A Genome-Wide Association Study Finds Genetic Associations with Broadly-Defined Headache in UK Biobank (N = 223,773)

BACKGROUND: Headache is the most common neurological symptom and a leading cause of years lived with disability. We sought to identify the genetic variants associated with a broadly-defined headache phenotype in 223,773 subjects from the UK Biobank cohort. METHODS: We defined headache based on a spe...

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Detalles Bibliográficos
Autores principales: Meng, Weihua, Adams, Mark J., Hebert, Harry L., Deary, Ian J., McIntosh, Andrew M., Smith, Blair H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5898025/
https://www.ncbi.nlm.nih.gov/pubmed/29397368
http://dx.doi.org/10.1016/j.ebiom.2018.01.023

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5898025/
https://www.ncbi.nlm.nih.gov/pubmed/29397368
http://dx.doi.org/10.1016/j.ebiom.2018.01.023

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