Cargando…
Novel hypotheses emerging from GWAS in migraine?
Recent technical advances in genetics made large-scale genome-wide association studies (GWAS) in migraine feasible and have identified over 40 common DNA sequence variants that affect risk for migraine types. Most of the variants, which are all single nucleotide polymorphisms (SNPs), show robust ass...
Autores principales: | van den Maagdenberg, Arn M. J. M., Nyholt, Dale R., Anttila, Verneri |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Milan
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6734558/ https://www.ncbi.nlm.nih.gov/pubmed/30634909 http://dx.doi.org/10.1186/s10194-018-0956-x |
Ejemplares similares
-
Linking migraine frequency with family history of migraine
por: Pelzer, Nadine, et al.
Publicado: (2018) -
Integrating eQTL and GWAS data characterises established and identifies novel migraine risk loci
por: Ghaffar, Ammarah, et al.
Publicado: (2023) -
Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants
por: Winsvold, Bendik S., et al.
Publicado: (2017) -
Genetics of migraine aura: an update
por: de Boer, Irene, et al.
Publicado: (2020) -
Migraine and neuroinflammation: the inflammasome perspective
por: Kursun, Oguzhan, et al.
Publicado: (2021)