Searching journal content for Lisanne Vervoort in author.

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  1. Research: Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndrome
    • Lisanne Vervoort,
    • Nicolas Dierckxsens,
    • Marta Sousa Santos,
    • Senne Meynants,
    • Erika Souche,
    • Ruben Cools,
    • Tracy Heung,
    • Koen Devriendt,
    • Hilde Peeters,
    • Donna M. McDonald-McGinn,
    • Ann Swillen,
    • Jeroen Breckpot,
    • Beverly S. Emanuel,
    • Hilde Van Esch,
    • Anne S. Bassett,
    • and Joris R. Vermeesch
    Genome Res. April 2025 35: 786-797; Published in Advance November 13, 2024, doi:10.1101/gr.279331.124
  2. Research: The 22q11 low copy repeats are characterized by unprecedented size and structural variability
    • Wolfram Demaerel,
    • Yulia Mostovoy,
    • Feyza Yilmaz,
    • Lisanne Vervoort,
    • Steven Pastor,
    • Matthew S. Hestand,
    • Ann Swillen,
    • Elfi Vergaelen,
    • Elizabeth A. Geiger,
    • Curtis R. Coughlin,
    • Stephen K. Chow,
    • Donna McDonald-McGinn,
    • Bernice Morrow,
    • Pui-Yan Kwok,
    • Ming Xiao,
    • Beverly S. Emanuel,
    • Tamim H. Shaikh,
    • and Joris R. Vermeesch
    Genome Res. September 2019 29: 1389-1401; doi:10.1101/gr.248682.119
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