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Author Details

Zolt??n Kutalik
University of Lausanne
2004
233
74
PMIDPaper TitleJournal TitlePublished Year
36658113Large scale phenotype imputation and in vivo functional validation implicate ADAMTS14 as an adiposity gene.Nat Commun2023
35670608The genetic etiology of periodic limb movement in sleep.Sleep2023
37586323Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic disease.Cell Rep Med2023
38093188Cannabis use and atherosclerotic cardiovascular disease: a Mendelian randomization study.BMC Cardiovasc Disord2023
36891970Exploiting the mediating role of the metabolome to unravel transcript-to-phenotype associations.Elife2023
36706759The impact of 22q11.2 copy-number variants on human traits in the general population.Am J Hum Genet2023
37188663Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy.Nat Commun2023
37002254Genetic insights into the causal relationship between physical activity and cognitive functioning.Sci Rep2023
37173452Identification of four novel loci associated with psychotropic drug-induced weight gain in a Swiss psychiatric longitudinal study: A GWAS analysis.Mol Psychiatry2023
36928782Partner choice, confounding and trait convergence all contribute to phenotypic partner similarity.Nat Hum Behav2023
37106081Participation bias in the UK Biobank distorts genetic associations and downstream analyses.Nat Hum Behav2023
37225732Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.NPJ Genom Med2023
37492104Multi-layered genetic approaches to identify approved drug targets.Cell Genom2023
37543033Genetic insights into the age-specific biological mechanisms governing human ovarian aging.Am J Hum Genet2023
37419093Response to Bassett et al.Am J Hum Genet2023
37036286Bias correction for inverse variance weighting Mendelian randomization.Genet Epidemiol2023
36658113Large scale phenotype imputation and in vivo functional validation implicate ADAMTS14 as an adiposity gene.Nat Commun2023
37492104Multi-layered genetic approaches to identify approved drug targets.Cell Genom2023
37586323Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic disease.Cell Rep Med2023
37543033Genetic insights into the age-specific biological mechanisms governing human ovarian aging.Am J Hum Genet2023
38093188Cannabis use and atherosclerotic cardiovascular disease: a Mendelian randomization study.BMC Cardiovasc Disord2023
35670608The genetic etiology of periodic limb movement in sleep.Sleep2023
37188663Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy.Nat Commun2023
37419093Response to Bassett et al.Am J Hum Genet2023
37173452Identification of four novel loci associated with psychotropic drug-induced weight gain in a Swiss psychiatric longitudinal study: A GWAS analysis.Mol Psychiatry2023
37106081Participation bias in the UK Biobank distorts genetic associations and downstream analyses.Nat Hum Behav2023
37036286Bias correction for inverse variance weighting Mendelian randomization.Genet Epidemiol2023
37002254Genetic insights into the causal relationship between physical activity and cognitive functioning.Sci Rep2023
37225732Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.NPJ Genom Med2023
36706759The impact of 22q11.2 copy-number variants on human traits in the general population.Am J Hum Genet2023
36928782Partner choice, confounding and trait convergence all contribute to phenotypic partner similarity.Nat Hum Behav2023
36891970Exploiting the mediating role of the metabolome to unravel transcript-to-phenotype associations.Elife2023
35953856Limited evidence for blood eQTLs in human sexual dimorphism.Genome Med2022
35715439Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.NPJ Genom Med2022
35653391Using genetic variation to disentangle the complex relationship between food intake and health outcomes.PLoS Genet2022
36173858Sex- and age-dependent genetics of longevity in a heterogeneous mouse population.Science2022
36035246Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations.HGG Adv2022
35953856Limited evidence for blood eQTLs in human sexual dimorphism.Genome Med2022
35832928Polynomial Mendelian randomization reveals non-linear causal effects for obesity-related traits.HGG Adv2022
35571679Improving polygenic prediction with genetically inferred ancestry.HGG Adv2022
35373152From pharmacogenetics to pharmaco-omics: Milestones and future directions.HGG Adv2022
36335127Parent-of-Origin inference for biobanks.Nat Commun2022
36131045Gene set enrichment analysis of pathophysiological pathways highlights oxidative stress in psychosis.Mol Psychiatry2022
36265482Liability-scale heritability estimation for biobank studies of low-prevalence disease.Am J Hum Genet2022
36059200Haematological changes from conception to childbirth: An indicator of major pregnancy complications.Eur J Haematol2022
36477627Quantifying the role of transcript levels in mediating DNA methylation effects on complex traits and diseases.Nat Commun2022
37118545Sphingolipids accumulate in aged muscle, and their reduction counteracts sarcopenia.Nat Aging2022
35653391Using genetic variation to disentangle the complex relationship between food intake and health outcomes.PLoS Genet2022
35373152From pharmacogenetics to pharmaco-omics: Milestones and future directions.HGG Adv2022
35832928Polynomial Mendelian randomization reveals non-linear causal effects for obesity-related traits.HGG Adv2022
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Collaborators

Peter Vollenweider
Lausanne University Hospital and University of Lausanne
Co-authored papers 79
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 66
Sven Bergmann
University of Lausanne
Co-authored papers 62
Cornelia M van Duijn
University of Oxford
Co-authored papers 59
Alexander Teumer
University Medicine Greifswald
Co-authored papers 59
Caroline Hayward
Co-authored papers 58
Tõnu Esko
Co-authored papers 57
Tamara B Harris
National Institute on Aging
Co-authored papers 55
Albert Hofman
Harvard T.H. Chan School of Public Health
Co-authored papers 54
Terho Lehtim??ki
Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University
Co-authored papers 53
Ruth J F Loos
Co-authored papers 53
Andres Metspalu
Co-authored papers 52
Vilmundur Gudnason
Co-authored papers 52
Albert V Smith
University of Michigan School of Public Health ann arbor
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Nicholas J Wareham
Co-authored papers 51
Olli T Raitakari
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G??rard Waeber
Centre hospitalier universitaire vaudois
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Tim D Spector
King's College London
Co-authored papers 48
Igor Rudan
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Paul M Ridker
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Fernando Rivadeneira
University Medical Center Rotterdam
Co-authored papers 46
Dorret I Boomsma
Co-authored papers 46
Christian Gieger
German Research Center for Cardiovascular Disease (DZHK)
Co-authored papers 45
James F Wilson
Co-authored papers 45
Daniel I Chasman
Harvard Medical School, Harvard University
Co-authored papers 45
Jing Hua Zhao
Co-authored papers 45
Ozren Polasek
Co-authored papers 44
Nicholas G Martin
Co-authored papers 44
Jouke-Jan Hottenga
Co-authored papers 44
Jian'an Luan
Co-authored papers 44
Release 1.2