Description
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.
Funder
National Institute of Neurological Disorders and Stroke
Research Topics
Related Studies
Using Electronic Health Records to Identify Gaps in Migraine Headache Care: A Step Towards Improving Patient Outcomes
Mindfulness and Migraine: A Randomized Controlled Trial
Investigator: Sylvia Sudat, PhD