R.A. Ophoff

Episodic Ataxia Type 2 (EA2) and Spinocerebellar Ataxia Type 6 (SCA6) Due to CAG Repeat Expansion in the CACNA1A Gene on Chromosome 19p

Carla Jodice, Elide Mantuano, Liana Veneziano et al. · Human Molecular Genetics · 1997 · 294 citations · Full text

Life Sciences, Genetics, Neurology +16

Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families.

Alexis Elbaz, J. Vale-Santos, Karin Jurkat‐Rott et al. · PubMed · 1995 · 113 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Familial Hemiplegic Migraine: A Clinical Comparison of Families Linked and Unlinked to Chromosome 19

GM Terwindt, R.A. Ophoff, J. Haan et al. · Cephalalgia · 1996 · 74 citations

Life Sciences, Genetics, Neurology +13

A genome-wide association study of anorexia nervosa

Vesna Boraska Perica, Christopher S. Franklin, James Floyd et al. · Research Portal (Queen's University Belfast) · 2014 · 74 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Partial Cosegregation of Familial Hemiplegic Migraine and a Benign Familial Infantile Epileptic Syndrome

G.M. Terwindt, R.A. Ophoff, Dick Lindhout et al. · Epilepsia · 1997 · 57 citations · Full text

Life Sciences, Genetics, Neurology +17