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Summarizing polygenic risks for complex diseases in a clinical whole-genome report.
Genet Med
31
2015
cardiomyopathy, common risk variants, complex diseases, pharmacogenomic variants, risk alleles
Alleles, Cardiomyopathies, Case-Control Studies, Genetic Association Studies, Genetic Predisposition to Disease, Genetic Testing, Genome, Human, Genome-Wide Association Study, Humans, Multifactorial Inheritance, Reproducibility of Results
Author NameAffiliation
Sek Won Kong1] Children's Hospital Informatics Program, Boston Children's Hospital, USA [2] Harvard Medical School
In-Hee Lee1] Children's Hospital Informatics Program, Boston Children's Hospital, USA [2] Harvard Medical School
In-Hee Lee1] Children's Hospital Informatics Program, Boston Children's Hospital, USA [2] Harvard Medical School
Ignaty Leshchiner1] Harvard Medical School, Brigham and Women's Hospital
Joel B Krier1] Harvard Medical School, Brigham and Women's Hospital
Peter KraftHarvard School of Public Health
Peter KraftHarvard School of Public Health
Heidi L Rehm1] Harvard Medical School, Brigham and Women's Hospital
Heidi L Rehm1] Harvard Medical School, Brigham and Women's Hospital
Robert C Green1] Harvard Medical School, Brigham and Women's Hospital
Isaac S Kohane1] Children's Hospital Informatics Program, Boston Children's Hospital, USA [2] Harvard Medical School
Isaac S Kohane1] Children's Hospital Informatics Program, Boston Children's Hospital, USA [2] Harvard Medical School
Calum A MacRae1] Harvard Medical School, Brigham and Women's Hospital
Calum A MacRae1] Harvard Medical School, Brigham and Women's Hospital
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