic loci for lung function ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• Narrow-sense heritability estimation of complex traits using identity-by-descent information ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2017
  not yet assessed
• Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation ↗

  Nature Genetics · 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
• 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
• Genomewide meta-analysis identifies loci associated with IGF-I and IGEBP-3 levels with impact on age-related traits (vol 15, pg 811, 2016) ↗

  Leiden Repository (Leiden University) · 2017
  not yet assessed
• Transcriptome-Wide Analysis Identifies Novel Associations With Blood Pressure

  Queensland's institutional digital repository (The University of Queensland) · 2017
  not yet assessed
• A reference panel of 64,976 haplotypes for genotype imputation ↗

  Nature Genetics · 2016 · PMID 27548312
  not yet assessed
• Genome-wide association study identifies 74 loci associated with educational attainment ↗

  Nature · 2016 · PMID 27225129
  not yet assessed
• Meta-analysis of genome-wide association studies of anxiety disorders ↗

  Molecular Psychiatry · 2016 · PMID 26754954
  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
• The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals ↗

  Nature Genetics · 2016 · PMID 27618452
  not yet assessed
• PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study ↗

  The Lancet Diabetes & Endocrinology · 2016 · PMID 27908689
  not yet assessed
• New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk ↗

  Nature Communications · 2016 · PMID 26833246
  not yet assessed
• Novel genetic loci underlying human intracranial volume identified through genome-wide association ↗

  Nature Neuroscience · 2016 · PMID 27694991
  not yet assessed
• <i>KLB</i> is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference ↗

  Proceedings of the National Academy of Sciences · 2016 · PMID 27911795
  not yet assessed
• Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium ↗

  Biological Psychiatry · 2016 · PMID 27519822
  not yet assessed
• Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies ↗

  The Lancet Neurology · 2016 · PMID 27068588
  not yet assessed
• Cystatin C and Cardiovascular Disease ↗

  Journal of the American College of Cardiology · 2016 · PMID 27561768
  not yet assessed
• Genetic variants linked to education predict longevity ↗

  Proceedings of the National Academy of Sciences · 2016 · PMID 27799538
  not yet assessed
• Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies ↗

  Gastroenterology · 2016 · PMID 27094239
  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
• Genomewide meta‐analysis identifies loci associated with <scp>IGF</scp> ‐I and <scp>IGFBP</scp> ‐3 levels with impact on age‐related traits ↗

  Aging Cell · 2016 · PMID 27329260
  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
• A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape ↗

  Nature Communications · 2016 · PMID 27876822
  not yet assessed
• Genetic Variants Associated with Circulating Parathyroid Hormone ↗

  Journal of the American Society of Nephrology · 2016 · PMID 27927781
  not yet assessed
• Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis ↗

  Circulation Cardiovascular Genetics · 2016 · PMID 27872105
  not yet assessed
• <scp>GWAS</scp> analysis of handgrip and lower body strength in older adults in the <scp>CHARGE</scp> consortium ↗

  Aging Cell · 2016 · PMID 27325353
  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
• Serum protease activity in chronic kidney disease patients: The GANI_MED renal cohort ↗

  Experimental Biology and Medicine · 2016 · PMID 28038565
  not yet assessed
• Exome Variant Analysis of Chronic Periodontitis in 2 Large Cohort Studies ↗

  Journal of Dental Research · 2016 · PMID 27655622
  not yet assessed
• Gene transcripts associated with muscle strength: a CHARGE meta-analysis of 7,781 persons ↗

  Physiological Genomics · 2016 · PMID 26487704
  not yet assessed
• The inverse link between genetic risk for schizophrenia and migraine through NMDA (N-methyl-D-aspartate) receptor activation via D-serine ↗

  European Neuropsychopharmacology · 2016 · PMID 27394076
  not yet assessed
• KLB is associated with alcohol drinking, and its gene product beta-Klotho is necessary for FGF21 regulation of alcohol preference

  Data Archiving and Networked Services (DANS) · 2016
  not yet assessed
• Angiopoietin‐2, its soluble receptor <scp>T</scp>ie‐2, and metabolic syndrome components in a population‐based sample ↗

  Obesity · 2016 · PMID 27601273
  not yet assessed
• Erratum: Meta-analysis of genome-wide association studies of anxiety disorders ↗

  Molecular Psychiatry · 2016
  not yet assessed
• Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study ↗

  PLoS Genetics · 2016
  not yet assessed
• Partial derivatives meta-analysis: pooled analyses when individual participant data cannot be shared ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 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
• GWAS for executive function and processing speed suggests involvement of the CADM2 gene

  Data Archiving and Networked Services (DANS) · 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
• Genome-wide association study identifies 74 loci associated with educational attainment

  e-space (Manchester Metropolitan University) · 2016
  not yet assessed
• Genome-wide association study identifies 74 loci associated with educational attainment

  RePEc: Research Papers in Economics · 2016
  not yet assessed
• Genetic studies of body mass index yield new insights for obesity biology ↗

  Nature · 2015 · PMID 25673413
  not yet assessed
• New genetic loci link adipose and insulin biology to body fat distribution ↗

  Nature · 2015 · PMID 25673412
  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
• Common genetic variants influence human subcortical brain structures ↗

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

  Nature Communications · 2015 · PMID 26490707
  not yet assessed
• 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
• 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
• 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
• 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
• Directional dominance on stature and cognition in diverse human populations ↗

  Nature · 2015 · PMID 26131930
  not yet assessed
• Multiethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI ↗

  Circulation Cardiovascular Genetics · 2015 · PMID 25663218
  not yet assessed
• Measuring Biological Age via Metabonomics: The Metabolic Age Score ↗

  Journal of Proteome Research · 2015 · PMID 26652958
  not yet assessed
• Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes ↗

  Diabetes · 2015 · PMID 26631737
  not yet assessed
• Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation ↗

  Nature Communications · 2015 · PMID 26635082
  not yet assessed
• GWAS for executive function and processing speed suggests involvement of the CADM2 gene ↗

  Molecular Psychiatry · 2015 · PMID 25869804
  not yet assessed
• Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders ↗

  Neuron · 2015 · PMID 26050039
  not yet assessed
• A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration ↗

  Human Molecular Genetics · 2015 · PMID 26561523
  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
• Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF ↗

  Blood · 2015 · PMID 26105150
  not yet assessed
• Using genetics to test the causal relationship of total adiposity and periodontitis: Mendelian randomization analyses in the Gene-Lifestyle Interactions and Dental Endpoints (GLIDE) Consortium ↗

  International Journal of Epidemiology · 2015 · PMID 26050256
  not yet assessed
• A Genetic Risk Score for Thyroid Peroxidase Antibodies Associates With Clinical Thyroid Disease in Community-Based Populations ↗

  The Journal of Clinical Endocrinology & Metabolism · 2015 · PMID 25719932
  not yet assessed
• Rare coding variants and X-linked loci associated with age at menarche ↗

  Nature Communications · 2015 · PMID 26239645
  not yet assessed
• No Association Between Polygenic Risk for Schizophrenia and Brain Volume in the General Population ↗

  Biological Psychiatry · 2015 · PMID 25917135
  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
• ABO blood type B and fucosyltransferase 2 non-secretor status as genetic risk factors for chronic pancreatitis ↗

  Gut · 2015 · PMID 26061595
  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
• Association of PNPLA3 rs738409 and TM6SF2 rs58542926 with health services utilization in a population-based study ↗

  BMC Health Services Research · 2015 · PMID 26847197
  not yet assessed
• Genome-Wide Association Study for Endothelial Growth Factors ↗

  Circulation Cardiovascular Genetics · 2015 · PMID 25552591
  not yet assessed
• Copy Number Variations and Cognitive Phenotypes in Unselected Populations ↗

  Obstetrical & Gynecological Survey · 2015
  not yet assessed
• Analyzing Illumina Gene Expression Microarray Data Obtained From Human Whole Blood Cell and Blood Monocyte Samples ↗

  Methods in molecular biology · 2015 · PMID 26614070
  not yet assessed
• Genome-wide association study of kidney function decline in individuals of European descent: the CKDGen Consortium. ↗

  Kidney International · 2015
  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
• Correction: Corrigendum: Rare coding variants and X-linked loci associated with age at menarche ↗

  Nature Communications · 2015 · PMID 26674845
  not yet assessed
• A reference panel of 64,976 haplotypes for genotype imputation ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2015
  not yet assessed
• Is there a male-specific effect on hypertension? ↗

  Human Genetics · 2015 · PMID 25560766
  not yet assessed
• Directional dominance on stature and cognition in diverse human populations ↗

  Archive ouverte UNIGE (University of Geneva) · 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
• 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
• Defining the role of common variation in the genomic and biological architecture of adult human height ↗

  Nature Genetics · 2014
  not yet assessed
• The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data ↗

  Brain Imaging and Behavior · 2014 · PMID 24399358
  not yet assessed
• Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche ↗

  Nature · 2014 · PMID 25231870
  not yet assessed
• Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption ↗

  Molecular Psychiatry · 2014 · PMID 25288136
  not yet assessed
• Identification of Novel Genetic Loci Associated with Thyroid Peroxidase Antibodies and Clinical Thyroid Disease ↗

  PLoS Genetics · 2014 · PMID 24586183
  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
• Genome-wide association analysis identifies six new loci associated with forced vital capacity ↗

  Nature Genetics · 2014 · PMID 24929828
  not yet assessed
• Defining the role of common variation in the genomic and biological architecture of adult human height. ↗

  PubMed · 2014 · PMID 25282103
  not yet assessed
• Genome-wide association study of kidney function decline in individuals of European descent ↗

  Kidney International · 2014 · PMID 25493955
  not yet assessed
• Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits ↗

  Nature Genetics · 2014 · PMID 24777453
  not yet assessed
• Asymmetry within and around the human planum temporale is sexually dimorphic and influenced by genes involved in steroid hormone receptor activity ↗

  Cortex · 2014 · PMID 25239853
  not yet assessed
• Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study ↗

  Molecular Psychiatry · 2014 · PMID 25469926
  not yet assessed
• Replicability and Robustness of Genome-Wide-Association Studies for Behavioral Traits ↗

  Psychological Science · 2014 · PMID 25287667
  not yet assessed
• Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium ↗

  Human Molecular Genetics · 2014 · PMID 24430505
  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
• Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations ↗

  The American Journal of Human Genetics · 2014 · PMID 24975945
  not yet assessed
• Fucosyltransferase 2 (FUT2) non-secretor status and blood group B are associated with elevated serum lipase activity in asymptomatic subjects, and an increased risk for chronic pancreatitis: a genetic association study ↗

  Gut · 2014 · PMID 25028398
  not yet assessed
• Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium ↗

  Biological Psychiatry · 2014 · PMID 25648963
  not yet assessed
• Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung Function ↗

  PLoS ONE · 2014 · PMID 24983941
  not yet assessed
• Genome-wide association and functional studies identify a role for IGFBP3 in hip osteoarthritis ↗

  Annals of the Rheumatic Diseases · 2014 · PMID 24928840
  not yet assessed
• A genome-wide association study of heparin-induced thrombocyto - penia using an electronic medical record ↗

  Thrombosis and Haemostasis · 2014 · PMID 25503805
  not yet assessed
• A genome‐wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus ↗

  Genes Brain & Behavior · 2014 · PMID 25130324
  not yet assessed
• Mitochondrial DNA Variants in Obesity ↗

  PLoS ONE · 2014 · PMID 24788344
  not yet assessed
• Genome-Wide Meta-Analyses of Plasma Renin Activity and Concentration Reveal Association With the Kininogen 1 and Prekallikrein Genes ↗

  Circulation Cardiovascular Genetics · 2014 · PMID 25477429
  not yet assessed
• Mapping the Genetic Architecture of Gene Regulation in Whole Blood ↗

  PLoS ONE · 2014 · PMID 24740359
  not yet assessed
• Impact of priming on the response of neutrophils to human neutrophil alloantigen‐3a antibodies ↗

  Transfusion · 2014 · PMID 25385443
  not yet assessed
• Genetic diversity is a predictor of mortality in humans ↗

  BMC Genetics · 2014 · PMID 25543667
  not yet assessed
• A common atopy‐associated variant in the Th2 cytokine locus control region impacts transcriptional regulation and alters <scp>SMAD</scp>3 and <scp>SP</scp>1 binding ↗

  Allergy · 2014 · PMID 24661001
  not yet assessed
• No Evidence for Genome-Wide Interactions on Plasma Fibrinogen by Smoking, Alcohol Consumption and Body Mass Index: Results from Meta-Analyses of 80,607 Subjects ↗

  PLoS ONE · 2014 · PMID 25551457
  not yet assessed
• Fucosyltransferase 2 (FUT2) non-secretor status and blood group B are associated with elevated serum lipase activity in asymptomatic subjects and an increased risk for chronic pancreatitis – a genetic association study ↗

  Pancreatology · 2014
  not yet assessed
• Rare Protein-Coding Variants Are Associated with Osteoporotic Fracture: An Exome-Chip Analysis of 44,130 Adult Caucasians in CHARGE and GEFOS Consortia.

  Journal of Bone and Mineral Research · 2014
  not yet assessed
• Abstract 35: Transcriptome-wide Association Study of Circulating Lipid Levels ↗

  Circulation · 2014
  not yet assessed
• Abstract 56: Genome-wide Association Studies of Incident Stroke: The Charge Consortium ↗

  Stroke · 2014
  not yet assessed
• Fucosyltransferase 2 (FUT2) "non-secretor"-Status und Blutgruppe B sind assoziiert mit erhöhter Serum Lipase Aktivität und einem erhöhten Risiko für die chronische Pankreatitis – Eine genetische Assoziationsstudie ↗

  Zeitschrift für Gastroenterologie · 2014 · PMID 25250410
  not yet assessed
• Replicability and Robustness of Genome-Wide-Association Studies for Behavioral Traits

  ERIM Top-Core Articles · 2014
  not yet assessed
• Asymmetry within and around the planum temporale is sexually dimorphic and influenced by genes involved in steroid biology

  Max Planck Digital Library · 2014
  not yet assessed
• Genome-wide association analysis identifies six new loci associated with forced vital capacity

  Maynooth University ePrints and eTheses Archive (Maynooth University) · 2014
  not yet assessed
• Identification of Novel Genetic Loci Associated with Thyroid Peroxidase Antibodies and Clinical Thyroid Disease

  UWA Profiles and Research Repository (University of Western Australia) · 2014
  not yet assessed
• Systematic identification of trans eQTLs as putative drivers of known disease associations ↗

  Nature Genetics · 2013 · PMID 24013639
  not yet assessed
• GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment ↗

  Science · 2013 · PMID 23722424
  not yet assessed
• Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture ↗

  Nature Genetics · 2013 · PMID 23563607
  not yet assessed
• Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits ↗

  PLoS Genetics · 2013 · PMID 23754948
  not yet assessed
• Meta-Analysis of Genome-Wide Association Studies Identifies Six New Loci for Serum Calcium Concentrations ↗

  PLoS Genetics · 2013 · PMID 24068962
  not yet assessed
• A Genome-Wide Association Study of Depressive Symptoms ↗

  Biological Psychiatry · 2013 · PMID 23290196
  not yet assessed
• A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy ↗

  European Heart Journal · 2013 · PMID 23853074
  not yet assessed
• Identification of Genetic Loci Associated With Helicobacter pylori Serologic Status ↗

  JAMA · 2013 · PMID 23652523
  not yet assessed
• Multiethnic Meta-Analysis of Genome-Wide Association Studies in &gt;100 000 Subjects Identifies 23 Fibrinogen-Associated Loci but No Strong Evidence of a Causal Association Between Circulating Fibrinogen and Cardiovascular Disease ↗

  Circulation · 2013 · PMID 23969696
  not yet assessed
• Genome‐wide association study of chronic periodontitis in a general German population ↗

  Journal Of Clinical Periodontology · 2013 · PMID 24024966
  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
• Causal and Synthetic Associations of Variants in the SERPINA Gene Cluster with Alpha1-antitrypsin Serum Levels ↗

  PLoS Genetics · 2013 · PMID 23990791
  not yet assessed
• Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets ↗

  Human Brain Mapping · 2013 · PMID 24827550
  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
• Overlap Between Common Genetic Polymorphisms Underpinning Kidney Traits and Cardiovascular Disease Phenotypes: The CKDGen Consortium ↗

  American Journal of Kidney Diseases · 2013 · PMID 23474010
  not yet assessed
• Distinct Loci in the <i>CHRNA5</i>/<i>CHRNA3</i>/<i>CHRNB4</i> Gene Cluster Are Associated With Onset of Regular Smoking ↗

  Genetic Epidemiology · 2013 · PMID 24186853
  not yet assessed
• Comparison of genotyping using pooled DNA samples (allelotyping) and individual genotyping using the affymetrix genome-wide human SNP array 6.0 ↗

  BMC Genomics · 2013 · PMID 23885805
  not yet assessed
• A genomewide association study of smoking relapse in four European population-based samples ↗

  Psychiatric Genetics · 2013 · PMID 23542338
  not yet assessed
• A Robust Method for Genome‐Wide Association Meta‐Analysis With the Application to Circulating Insulin‐Like Growth Factor I Concentrations ↗

  Genetic Epidemiology · 2013 · PMID 24446417
  not yet assessed
• Distinct Loci in the CHRNA5/CHRNA3/CHRNB4 Gene Cluster Are Associated With Onset of Regular Smoking ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2013
  not yet assessed
• A mega-analysis of genome-wide association studies for major depressive disorder

  EUR Research Repository (Erasmus University Rotterdam) · 2013
  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
• Supplementary Material 15

  2013
  not yet assessed
• Mendelian randomization suggests non-causal associations of testosterone with cardiometabolic risk factors and mortality ↗

  Endocrine Abstracts · 2013
  not yet assessed
• GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment

  RePEc: Research Papers in Economics · 2013
  not yet assessed
• Genome-wide association scanning for asymmetry of the human planum temporale

  MPG.PuRe (Max Planck Society) · 2013
  not yet assessed
• Between Circulating Fibrinogen and Cardiovascular Disease Identifies 23 Fibrinogen-Associated Loci but No Strong Evidence of a Causal Association Multiethnic Meta-Analysis of Genome-Wide Association Studies in >100 000 Subjects

  2013
  not yet assessed
• Causal and synthetic associations of variants in the SERPINA gene cluster with alpha1-antitrypsin serum levels ↗

  UWA Profiles and Research Repository (University of Western Australia) · 2013
  not yet assessed
• A mega-analysis of genome-wide association studies for major depressive disorder ↗

  Molecular Psychiatry · 2012 · PMID 22472876
  not yet assessed
• Genome-wide association analyses identify 18 new loci associated with serum urate concentrations ↗

  Nature Genetics · 2012 · PMID 23263486
  not yet assessed
• Identification of common variants associated with human hippocampal and intracranial volumes ↗

  Nature Genetics · 2012 · PMID 22504417
  not yet assessed
• FTO genotype is associated with phenotypic variability of body mass index ↗

  Nature · 2012 · PMID 22982992
  not yet assessed
• Seventy-five genetic loci influencing the human red blood cell ↗

  Nature · 2012 · PMID 23222517
  not yet assessed
• A Genome-Wide Association Meta-Analysis of Circulating Sex Hormone–Binding Globulin Reveals Multiple Loci Implicated in Sex Steroid Hormone Regulation ↗

  PLoS Genetics · 2012 · PMID 22829776
  not yet assessed
• Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function ↗

  PLoS Genetics · 2012 · PMID 22479191
  not yet assessed
• Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region ↗

  Annals of the Rheumatic Diseases · 2012 · PMID 22956598
  not yet assessed
• Analyzing Illumina Gene Expression Microarray Data from Different Tissues: Methodological Aspects of Data Analysis in the MetaXpress Consortium ↗

  PLoS ONE · 2012 · PMID 23236413
  not yet assessed
• Increased Genetic Vulnerability to Smoking at CHRNA5 in Early-Onset Smokers ↗

  Archives of General Psychiatry · 2012 · PMID 22868939
  not yet assessed
• Myocardial gene expression profiles and cardiodepressant autoantibodies predict response of patients with dilated cardiomyopathy to immunoadsorption therapy ↗

  European Heart Journal · 2012 · PMID 23100283
  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
• Mendelian randomization suggests non‐causal associations of testosterone with cardiometabolic risk factors and mortality ↗

  Andrology · 2012 · PMID 23258625
  not yet assessed
• Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function ↗

  Human Molecular Genetics · 2012 · PMID 22494929
  not yet assessed
• Genome-wide meta-analysis of common variant differences between men and women ↗

  Human Molecular Genetics · 2012 · PMID 22843499
  not yet assessed
• A description of large-scale metabolomics studies: increasing value by combining metabolomics with genome-wide SNP genotyping and transcriptional profiling ↗

  Journal of Endocrinology · 2012 · PMID 22782382
  not yet assessed
• Pooled Sample-Based GWAS: A Cost-Effective Alternative for Identifying Colorectal and Prostate Cancer Risk Variants in the Polish Population ↗

  PLoS ONE · 2012 · PMID 22532847
  not yet assessed
• A SULT2A1 genetic variant identified by GWAS as associated with low serum DHEAS does not impact on the actual DHEA/DHEAS ratio ↗

  Journal of Molecular Endocrinology · 2012 · PMID 23132913
  not yet assessed
• Genome-Wide Association Study to Identify Common Variants Associated with Brachial Circumference: A Meta-Analysis of 14 Cohorts ↗

  PLoS ONE · 2012 · PMID 22479309
  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
• A Genome-Wide Association Meta-Analysis of Circulating Sex Hormone-Binding Globulin Reveals Multiple Loci Implicated in Sex Steroid Hormone Regulation

  Tampere University Institutional Repository (Tampere University) · 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
• Erratum: DIRAS2 is Associated with Adult ADHD, Related Traits, and Co-Morbid Disorders ↗

  Neuropsychopharmacology · 2012
  not yet assessed
• A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple loci implicated in s

  2012
  not yet assessed
• Genome-wide association and functional follow-up reveals new loci for kidney function ↗

  University of Chicago · 2012
  not yet assessed
• Genome-wide association and functional follow-up reveals new loci for kidney function ↗

  University of Chicago · 2012
  not yet assessed
• Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk ↗

  Nature · 2011 · PMID 21909115
  not yet assessed
• Meta-Analysis of Genome-Wide Association Studies in &gt;80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels ↗

  Circulation · 2011 · PMID 21300955
  not yet assessed
• New gene functions in megakaryopoiesis and platelet formation ↗

  Nature · 2011 · PMID 22139419
  not yet assessed
• A genome-wide association study of metabolic traits in human urine ↗

  Nature Genetics · 2011 · PMID 21572414
  not yet assessed
• CUBN Is a Gene Locus for Albuminuria ↗

  Journal of the American Society of Nephrology · 2011 · PMID 21355061
  not yet assessed
• Moderation of Adult Depression by a Polymorphism in the FKBP5 Gene and Childhood Physical Abuse in the General Population ↗

  Neuropsychopharmacology · 2011 · PMID 21654733
  not yet assessed
• Genetic Determinants of Serum Testosterone Concentrations in Men ↗

  PLoS Genetics · 2011 · PMID 21998597
  not yet assessed
• Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD ↗

  PLoS Genetics · 2011 · PMID 21980298
  not yet assessed
• Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study ↗

  Human Molecular Genetics · 2011 · PMID 21378095
  not yet assessed
• Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM ↗

  Molecular Psychiatry · 2011 · PMID 21876539
  not yet assessed
• Multiple Loci Are Associated with White Blood Cell Phenotypes ↗

  PLoS Genetics · 2011 · PMID 21738480
  not yet assessed
• Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies ↗

  Circulation Cardiovascular Genetics · 2011 · PMID 22199011
  not yet assessed
• Genetic epistasis between the brain-derived neurotrophic factor Val66Met polymorphism and the 5-HTT promoter polymorphism moderates the susceptibility to depressive disorders after childhood abuse ↗

  Progress in Neuro-Psychopharmacology and Biological Psychiatry · 2011 · PMID 21996278
  not yet assessed
• Eight Common Genetic Variants Associated with Serum DHEAS Levels Suggest a Key Role in Ageing Mechanisms ↗

  PLoS Genetics · 2011 · PMID 21533175
  not yet assessed
• A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3 ↗

  Human Molecular Genetics · 2011 · PMID 21216879
  not yet assessed
• Genome-wide Association Study Identifies Four Genetic Loci Associated with Thyroid Volume and Goiter Risk ↗

  The American Journal of Human Genetics · 2011 · PMID 21565293
  not yet assessed
• DIRAS2 is Associated with Adult ADHD, Related Traits, and Co-Morbid Disorders ↗

  Neuropsychopharmacology · 2011 · PMID 21750579
  not yet assessed
• Common variants at 10 genomic loci influence hemoglobin A1C levels via glycemic and nonglycemic pathways (Diabetes (2010) 59, (3229-3239))

  Oxford University Research Archive (ORA) (University of Oxford) · 2011
  not yet assessed
• The effect of <i>catechol‐<scp>O</scp>‐methyltransferase</i> polymorphisms on pain is modified by depressive symptoms ↗

  European Journal of Pain · 2011 · PMID 22337325
  not yet assessed
• Meta-Analysis of Genome-Wide Association Studies in > 80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels ↗

  Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2011
  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
• Genome-Wide Association Study Identified New Variants Associated With Colorectal Cancer ↗

  Gastroenterology · 2011
  not yet assessed
• S202 A GENOME WIDE ASSOCIATION STUDY ON CHRONIC WIDESPREAD PAIN: EVIDENCE FOR INVOLVEMENT OF THE 5P15.2 REGION ↗

  European Journal of Pain Supplements · 2011
  not yet assessed
• Genome-Wide Interaction Study With Cigarette Smoking In Relation To Pulmonary Function ↗

  2011
  not yet assessed
• EIGHT COMMON GENETIC VARIANTS ASSOCIATED WITH SERUM DHEAS LEVELS SUGGESTS A KEY ROLE IN AGEING MECHANISMS

  Research Portal (King's College London) · 2011
  not yet assessed
• Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk ↗

  Archive ouverte UNIGE (University of Geneva) · 2011
  not yet assessed
• Cohort Profile: The Study of Health in Pomerania ↗

  International Journal of Epidemiology · 2010 · PMID 20167617
  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
• New loci associated with kidney function and chronic kidney disease ↗

  Nature Genetics · 2010 · PMID 20383146
  not yet assessed
• Meta-analysis and imputation refines the association of 15q25 with smoking quantity ↗

  Nature Genetics · 2010 · PMID 20418889
  not yet assessed
• Genome-Wide Association Study of Blood Pressure Extremes Identifies Variant near UMOD Associated with Hypertension ↗

  PLoS Genetics · 2010 · PMID 21082022
  not yet assessed
• Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction ↗

  Nature Genetics · 2010 · PMID 21076409
  not yet assessed
• Childhood maltreatment, the corticotropin‐releasing hormone receptor gene and adult depression in the general population ↗

  American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2010 · PMID 20957648
  not yet assessed
• Replication of the association of chromosomal region 9p21.3with generalized aggressive periodontitis (gAgP) using an independent case-control cohort ↗

  BMC Medical Genetics · 2010 · PMID 20696043
  not yet assessed
• Multiple new genetic loci associated with kidney function and Chronic Kidney Disease: The CKDGen Consortium ↗

  Das Gesundheitswesen · 2010
  not yet assessed
• Protecs, a comprehensive and powerful storage and analysis system for OMICS data, applied for profiling the anaerobiosis response of <i>Staphylococcus aureus</i> COL ↗

  PROTEOMICS · 2010 · PMID 20662099
  not yet assessed
• A risk marker for alcohol dependence on chromosome 2q35 is related to neuroticism in the general population ↗

  Molecular Psychiatry · 2010 · PMID 20351720
  not yet assessed
• 50 A Genome-Wide Scan Identifies TM4SF4 (Intestine and Liver Tetraspan Membrane Protein 4) as a Susceptibility Locus for Gallstone Disease ↗

  Gastroenterology · 2010
  not yet assessed
• Genomweite Analyse identifiziert TM4SF4 (intestine and liver tetraspan membrane protein 4) als Risikogen für das Gallensteinleiden ↗

  Zeitschrift für Gastroenterologie · 2010
  not yet assessed
• W48 GENETIC VARIATION WITHIN ADIPONUTRIN IS ASSOCIATED WITH LIPOPROTEIN METABOLISM AND LIVER FUNCTION ↗

  Atherosclerosis Supplements · 2010
  not yet assessed
• Genome-wide association study identifies eight loci associated with blood pressure ↗

  Nature Genetics · 2009 · PMID 19430483
  not yet assessed
• Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations ↗

  PLoS Genetics · 2009 · PMID 19503597
  not yet assessed
• Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium ↗

  Nature Genetics · 2009 · PMID 19862010
  not yet assessed
• Genetic Variants Associated With Cardiac Structure and Function ↗

  JAMA · 2009 · PMID 19584346
  not yet assessed
• Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein B-containing lipoproteins ↗

  Human Molecular Genetics · 2009 · PMID 19729411
  not yet assessed
• A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium ↗

  Nature Genetics · 2009 · PMID 19820697
  not yet assessed
• Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

  2009
  not yet assessed
• Monitoring of changes in the membrane proteome during stationary phase adaptation of <b><i>Bacillus subtilis</i></b> using <b><i>in vivo</i></b> labeling techniques ↗

  PROTEOMICS · 2008 · PMID 18491319
  not yet assessed