Erwan WATRIN

Information

Staff scientist

Véronique DAVID Group

+33 (0)2 23 23 43 32

Villejean Campus / Building 4 /  Room 207

Major publications

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

    Parenti 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.
    Expanding the clinical spectrum of the "HDAC8-phenotype" - Implications for molecular diagnostics, counselling and risk prediction.
    Clin Genet. 2015 

    Parenti 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. 
    Broadening of  cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotype.
    Clin Genet. 2015 Feb 4. 

    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. 
    Hidden mutations in Cornelia de Lange syndrome limitations of sanger sequencing in molecular diagnostics.
    Hum Mutat. 2015 Jan;36(1):26-9.

    Watrin E, Demidova M, Watrin T, Hu Z, Prigent C.
    Sororin pre-mRNA splicing is required for proper sister chromatid cohesion in human cells.
    EMBO Rep. 2014 Sep;15(9):948-55.

    Deardorff MA*, Bando M*, Nakato R*, Watrin E*, Itoh T, Minamino M, Saitoh K, Komata M, Katou Y, Clark D, Cole KE, De Baere E, Decroos C, Di Donato N, Ernst S, Francey LJ, Gyftodimou Y, Hirashima K, Hullings M, Ishikawa Y, Jaulin C, Kaur M,  Kiyono T, Lombardi PM, Magnaghi-Jaulin L, Mortier GR, Nozaki N, Petersen MB, Seimiya H, Siu VM, Suzuki Y, Takagaki K, Wilde JJ, Willems PJ, Prigent C, Gillessen-Kaesbach G, Christianson DW, Kaiser FJ, Jackson LG, Hirota T, Krantz ID, Shirahige K.
    HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle.
    Nature. 2012 Sep 13;489(7415):313-7. (* co-premier auteur)

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