Staff scientist

Véronique DAVID Group

+33 (0)2 23 23 43 32

Villejean Campus / Building 4 /  Room 207

Major publications

  • 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 Am J Med Genet. C. 2018 May.

    Aurora A kinase activity is required to maintain an active spindle assembly checkpoint during prometaphase. Courtheoux T, Diallo A, Damodaran AP, Reboutier D, Watrin E, Prigent C. J cell Sci. 2018 Apr.

    Regulation of the cohesin-loading factor NIPBL: Role of the lncRNA NIPBL-AS1 and identification of a distal enhancer element. Zuin J, Casa V, Pozojevic J, Kolovos P, van den Hout MCGN, van Ijcken WFJ, Parenti I, Braunholz D, Baron Y, Watrin E, Kaiser FJ, Wendt KS. PLoS Genetics 2017 Dec

    Novel mosaic variants in two patients with Cornelia de Lange syndrome. Pozojevic J, Parenti I, Graul-Neumann L, Ruiz Gil S, Watrin E, Wendt KS, Werner R, Strom TM, Gillessen-Kaesbach G, Kaiser FJ. Eur J Med Genet. 2017 Nov

    Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes. Parenti I, Teresa-Rodrigo ME, Pozojevic J, Ruiz Gil S, Bader I, Braunholz D, Bramswig NC, Gervasini C, Larizza L, Pfeiffer L, Ozkinay F, Ramos F, Reiz B, Rittinger O, Strom TM, Watrin E, Wendt K, Wieczorek D, Wollnik B, Baquero-Montoya C, Pié J, Deardorff MA, Gillessen-Kaesbach G, Kaiser FJ. Hum Genet. 2017 Mar

    Gene regulation and chromatin organization: Relevance of cohesin mutations to human disease. Watrin E, Kaiser F and Wendt KS. Curr Opin Genet Dev. 2016 Apr

    Expanding the clinical spectrum of the "HDAC8-phenotype" - Implications for molecular diagnostics, counselling and risk predictionParenti I, Gervasini C, Pozojevic J, Wendt KS, Watrin E, Azzollini J, Braunholz D, Buiting K, Cereda A, Engels H, Garavelli L, Glazar R, Graffmann B, Larizza L, Lüdecke HJ, Mariani M, Masciadri M, Pié J, Ramos FJ, Russo S, Selicorni A, Stefanova M, Strom TM, Werner R, Wierzba J, Zampino G, Gillessen-Kaesbach G, Wieczorek D, Kaiser FJ. Clin Genet. 2016 May

    Broadening of  cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotypeParenti I, Gervasini C, Pozojevic J, Graul-Neumann L, Azzollini J, Braunholz D, Watrin E, Wendt KS, Cereda A, Cittaro D, Gillessen-Kaesbach G, Lazarevic D, Mariani M, Russo S, Werner R, Krawitz P, Larizza L, Selicorni A, Kaiser FJ. Clin Genet. 2015 Feb

    Hidden mutations in Cornelia de Lange syndrome limitations of sanger sequencing in molecular diagnostics. Braunholz D, Obieglo C, Parenti I, Pozojevic J, Eckhold J, Reiz B, Braenne I, Wendt KS, Watrin E, Vodopiutz J, Rieder H, Gillessen-Kaesbach G, Kaiser FJ. Hum Mutat. 2015 Jan

    Sororin pre-mRNA splicing is required for proper sister chromatid cohesion in human cells. Watrin E, Demidova M, Watrin T, Hu Z, Prigent C. EMBO Rep. 2014 Sep

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