Publikationen in Zusammenarbeit mit Forschern von KU Leuven (5)

2023

  1. Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes

    The Lancet. Oncology, Vol. 24, Núm. 1, pp. 91-106

2017

  1. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

    Nature Genetics, Vol. 49, Núm. 12, pp. 1767-1778

2015

  1. Infectious and Immunologic Phenotype of MECP2 Duplication Syndrome

    Journal of Clinical Immunology, Vol. 35, Núm. 2, pp. 168-181

2011

  1. A child with mild X-linked intellectual disability and a microduplication at Xp22.12 including RPS6KA3

    Pediatrics, Vol. 128, Núm. 4

2009

  1. A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

    Nature Genetics, Vol. 41, Núm. 5, pp. 535-543