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
September 01, 2012
August 31, 2016
Using Electronic Health Records to Identify Gaps in Migraine Headache Care: A Step Towards Improving Patient Outcomes
Investigator: Alice R. Pressman, Ph.D., M.S.