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David R. Crosslin
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Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
JC Denny, L Bastarache, MD Ritchie, RJ Carroll, R Zink, JD Mosley, ...
Nature biotechnology 31 (12), 1102-1111, 2013
9842013
Detectable clonal mosaicism from birth to old age and its relationship to cancer
CC Laurie, CA Laurie, K Rice, KF Doheny, LR Zelnick, CP McHugh, ...
Nature genetics 44 (6), 642-650, 2012
6392012
The electronic medical records and genomics (eMERGE) network: past, present, and future
O Gottesman, H Kuivaniemi, G Tromp, WA Faucett, R Li, TA Manolio, ...
Genetics in Medicine 15 (10), 761-771, 2013
5892013
Association of a peripheral blood metabolic profile with coronary artery disease and risk of subsequent cardiovascular events
SH Shah, JR Bain, MJ Muehlbauer, RD Stevens, DR Crosslin, C Haynes, ...
Circulation: Cardiovascular Genetics 3 (2), 207-214, 2010
4952010
Return of genomic results to research participants: the floor, the ceiling, and the choices in between
GP Jarvik, LM Amendola, JS Berg, K Brothers, EW Clayton, W Chung, ...
The American Journal of Human Genetics 94 (6), 818-826, 2014
4232014
Branched-chain amino acid levels are associated with improvement in insulin resistance with weight loss
SH Shah, DR Crosslin, CS Haynes, S Nelson, CB Turer, RD Stevens, ...
Diabetologia 55, 321-330, 2012
3872012
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study
AF Schmidt, DI Swerdlow, MV Holmes, RS Patel, Z Fairhurst-Hunter, ...
The lancet Diabetes & endocrinology 5 (2), 97-105, 2017
3832017
Actionable exomic incidental findings in 6503 participants: challenges of variant classification
LM Amendola, MO Dorschner, PD Robertson, JS Salama, R Hart, ...
Genome research 25 (3), 305-315, 2015
3692015
The phenotypic legacy of admixture between modern humans and Neandertals
CN Simonti, B Vernot, L Bastarache, E Bottinger, DS Carrell, RL Chisholm, ...
Science 351 (6274), 737-741, 2016
3482016
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study
AN Kho, MG Hayes, L Rasmussen-Torvik, JA Pacheco, WK Thompson, ...
Journal of the American Medical Informatics Association 19 (2), 212-218, 2012
3262012
Design and anticipated outcomes of the eMERGE‐PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems
LJ Rasmussen‐Torvik, SC Stallings, AS Gordon, B Almoguera, ...
Clinical Pharmacology & Therapeutics 96 (4), 482-489, 2014
2542014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ...
The American Journal of Human Genetics 94 (2), 233-245, 2014
2362014
GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies
SM Gogarten, T Bhangale, MP Conomos, CA Laurie, CP McHugh, ...
Bioinformatics 28 (24), 3329-3331, 2012
2102012
Staphylococcus aureus bacteremia in patients with prosthetic devices: costs and outcomes
VH Chu, DR Crosslin, JY Friedman, SD Reed, CH Cabell, RI Griffiths, ...
The American journal of medicine 118 (12), 1416. e19-1416. e24, 2005
1952005
Association of arrhythmia-related genetic variants with phenotypes documented in electronic medical records
SL Van Driest, QS Wells, S Stallings, WS Bush, A Gordon, DA Nickerson, ...
Jama 315 (1), 47-57, 2016
1892016
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels
TO Kilpeläinen, JFM Carli, AA Skowronski, Q Sun, J Kriebel, MF Feitosa, ...
Nature communications 7 (1), 10494, 2016
1832016
Genetic variation among 82 pharmacogenes: the PGRNseq data from the eMERGE network
WS Bush, DR Crosslin, A Owusu‐Obeng, J Wallace, B Almoguera, ...
Clinical Pharmacology & Therapeutics 100 (2), 160-169, 2016
1822016
Meta-analysis of genome-wide association studies for abdominal aortic aneurysm identifies four new disease-specific risk loci
GT Jones, G Tromp, H Kuivaniemi, S Gretarsdottir, AF Baas, B Giusti, ...
Circulation research 120 (2), 341-353, 2017
1782017
Clinical sequencing exploratory research consortium: accelerating evidence-based practice of genomic medicine
RC Green, KAB Goddard, GP Jarvik, LM Amendola, PS Appelbaum, ...
The American Journal of Human Genetics 98 (6), 1051-1066, 2016
1692016
Genome-wide association scan for childhood caries implicates novel genes
JR Shaffer, X Wang, E Feingold, M Lee, F Begum, DE Weeks, KT Cuenco, ...
Journal of dental research 90 (12), 1457-1462, 2011
1602011
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