Wout H. Deelen

A novel <i>tau</i> mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease

Sonia M. Rosso, Esther van Herpen, Wout H. Deelen et al. · Annals of Neurology · 2002 · 97 citations

Life Sciences, Genetics, Neurology +16

DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR‐1 gene

Ans M.W. van den Ouweland, Bert B.A. de Vries, P. Lida G. Bakker et al. · American Journal of Medical Genetics · 1994 · 56 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome.

E.J. Meijers-Heijboer, L. Sandkuijl, Han G. Brunner et al. · Journal of Medical Genetics · 1992 · 50 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes

Ans M.W. van den Ouweland, Wout H. Deelen, Catherine B. Kunst et al. · Human Molecular Genetics · 1994 · 47 citations

Life Sciences, Genetics, Molecular Genetics +16

Founder effect in a Belgian-Dutch fragile X population

Sonja Buyle, Edwin Reyniers, Lieve Vits et al. · Human Genetics · 1993 · 43 citations

Life Sciences, Genetics, Human Genetics +5