Ruben van’t Slot

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

Myosin Ixb Variant, Autoimmune Disease, Pathogenesis +8

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

Michael A. van Es, Paul WJ van Vught, Hylke M. Blauw et al. · Nature Genetics · 2007 · 218 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Genetics +9

Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder

Martin Poot, Vera Beyer, Ira Schwaab et al. · Neurogenetics · 2009 · 135 citations

Neurodevelopmental Disorders, Syndromic Autism, Genetic Disorder +9

An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia

Bart J. Jungerius, Mechteld L.C. Hoogendoorn, S C Bakker et al. · Molecular Psychiatry · 2007 · 107 citations

Psychiatry, Genetic Disorder, Medicine +11

Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients

Carolien G. F. de Kovel, Eva H. Brilstra, Marjan J. A. van Kempen et al. · Molecular Genetics & Genomic Medicine · 2016 · 89 citations · Full text