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  1. Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

    Article • October 2020, Cold Spring Harbor Laboratory Press

    MSc Laurens Wiel

  2. Evidence for 28 genetic disorders discovered by combining healthcare and research data

    Article • Nature, October 2020, Springer Science + Business Media

    MSc Laurens Wiel

  3. Front Cover, Volume 40, Issue 8

    Article • Human Mutation, August 2019, Wiley

    MSc Laurens Wiel

  4. MetaDome: Pathogenicity analysis of genetic variants through aggregation of homologous human protein domains

    Article • Human Mutation, May 2019, Wiley

    MSc Laurens Wiel

  5. Spatial Clustering of de Novo Missense Mutations Identifies Candidate Neurodevelopmental Disorder-Associated Genes

    Article • The American Journal of Human Genetics, September 2017, Elsevier

    MSc Laurens Wiel

  6. Human homologue protein domains aid in interpreting genetic variants

    Article • Human Mutation, August 2017, Wiley

    MSc Laurens Wiel

  7. Genome-scale detection of positive selection in nine primates predicts human-virus evolutionary conflicts

    Article • Nucleic Acids Research, August 2017, Oxford University Press (OUP)

    MSc Laurens Wiel

  8. Genome-scale detection of positive selection in 9 primates predicts human-virus evolutionary conflicts

    Article • April 2017, Cold Spring Harbor Laboratory Press

    MSc Laurens Wiel

  9. KeCo: Kernel-Based Online Co-agreement Algorithm

    Article • January 2015, Springer Science + Business Media

    MSc Laurens Wiel