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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Hlavní autoři: Pathak, Jyotishman, Pan, Helen, Wang, Janey, Kashyap, Sudha, Schad, Peter A., Hamilton, Carol M., Masys, Daniel R., Chute, Christopher G.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Medical Informatics Association 2011
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3248754/
https://ncbi.nlm.nih.gov/pubmed/22211178
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