Articles with public access mandates - Ron DoLearn more
OverallNIHMRCAHACIHRBHFNIHRWellcomeVALeducq Foundation, USAEuropean CommissionFRQSUK Research & InnovationSwedish Research CouncilCancer Research UKHSFHHMIGenome CanadaDFGANRGovernment of ItalyDoDNSERCDFFINSERMBBSRCESRCParkinson's UKZonMwDoris Duke Charitable FoundationState of CalifoniaHealth Data Research, UKFWODSFAcademy of FinlandHRBNWOProstate Cancer UKRCNRWJFAIRC Foundation for Cancer Research in ItalyOICRCZISusan G. Komen
Not available anywhere: 5
Squalene synthase: a critical enzyme in the cholesterol biosynthesis pathway
R Do, RS Kiss, D Gaudet, JC Engert
Clinical genetics 75 (1), 19-29, 2009
Mandates: Canadian Institutes of Health Research, Fonds de recherche du Québec - Santé
Using full genomic information to predict disease: breaking down the barriers between complex and Mendelian diseases
DM Jordan, R Do
Annual Review of Genomics and Human Genetics 19 (1), 289-301, 2018
Mandates: US National Institutes of Health, American Heart Association
Estimation of metabolic syndrome heritability in three large populations including full pedigree and genomic information
F Graziano, G Biino, MT Bonati, BM Neale, R Do, MP Concas, ...
Human Genetics 138, 739-748, 2019
Mandates: US National Institutes of Health, Government of Italy
Development of a human genetics-guided priority score for 19,365 genes and 399 drug indications
Á Duffy, BO Petrazzini, D Stein, JK Park, IS Forrest, K Gibson, HM Vy, ...
Nature Genetics 56 (1), 51-59, 2024
Mandates: Agence Nationale de la Recherche
Prediction of incident heart failure in TTR Val122Ile carriers one year ahead of diagnosis in a multiethnic biobank
K Chaudhary, BO Petrazzini, J Narula, GN Nadkarni, R Do
The American Journal of Cardiology 142, 151, 2021
Mandates: US National Institutes of Health
Available somewhere: 126
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
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases
M Verbanck, CY Chen, B Neale, R Do
Nature genetics 50 (5), 693-698, 2018
Mandates: US National Institutes of Health, American Heart Association, National …
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
Mandates: US National Institutes of Health, British Heart Foundation, UK Economic and …
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
Mandates: US National Institutes of Health, British Heart Foundation
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
Mandates: US National Institutes of Health, British Heart Foundation
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
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
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
Mandates: US National Institutes of Health
Large-scale association analysis identifies new risk loci for coronary artery disease
CARDIoGRAMplusC4D Consortium, P Deloukas, S Kanoni, C Willenborg, ...
Nature genetics 45 (1), 25-33, 2013
Mandates: US National Institutes of Health, National Institute of Health and Medical …
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
Mandates: US National Institutes of Health, Danish Council for Independent Research …
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Heart Attack Risk in Puget Sound. Schwartz Stephen M 20 26 Siscovick David S ...
Nature genetics 41 (3), 334-341, 2009
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
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
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
TG and HDL Working Group of the Exome Sequencing Project, National Heart ...
New England Journal of Medicine 371 (1), 22-31, 2014
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Genetic analyses of diverse populations improves discovery for complex traits
GL Wojcik, M Graff, KK Nishimura, R Tao, J Haessler, CR Gignoux, ...
Nature 570 (7762), 514-518, 2019
Mandates: US National Institutes of Health
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
Mandates: US National Institutes of Health, Canadian Institutes of Health Research
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
Mandates: US National Institutes of Health, Health Research Board, Ireland, UK Medical …
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