Ron Do
Ron Do
The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
Verified email at broadinstitute.org - Homepage
TitleCited byYear
Analysis of protein-coding genetic variation in 60,706 humans
M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ...
Nature 536 (7616), 285-291, 2016
55892016
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
BF Voight, GM Peloso, M Orho-Melander, R Frikke-Schmidt, M Barbalic, ...
The Lancet 380 (9841), 572-580, 2012
17102012
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
H Schunkert, IR König, S Kathiresan, MP Reilly, TL Assimes, H Holm, ...
Nature genetics 43 (4), 333-338, 2011
15712011
Discovery and refinement of loci associated with lipid levels
CJ Willer, EM Schmidt, S Sengupta, GM Peloso, S Gustafsson, S Kanoni, ...
Nature genetics 45 (11), 1274, 2013
14652013
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
JA Tennessen, AW Bigham, TD O’Connor, W Fu, EE Kenny, S Gravel, ...
science 337 (6090), 64-69, 2012
14602012
A high-coverage genome sequence from an archaic Denisovan individual
M Meyer, M Kircher, MT Gansauge, H Li, F Racimo, S Mallick, ...
Science 338 (6104), 222-226, 2012
13542012
Large-scale association analysis identifies new risk loci for coronary artery disease
P Deloukas, S Kanoni, C Willenborg, M Farrall, TL Assimes, ...
Nature genetics 45 (1), 25-33, 2013
11732013
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Myocardial Infarction Genetics Consortium
Nature genetics 41 (3), 334, 2009
10492009
Common variants associated with plasma triglycerides and risk for coronary artery disease
R Do, CJ Willer, EM Schmidt, S Sengupta, C Gao, GM Peloso, ...
Nature genetics 45 (11), 1345-1352, 2013
6022013
Upper Palaeolithic Siberian genome reveals dual ancestry of Native Americans
M Raghavan, P Skoglund, KE Graf, M Metspalu, A Albrechtsen, I Moltke, ...
Nature 505 (7481), 87-91, 2014
5332014
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia
K Musunuru, JP Pirruccello, R Do, GM Peloso, C Guiducci, C Sougnez, ...
New England Journal of Medicine 363 (23), 2220-2227, 2010
4932010
Searching for missing heritability: designing rare variant association studies
O Zuk, SF Schaffner, K Samocha, R Do, E Hechter, S Kathiresan, MJ Daly, ...
Proceedings of the National Academy of Sciences 111 (4), E455-E464, 2014
4692014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, PA Merlini, A Kiezun, ...
Nature 518 (7537), 102-106, 2015
4542015
Exome sequencing and the genetic basis of complex traits
A Kiezun, K Garimella, R Do, NO Stitziel, BM Neale, PJ McLaren, N Gupta, ...
Nature genetics 44 (6), 623, 2012
4042012
Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus
W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ...
PLoS genetics 6 (2), 2010
3732010
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis
EA Stahl, D Wegmann, G Trynka, J Gutierrez-Achury, R Do, BF Voight, ...
Nature genetics 44 (5), 483, 2012
3712012
Modeling linkage disequilibrium increases accuracy of polygenic risk scores
BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ...
The american journal of human genetics 97 (4), 576-592, 2015
3372015
Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease
Myocardial Infarction Genetics Consortium Investigators
New England Journal of Medicine 371 (22), 2072-2082, 2014
3172014
Genetic variants of FTO influence adiposity, insulin sensitivity, leptin levels, and resting metabolic rate in the Quebec Family Study
R Do, SD Bailey, K Desbiens, A Belisle, A Montpetit, C Bouchard, ...
Diabetes 57 (4), 1147-1150, 2008
2622008
Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia
VG Sankaran, R Ghazvinian, R Do, P Thiru, JA Vergilio, AH Beggs, ...
The Journal of clinical investigation 122 (7), 2439-2443, 2012
2602012
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Articles 1–20