Véronique David

Véronique David publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Véronique David sits on this spectrum.

Véronique David D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Véronique David sits on this spectrum.

Overview

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

  518
  Citations

• 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

  289
  Citations

• 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

  212
  Citations

• 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

  192
  Citations

• 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

  183
  Citations

• 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

  177
  Citations

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

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

  164
  Citations

• Analysis of genotype-phenotype correlations in human holoprosencephaly.

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

  151
  Citations

• 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

  144
  Citations

• 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

  137
  Citations

• 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

  130
  Citations

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

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

  125
  Citations

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

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

  125
  Citations

• Functional Characterization of Sonic Hedgehog Mutations Associated with Holoprosencephaly

  Elisabeth Traiffort;Christèle Dubourg;Hélène Faure;Didier Rognan

  118
  Citations

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

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

  117
  Citations

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

  Laurent Pasquier;Pascale Marcorelles;Philippe Loget;Fanny Pelluard

  113
  Citations

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

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

  111
  Citations

• 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

  107
  Citations

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

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

  102
  Citations

• Phenotypic and molecular variability of the holoprosencephalic spectrum.

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

  95
  Citations