Clinical Trial FAQs
Information for patients and study volunteers, including frequently asked questions.
The primary aim of this study is to identify common genetic variants for migraine to determine whether there are single nucleotide polymorphisms associated with migraine by applying genome-wide association study methodology to compare Kaiser Permanente Northern California members with migraine to a control group of unaffected members.
National Institute of Neurological Disorders and Stroke
Using Electronic Health Records to Identify Gaps in Migraine Headache Care: A Step Towards Improving Patient Outcomes
Investigator: Sylvia Sudat, PhD