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RO

Roel A. Ophoff

Independent Researcher

ORCID iD 0000-0002-8287-6457
533
Publications
70,209
Citations
118
H-Index
320
i10-Index
6.82
2yr Mean Cite
-
Cite/Paper
Data combined from OpenAlex . OA = OpenAlex S2 = Semantic Scholar
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Publication & Citation Trends

Publications

437 total

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

Roel A. Ophoff, Gisela M. Terwindt, Monique N. Vergouwe, Ronald van Eijk, Peter J. Oefner et al. - Cell, 1996
Cited by 2,336 OpenAlex

Research Topics

Genetic Associations and Epidemiology (162) Genomic variations and chromosomal abnormalities (79) Genetics and Neurodevelopmental Disorders (61) Genomics and Rare Diseases (58) Bipolar Disorder and Treatment (55)

Affiliations

Rutgers, The State University of New Jersey
US 2025 - 2025
Broad Institute
US 2021 - 2017
University of North Carolina at Chapel Hill
US 2019 - 2019
Leiden University
NL 1998 - 1994
Dalhousie University
CA 2024 - 2024

External Profiles

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