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Véronique David

Véronique David

D-Index & Metrics

Genetics

D-Index
51
Citations
6720
World Ranking
3881
National Ranking
201

Overview

Véronique David is affiliated with Université de Rennes in France and has contributed extensively to the fields of medicine, biochemistry, genetics, and molecular biology. Their work spans multiple subfields including nephrology, molecular biology, genetics, surgery, and pathology and forensic medicine.

Their research topics primarily address parathyroid disorders and treatments, fibroblast growth factor research, genetic syndromes and imprinting, biomedical research and pathophysiology, connective tissue disorders research, intraperitoneal and appendiceal malignancies, and epigenetics and DNA methylation.

Some of the recent papers authored by Véronique David include:

  • Lipocalin 2 stimulates bone fibroblast growth factor 23 production in chronic kidney disease, 2021, Bone Research
  • Iron status, fibroblast growth factor 23 and cardiovascular and kidney outcomes in chronic kidney disease, 2021, Kidney International
  • Bone-derived C-terminal FGF23 cleaved peptides increase iron availability in acute inflammation, 2023, Blood
  • Effects of ferric carboxymaltose on markers of mineral and bone metabolism: A single-center prospective observational study of women with iron deficiency, 2020, Bone
  • Antagonism Between PEDF and TGF-β Contributes to Type VI Osteogenesis Imperfecta Bone and Vascular Pathogenesis, 2020, Journal of Bone and Mineral Research

Véronique David frequently collaborates with several co-authors, including:

  • Aline Martin
  • Guillaume Courbon
  • Jadeah J. Spindler
  • Marta Martínez-Calle
  • Bridget Hunt-Tobey

The researcher often publishes in well-known venues, with multiple contributions to:

  • Journal of the American Society of Nephrology
  • Current Opinion in Nephrology & Hypertension
  • Annals of Surgical Oncology
  • Kidney International
  • Journal of Clinical Investigation

Best Publications

  • Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.

    Audrey Guilmatre;Christèle Dubourg;Anne-Laure Mosca;Solenn Legallic

  • MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations

    Nathalie Le Meur;Muriel Holder-Espinasse;Sylvie Jaillard;Alice Goldenberg

  • Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination

    Lúcia Y. Brown;Sylvie Odent;Véronique David;Martine Blayau

  • Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.

    Christèle Dubourg;Leïla Lazaro;Laurent Pasquier;Claude Bendavid

  • Expression of the Sonic hedgehog (SHH) Gene during Early Human Development and Phenotypic Expression of New Mutations Causing Holoprosencephaly

    S. Odent;T. Attié-Bitach;M. Blayau;M. Mathieu

  • Phenotypic expression of HFE mutations: A French study of 1110 unrelated iron-overloaded patients and relatives ☆ ☆☆

    Romain Moirand;Anne-Marie Jouanolle;Pierre Brissot;Jean-Yves Le Gall

  • A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.

    A M Jouanolle;P Fergelot;G Gandon;J Yaouanq

  • Analysis of genotype-phenotype correlations in human holoprosencephaly.

    Benjamin D. Solomon;Sandra Mercier;Jorge I. Vélez;Daniel E. Pineda-Alvarez

  • Neonatal Screening for Cystic Fibrosis in Brittany, France: Assessment of 10 Years’ Experience and Impact on Prenatal Diagnosis

    Virginie Scotet;Marc de Braekeleer;Michel Roussey;Gilles Rault

  • Common Variants in the BMP2, BMP4, and HJV Genes of the Hepcidin Regulation Pathway Modulate HFE Hemochromatosis Penetrance

    Jacqueline Milet;Valérie Déhais;Catherine Bourgain;Catherine Bourgain;Anne Marie Jouanolle

  • Comparing the clinical evolution of cystic fibrosis screened neonatally to that of cystic fibrosis diagnosed from clinical symptoms: a 10-year retrospective study in a French region (Brittany).

    D Siret;G Bretaudeau;B Branger;A Dabadie

  • A genotypic study of 217 unrelated probands diagnosed as “genetic hemochromatosis” on “classical” phenotypic criteria

    Pierre Brissot;Romain Moirand;Anne-Marie Jouanolle;Dominique Guyader

  • Venesection therapy of insulin resistance-associated hepatic iron overload.

    Anne Guillygomarc'h;Michel Henri Mendler;Romain Moirand;Fabrice Lainé

  • Functional Characterization of Sonic Hedgehog Mutations Associated with Holoprosencephaly

    Elisabeth Traiffort;Christèle Dubourg;Hélène Faure;Didier Rognan

  • New findings for phenotype–genotype correlations in a large European series of holoprosencephaly cases

    Sandra Mercier;Christèle Dubourg;Nicolas Garcelon;Boris Campillo-Gimenez

  • Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal cases

    Laurent Pasquier;Pascale Marcorelles;Philippe Loget;Fanny Pelluard

  • Twelve new patients with 13q deletion syndrome: genotype-phenotype analyses in progress.

    Chloé Quélin;Claude Bendavid;Christèle Dubourg;Céline de la Rochebrochard

  • Gender-specific phenotypic expression and screening strategies in C282Y-linked haemochromatosis: a study of 9396 French people.

    Yves Deugnier;Anne-Marie Jouanolle;Jacques Chaperon;Romain Moirand

  • Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload.

    Anne-Marie Jouanolle;Véronique Douabin-Gicquel;Chantal Halimi;Olivier Loréal

  • Phenotypic and molecular variability of the holoprosencephalic spectrum.

    Leila Lazaro;Christéle Dubourg;Laurent Pasquier;Franck Le Duff

Frequent Co-Authors

Christèle Dubourg
Christèle Dubourg University of Rennes
Sylvie Odent
Sylvie Odent University of Rennes
Pierre Brissot
Pierre Brissot University of Rennes
Laurent Pasquier
Laurent Pasquier University of Rennes
Maximilian Muenke
Maximilian Muenke American College of Medical Genetics
Erich Roessler
Erich Roessler National Institutes of Health
Pierre Pontarotti
Pierre Pontarotti Aix-Marseille University
Annick Toutain
Annick Toutain François Rabelais University
Thierry Frebourg
Thierry Frebourg Grenoble Alpes University
Sherri J. Bale
Sherri J. Bale OPKO Health (United States)

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