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Stephen S Rich
Stephen S Rich
Professor & Director, Center for Public Health Genomics, University of Virginia
Verified email at virginia.edu
Title
Cited by
Cited by
Year
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
3114*2013
Robust relationship inference in genome-wide association studies
A Manichaikul, JC Mychaleckyj, SS Rich, K Daly, M Sale, WM Chen
Bioinformatics 26 (22), 2867-2873, 2010
31102010
Personality similarity in twins reared apart and together
A Tellegen, DT Lykken, TJ Bouchard, KJ Wilcox, NL Segal, S Rich
Personality and Personality Disorders, 235-243, 2013
25892013
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
JC Barrett, DG Clayton, P Concannon, B Akolkar, JD Cooper, HA Erlich, ...
Nature genetics 41 (6), 703-707, 2009
22252009
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
17252021
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
R Malik, G Chauhan, M Traylor, M Sargurupremraj, Y Okada, A Mishra, ...
Nature genetics 50 (4), 524-537, 2018
14652018
Familial clustering of diabetic kidney disease
ER Seaquist, FC Goetz, S Rich, J Barbosa
New England Journal of Medicine 320 (18), 1161-1165, 1989
13611989
Gut microbiomes of Malawian twin pairs discordant for kwashiorkor
MI Smith, T Yatsunenko, MJ Manary, I Trehan, R Mkakosya, J Cheng, ...
Science 339 (6119), 548-554, 2013
13362013
The health status of adults on the autism spectrum
LA Croen, O Zerbo, Y Qian, ML Massolo, S Rich, S Sidney, C Kripke
Autism 19 (7), 814-823, 2015
12662015
Functional aspects of meningeal lymphatics in ageing and Alzheimer’s disease
S Da Mesquita, A Louveau, A Vaccari, I Smirnov, RC Cornelison, ...
Nature 560 (7717), 185-191, 2018
11852018
Corrigendum: genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
A Okbay, BML Baselmans, JE De Neve, P Turley, MG Nivard, MA Fontana, ...
Nature Genetics 48 (8), 970, 2016
1154*2016
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
10722013
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
G Trynka, KA Hunt, NA Bockett, J Romanos, V Mistry, A Szperl, SF Bakker, ...
Nature genetics 43 (12), 1193-1201, 2011
10042011
Early-onset stroke and vasculopathy associated with mutations in ADA2
Q Zhou, D Yang, AK Ombrello, AV Zavialov, C Toro, AV Zavialov, ...
New England Journal of Medicine 370 (10), 911-920, 2014
8722014
A structural variation reference for medical and population genetics
RL Collins, H Brand, KJ Karczewski, X Zhao, J Alföldi, LC Francioli, ...
Nature 581 (7809), 444-451, 2020
8702020
Mendelian randomization of blood lipids for coronary heart disease
MV Holmes, FW Asselbergs, TM Palmer, F Drenos, MB Lanktree, ...
European heart journal 36 (9), 539-550, 2015
8222015
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis
S Eyre, J Bowes, D Diogo, A Lee, A Barton, P Martin, A Zhernakova, ...
Nature genetics 44 (12), 1336-1340, 2012
7962012
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, P Angelica Merlini, ...
Nature 518 (7537), 102-106, 2015
7852015
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
S Onengut-Gumuscu, WM Chen, O Burren, NJ Cooper, AR Quinlan, ...
Nature genetics 47 (4), 381-386, 2015
7322015
Imputing amino acid polymorphisms in human leukocyte antigens
X Jia, B Han, S Onengut-Gumuscu, WM Chen, PJ Concannon, SS Rich, ...
PloS one 8 (6), e64683, 2013
7282013
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