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
Coverage, Price, and Reimbursement for Multigene Tests for Cancer and Related Conditions
Our objective is to examine “coverage, price, and reimbursement” for multigene tests broadly and for cancer-related indications.
Investigator: Su-Ying Liang, Ph.D.
Implementing Universal Lynch Syndrome Screening Across Multiple Healthcare Systems: Identifying Strategies to Facilitate and Maintain Programs in Different Organizations Contexts
To describe and explain variations in Lynch syndrome (LS) screening implementation across healthcare systems and create a toolkit for implementing LS screening.
Investigators: External PI, Principal Investigator, Su-Ying Liang, Ph.D., Monique de Bruin, M.D., MPH
Precision Medicine for Multiple Sclerosis: Making It Work (MS-SHARE)
Develop an app that support access to clinical data and shared decision-making, predict disease course, and guide disease management.
Investigators: Xiaowei (Sherry) Yan, PhD, MS, J.B. Jones, PhD, MBA
Risk-Benefit Trade-Offs for Whole Genome Sequencing
Describe the clinical pathway of genetic testing at PAMF, and assess and obtain preliminary data on the use of genetic tests at PAMF.
Investigators: Su-Ying Liang, Ph.D., External PI, Principal Investigator
Understanding the Experiences of Patients Undergoing Genetic Counseling and Testing for BRCA
This project investigates how patients deliberate, decide, & act upon genetic counseling & testing to determine their personal risk for breast & ovarian cancer.