Informing disease modelling with brain-relevant functional genomic annotations

The past decade has seen a surge in the number of disease/trait-associated variants, largely because of the union of studies to share genetic data and the availability of electronic health records from large cohorts for research use. Variant discovery for neurological and neuropsychiatric genome-wid...

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Detalles Bibliográficos
Autores principales: Reynolds, Regina H, Hardy, John, Ryten, Mina, Gagliano Taliun, Sarah A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885670/
https://www.ncbi.nlm.nih.gov/pubmed/31603214
http://dx.doi.org/10.1093/brain/awz295

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885670/
https://www.ncbi.nlm.nih.gov/pubmed/31603214
http://dx.doi.org/10.1093/brain/awz295

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