Electronic health records: the next wave of complex disease genetics

Author:

Wolford Brooke N12,Willer Cristen J1234,Surakka Ida3

Affiliation:

1. Department of Computational Medicine and Bioinformatics, Ann Arbor, MI, USA

2. Center for Statistical Genetics, Ann Arbor, MI, USA

3. Division of Cardiovascular Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA

4. Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference61 articles.

1. Using electronic health records to drive discovery in disease genomics;Kohane;Nat. Rev. Genet,2011

2. PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associations;Denny;Bioinformatics,2010

3. Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies;Zhou;bioRxiv,2017

4. An Icelandic saga on a centralized healthcare database and democratic decision making;Gulcher;Nat. Biotechnol,1999

5. Principles of human subjects protections applied in an opt-out, de-identified biobank;Pulley;Clin. Transl. Sci,2010

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