Marie DE TAYRAC

Information

Research professor

Véronique DAVID Group

+33 (0)2 23 23 38 07

Major publications

  • Integrated Clinical and Omics Approach to Rare Diseases : Novel Genes and Oligogenic Inheritance in Holoprosencephaly. Kim A, Savary C, Dubourg C, Carré W, Mouden C, Hamdi-Rozé H, Guyodo H, Le Douce J, Frex Consortium, GoNL Consortium, Pasquier L, Flori E, Gonzales M, Bénéteau C, Boute 0, Attié-Bitach T, Roume J, Goujon L, Akloul L, Odent S, Watrin E, Dupé V, de Tayrac M, David V. Brain. 2019 Jan.

    Recent advances in understanding inheritance of holoprosencephaly. Dubourg C, Kim A, Watrin E, de Tayrac M, Odent S, David V, Dupé V. Am J Med Genet. C. 2018 May.

    [From cyclops to reality: a fresh look at the genetics of holoprosencephaly]. Dupé V, Dubourg C, de Tayrac M, David V. Médecine/Science. 2017 Nov. French

    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.

    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.

    Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis. 
    de Tayrac M, Roth MP, Jouanolle M, Coppin H, le Gac G, Piperno a, Férec C, Pelucchi S, Scotet V, Bardou-Jacquet E, Ropert M, Bouvet R, Génin E, Mosser J, Deugnier Y.
    J. Hepatol. 2015 Mar.

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