Kees van Roozendaal

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling

Lot Snijders Blok, Erik Madsen, Jane Juusola et al. · The American Journal of Human Genetics · 2015 · 339 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Further characterization of the first seminoma cell line TCam‐2

Jeroen de Jong, Hans Stoop, Ad Gillis et al. · Genes Chromosomes and Cancer · 2007 · 145 citations

Medicine, Genetics, Oncology +13

Rett syndrome in females with CTS hot spot deletions: A disorder profile

E. Smeets, Pauline Terhal, A.A.W. Peters et al. · American Journal of Medical Genetics Part A · 2004 · 80 citations

Life Sciences, Genetics, Neuroscience +16

Expression of the <i>PDGF α‐receptor</i> 1.5 kb transcript, <i>OCT‐4</i>, and c‐<i>KIT</i> in human normal and malignant tissues. Implications for the early diagnosis of testicular germ cell tumours and for our understanding of regulatory mechanisms

Camilla Palumbo, Kees van Roozendaal, Ad Gillis et al. · The Journal of Pathology · 2002 · 79 citations · Full text

Medicine, Molecular Biology, Oncology +17

MCT8 mutation analysis and identification of the first female with Allan–Herndon–Dudley syndrome due to loss of MCT8 expression

Suzanna G.M. Frints, Steffen Lenzner, Mareike Bauters et al. · European Journal of Human Genetics · 2008 · 71 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7