Bert van der Zwaag

Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome

Daniel Beltrán-Valero de Bernabé, Sophie Currier, Alice Steinbrecher et al. · The American Journal of Human Genetics · 2002 · 684 citations · Full text

Molecular Neuroscience, Developmental Biology, Mendelian Disorder +8

Mobius syndrome redefined

H. T. F. M. Verzijl, Bert van der Zwaag, J.R.M. Cruysberg et al. · Neurology · 2003 · 300 citations

Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis

Anneke I. den Hollander, Robert K. Koenekoop, Moin Mohamed et al. · Nature Genetics · 2007 · 199 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1

Erwin van Wijk, Bert van der Zwaag, Theo Peters et al. · Human Molecular Genetics · 2006 · 185 citations

Signal Transduction, Developmental Biology, Signaling Pathway +14

Contact in the genetics of autism and schizophrenia

J. Peter H. Burbach, Bert van der Zwaag · Trends in Neurosciences · 2009 · 165 citations

Psychiatry, Syndromic Autism, Genetics +8