Improving the power of genetic association tests with imperfect phenotype derived from electronic medical records
To reduce costs and improve clinical relevance of genetic studies, there has been increasing interest in performing such studies in hospital-based cohorts by linking phenotypes extracted from electronic medical records (EMRs) to genotypes assessed in routinely collected medical samples. A fundamenta...
| Main Authors: | , , , , , , , , , , , , |
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| Other Authors: | |
| Format: | Article |
| Language: | en_US |
| Published: |
Springer-Verlag
2016
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| Online Access: | http://hdl.handle.net/1721.1/101048 https://orcid.org/0000-0001-8411-6403 |