1.
Opportunities for genomic clinical decision support interventions
by Overby, Casey Lynnette
Genetics in medicine, 2013, Vol.15 (10), p.817-823
2.
Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network
by Gallego, Carlos J
American journal of human genetics, 2015, Vol.97 (4), p.512-520
3.
PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability
by Kirby, Jacqueline C
Journal of the American Medical Informatics Association : JAMIA, 2016, Vol.23 (6), p.1046-1052
4.
The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future
by Gottesman, Omri
Genetics in medicine, 2013, Vol.15 (10), p.761-771
5.
A collaborative approach to developing an electronic health record phenotyping algorithm for drug-induced liver injury
by Overby, Casey Lynnette
Journal of the American Medical Informatics Association : JAMIA, 2013, Vol.20 (e2), p.e243-e252
6.
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development
by Nielsen, Jonas B
American journal of human genetics, 2018, Vol.102 (1), p.103-115
7.
Transethnic Genetic-Correlation Estimates from Summary Statistics
by Brown, Brielin C
American journal of human genetics, 2016, Vol.99 (1), p.76-88
8.
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
by Lange, Leslie A
American journal of human genetics, 2014, Vol.94 (2), p.233-45
9.
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks
by Peloso, Gina M
American journal of human genetics, 2014, Vol.94 (2), p.223-32
