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Zoltán Kutalik

Name	Zoltán Kutalik
Zeit	2004- (Wirkungsdaten)
Ort	Schweiz Großbritannien
Geschlecht	männlich
Akademischer Grad bzw. Titel	Dr.
Variante	Zoltan Kutalik
Beziehung	Université de Lausanne Unisanté University of Exeter SIB Swiss Institute of Bioinformatics Statistik (Thema) Genetik (Thema)
Datensatztyp	Person
GND-Nummer	1261049748
Datensatz-ID	1261049748
Beteiligt an alle anzeigen DNA methylation may partly explain psychotropic drug-induced metabolic side effects: results from a prospective 1-month observational study Rare copy-number variants as modulators of common disease susceptibility Cannabis use and atherosclerotic cardiovascular disease: a Mendelian randomization study Identification of four novel loci associated with psychotropic drug-induced weight gain in a Swiss psychiatric longitudinal study: A GWAS analysis Genetic insights into the causal relationship between physical activity and cognitive functioning Quantifying the role of transcript levels in mediating DNA methylation effects on complex traits and diseases Parent-of-Origin inference for biobanks Gene set enrichment analysis of pathophysiological pathways highlights oxidative stress in psychosis Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention Limited evidence for blood eQTLs in human sexual dimorphism Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts HSD17B7 gene in self‐renewal and oncogenicity of keratinocytes from Black versus White populations Heterogeneity in Obesity: Genetic Basis and Metabolic Consequences 48th European Mathematical Genetics Meeting (EMGM) 2020 Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour Mendelian randomisation analyses find pulmonary factors mediate the effect of height on coronary artery disease Dysregulation of a long noncoding RNA reduces leptin leading to a leptin-responsive form of obesity Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution Assessment of network module identification across complex diseases Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Addendum: A joint view on genetic variants for adiposity differentiates subtypes with distinct metabolic implications A joint view on genetic variants for adiposity differentiates subtypes with distinct metabolic implications Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Genetic and clinic predictors of new onset diabetes mellitus after transplantation Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits Large meta-analysis of genome-wide association studies identifies five loci for lean body mass 1000 genomes-based meta-analysis identifies 10 novel loci for kidney function The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder Genetic analyses reveal a role for vitamin D insufficiency in HCV-associated hepatocellular carcinoma development Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort Comparative modular analysis of gene expression in vertebrate organs A genetic validation study reveals a role of vitamin D metabolism in the response to interferon-alfa-based therapy of chronic hepatitis C

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Katalog der Deutschen Nationalbibliothek

Zoltán Kutalik

DNA methylation may partly explain psychotropic drug-induced metabolic side effects: results from a prospective 1-month observational study

Rare copy-number variants as modulators of common disease susceptibility

Cannabis use and atherosclerotic cardiovascular disease: a Mendelian randomization study

Identification of four novel loci associated with psychotropic drug-induced weight gain in a Swiss psychiatric longitudinal study: A GWAS analysis

Genetic insights into the causal relationship between physical activity and cognitive functioning

Quantifying the role of transcript levels in mediating DNA methylation effects on complex traits and diseases

Parent-of-Origin inference for biobanks

Gene set enrichment analysis of pathophysiological pathways highlights oxidative stress in psychosis

Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

Limited evidence for blood eQTLs in human sexual dimorphism

Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts

HSD17B7 gene in self‐renewal and oncogenicity of keratinocytes from Black versus White populations

Heterogeneity in Obesity: Genetic Basis and Metabolic Consequences

48th European Mathematical Genetics Meeting (EMGM) 2020

Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals

A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour

Mendelian randomisation analyses find pulmonary factors mediate the effect of height on coronary artery disease

Dysregulation of a long noncoding RNA reduces leptin leading to a leptin-responsive form of obesity

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

Assessment of network module identification across complex diseases

Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD

Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Addendum: A joint view on genetic variants for adiposity differentiates subtypes with distinct metabolic implications

A joint view on genetic variants for adiposity differentiates subtypes with distinct metabolic implications

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Genetic and clinic predictors of new onset diabetes mellitus after transplantation

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders

Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

1000 genomes-based meta-analysis identifies 10 novel loci for kidney function

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT

KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference

A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder

Genetic analyses reveal a role for vitamin D insufficiency in HCV-associated hepatocellular carcinoma development

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort

Comparative modular analysis of gene expression in vertebrate organs

A genetic validation study reveals a role of vitamin D metabolism in the response to interferon-alfa-based therapy of chronic hepatitis C