Zoltán Kutalik
Reproducibility track record
1
assessed papers
100/100
mean reproducibility
1
reproduced (C1–C2)
0
flagged
139
total citations
flag rate:
0%
(0/1)
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.
Authorship role
first author: 0
last author: 1
Topics
Funders
—
Frequent co-authors
Matthias Nauck 1Stefania Bandinelli 1Chiara Auwerx 1Uwe Völker 1Federico Santoni 1Alexander Teumer 1Andres Metspalu 1Toshiko Tanaka 1Eleonora Porcu 1Antoine Weihs 1
Institutions
SIB Swiss Institute of Bioinformatics 1University of Lausanne 1University of Tartu 1University of Exeter 1Universitätsmedizin Greifswald 1École Polytechnique Fédérale de Lausanne 1
Geography (author institutions)
CH 1EE 1GB 1DE 1IT 1US 1
Co-author network
Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.
How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.
Assessed papers (1)
Complete publication record (610)
Request a reproduction →1 assessed by us (1 reproduced) · 609 not yet assessed — every PubMed paper on record, linked below.
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Genetic analysis of circulating metabolic traits in 619,372 individuals ↗Nature · 2026 · PMID 42162431not yet assessed
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Integration of genetic evidence to identify approved drug targets ↗Genome Medicine · 2026 · PMID 42410617not yet assessed
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Mendelian randomization linking metabolites with enzymes reveals pathway regulation and therapeutic avenues ↗The American Journal of Human Genetics · 2026 · PMID 41650937not yet assessed
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Lipid transport is necessary for neocortical lamination ↗Genes & Diseases · 2026not yet assessed
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<i>Trans</i> -eQTLs reveal the architecture of human gene regulatory networks ↗medRxiv · 2026 · PMID 42051578not yet assessed
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Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium ↗UNC Libraries · 2026not yet assessed
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not yet assessed
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Mapping corpus callosum architecture: developmental, genetic, and cognitive correlates in youth ↗bioRxiv (Cold Spring Harbor Laboratory) · 2026 · PMID 42094545not yet assessed
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Sex differences in the genetic basis of human recombination within 190,000 parent-child pairs ↗bioRxiv (Cold Spring Harbor Laboratory) · 2026not yet assessed
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CYP4F2-mediated ω-hydroxylation of 1-deoxysphingolipids reveals a new hepatic detoxification pathway ↗bioRxiv (Cold Spring Harbor Laboratory) · 2026not yet assessed
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Using human genetics to understand the effect of modulating targets of antihypertensive drugs in pregnancy ↗medRxiv · 2026 · PMID 42238470not yet assessed
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Evaluating anonymized genome re-identification using polygenic predictions and its implications for data privacy ↗bioRxiv (Cold Spring Harbor Laboratory) · 2026not yet assessed
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Advancing Clinical Implementation of Cardiovascular Polygenic Risk Scores Through Patient-Level Robustness Assessment ↗medRxiv · 2026not yet assessed
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Additional file 1 of Integration of genetic evidence to identify approved drug targets ↗Figshare · 2026not yet assessed
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Additional file 2 of Integration of genetic evidence to identify approved drug targets ↗Figshare · 2026not yet assessed
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Additional file 1 of Integration of genetic evidence to identify approved drug targets ↗Figshare · 2026not yet assessed
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Additional file 2 of Integration of genetic evidence to identify approved drug targets ↗Figshare · 2026not yet assessed
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LiMA: Robust inference of molecular mediation from summary statistics ↗The American Journal of Human Genetics · 2026 · PMID 41512839not yet assessed
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Dataset_CoLaus|PsyCoLaus_study_and_satellite_studies ↗Open MIND · 2026not yet assessed
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Dataset_CoLaus|PsyCoLaus_study_and_satellite_studies ↗Zenodo (CERN European Organization for Nuclear Research) · 2026not yet assessed
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not yet assessed
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Trans-ancestry genome-wide study of depression identifies 697 associations implicating cell types and pharmacotherapies ↗Cell · 2025 · PMID 39814019not yet assessed
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Polygenic prediction of body mass index and obesity through the life course and across ancestries ↗Nature Medicine · 2025 · PMID 40691366not yet assessed
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Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery ↗Nature Medicine · 2025 · PMID 40251273not yet assessed
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Associations between common genetic variants and income provide insights about the socio-economic health gradient ↗Nature Human Behaviour · 2025 · PMID 39875632not yet assessed
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Parent-of-origin effects on complex traits in up to 236,781 individuals ↗Nature · 2025 · PMID 40770099not yet assessed
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Leveraging large-scale biobank EHRs to enhance pharmacogenetics of cardiometabolic disease medications ↗Nature Communications · 2025 · PMID 40133288not yet assessed
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Non-linear Mendelian randomization: evaluation of effect modification in the residual and doubly-ranked methods with simulated and empirical examples ↗European Journal of Epidemiology · 2025 · PMID 40455395not yet assessed
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Clinical lipidomics reveals high individuality and sex specificity of circulatory lipid signatures: a prospective healthy population study ↗Journal of Lipid Research · 2025 · PMID 40112951not yet assessed
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Combining cross-sectional and longitudinal genomic approaches to identify determinants of cognitive and physical decline ↗Nature Communications · 2025 · PMID 40374629not yet assessed
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The Role of Energy Homeostasis in Depression Pathophysiology and Its Heterogeneity ↗JAMA Psychiatry · 2025 · PMID 40768164not yet assessed
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Incorporating genetic data improves target trial emulations and informs the use of polygenic scores in randomized controlled trial design ↗Nature Genetics · 2025 · PMID 40533517not yet assessed
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Periodic limb movements during sleep, restless legs syndrome, and cognitive changes in older adults: a population-based longitudinal study ↗SLEEP · 2025 · PMID 41105131not yet assessed
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Genetic determinants of zinc homeostasis and its role in cardiometabolic diseases ↗PLoS Genetics · 2025 · PMID 41325371not yet assessed
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Identification of effect modifiers using a stratified Mendelian randomization algorithmic framework ↗European Journal of Epidemiology · 2025 · PMID 40072671not yet assessed
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Familial and genetic relationships of major depressive disorders and adiposity markers in the community ↗Translational Psychiatry · 2025 · PMID 41173844not yet assessed
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Urinary Copper Is Associated with Dyslipidemia, and This Association Is Mediated by Inflammation ↗Biological Trace Element Research · 2025 · PMID 40172775not yet assessed
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A large-scale genome-wide study of gene-sleep duration interactions for blood pressure in 811,405 individuals from diverse populations ↗Molecular Psychiatry · 2025 · PMID 40181193not yet assessed
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Expectations for papers performing Mendelian randomization analyses ↗PLoS Genetics · 2025 · PMID 40674297not yet assessed
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Author Correction: Incorporating genetic data improves target trial emulations and informs the use of polygenic scores in randomized controlled trial design ↗Nature Genetics · 2025 · PMID 40579539not yet assessed
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Design and model choices shape inference of age-varying genetic effects on complex traits ↗medRxiv · 2025not yet assessed
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Parental haplotypes reconstruction in up to 440,209 individuals reveals recent assortative mating dynamics ↗bioRxiv (Cold Spring Harbor Laboratory) · 2025not yet assessed
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Parent-of-Origin inference and its role in the genetic architecture of complex traits: evidence from ~265,000 individuals ↗Research Square · 2025not yet assessed
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Exploring the mediating role of inflammation in the link between urinary copper and dyslipidemia ↗European Journal of Preventive Cardiology · 2025not yet assessed
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The role of common and rare genetic variation on adiposity across childhood. ↗Research Square · 2025not yet assessed
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Mendelian randomization linking metabolites with enzymes reveals known and novel pathway regulation and therapeutic avenues ↗medRxiv · 2025not yet assessed
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Compounding of rare pathogenic copy-number variants and polygenic background is consistent with assortative mating ↗medRxiv · 2025not yet assessed
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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. ↗UNC Libraries · 2025not yet assessed
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MR-link-2: pleiotropy robust cis Mendelian randomization validated in three independent reference datasets of causality ↗Nature Communications · 2025 · PMID 40610416not yet assessed
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Polygenic Scores Derived from ~150,000 UK Biobank individuals - Hofmeister et al., 2025 ↗Zenodo (CERN European Organization for Nuclear Research) · 2025not yet assessed
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Polygenic Scores Derived from ~150,000 UK Biobank individuals - Hofmeister et al., 2025 ↗Zenodo (CERN European Organization for Nuclear Research) · 2025not yet assessed
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Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits ↗Nature Genetics · 2024 · PMID 38689001not yet assessed
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Causality-enriched epigenetic age uncouples damage and adaptation ↗Nature Aging · 2024 · PMID 38243142not yet assessed
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Rare copy-number variants as modulators of common disease susceptibility ↗Genome Medicine · 2024 · PMID 38185688not yet assessed
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PheWAS-based clustering of Mendelian Randomisation instruments reveals distinct mechanism-specific causal effects between obesity and educational attainment ↗Nature Communications · 2024 · PMID 38360877not yet assessed
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The impact of self-report inaccuracy in the UK Biobank and its interplay with selective participation ↗Nature Human Behaviour · 2024 · PMID 39695248not yet assessed
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Breaking down causes, consequences, and mediating effects of telomere length variation on human health ↗Genome biology · 2024 · PMID 38760657not yet assessed
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The pleiotropic spectrum of proximal 16p11.2 CNVs ↗The American Journal of Human Genetics · 2024 · PMID 39332410not yet assessed
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DNA methylation may partly explain psychotropic drug-induced metabolic side effects: results from a prospective 1-month observational study ↗Clinical Epigenetics · 2024 · PMID 38419113not yet assessed
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Disentangling mechanisms behind the pleiotropic effects of proximal 16p11.2 BP4-5 CNVs ↗The American Journal of Human Genetics · 2024 · PMID 39332408not yet assessed
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SMIM1 absence is associated with reduced energy expenditure and excess weight ↗Med · 2024 · PMID 38906141not yet assessed
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Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure ↗Kidney International Reports · 2024 · PMID 38899223not yet assessed
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Identification of rare disease genes as drivers of common diseases through tissue-specific gene regulatory networks ↗Scientific Reports · 2024 · PMID 39632930not yet assessed
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A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure ↗UNC Libraries · 2024not yet assessed
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Lipid disturbances induced by psychotropic drugs: clinical and genetic predictors for early worsening of lipid levels and new-onset dyslipidaemia in Swiss psychiatric samples ↗BJPsych Open · 2024 · PMID 39635766not yet assessed
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Menopause increases the risk of diabetes, and this association might be due to iron metabolism ↗European Journal of Preventive Cardiology · 2024not yet assessed
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The power of genetic diversity in genome-wide association studies of lipids ↗UNC Libraries · 2024not yet assessed
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Psychotropic-induced weight gain and telomere length: results from a one-year longitudinal study and a large population-based cohort ↗Translational Psychiatry · 2024 · PMID 39548087not yet assessed
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Genome-wide association study for circulating metabolic traits in 619,372 individuals ↗medRxiv · 2024 · PMID 40297438not yet assessed
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Leveraging large-scale biobank EHRs to enhance pharmacogenetics of cardiometabolic disease medications ↗medRxiv · 2024 · PMID 38633781not yet assessed
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Associations between common genetic variants and income provide insights about the socioeconomic health gradient ↗bioRxiv (Cold Spring Harbor Laboratory) · 2024not yet assessed
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MR-link-2: pleiotropy robust <i>cis</i> Mendelian randomization validated in four independent gold-standard datasets of causality ↗medRxiv · 2024not yet assessed
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Delphi: Deep Learning for Polygenic Risk Prediction ↗medRxiv · 2024not yet assessed
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Disentangling mechanisms behind the pleiotropic effects of proximal 16p11.2 BP4-5 CNVs ↗medRxiv · 2024not yet assessed
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Breaking down causes, consequences, and mediating effects of age-related telomere shortening on human health ↗medRxiv · 2024not yet assessed
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Parent-of-Origin inference and its role in the genetic architecture of complex traits: evidence from ∼265,000 individuals ↗medRxiv · 2024not yet assessed
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Associations between common genetic variants and income provide insights about the socioeconomic health gradient ↗Research Square · 2024not yet assessed
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A Large-Scale Genome-Wide Study of Gene-Sleep Duration Interactions for Blood Pressure in 811,405 Individuals from Diverse Populations ↗medRxiv · 2024 · PMID 38496537not yet assessed
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not yet assessed
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not yet assessed
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Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity ↗Digital Commons@Becker (Washington University School of Medicine) · 2024not yet assessed
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Genetic insights into biological mechanisms governing human ovarian ageing ↗UNC Libraries · 2024not yet assessed
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Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression ↗UNC Libraries · 2024not yet assessed
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Genetic comorbidity between major depression and cardio-metabolic traits, stratified by age at onset of major depression ↗UNC Libraries · 2024not yet assessed
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A Large-Scale Genome-Wide Study of Gene-Sleep Duration Interactions for Blood Pressure in 811,405 Individuals from Diverse Populations ↗Research Square · 2024 · PMID 39070651not yet assessed
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Widespread natural selection on metabolite levels in humans ↗Genome Research · 2024 · PMID 39152035not yet assessed
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Widespread environment-specific causal effects detected in the UK Biobank ↗Research Square · 2024not yet assessed
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65. DISENTANGLING MECHANISMS BEHIND THE PLEIOTROPIC EFFECTS OF PROXIMAL 16P11.2 BP4-5 COPY-NUMBER VARIANTS ↗European Neuropsychopharmacology · 2024not yet assessed
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not yet assessed
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ↗UNC Libraries · 2024not yet assessed
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Author Correction: The power of genetic diversity in genome-wide association studies of lipids ↗RePEc: Research Papers in Economics · 2024not yet assessed
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SMIM1 absence is associated with reduced energy expenditure and excess weightFigshare · 2024not yet assessed
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Guidelines for performing Mendelian randomization investigations: update for summer 2023 ↗Wellcome Open Research · 2023not yet assessed
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Bias correction for inverse variance weighting Mendelian randomization ↗Genetic Epidemiology · 2023 · PMID 37036286not yet assessed
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Participation bias in the UK Biobank distorts genetic associations and downstream analyses ↗Nature Human Behaviour · 2023 · PMID 37106081not yet assessed
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Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy ↗Nature Communications · 2023 · PMID 37188663not yet assessed
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OTTERS: a powerful TWAS framework leveraging summary-level reference data ↗Nature Communications · 2023 · PMID 36882394not yet assessed
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Multi-layered genetic approaches to identify approved drug targets ↗Cell Genomics · 2023 · PMID 37492104not yet assessed
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Genetic insights into the causal relationship between physical activity and cognitive functioning ↗Scientific Reports · 2023 · PMID 37002254not yet assessed
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Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic disease ↗Cell Reports Medicine · 2023 · PMID 37586323not yet assessed
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Exploiting the mediating role of the metabolome to unravel transcript-to-phenotype associations ↗eLife · 2023 · PMID 36891970not yet assessed
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Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity ↗Stroke · 2023 · PMID 36655558not yet assessed
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Polygenic risk prediction: why and when out-of-sample prediction R2 can exceed SNP-based heritability ↗The American Journal of Human Genetics · 2023 · PMID 37379836not yet assessed
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The impact of 22q11.2 copy-number variants on human traits in the general population ↗The American Journal of Human Genetics · 2023 · PMID 36706759not yet assessed
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Identification of four novel loci associated with psychotropic drug-induced weight gain in a Swiss psychiatric longitudinal study: A GWAS analysis ↗Molecular Psychiatry · 2023 · PMID 37173452not yet assessed
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Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH ↗Diabetologia · 2023 · PMID 37233759not yet assessed
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Partner choice, confounding and trait convergence all contribute to phenotypic partner similarity ↗Nature Human Behaviour · 2023 · PMID 36928782not yet assessed
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Genetic insights into the age-specific biological mechanisms governing human ovarian aging ↗The American Journal of Human Genetics · 2023 · PMID 37543033not yet assessed
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Cannabis use and atherosclerotic cardiovascular disease: a Mendelian randomization study ↗BMC Cardiovascular Disorders · 2023 · PMID 38093188not yet assessed
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Large scale phenotype imputation and in vivo functional validation implicate ADAMTS14 as an adiposity gene ↗Nature Communications · 2023 · PMID 36658113not yet assessed
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Author Correction: The power of genetic diversity in genome-wide association studies of lipids ↗Nature · 2023 · PMID 37237109not yet assessed
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Self-report inaccuracy in the UK Biobank: Impact on inference and interplay with selective participation ↗medRxiv · 2023not yet assessed
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not yet assessed
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not yet assessed
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Incorporating discovery and replication GWAS into summary data Mendelian randomization studies: A review of current methods and a simple, general and powerful alternative ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Widespread natural selection on metabolite levels in humans ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Cannabis use and atherosclerotic cardiovascular disease: a Mendelian randomization study ↗medRxiv · 2023not yet assessed
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Genetic insights into the age-specific biological mechanisms governing human ovarian ageing ↗medRxiv · 2023not yet assessed
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not yet assessed
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Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts ↗npj Genomic Medicine · 2023 · PMID 37225732not yet assessed
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Cannabis use and risk of atherosclerosis cardiovascular disease: a two-sample mendelian randomization study ↗European Journal of Preventive Cardiology · 2023not yet assessed
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Response to Bassett et al. ↗The American Journal of Human Genetics · 2023 · PMID 37419093not yet assessed
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T71. EXPLORING CORRELATES AND CAUSES OF SELF-REPORT ERROR IN BIOBANK-SCALE DATA ↗European Neuropsychopharmacology · 2023not yet assessed
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Identification of four novel loci associated with psychotropic drug-induced weight gain in a Swiss psychiatric longitudinal study: A GWAS analysis ↗Zenodo (CERN European Organization for Nuclear Research) · 2023not yet assessed
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Identification of four novel loci associated with psychotropic drug-induced weight gain in a Swiss psychiatric longitudinal study: A GWAS analysis ↗Zenodo (CERN European Organization for Nuclear Research) · 2023not yet assessed
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Additional file 28 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 21 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 25 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 18 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 27 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 10 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 29 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 19 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (UWA) · 2023not yet assessed
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Additional file 4 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 17 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 2 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 33 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 32 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 5 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 30 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 7 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 8 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 20 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 22 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 23 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 1 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 12 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Correction to: The power of genetic diversity in genome-wide association studies of lipids (Nature, (2021), 600, 7890, (675-679), 10.1038/s41586-021-04064-3)Institutional Repositories DataBase (IRDB) · 2023not yet assessed
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A saturated map of common genetic variants associated with human height ↗Nature · 2022 · PMID 36224396not yet assessed
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Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals ↗Nature Genetics · 2022 · PMID 35361970not yet assessed
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A cross-disorder dosage sensitivity map of the human genome ↗Cell · 2022 · PMID 35917817not yet assessed
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Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention ↗Nature Genetics · 2022 · PMID 36071172not yet assessed
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The individual and global impact of copy-number variants on complex human traits ↗The American Journal of Human Genetics · 2022 · PMID 35240056not yet assessed
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Sex- and age-dependent genetics of longevity in a heterogeneous mouse population ↗Science · 2022 · PMID 36173858not yet assessed
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Using genetic variation to disentangle the complex relationship between food intake and health outcomes ↗PLoS Genetics · 2022 · PMID 35653391not yet assessed
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From pharmacogenetics to pharmaco-omics: Milestones and future directions ↗Human Genetics and Genomics Advances · 2022 · PMID 35373152not yet assessed
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ↗The American Journal of Human Genetics · 2022 · PMID 35931049not yet assessed
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Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Genome biology · 2022 · PMID 36575460not yet assessed
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Sphingolipids accumulate in aged muscle, and their reduction counteracts sarcopenia ↗Nature Aging · 2022 · PMID 37118545not yet assessed
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Parent-of-Origin inference for biobanks ↗Nature Communications · 2022 · PMID 36335127not yet assessed
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The genetic etiology of periodic limb movement in sleep ↗SLEEP · 2022 · PMID 35670608not yet assessed
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Quantifying the role of transcript levels in mediating DNA methylation effects on complex traits and diseases ↗Nature Communications · 2022 · PMID 36477627not yet assessed
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Novel Biological Insights Into the Common Heritable Liability to Substance Involvement: A Multivariate Genome-wide Association Study ↗Biological Psychiatry · 2022not yet assessed
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Polynomial Mendelian randomization reveals non-linear causal effects for obesity-related traits ↗Human Genetics and Genomics Advances · 2022 · PMID 35832928not yet assessed
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Gene set enrichment analysis of pathophysiological pathways highlights oxidative stress in psychosis ↗Molecular Psychiatry · 2022 · PMID 36131045not yet assessed
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Limited evidence for blood eQTLs in human sexual dimorphism ↗Genome Medicine · 2022 · PMID 35953856not yet assessed
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Liability-scale heritability estimation for biobank studies of low-prevalence disease ↗The American Journal of Human Genetics · 2022 · PMID 36265482not yet assessed
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Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations ↗Human Genetics and Genomics Advances · 2022 · PMID 36035246not yet assessed
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Haematological changes from conception to childbirth: An indicator of major pregnancy complications ↗European Journal Of Haematology · 2022 · PMID 36059200not yet assessed
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Improving polygenic prediction with genetically inferred ancestry ↗Human Genetics and Genomics Advances · 2022 · PMID 35571679not yet assessed
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Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts ↗npj Genomic Medicine · 2022 · PMID 35715439not yet assessed
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Correction for participation bias in the UK Biobank reveals non-negligible impact on genetic associations and downstream analyses ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Causality-Enriched Epigenetic Age Uncouples Damage and Adaptation ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Genome-wide analysis in over 1 million individuals reveals over 2,000 independent genetic signals for blood pressure ↗Research Square · 2022not yet assessed
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Liability-scale heritability estimation for biobank studies of low prevalence disease ↗medRxiv · 2022not yet assessed
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Polynomial Mendelian Radomization reveals widespreadnon-linear causal effects in the UK Biobank ↗Research Square · 2022not yet assessed
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Novel discoveries and enhanced genomic prediction from modelling genetic risk of cancer age-at-onset ↗medRxiv · 2022not yet assessed
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The contribution of mate-choice, couple convergence and confounding to assortative mating ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Exploiting the mediating role of the metabolome to unravel transcript-to-phenotype associations ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Omics-informed CNV calls reduce false positive rate and improve power for CNV-trait associations ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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A polygenic risk score to predict sudden cardiac arrest in patients with coronary artery disease ↗medRxiv · 2022not yet assessed
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The impact of 22q11.2 copy number variants on human traits in the general population ↗medRxiv · 2022not yet assessed
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A cross-disorder dosage sensitivity map of the human genome ↗Zenodo (CERN European Organization for Nuclear Research) · 2022not yet assessed
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The contribution of mate-choice, couple convergence and confounding to assortative mating ↗Research Square · 2022not yet assessed
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DNA methylation may mediate psychotropic drug-induced metabolic side effects: results from a 1-month observational study ↗European Psychiatry · 2022not yet assessed
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T13. GENE SET ENRICHMENT ANALYSIS OF PATHOPHYSIOLOGICAL PATHWAYS HIGHLIGHTS OXIDATIVE STRESS IN PSYCHOSIS ↗European Neuropsychopharmacology · 2022not yet assessed
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Genetic Insights into the Causal Relationship between Physical Activity and Cognitive Functioning ↗SSRN Electronic Journal · 2022not yet assessed
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not yet assessed
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A cross-disorder dosage sensitivity map of the human genome ↗Zenodo (CERN European Organization for Nuclear Research) · 2022not yet assessed
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not yet assessed
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Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression ↗Nature Genetics · 2021 · PMID 34475573not yet assessed
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The power of genetic diversity in genome-wide association studies of lipids ↗Nature · 2021 · PMID 34887591not yet assessed
-
The trans-ancestral genomic architecture of glycemic traits ↗Nature Genetics · 2021 · PMID 34059833not yet assessed
-
Genetic insights into biological mechanisms governing human ovarian ageing ↗Nature · 2021 · PMID 34349265not yet assessed
-
Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ↗Biological Psychiatry · 2021 · PMID 34861974not yet assessed
-
A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts ↗Biological Psychiatry · 2021 · PMID 34304866not yet assessed
-
The Genetic Architecture of Depression in Individuals of East Asian Ancestry ↗JAMA Psychiatry · 2021 · PMID 34586374not yet assessed
-
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour ↗Nature Human Behaviour · 2021 · PMID 34211149not yet assessed
-
Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptomeNature Communications · 2021 · PMID 34561431L1 100/100
-
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders ↗Biological Psychiatry · 2021 · PMID 34099189not yet assessed
-
Identifying the Common Genetic Basis of Antidepressant Response ↗Biological Psychiatry Global Open Science · 2021 · PMID 35712048not yet assessed
-
Simultaneous estimation of bi-directional causal effects and heritable confounding from GWAS summary statistics ↗Nature Communications · 2021 · PMID 34907193not yet assessed
-
Obesity and atypical depression symptoms: findings from Mendelian randomization in two European cohorts ↗Translational Psychiatry · 2021 · PMID 33542229not yet assessed
-
Genome-wide association study of circulating interleukin 6 levels identifies novel loci ↗Human Molecular Genetics · 2021 · PMID 33517400not yet assessed
-
Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease ↗Neurology · 2021 · PMID 34845052not yet assessed
-
Mendelian randomization to assess causality between uromodulin, blood pressure and chronic kidney disease ↗Kidney International · 2021 · PMID 34634361not yet assessed
-
Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits ↗Nature Communications · 2021 · PMID 34848700not yet assessed
-
Triangulating evidence from longitudinal and Mendelian randomization studies of metabolomic biomarkers for type 2 diabetes ↗Scientific Reports · 2021 · PMID 33737653not yet assessed
-
Composite trait Mendelian randomization reveals distinct metabolic and lifestyle consequences of differences in body shape ↗Communications Biology · 2021 · PMID 34518635not yet assessed
-
HSD17B7 gene in self‐renewal and oncogenicity of keratinocytes from Black versus White populations ↗EMBO Molecular Medicine · 2021 · PMID 34185380not yet assessed
-
Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis ↗Nature Communications · 2021 · PMID 33879782not yet assessed
-
Untargeted Metabolome- and Transcriptome-Wide Association Study Suggests Causal Genes Modulating Metabolite Concentrations in Urine ↗Journal of Proteome Research · 2021 · PMID 34699229not yet assessed
-
Socio-economic position as a moderator of cardiometabolic outcomes in patients receiving psychotropic treatment associated with weight gain: results from a prospective 12-month inception cohort study and a large population-based cohort ↗Translational Psychiatry · 2021 · PMID 34226496not yet assessed
-
Gene regulation contributes to explain the impact of early life socioeconomic disadvantage on adult inflammatory levels in two cohort studies ↗Scientific Reports · 2021 · PMID 33542415not yet assessed
-
Using genetic variation to disentangle the complex relationship between food intake and health outcomes. ↗DOAJ (DOAJ: Directory of Open Access Journals) · 2021not yet assessed
-
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expressionFigshare · 2021not yet assessed
-
not yet assessed
-
Bias correction for inverse variance weighting Mendelian randomization ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
-
not yet assessed
-
not yet assessed
-
Parent-of-origin effects in the UK Biobank ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
-
Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗medRxiv · 2021not yet assessed
-
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
-
Novel insights into the common heritable liability to addiction: a multivariate genome-wide association study ↗medRxiv · 2021not yet assessed
-
Quantifying mediation between omics layers and complex traits ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
-
Polynomial Mendelian Randomization reveals widespread non-linear causal effects in the UK Biobank ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
-
Correction: Socio-economic position as a moderator of cardiometabolic outcomes in patients receiving psychotropic treatment associated with weight gain: results from a prospective 12-month inception cohort study and a large population-based cohort ↗Translational Psychiatry · 2021not yet assessed
-
The trans-ancestral genomic architecture of glycemic traits. ↗UCL Discovery (University College London) · 2021not 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 34321615not yet assessed
-
Parent-of-origin effects in the UK Biobank ↗Research Square · 2021not yet assessed
-
Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity ↗UNC Libraries · 2021not yet assessed
-
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology ↗UNC Libraries · 2021not yet assessed
-
GWAS summary statistics for waist-to-hip ratio and body principal components ↗Zenodo (CERN European Organization for Nuclear Research) · 2021not yet assessed
-
GWAS summary statistics for waist-to-hip ratio and body principal components ↗Zenodo (CERN European Organization for Nuclear Research) · 2021not yet assessed
-
GWAS summary statistics for waist-to-hip ratio and body principal components ↗Zenodo (CERN European Organization for Nuclear Research) · 2021not yet assessed
-
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank ↗Molecular Psychiatry · 2020 · PMID 31969693not yet assessed
-
Genome-wide association study identifies 48 common genetic variants associated with handedness ↗Nature Human Behaviour · 2020 · PMID 32989287not yet assessed
-
A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank ↗Nature Communications · 2020 · PMID 32385265not yet assessed
-
Association of polygenic score for major depression with response to lithium in patients with bipolar disorder ↗Molecular Psychiatry · 2020 · PMID 32203155not yet assessed
-
Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression ↗American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2020 · PMID 32681593not yet assessed
-
Quantification of the overall contribution of gene-environment interaction for obesity-related traits ↗Nature Communications · 2020 · PMID 32170055not yet assessed
-
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity ↗Diabetes · 2020 · PMID 32917775not yet assessed
-
Heterogeneity in Obesity: Genetic Basis and Metabolic Consequences ↗Current Diabetes Reports · 2020 · PMID 31970540not yet assessed
-
Influence of Genetic Ancestry on Human Serum Proteome ↗The American Journal of Human Genetics · 2020 · PMID 32059761not 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 32684367not yet assessed
-
bGWAS: an R package to perform Bayesian genome wide association studies ↗Bioinformatics · 2020 · PMID 32470106not yet assessed
-
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape ↗UNC Libraries · 2020not yet assessed
-
Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent ↗UNC Libraries · 2020not yet assessed
-
Causal Inference Methods to Integrate Omics and Complex Traits ↗Cold Spring Harbor Perspectives in Medicine · 2020 · PMID 32816877not yet assessed
-
Simultaneous estimation of bi-directional causal effects and heritable confounding from GWAS summary statistics ↗medRxiv · 2020not yet assessed
-
Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits ↗medRxiv · 2020not yet assessed
-
The Trans-Ancestral Genomic Architecture of Glycaemic Traits ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
-
Composite trait Mendelian Randomization reveals distinct metabolic and lifestyle consequences of differences in body shape ↗medRxiv · 2020not yet assessed
-
Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome ↗medRxiv · 2020not yet assessed
-
Commentary on: “The contribution of tissue-specific BMI-associated gene sets to cardiometabolic disease risk: a Mendelian randomization study” ↗International Journal of Epidemiology · 2020 · PMID 32386404not yet assessed
-
Genetic insights into the causal relationship between physical activity and cognitive functioning ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
-
The role of gene expression on human sexual dimorphism: too early to call ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
-
Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank ↗Molecular Psychiatry · 2020 · PMID 32424234not yet assessed
-
Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis ↗medRxiv · 2020not yet assessed
-
Untargeted metabolome- and transcriptome-wide association study identifies causal genes modulating metabolite concentrations in urine ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
-
Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity ↗2020not yet assessed
-
Genome-wide associations for birth weight and correlations with adult disease ↗UNC Libraries · 2020not yet assessed
-
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism ↗UNC Libraries · 2020not yet assessed
-
not yet assessed
-
not yet assessed
-
Antibodies against the c-terminus of apoA-1 as predictors of death in the general population but not as therapeutic targets actionable through cognate peptides immunomodulation ↗European Heart Journal · 2020not yet assessed
-
Genome wide association study of circulating interleukin 6 levels identifies novel lociMurdoch Research Repository (Murdoch University) · 2020not yet assessed
-
Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity ↗2020not yet assessed
-
Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity ↗2020not yet assessed
-
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution ↗UNC Libraries · 2020not yet assessed
-
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals ↗UNC Libraries · 2020not yet assessed
-
Quality control and conduct of genome-wide association meta-analyses ↗UNC Libraries · 2020not yet assessed
-
Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults ↗UNC Libraries · 2020not yet assessed
-
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass ↗UNC Libraries · 2020not yet assessed
-
Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk: A Meta-Analysis of 218,166 Adults and 19,268 Children ↗UNC Libraries · 2020not 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) · 2020not yet assessed
-
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies ↗UNC Libraries · 2020not yet assessed
-
No Interactions Between Previously Associated 2-Hour Glucose Gene Variants and Physical Activity or BMI on 2-Hour Glucose Levels ↗UNC Libraries · 2020not yet assessed
-
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits ↗Digital Commons@Becker (Washington University School of Medicine) · 2020not yet assessed
-
A genome-wide association study of early menopause and the combined impact of identified variants ↗UNC Libraries · 2020not yet assessed
-
Defining the role of common variation in the genomic and biological architecture of adult human height ↗UNC Libraries · 2020not yet assessed
-
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity ↗UNC Libraries · 2020not 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 · 2020not 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 · 2020not yet assessed
-
Approaches to detect genetic effects that differ between two strata in genome-wide meta-analyses: Recommendations based on a systematic evaluation ↗UNC Libraries · 2020not yet assessed
-
Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene ↗UNC Libraries · 2020not yet assessed
-
An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype ↗UNC Libraries · 2020not yet assessed
-
Across-cohort QC analyses of GWAS summary statistics from complex traits ↗UNC Libraries · 2020not yet assessed
-
New genetic loci link adipose and insulin biology to body fat distribution ↗White Rose Research Online (University of Leeds, The University of Sheffield, University of York) · 2020not yet assessed
-
Genetic studies of body mass index yield new insights for obesity biology ↗UNC Libraries · 2020not yet assessed
-
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ↗Nature Genetics · 2019 · PMID 31043758not yet assessed
-
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ↗Nature Communications · 2019 · PMID 31341166not yet assessed
-
Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour ↗Nature Communications · 2019 · PMID 30952852not yet assessed
-
Assessment of network module identification across complex diseases ↗Nature Methods · 2019not yet assessed
-
Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances ↗eLife · 2019 · PMID 30642433not 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 31926635not yet assessed
-
Associations of autozygosity with a broad range of human phenotypes ↗Nature Communications · 2019 · PMID 31673082not yet assessed
-
Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns ↗Nature Communications · 2019 · PMID 31186427not yet assessed
-
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution ↗Nature Genetics · 2019 · PMID 30778226not yet assessed
-
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity ↗Nature Communications · 2019 · PMID 30670697not yet assessed
-
Dysregulation of a long noncoding RNA reduces leptin leading to a leptin-responsive form of obesity ↗Nature Medicine · 2019 · PMID 30842678not yet assessed
-
Mendelian randomisation analyses find pulmonary factors mediate the effect of height on coronary artery disease ↗Communications Biology · 2019 · PMID 30937401not yet assessed
-
FADS3 is a Δ14Z sphingoid base desaturase that contributes to gender differences in the human plasma sphingolipidome ↗Journal of Biological Chemistry · 2019 · PMID 31862735not yet assessed
-
A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy ↗Nature Communications · 2019 · PMID 31253780not yet assessed
-
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals ↗The American Journal of Human Genetics · 2019 · PMID 31668704not yet assessed
-
A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure ↗Human Molecular Genetics · 2019 · PMID 31127295not yet assessed
-
Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders ↗Molecular Psychiatry · 2019 · PMID 31712721not yet assessed
-
Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression ↗Biological Psychiatry · 2019 · PMID 31570195not yet assessed
-
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology ↗The American Journal of Human Genetics · 2019 · PMID 31178129not yet assessed
-
Cross-species functional modules link proteostasis to human normal aging ↗PLoS Computational Biology · 2019 · PMID 31269015not yet assessed
-
Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals ↗Scientific Reports · 2019 · PMID 31263163not yet assessed
-
Weight Loss Directly Influences Intermediate-Term Remission of Diabetes Mellitus After Bariatric Surgery: A Retrospective Case-Control Study ↗Obesity Surgery · 2019 · PMID 31754925not yet assessed
-
rs34567942 a Novel Susceptibility Single Nucleotide Polymorphism for Cutaneous Squamous Cell Carcinoma in Organ Transplant Recipients ↗Acta Dermato Venereologica · 2019 · PMID 31573663not yet assessed
-
Using instrumental variables to estimate the attributable fraction ↗Statistical Methods in Medical Research · 2019 · PMID 31640504not yet assessed
-
Dysregulation of a long noncoding RNA reduces leptin leading to a leptin-responsive form of obesity ↗Yearbook of pediatric endocrinology · 2019not yet assessed
-
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influencesKölner Universitäts PublikationsServer (Universität zu Köln) · 2019not yet assessed
-
48th European Mathematical Genetics Meeting (EMGM) 2020 ↗Human Heredity · 2019 · PMID 32268327not yet assessed
-
Genome-wide association study identifies 48 common genetic variants associated with handedness ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2019not yet assessed
-
Correction: Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid BiologyTechnical University of Denmark, DTU Orbit (Technical University of Denmark, DTU) · 2019not yet assessed
-
Leveraging biobank-scale rare and common variant analyses to identify <i>ASPHD1</i> as the main driver of reproductive traits in the 16p11.2 locus ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Genetic comorbidity between major depression and cardio-metabolic disease, stratified by age at onset of major depression ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
The human-specific <i>BOLA2</i> duplication modifies iron homeostasis and anemia predisposition in chromosome 16p11.2 autism patients ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. ↗Archive ouverte UNIGE (University of Geneva) · 2019not yet assessed
-
Disentangling the genetics of lean massPure Amsterdam UMC · 2019not yet assessed
-
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology ↗The American Journal of Human Genetics · 2019not yet assessed
-
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traitsData Archiving and Networked Services (DANS) · 2019not yet assessed
-
Early life socioeconomic position and adult systemic inflammation: the role of gene regulation ↗European Journal of Public Health · 2019not yet assessed
-
Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals. ↗Apollo (University of Cambridge) · 2019not yet assessed
-
Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-bornsQUT ePrints (Queensland University of Technology) · 2019not yet assessed
-
Coding Variant In&nbsp; <i>LEP</i>&nbsp;Associated with Lower Leptin Concentrations Implicates Leptin in the Regulation of Early Adiposity ↗SSRN Electronic Journal · 2019not yet assessed
-
Maximum likelihood method quantifies the overall contribution of gene-environment interaction to continuous traits: an application to complex traits in the UK Biobank ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression ↗Nature Genetics · 2018 · PMID 29700475not yet assessed
-
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits ↗Nature Genetics · 2018 · PMID 30224653not yet assessed
-
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries ↗PLoS ONE · 2018 · PMID 29912962not yet assessed
-
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes ↗Nature Communications · 2018 · PMID 30054458not yet assessed
-
Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood ↗Nature Communications · 2018 · PMID 29891976not yet assessed
-
Genome Analyses of >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 30388399not yet assessed
-
Evaluation and application of summary statistic imputation to discover new height-associated loci ↗PLoS Genetics · 2018 · PMID 29782485not yet assessed
-
Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels ↗Nature Communications · 2018 · PMID 30315176not yet assessed
-
A joint view on genetic variants for adiposity differentiates subtypes with distinct metabolic implications ↗Nature Communications · 2018 · PMID 29769528not yet assessed
-
Disentangling the genetics of lean mass ↗American Journal of Clinical Nutrition · 2018 · PMID 30721968not yet assessed
-
Addendum: A joint view on genetic variants for adiposity differentiates subtypes with distinct metabolic implications ↗Nature Communications · 2018 · PMID 30030451not yet assessed
-
Copy Number Variation ↗Methods in molecular biology · 2018 · PMID 29876900not 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 · 2018not 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 30197049not yet assessed
-
Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder ↗Communications Biology · 2018 · PMID 30320231not yet assessed
-
Genetic immune and inflammatory markers associated with diabetes in solid organ transplant recipients ↗American Journal of Transplantation · 2018 · PMID 29920932not yet assessed
-
not yet assessed
-
Associations of autozygosity with a broad range of human phenotypes ↗Apollo (University of Cambridge) · 2018not yet assessed
-
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Mendelian Randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits ↗Nature Genetics · 2018 · PMID 30429575not yet assessed
-
Protein-Coding Variants Implicate Novel Genes Related to Lipid Homeostasis Contributing to Body Fat Distribution ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Narcolepsy risk loci are enriched in immune cells and suggest autoimmune modulation of the T cell receptor repertoire ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Genetic studies of accelerometer-based sleep measures in 85,670 individuals yield new insights into human sleep behaviour ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not 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 29549329not 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 29549330not yet assessed
-
A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Genomic underpinnings of lifespan allow prediction and reveal basis in modern risks ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Genetic variation in the Major Histocompatibility Complex and association with depression ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
not yet assessed
-
Cross-species functional modules link proteostasis to human normal aging ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
A Five-Decision Testing Procedure to Infer the Value of a Unidimensional Parameter ↗The American Statistician · 2018not 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) · 2018not yet assessed
-
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K iPLoS ONE · 2018not yet assessed
-
Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics ConsortiumOpen MIND · 2018not yet assessed
-
Rare and low-frequency coding variants alter human adult height ↗Nature · 2017 · PMID 28146470not 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 28436984not yet assessed
-
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2017 · PMID 29273807not yet assessed
-
Genetic evidence of assortative mating in humans ↗Nature Human Behaviour · 2017not yet assessed
-
Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults ↗PLoS Genetics · 2017 · PMID 28448500not yet assessed
-
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits ↗Nature Communications · 2017 · PMID 28443625not yet assessed
-
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass ↗Nature Communications · 2017 · PMID 28724990not yet assessed
-
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity ↗Nature Communications · 2017 · PMID 29030599not 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 28739976not yet assessed
-
Rare and low-frequency coding variants alter human adult height ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2017not 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 29129318not yet assessed
-
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function ↗Scientific Reports · 2017 · PMID 28452372not yet assessed
-
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits ↗Nature Communications · 2017 · PMID 28963451not yet assessed
-
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness ↗Nature Communications · 2017 · PMID 28272467not 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 29077507not yet assessed
-
Bayesian association scan reveals loci associated with human lifespan and linked biomarkers ↗Nature Communications · 2017 · PMID 28748955not yet assessed
-
The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders ↗Molecular Psychiatry · 2017 · PMID 28070120not yet assessed
-
cis-Acting Complex-Trait-Associated lincRNA Expression Correlates with Modulation of Chromosomal Architecture ↗Cell Reports · 2017 · PMID 28249171not yet assessed
-
Interaction between the <i>FTO</i> gene, body mass index and depression: meta-analysis of 13701 individuals ↗The British Journal of Psychiatry · 2017 · PMID 28642257not yet assessed
-
Approaches to detect genetic effects that differ between two strata in genome-wide meta-analyses: Recommendations based on a systematic evaluation ↗PLoS ONE · 2017 · PMID 28749953not yet assessed
-
Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes ↗Scientific Reports · 2017 · PMID 29127340not yet assessed
-
C-reactive protein upregulates the whole blood expression of CD59 - an integrative analysis ↗PLoS Computational Biology · 2017 · PMID 28922377not yet assessed
-
An Integrated Systems Genetics and Omics Toolkit to Probe Gene Function ↗Cell Systems · 2017 · PMID 29199021not yet assessed
-
Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes ↗Journal of the American Society of Nephrology · 2017 · PMID 29093028not yet assessed
-
A systematic review and meta‐analysis of <scp>HCV</scp> clearance ↗Liver International · 2017 · PMID 28261910not yet assessed
-
Risk prediction of developing venous thrombosis in combined oral contraceptive users ↗PLoS ONE · 2017 · PMID 28750087not yet assessed
-
Anti-Apolipoprotein A-1 IgG Predict All-Cause Mortality and Are Associated with Fc Receptor-Like 3 Polymorphisms ↗Frontiers in Immunology · 2017 · PMID 28458671not yet assessed
-
Genome-Wide Association between Transcription Factor Expression and Chromatin Accessibility Reveals Regulators of Chromatin Accessibility ↗PLoS Computational Biology · 2017 · PMID 28118358not yet assessed
-
Impact of CD14 Polymorphisms on Anti-Apolipoprotein A-1 IgG-Related Coronary Artery Disease Prediction in the General Population ↗Arteriosclerosis Thrombosis and Vascular Biology · 2017 · PMID 29074586not yet assessed
-
NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality ↗Journal of the American Society of Nephrology · 2017 · PMID 28360221not yet assessed
-
Metabomatching: Using genetic association to identify metabolites in proton NMR spectroscopy ↗PLoS Computational Biology · 2017 · PMID 29194434not yet assessed
-
Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders ↗Translational Psychiatry · 2017 · PMID 29225345not yet assessed
-
Genetic and clinic predictors of new onset diabetes mellitus after transplantation ↗The Pharmacogenomics Journal · 2017 · PMID 29282365not yet assessed
-
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (vol 8, 80, 2017)eScholarship (California Digital Library) · 2017not yet assessed
-
SQC: secure quality control for meta-analysis of genome-wide association studies ↗Bioinformatics · 2017 · PMID 28379351not yet assessed
-
Impact of CD14 polymorphisms on anti-apolipoprotein A-1 IGG-related coronary heart disease prediction in the general population ↗Atherosclerosis · 2017not 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) · 2017not yet assessed
-
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the KidneyArchive ouverte UNIGE (University of Geneva) · 2017not yet assessed
-
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. ↗Duo Research Archive (University of Oslo) · 2017not yet assessed
-
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depressive disorder ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Genetic analysis of over one million people identifies 535 novel loci for blood pressure ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults ↗PLoS Genetics · 2017 · PMID 28832619not yet assessed
-
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass ↗Nature Communications · 2017not yet assessed
-
GenoShare: Supporting Privacy-Informed Decisions for Sharing Exact Genomic DataInfoscience (Ecole Polytechnique Fédérale de Lausanne) · 2017not yet assessed
-
Correction: Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function ↗Scientific Reports · 2017 · PMID 28548086not yet assessed
-
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (Nature Communications 8:80)STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2017not yet assessed
-
Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Anti-apolipoprotein A-1 IgG predict all-cause mortality and are associated with FCRL3 polymorphisms ↗Atherosclerosis · 2017not yet assessed
-
Metabomatching: Using Genetic Association To Identify Metabolites In Proton Nmr Spectroscopy. Colaus Pseudospectra. ↗Zenodo (CERN European Organization for Nuclear Research) · 2017not yet assessed
-
A five-decision testing procedure to infer on unidimensional parameter ↗arXiv (Cornell University) · 2017not yet assessed
-
Disease-Informed Bayesian Association Scan Reveals Novel Loci Associated with Human Lifespan and Linked BiomarkersInfoscience (Ecole Polytechnique Fédérale de Lausanne) · 2017not 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) · 2017not yet assessed
-
Association of genetic risk scores with body mass index in Swiss psychiatric cohorts ↗Archive ouverte UNIGE (University of Geneva) · 2017not yet assessed
-
New Quality Measure for CNV : A Multi-Omics ApproachData Archiving and Networked Services (DANS) · 2017not yet assessed
-
Evaluation and application of summary statistic imputation to discover new height-associated loci ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Metabomatching: Using Genetic Association To Identify Metabolites In Proton Nmr Spectroscopy. Colaus Pseudospectra. ↗Zenodo (CERN European Organization for Nuclear Research) · 2017not yet assessed
-
Referee report. For: Replication of the principal component analyses of the human genome diversity panel [version 1; referees: 1 approved] ↗Faculty of 1000 Research Ltd · 2017not yet assessed
-
Improved imputation of summary statistics for admixed populations ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Genome-wide association study identifies 74 loci associated with educational attainment ↗Nature · 2016 · PMID 27225129not yet assessed
-
Meta-analysis of genome-wide association studies of anxiety disorders ↗Molecular Psychiatry · 2016 · PMID 26754954not yet assessed
-
Genome-wide associations for birth weight and correlations with adult disease ↗Nature · 2016 · PMID 27680694not yet assessed
-
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals ↗Nature Genetics · 2016 · PMID 27618452not yet assessed
-
Tissue-specific regulatory circuits reveal variable modular perturbations across complex diseases ↗Nature Methods · 2016 · PMID 26950747not yet assessed
-
Genome-wide analysis identifies 12 loci influencing human reproductive behavior ↗Nature Genetics · 2016 · PMID 27798627not yet assessed
-
Fast and Rigorous Computation of Gene and Pathway Scores from SNP-Based Summary Statistics ↗PLoS Computational Biology · 2016 · PMID 26808494not 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 27911795not yet assessed
-
Gene–obesogenic environment interactions in the UK Biobank study ↗International Journal of Epidemiology · 2016 · PMID 28073954not 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 27519822not yet assessed
-
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels ↗Nature Communications · 2016 · PMID 26833098not yet assessed
-
Genetic variants linked to education predict longevity ↗Proceedings of the National Academy of Sciences · 2016 · PMID 27799538not yet assessed
-
TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT ↗EMBO Molecular Medicine · 2016 · PMID 27861123not yet assessed
-
An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype ↗Biological Psychiatry · 2016 · PMID 28049566not yet assessed
-
Narcolepsy-Associated HLA Class I Alleles Implicate Cell-Mediated Cytotoxicity ↗SLEEP · 2016 · PMID 26518595not yet assessed
-
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape ↗Nature Communications · 2016 · PMID 27876822not yet assessed
-
New quality measure for SNP array based CNV detection ↗Bioinformatics · 2016 · PMID 27402902not yet assessed
-
Quantifying the extent to which index event biases influence large genetic association studies ↗Human Molecular Genetics · 2016 · PMID 28040731not yet assessed
-
Across-cohort QC analyses of GWAS summary statistics from complex traits ↗European Journal of Human Genetics · 2016 · PMID 27552965not yet assessed
-
ORMDL3 expression levels have no influence on the activity of serine palmitoyltransferase ↗The FASEB Journal · 2016 · PMID 27645259not yet assessed
-
Weighted Genetic Risk Scores and Prediction of Weight Gain in Solid Organ Transplant Populations ↗PLoS ONE · 2016 · PMID 27788139not yet assessed
-
KLB is associated with alcohol drinking, and its gene product beta-Klotho is necessary for FGF21 regulation of alcohol preferenceData Archiving and Networked Services (DANS) · 2016not yet assessed
-
Association of genetic risk scores with body mass index in Swiss psychiatric cohorts ↗Pharmacogenetics and Genomics · 2016 · PMID 26918956not yet assessed
-
Erratum: Meta-analysis of genome-wide association studies of anxiety disorders ↗Molecular Psychiatry · 2016not 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 · 2016not yet assessed
-
Quantifying the extent to which index event biases influence large genetic association studies ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not 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) · 2016not yet assessed
-
Evidence that lower socioeconomic position accentuates genetic susceptibility to obesity ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
-
Genome-wide association between transcription factor expression and chromatin accessibility reveals chromatin state regulators ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
-
Genome- wide뀀Ƞassociation뀀Ƞbetween뀀Ƞtranscription뀀Ƞfactor뀀Ƞ expression뀀Ƞand뀀Ƞchromatin뀀Ƞaccessibility뀀Ƞreveals뀀Ƞchromatin뀀Ƞ state뀀Ƞregulators 뀀Ƞ2016not yet assessed
-
Tissue-specific regulatory circuits reveal variable modular perturbations across complex diseasesDSpace@MIT (Massachusetts Institute of Technology) · 2016not yet assessed
-
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels ↗University of Southern Denmark Research Portal (University of Southern Denmark) · 2016not 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) · 2016not yet assessed
-
Genome-wide association study identifies 74 loci associated with educational attainmente-space (Manchester Metropolitan University) · 2016not yet assessed
-
Genome-wide association study identifies 74 loci associated with educational attainmentRePEc: Research Papers in Economics · 2016not yet assessed
-
Genetic studies of body mass index yield new insights for obesity biology ↗Nature · 2015 · PMID 25673413not yet assessed
-
New genetic loci link adipose and insulin biology to body fat distribution ↗Nature · 2015 · PMID 25673412not yet assessed
-
Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans ↗PLoS ONE · 2015 · PMID 25811787not 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 26426971not yet assessed
-
Copy Number Variations and Cognitive Phenotypes in Unselected Populations ↗JAMA · 2015 · PMID 26010633not yet assessed
-
Prevalence and determinants of periodic limb movements in the general population ↗Annals of Neurology · 2015 · PMID 26703954not yet assessed
-
Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes ↗Diabetes · 2015 · PMID 26631737not yet assessed
-
Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders ↗Neuron · 2015 · PMID 26050039not yet assessed
-
The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects ↗Molecular Psychiatry · 2015 · PMID 25917368not yet assessed
-
A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder ↗BMC Medicine · 2015 · PMID 25903154not yet assessed
-
A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology ↗The American Journal of Human Genetics · 2015 · PMID 25937446not yet assessed
-
not yet assessed
-
Influence of MCHR2 and MCHR2-AS1 Genetic Polymorphisms on Body Mass Index in Psychiatric Patients and In Population-Based Subjects with Present or Past Atypical Depression ↗PLoS ONE · 2015 · PMID 26461262not yet assessed
-
Heritability of ambulatory and office blood pressure in the Swiss population ↗Journal of Hypertension · 2015 · PMID 26203966not yet assessed
-
Impact of HSD11B1 polymorphisms on BMI and components of the metabolic syndrome in patients receiving psychotropic treatments ↗Pharmacogenetics and Genomics · 2015 · PMID 25751397not yet assessed
-
CRTC2 polymorphism as a risk factor for the incidence of metabolic syndrome in patients with solid organ transplantation ↗The Pharmacogenomics Journal · 2015 · PMID 26644205not yet assessed
-
Impact of a <i>cis</i>-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance ↗The British Journal of Psychiatry · 2015 · PMID 26338991not yet assessed
-
Copy Number Variations and Cognitive Phenotypes in Unselected Populations ↗Obstetrical & Gynecological Survey · 2015not yet assessed
-
Association of PCK1 with Body Mass Index and Other Metabolic Features in Patients With Psychotropic Treatments ↗Journal of Clinical Psychopharmacology · 2015 · PMID 26280835not yet assessed
-
Correction: Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis ↗Nature Communications · 2015 · PMID 25817829not yet assessed
-
Across-cohort QC analyses of genome-wide association study summary statistics from complex traits ↗bioRxiv (Cold Spring Harbor Laboratory) · 2015not yet assessed
-
Correction: Corrigendum: Reduced IFNλ4 activity is associated with improved HCV clearance and reduced expression of interferon-stimulated genes ↗Nature Communications · 2015not yet assessed
-
Defining the role of common variation in the genomic and biological architecture of adult human height ↗Nature Genetics · 2014not yet assessed
-
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche ↗Nature · 2014 · PMID 25231870not yet assessed
-
Quality control and conduct of genome-wide association meta-analyses ↗Nature Protocols · 2014 · PMID 24762786not yet assessed
-
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption ↗Molecular Psychiatry · 2014 · PMID 25288136not yet assessed
-
Multilayered Genetic and Omics Dissection of Mitochondrial Activity in a Mouse Reference Population ↗Cell · 2014 · PMID 25215496not yet assessed
-
The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity ↗Molecular Psychiatry · 2014 · PMID 25421402not yet assessed
-
DQB1 Locus Alone Explains Most of the Risk and Protection in Narcolepsy with Cataplexy in Europe ↗SLEEP · 2014 · PMID 24381371not 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) · 2014not yet assessed
-
Gene-Age Interactions in Blood Pressure Regulation: A Large-Scale Investigation with the CHARGE, Global BPgen, and ICBP Consortia ↗The American Journal of Human Genetics · 2014 · PMID 24954895not yet assessed
-
Defining the role of common variation in the genomic and biological architecture of adult human height. ↗PubMed · 2014 · PMID 25282103not yet assessed
-
Genome-wide association study of kidney function decline in individuals of European descent ↗Kidney International · 2014 · PMID 25493955not yet assessed
-
Reduced IFNλ4 activity is associated with improved HCV clearance and reduced expression of interferon-stimulated genes ↗Nature Communications · 2014 · PMID 25534433not yet assessed
-
EasyStrata: evaluation and visualization of stratified genome-wide association meta-analysis data ↗Bioinformatics · 2014 · PMID 25260699not yet assessed
-
Impact of common risk factors of fibrosis progression in chronic hepatitis C ↗Gut · 2014 · PMID 25214320not yet assessed
-
Common Variants in UMOD Associate with Urinary Uromodulin Levels ↗Journal of the American Society of Nephrology · 2014 · PMID 24578125not 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 25078964not yet assessed
-
Genome-Wide Association Study of Metabolic Traits Reveals Novel Gene-Metabolite-Disease Links ↗PLoS Genetics · 2014 · PMID 24586186not yet assessed
-
IL1B and DEFB1 Polymorphisms Increase Susceptibility to Invasive Mold Infection After Solid-Organ Transplantation ↗The Journal of Infectious Diseases · 2014 · PMID 25398456not yet assessed
-
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis ↗Nature Communications · 2014 · PMID 25352340not yet assessed
-
75 ↗Cytokine · 2014not yet assessed
-
P196 INVESTIGATION OF HEPATITIS C VIRUS ADAPTATION TO HOST GENETIC POLYMORPHISMS ↗Journal of Hepatology · 2014not yet assessed
-
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment ↗Science · 2013 · PMID 23722424not yet assessed
-
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture ↗Nature Genetics · 2013 · PMID 23563607not 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 23754948not yet assessed
-
Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders ↗Nature Genetics · 2013 · PMID 23583979not yet assessed
-
Clinical, polysomnographic and genome‐wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study ↗Journal of Sleep Research · 2013 · PMID 23496005not yet assessed
-
A genome-to-genome analysis of associations between human genetic variation, HIV-1 sequence diversity, and viral control ↗eLife · 2013 · PMID 24171102not yet assessed
-
Meta-Analysis of Genome-Wide Association Studies Identifies Six New Loci for Serum Calcium Concentrations ↗PLoS Genetics · 2013 · PMID 24068962not yet assessed
-
A genome-wide association study of early menopause and the combined impact of identified variants ↗Human Molecular Genetics · 2013 · PMID 23307926not yet assessed
-
The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation ↗Frontiers in Genetics · 2013 · PMID 23750167not yet assessed
-
Comparative genetic analyses point to HCP5 as susceptibility locus for HCV-associated hepatocellular carcinoma ↗Journal of Hepatology · 2013 · PMID 23665287not yet assessed
-
Genetic Analyses Reveal a Role for Vitamin D Insufficiency in HCV-Associated Hepatocellular Carcinoma Development ↗PLoS ONE · 2013 · PMID 23734184not yet assessed
-
Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent ↗American Journal of Epidemiology · 2013 · PMID 23558354not yet assessed
-
GWAS of human bitter taste perception identifies new loci and reveals additional complexity of bitter taste genetics ↗Human Molecular Genetics · 2013 · PMID 23966204not yet assessed
-
Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function ↗Journal of the American Society of Nephrology · 2013 · PMID 24029420not yet assessed
-
Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk: A Meta-Analysis of 218,166 Adults and 19,268 ChildrenResearch Portal (King's College London) · 2013not yet assessed
-
Discovery and replication of several loci significantly associated with lean body mass: a large meta-analysis of genome wide association studies (GWAS) from the 'charge' and 'gefos' consortia ↗Bone Abstracts · 2013not yet assessed
-
Genome-wide association analyses identify 18 new loci associated with serum urate concentrationsUCL Discovery (University College London) · 2013not 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) · 2013not yet assessed
-
Supplementary Material 152013not yet assessed
-
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational AttainmentLondon School of Economics and Political Science Research Online (London School of Economics and Political Science) · 2013not yet assessed
-
not yet assessed
-
Liver, Pancreas, and Biliary Tract ゲノムワイド関連解析で見いだされたC型肝炎ウイルス感染による線維化進展と関連する遺伝子多型Review of gastroenterology & clinical gastroenterology and hepatology · 2013not yet assessed
-
A mega-analysis of genome-wide association studies for major depressive disorder ↗Molecular Psychiatry · 2012 · PMID 22472876not yet assessed
-
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations ↗Nature Genetics · 2012 · PMID 23263486not yet assessed
-
FTO genotype is associated with phenotypic variability of body mass index ↗Nature · 2012 · PMID 22982992not yet assessed
-
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways ↗Nature Genetics · 2012 · PMID 22267201not yet assessed
-
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders ↗Journal of Medical Genetics · 2012 · PMID 23054248not yet assessed
-
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism ↗Nature Genetics · 2012 · PMID 23202124not yet assessed
-
Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function ↗PLoS Genetics · 2012 · PMID 22479191not yet assessed
-
Genome-Wide Association Study Identifies Variants Associated With Progression of Liver Fibrosis From HCV Infection ↗Gastroenterology · 2012 · PMID 22841784not yet assessed
-
The protective effect of the obesity-associated rs9939609 A variant in fat mass- and obesity-associated gene on depression ↗Molecular Psychiatry · 2012 · PMID 23164817not yet assessed
-
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways ↗QUT ePrints (Queensland University of Technology) · 2012not yet assessed
-
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function ↗Human Molecular Genetics · 2012 · PMID 22962313not yet assessed
-
Caffeine intake and CYP1A2 variants associated with high caffeine intake protect non-smokers from hypertension ↗Human Molecular Genetics · 2012 · PMID 22492992not yet assessed
-
A Genetic Validation Study Reveals a Role of Vitamin D Metabolism in the Response to Interferon-Alfa-Based Therapy of Chronic Hepatitis C ↗PLoS ONE · 2012 · PMID 22808108not yet assessed
-
A Multi-SNP Locus-Association Method Reveals a Substantial Fraction of the Missing Heritability ↗The American Journal of Human Genetics · 2012 · PMID 23122585not yet assessed
-
Genome-wide meta-analysis of common variant differences between men and women ↗Human Molecular Genetics · 2012 · PMID 22843499not yet assessed
-
No Interactions Between Previously Associated 2-Hour Glucose Gene Variants and Physical Activity or BMI on 2-Hour Glucose Levels ↗Diabetes · 2012 · PMID 22415877not yet assessed
-
Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort ↗BMC Genomics · 2012 · PMID 22702538not yet assessed
-
Comparative modular analysis of gene expression in vertebrate organs ↗BMC Genomics · 2012 · PMID 22458817not yet assessed
-
1401 GENOME-WIDE ASSOCIATION STUDY IDENTIFIES VARIANTS ASSOCIATED WITH LIVER FIBROSIS PROGRESSION IN HCV-INFECTED PATIENTS ↗Journal of Hepatology · 2012not yet assessed
-
A Missense Mutation in Myelin Oligodendrocyte Glycoprotein as a Cause of Familial Narcolepsy with Cataplexy ↗The American Journal of Human Genetics · 2012not yet assessed
-
To Stratify Or Not To Stratify: What Can Be Learned From Power Considerations And A Practical Genome-Wide Search On Sex-Difference In The GIANT ConsortiumOxford University Research Archive (ORA) (University of Oxford) · 2012not yet assessed
-
Genome-Wide Association Study to Identify Common Variants Associated with Brachial Circumference: A Meta-Analysis of 14 Cohorts ↗PLoS ONE · 2012 · PMID 22479309not yet assessed
-
Abstract MP067: Six Novel Loci With Evidence For Sexual Dimorphism For Human Anthropometric Traits From Genome-wide Meta Analyses Across 270,722 Individuals ↗Circulation · 2012not yet assessed
-
FTO genotype is associated with phenotypic variability of body mass indexUniversity of Regensburg Publication Server (University of Regensburg) · 2012not yet assessed
-
Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk: A Meta-Analysis of 218,166 Adults and 19,268 Children ↗PLoS Medicine · 2011 · PMID 22069379not yet assessed
-
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus ↗Nature · 2011 · PMID 21881559not yet assessed
-
CUBN Is a Gene Locus for Albuminuria ↗Journal of the American Society of Nephrology · 2011 · PMID 21355061not yet assessed
-
Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD ↗PLoS Genetics · 2011 · PMID 21980298not yet assessed
-
Genomewide Association Study Using a High-Density Single Nucleotide Polymorphism Array and Case-Control Design Identifies a Novel Essential Hypertension Susceptibility Locus in the Promoter Region of Endothelial NO Synthase ↗Hypertension · 2011 · PMID 22184326not yet assessed
-
IL28B Alleles Associated With Poor Hepatitis C Virus (HCV) Clearance Protect Against Inflammation and Fibrosis in Patients Infected With Non-1 HCV Genotypes ↗Hepatology · 2011 · PMID 22180014not yet assessed
-
A Missense Mutation in Myelin Oligodendrocyte Glycoprotein as a Cause of Familial Narcolepsy with Cataplexy ↗The American Journal of Human Genetics · 2011 · PMID 21907016not yet assessed
-
Sensitivity of Genome-Wide-Association Signals to Phenotyping Strategy: The PROP-TAS2R38 Taste Association as a Benchmark ↗PLoS ONE · 2011 · PMID 22132133not yet assessed
-
Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy ↗Hepatology · 2011 · PMID 22095909not yet assessed
-
Genome-wide association study identifies two loci strongly affecting transferrin glycosylation ↗Human Molecular Genetics · 2011 · PMID 21665994not yet assessed
-
A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol ↗PLoS Genetics · 2011 · PMID 22028671not yet assessed
-
Novel method to estimate the phenotypic variation explained by genome-wide association studies reveals large fraction of the missing heritability ↗Genetic Epidemiology · 2011 · PMID 21465548not yet assessed
-
Variant Within the Promoter Region of the CHRNA3 Gene Associated With FTN Dependence Is Not Related to Self-Reported Willingness to Quit Smoking ↗Nicotine & Tobacco Research · 2011 · PMID 21511889not yet assessed
-
Comparison of Strategies to Detect Epistasis from eQTL Data ↗PLoS ONE · 2011 · PMID 22205949not yet assessed
-
the Swiss Hepatitis C Cohort Study GroupBern Open Repository and Information System (University of Bern) · 2011not yet assessed
-
1361 IL28B POLYMORPHISMS LINKED TO POOR RESPONSE TO TREATMENT ARE ASSOCIATED WITH LOW NECROINFLAMMATORY ACTIVITY AND SLOW FIBROSIS PROGRESSION IN HCV GENOTYPE NON-1-INFECTED PATIENTS ↗Journal of Hepatology · 2011not yet assessed
-
1357 A LARGE-SCALE GENETIC VALIDATION STUDY COUPLED WITH IN-VITRO ANALYSES REVEAL A ROLE OF VITAMIN D-SIGNALING IN THE PATHOGENESIS AND TREATMENT OF CHRONIC HEPATITIS C ↗Journal of Hepatology · 2011not 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 · 2011not yet assessed
-
Erratum: Corrigendum: Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy ↗Nature Genetics · 2011not yet assessed
-
A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total CholesterolTampere University Institutional Repository (Tampere University) · 2011not yet assessed
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index ↗Nature Genetics · 2010 · PMID 20935630not yet assessed
-
Hundreds of variants clustered in genomic loci and biological pathways affect human height ↗Nature · 2010 · PMID 20881960not yet assessed
-
Genetic Variation in IL28B Is Associated With Chronic Hepatitis C and Treatment Failure: A Genome-Wide Association Study ↗Gastroenterology · 2010 · PMID 20060832not 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 · 2010not yet assessed
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2010not yet assessed
-
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies ↗Nature Genetics · 2010 · PMID 21102462not yet assessed
-
Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy ↗Nature Genetics · 2010 · PMID 20711174not yet assessed
-
Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene ↗PLoS Genetics · 2010 · PMID 20661308not yet assessed
-
Modular analysis of gene expression data with R ↗Bioinformatics · 2010 · PMID 20371495not yet assessed
-
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. ↗PubMed · 2010 · PMID 20935629not yet assessed
-
Methods for testing association between uncertain genotypes and quantitative traits ↗Biostatistics · 2010 · PMID 20543033not yet assessed
-
ExpressionView—an interactive viewer for modules identified in gene expression data ↗Bioinformatics · 2010 · PMID 20671149not yet assessed
-
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2010not yet assessed
-
W48 GENETIC VARIATION WITHIN ADIPONUTRIN IS ASSOCIATED WITH LIPOPROTEIN METABOLISM AND LIVER FUNCTION ↗Atherosclerosis Supplements · 2010not yet assessed
-
Hundreds of variants clustered in genomic loci and biological pathways affect human heightUWA Profiles and Research Repository (University of Western Australia) · 2010not yet assessed
-
Liver, Pancreas, and Biliary tract IL28B遺伝子の多型はC型肝炎の慢性化と治療不成功に関連するReview of gastroenterology & clinical gastroenterology and hepatology · 2010not yet assessed
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Penetrance of marked cognitive impairment in older male carriers of the <i>FMR1</i> gene premutation ↗Journal of Medical Genetics · 2009 · PMID 19542082not yet assessed
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Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein B-containing lipoproteins ↗Human Molecular Genetics · 2009 · PMID 19729411not yet assessed
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Parameter estimation for the distribution of single cell lag times ↗Journal of Theoretical Biology · 2009 · PMID 19328813not yet assessed
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Cardiovascular Response to Beta-Adrenergic Blockade or Activation in 23 Inbred Mouse Strains ↗PLoS ONE · 2009 · PMID 19672458not yet assessed
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Genes mirror geography within Europe ↗Nature · 2008 · PMID 18758442not yet assessed
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A modular approach for integrative analysis of large-scale gene-expression and drug-response data ↗Nature Biotechnology · 2008 · PMID 18464786not yet assessed
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Genes mirror geography within Europe ↗Nature · 2008not yet assessed
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Prévalence des troubles cognitifs chez les sujets porteurs de la prémutation du gène fmr1 ↗Revue Neurologique · 2008not yet assessed
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S-system parameter estimation for noisy metabolic profiles using Newton-flow analysis ↗IET Systems Biology · 2007 · PMID 17591176not yet assessed
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Estimating parameters for generalized mass action models using constraint propagation ↗Mathematical Biosciences · 2006 · PMID 17306307not yet assessed
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Stochastic modelling of individual cell growth using flow chamber microscopy images ↗International Journal of Food Microbiology · 2005 · PMID 16091296not yet assessed
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Optimal sampling time selection for parameter estimation in dynamic pathway modeling ↗Biosystems · 2004 · PMID 15245803not yet assessed
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Connection between stochastic and deterministic modelling of microbial growth ↗Journal of Theoretical Biology · 2004 · PMID 15530497not yet assessed
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Advanced significance analysis of microarray data based on weighted resampling: a comparative study and application to gene deletions in <i>Mycobacterium bovis</i> ↗Bioinformatics · 2004 · PMID 14960462not yet assessed
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Occluding Convex Image Segmentation For E.Coli Microscopy Images ↗UEA Digital Repository (University of East Anglia) · 2004not yet assessed
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Automated spatial and temporal image analysis of bacterial cell growthUEA Digital Repository (University of East Anglia) · 2004not yet assessed
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A novel statistical approach in comparative genomics to reveal new immunogenic antigens in M. bovis ↗UEA Digital Repository (University of East Anglia) · 2004not yet assessed
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Level sets and minimum volume sets of probability density functions ↗International Journal of Approximate Reasoning · 2003not yet assessed
Full bibliography from OpenAlex; reproducibility verdicts matched by PMID.
Author attribution follows OpenAlex disambiguation, which is imperfect — a researcher's papers can be split across profiles or mixed with a namesake.
Merged across profiles sharing this ORCID where present. See every “Kutalik Z” paper on PubMed ↗