Raoul van de Graaf

A Mutation in the Fibroblast Growth Factor 14 Gene Is Associated with Autosomal Dominant Cerebral Ataxia

John C. van Swieten, Esther Brusse, Bianca M. de Graaf et al. · The American Journal of Human Genetics · 2003 · 295 citations · Full text

Life Sciences, Genetics, Neurology +13

Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies

Lars T. van der Veken, Marianne MJ Dieleman, Hannie Douben et al. · Molecular Cytogenetics · 2010 · 97 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Variable phenotypic expression and extensive tau pathology in two families with the novel <i>tau</i> mutation L315R

Esther van Herpen, Sonia M. Rosso, Lies‐Anne Serverijnen et al. · Annals of Neurology · 2003 · 83 citations

Life Sciences, Neurology, Neuroscience +17

Cortical Brain Malformations

Marie Claire Yvette de Wit, Maarten H. Lequin, I.F.M. de Coo et al. · Archives of Neurology · 2008 · 32 citations

Medicine, Genetics, Pediatrics +17

Identification of a large rearrangement in CYLD as a cause of familial cylindromatosis

Ans M.W. van den Ouweland, Peter Elfferich, R. J. Lamping et al. · Familial Cancer · 2010 · 29 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17