Suivre
Stephen S Rich
Stephen S Rich
Professor & Director, Center for Public Health Genomics, University of Virginia
Adresse e-mail validée de virginia.edu
Titre
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Année
Discovery and refinement of loci associated with lipid levels
Nature genetics 45 (11), 1274-1283, 2013
29432013
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
27082010
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
25102013
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
21522009
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
13872021
Familial clustering of diabetic kidney disease
ER Seaquist, FC Goetz, S Rich, J Barbosa
New England Journal of Medicine 320 (18), 1161-1165, 1989
13511989
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
12802013
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
12792018
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
11382015
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
1058*2016
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
10252018
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
10252013
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
9522011
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
8062014
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
7742015
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
7652015
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
7622012
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
7302020
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
6912013
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
6812015
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