Martine J. van Belzen

Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect

Alienke J. Monsuur, Paul I. W. de Bakker, Behrooz Z. Alizadeh et al. · Nature Genetics · 2005 · 243 citations

Life Sciences, Genetics, Molecular Genetics +16

Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients

Gijs W.E. Santen, Emmelien Aten, Anneke T. Vulto‐van Silfhout et al. · Human Mutation · 2013 · 220 citations

Life Sciences, Genetics, Molecular Genetics +17

Archetypal <i>NOTCH3</i> mutations frequent in public exome: implications for CADASIL

Julie W. Rutten, Hans G. Dauwerse, Gido Gravesteijn et al. · Annals of Clinical and Translational Neurology · 2016 · 204 citations · Full text

Life Sciences, Molecular Genetics, Neurology +15

A major non-HLA locus in celiac disease maps to chromosome 191 1This study is dedicated to the memory of Lodewijk Sandkuijl (1953–2002), who died shortly after its completion. He was an inspiration to us and was a world expert on biostatistics.

Martine J. van Belzen, Jos W. R. Meijer, Lodewijk A. Sandkuijl et al. · Gastroenterology · 2003 · 144 citations · Full text

Life Sciences, Genetics, Immunology +12

The SNAP-25 gene is associated with cognitive ability: evidence from a family-based study in two independent Dutch cohorts

M.F. Gosso, Eco J. C. de Geus, Martine J. van Belzen et al. · Molecular Psychiatry · 2006 · 94 citations · Full text

Life Sciences, Genetics, Psychology +15