Clinical Domain Working Groups
Brugada Syndrome Gene Curation Expert Panel Inactive
Membership DocumentsThis Expert Panel is currently inactive. Click here to learn about this designation.
The Brugada Syndrome GCEP was formed in 2017, and their initial scope of work included 21 genes thought to be associated with Brugada syndrome. The group completed evaluation of these genes in 2018, and their findings are described in Hosseini et al. 2018 (PMID:29959160). The Hereditary Cardiovascular Disease GCEP now re-evaluates these curations on a periodic basis, as described in the ClinGen recuration procedure. Inactive date - 12/20/21
Expert Panel Status - Approved Expert Panel
Documents
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Gene-Disease Validity Standard Operating Procedures, Version 6 (Archived)Curation Activity Procedures - August 29, 2018 Archived Document
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Expert Panel Membership
Membership spans many fields, including genetics, medical, academia, and industry.
Michael Gollob, MD
Ray Hershberger, MD
Arthur Wilde MD, PhD
Melanie Care, MSc, CGC
John Garcia, PhD
Jenny Goldstein, PhD, CGC
Valeria Novelli PhD
Amy Sturm, MS, LGC
James Ware, MD, PhD
C. Lisa Kurtz, PhD