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A genome-wide association study of heparin-induced thrombocytopenia using an electronic medical record

artículo científico publicado en 2014

A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers

artículo científico publicado en 2018

Biobanks and electronic medical records: enabling cost-effective research

artículo científico publicado en 2014

Comparison of HLA allelic imputation programs.

artículo científico publicado en 2017

Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults.

artículo científico publicado en 2017

Identifying genetically driven clinical phenotypes using linear mixed models

artículo científico publicado en 2016

Influence of human leukocyte antigen (HLA) alleles and killer cell immunoglobulin-like receptors (KIR) types on heparin-induced thrombocytopenia (HIT).

artículo científico publicado en 2017

Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data

artículo científico publicado en 2013

Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants.

artículo científico publicado en 2017

Single nucleotide polymorphisms in the MYLKP1 pseudogene are associated with increased colon cancer risk in African Americans

scientific article published on 30 August 2018

Using systems approaches to address challenges for clinical implementation of pharmacogenomics

Using systems approaches to address challenges for clinical implementation of pharmacogenomics.

artículo científico publicado en 2013

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