List of works - Veronique Vitart

Discovery and fine mapping of serum protein loci through transethnic meta-analysis

scientific article

Localising loci underlying complex trait variation using Regional Genomic Relationship Mapping

scientific article

Evidence of inbreeding depression on human height

scientific article

Genome-wide association uncovers shared genetic effects among personality traits and mood states

scientific article published on 24 May 2012

Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

scientific article

Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

scientific article published on 29 March 2016

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

scientific article

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

scientific article published on 8 September 2012

Genome-wide association study of biochemical traits in Korcula Island, Croatia

scientific article

Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration

scientific article

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

scientific article

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error

scientific article

Bayesian methods for instrumental variable analysis with genetic instruments ('Mendelian randomization'): example with urate transporter SLC2A9 as an instrumental variable for effect of urate levels on metabolic syndrome

scientific article

A comprehensive evaluation of potential lung function associated genes in the SpiroMeta general population sample

scientific article

Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's disease

scientific article

Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels

scientific article

A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level

scientific article

Recent genomic heritage in Scotland

scientific article

Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation

scientific article published on 2 February 2016

Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci

scientific article

The power of regional heritability analysis for rare and common variant detection: simulations and application to eye biometrical traits

scientific article

Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data

scientific article

Genome-wide analysis of epistasis in body mass index using multiple human populations

scientific article

Genome-wide association study of anthropometric traits in Korcula Island, Croatia

scientific article

Quantifying the increase in average human heterozygosity due to urbanisation

scientific article

Genetic predictors of fibrin D-dimer levels in healthy adults

scientific article

The TCF7L2 diabetes risk variant is associated with HbA₁(C) levels: a genome-wide association meta-analysis

scientific article

Modulation of genetic associations with serum urate levels by body-mass-index in humans

scientific article

Genes predict village of origin in rural Europe

scientific article

Common variants in Mendelian kidney disease genes and their association with renal function

scientific article published on 12 September 2013

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

scientific article published on 23 November 2016

Integrative pathway genomics of lung function and airflow obstruction

scientific article

Copy number variation across European populations

scientific article

Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

scientific article

Increased level of linkage disequilibrium in rural compared with urban communities: a factor to consider in association-study design

scientific article

Homozygous loss-of-function variants in European cosmopolitan and isolate populations

scientific article

The association between galactosylation of immunoglobulin G and body mass index

scientific article

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

scientific article

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

scientific article

Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models

scientific article

Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.

scientific article

Inference of identity by descent in population isolates and optimal sequencing studies

scientific article published on 30 January 2013

Heritabilities of ocular biometrical traits in two croatian isolates with extended pedigrees

scientific article

When do myopia genes have their effect? Comparison of genetic risks between children and adults

scientific article published on 9 September 2016

Multicohort analysis of the maternal age effect on recombination

scientific article

Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolates

scientific article

Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studies

scientific article

Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits

scientific article published on 3 August 2011

Historic, demographic, and genetic evidence for increased population frequencies of CCR5Delta32 mutation in Croatian Island isolates after lethal 15th century epidemics

scientific article

Whole-exome sequencing in an isolated population from the Dalmatian island of Vis

scientific article published on 06 April 2016

List of works by Veronique Vitart

Discovery and fine mapping of serum protein loci through transethnic meta-analysis

Localising loci underlying complex trait variation using Regional Genomic Relationship Mapping

Evidence of inbreeding depression on human height

Genome-wide association uncovers shared genetic effects among personality traits and mood states

Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

Genome-wide association study of biochemical traits in Korcula Island, Croatia

Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error

Bayesian methods for instrumental variable analysis with genetic instruments ('Mendelian randomization'): example with urate transporter SLC2A9 as an instrumental variable for effect of urate levels on metabolic syndrome

A comprehensive evaluation of potential lung function associated genes in the SpiroMeta general population sample

Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's disease

Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels

A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level

Recent genomic heritage in Scotland

Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation

Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci

The power of regional heritability analysis for rare and common variant detection: simulations and application to eye biometrical traits

Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data

Genome-wide analysis of epistasis in body mass index using multiple human populations

Genome-wide association study of anthropometric traits in Korcula Island, Croatia

Quantifying the increase in average human heterozygosity due to urbanisation

Genetic predictors of fibrin D-dimer levels in healthy adults

The TCF7L2 diabetes risk variant is associated with HbA₁(C) levels: a genome-wide association meta-analysis

Modulation of genetic associations with serum urate levels by body-mass-index in humans

Genes predict village of origin in rural Europe

Common variants in Mendelian kidney disease genes and their association with renal function

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

Integrative pathway genomics of lung function and airflow obstruction

Copy number variation across European populations

Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

Increased level of linkage disequilibrium in rural compared with urban communities: a factor to consider in association-study design

Homozygous loss-of-function variants in European cosmopolitan and isolate populations

The association between galactosylation of immunoglobulin G and body mass index

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models

Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.

Inference of identity by descent in population isolates and optimal sequencing studies

Heritabilities of ocular biometrical traits in two croatian isolates with extended pedigrees

When do myopia genes have their effect? Comparison of genetic risks between children and adults

Multicohort analysis of the maternal age effect on recombination

Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolates

Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studies

Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits

Historic, demographic, and genetic evidence for increased population frequencies of CCR5Delta32 mutation in Croatian Island isolates after lethal 15th century epidemics

Whole-exome sequencing in an isolated population from the Dalmatian island of Vis