Gisela M. Terwindt

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

Roel A. Ophoff, Gisela M. Terwindt, Monique N. Vergouwe et al. · Cell · 1996 · 2.3K citations · Full text

Channelopathies, Genetic Disorder, Genetics +5

Analysis of shared heritability in common disorders of the brain

Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane et al. · Science · 2018 · 2K citations · Full text

Brain Function, Psychiatric Disorders, Genetics +23

The prevalence and characteristics of migraine in a population-based cohort

Lenore J. Launer, Gisela M. Terwindt, Michel D. Ferrari · Neurology · 1999 · 577 citations

C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

Anna Richards, Arn M. J. M. van den Maagdenberg, Joanna C. Jen et al. · Nature Genetics · 2007 · 444 citations

Ocular Disease, C-terminal Truncations, Retina +8

Genome-wide association study reveals three susceptibility loci for common migraine in the general population

Daniel I. Chasman, Markus Schürks, Verneri Anttila et al. · Nature Genetics · 2011 · 420 citations · Full text

Genome-wide Association Study, Cluster Headache, Genotype-phenotype Association +10