Author details

Full Name

Veronique Vitart

Affiliation

ORCID

Career Start Year

1990

Papers

180

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37503126	Understanding the genetic complexity of puberty timing across the allele frequency spectrum.	medRxiv	2023
37749248	Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.	Nat Genet	2023
37881452	Typing myalgic encephalomyelitis by infection at onset: A DecodeME study.	NIHR Open Res	2023
37621707	Colocalization of corneal resistance factor GWAS loci with GTEx e/sQTLs highlights plausible candidate causal genes for keratoconus postnatal corneal stroma weakening.		2023
35022422	A multi-omics study of circulating phospholipid markers of blood pressure.	Sci Rep	2022
35697829	Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.	Commun Biol	2022
35854226	DecodeME: community recruitment for a large genetics study of myalgic encephalomyelitis / chronic fatigue syndrome.	BMC Neurology	2022
34368841	A mouse model of brittle cornea syndrome caused by mutation in Zfp469.	Dis Model Mech	2021
33909031	IMI 2021 Yearly Digest.	Invest Ophthalmol Vis Sci	2021
33627673	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Nat Commun	2021
33558525	Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
33307546	Genetic mechanisms of critical illness in COVID-19.	Nature	2021
33402679	Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
33311554	Fine-mapping and cell-specific enrichment at corneal resistance factor loci prioritize candidate causal regulatory variants.	Communications Biology	2020
31959993	Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.	Nat Genet	2020
32128391	Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseases.	Sci Adv	2020
32231278	Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia.	Nat Genet	2020
31358886	An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort.	Sci Rep	2019
31597446	Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease.	Arterioscler Thromb Vasc Biol	2019
31765389	Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.	PLoS Genet	2019
30804560	New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.	Nat Genet	2019
31121135	Genetic Correlations Between Diabetes and Glaucoma: An Analysis of Continuous and Dichotomous Phenotypes.	Am J Ophthalmol	2019
31160809	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2019
31152163	A catalog of genetic loci associated with kidney function from analyses of a million individuals.	Nat Genet	2019
31481615	The genetic landscape of Scotland and the Isles.	Proc Natl Acad Sci U S A	2019
29847655	Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus.	Invest Ophthalmol Vis Sci	2018
30429575	Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.	Nat Genet	2018
29912962	Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.	PLoS One	2018
30224653	Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.	Nat Genet	2018
29093028	Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes.	J Am Soc Nephrol	2018
29549330	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29549329	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29273807	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29808027	Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.	Nat Genet	2018
28146470	Rare and low-frequency coding variants alter human adult height.	Nature	2017
28509723	Determinants of retinal microvascular features and their relationships in two European populations.	Journal of Hypertension	2017
28986520	Regional variation in health is predominantly driven by lifestyle rather than genetics.	Nature Communications	2017
28939808	Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degeneration.	Sci Rep	2017
28448500	Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.	PLoS Genet	2017
28443625	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	Nat Commun	2017
28832619	Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.	PLoS Genet	2017
28739976	Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.	Hypertension	2017
28436984	Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.	Nat Genet	2017
29062915	Electronic health record and genome-wide genetic data in Generation Scotland participants.	Wellcome Open Research	2017
28270201	Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.	Genome Med	2017
28073927	New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.	Hum Mol Genet	2017
28196069	Correction: Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation.	PLoS Genetics	2017
28166213	Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.	Nat Genet	2017
27618452	The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.	Nat Genet	2016
25869804	GWAS for executive function and processing speed suggests involvement of the CADM2 gene.	Mol Psychiatry	2016