Genomics of migraine
In contrast to the candidate gene studies carried out since the mid-1990s, the last few years have seen the rise of genetic studies, which assume that polygenic variability with a small effect is of importance in human disease. Genotyping allows researchers to study genetic variations and mutations that may contribute to migraines.
A genomic library is a collection of biological samples, such as blood, and health information that is used in research to gain a better understanding of how a person's genes (DNA) may influence overall health and wellness.
The Mayo Clinic Migraine Genomic Library focuses on identifying genetic differences that might affect a person's risk of experiencing certain migraine symptoms and examining how differences in DNA influence responses to different migraine medications. By gaining a deeper understanding of the genetic causes of migraine, physicians can better treat people with migraines.
Introducing the Genetic Clues Behind Migraines and the Resulting Research Project