Véronique DAVID

Information

Group leader

Véronique DAVID Group

+33 (0)2 23 23 45 43

Villejean campus / Building 4 / Room 207

Major publications

  • Mutational Spectrum in Holoprosencephaly Shows That Fgf is a New Major Signaling Pathway. 
    Dubourg C, Carré W, Hamdi-Rozé H, Mouden C, Roume J, Abdelmajid B, Amram D, Baumann C, Chassaing N, Coubes C, Faivre-Olivier L, Ginglinger E, Gonzales M, Levy-Mozziconacci A, Lynch SA, Naudion S, Pasquier L, Poidvin A, Prieur F, Sarda P, Toutain A, Dupé V, Akloul L, Odent S, de Tayrac M, David V. Hum. Mutat. 2016 Jul.

    Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing.
    Mouden C, Dubourg C, Carré W, Rose S, Quelin c, Akloul L, Viot G, Salhi H, Darnault P, Odent S, Dupé V, David V. Clin. Genet. 2016 Jan.

    Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings. 
    Mouden C, de Tayrac M, Dubourg C, Rose S, Carré W, Hamdi-Rozé H, Akloul L, Héron B, Odent S, Dupé V, Giet R, David V. PLoS One. 2015 Feb.

    Identification of nine new RAI1truncating mutations in Smith-Magenis syndrome patients without 17p11.2 deletions.
    Dubourg C, Bonnet-Brilhault F, Toutain A, Mignot C, Jacquette A, Dieux A, Gérard-Banluet M, Beaumont-Epinette M, Julia S, Isidor B, Rossi M, Odent S, Bendavid C, Barthélémy C, Verloes A, David V. Mol Syndromol. 2014 Feb.

    Array-CGH analysis suggests genetic heterogeneity in Rhombencephalosynapsis.
    Démurger F, Pasquier L, Dubourg C, Dupé V, Gicquel I, Evain C, Ratié L, Jaillard S, Beri M, Leheup B, Lespinasse J, Martin-Coignard D, Mercier S, Quelin C, Loget P, Marcorelles P, Laquerrière A, Bendavid C, Odent S, David V. Molecular Syndromology. 2013 Sep

    NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryo. 
    Mercier S, David V, Ratié L, Gicquel I, Odent S, Dupé V. Dis Model Mech. 2013 Mar.

    NOTCH, a new signaling pathway implicated in holoprosencephaly. 
    Dupé V, Rochard L, Mercier S, Le Pétillon Y, Gicquel I, Bendavid C, Bourrouillou G, Usha K, Thauvin-Robinet C, Bohan T, Odent S, Dubourg C, David V.
    Hum Mol Genet. 2011 Mar.

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