Evaluating Phenotypic Data Elements for Genetics and Epidemiological Research: Experiences from the eMERGE and PhenX Network Projects

Combining genome-wide association studies (GWAS) data with clinical information from the electronic medical record (EMR) provide unprecedented opportunities to identify genetic variants that influence susceptibility to common, complex diseases. While mining the vastness of EMR greatly expands the po...

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Detalles Bibliográficos
Autores principales: Pathak, Jyotishman, Pan, Helen, Wang, Janey, Kashyap, Sudha, Schad, Peter A., Hamilton, Carol M., Masys, Daniel R., Chute, Christopher G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Informatics Association 2011
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248754/
https://www.ncbi.nlm.nih.gov/pubmed/22211178

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248754/
https://www.ncbi.nlm.nih.gov/pubmed/22211178

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