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Santhi K. Ganesh
Santhi K. Ganesh
Associate Professor
Verified email at umich.edu
Title
Cited by
Cited by
Year
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
GB Ehret, PB Munroe, KM Rice, M Bochud, AD Johnson, DI Chasman, ...
Nature 478 (7367), 103, 2011
23262011
Association of elevated serum PO4, Ca× PO4 product, and parathyroid hormone with cardiac mortality risk in chronic hemodialysis patients
SK Ganesh, AG Stack, NW Levin, T Hulbert-Shearon, FK Port
Journal of the American Society of Nephrology 12 (10), 2131-2138, 2001
16672001
Genome-wide association study of blood pressure and hypertension
D Levy, GB Ehret, K Rice, GC Verwoert, LJ Launer, A Dehghan, ...
Nature genetics 41 (6), 677, 2009
16462009
Exome-wide association study of plasma lipids in> 300,000 individuals
DJ Liu, GM Peloso, H Yu, AS Butterworth, X Wang, A Mahajan, ...
Nature genetics 49 (12), 1758, 2017
5592017
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
C Pattaro, A Teumer, M Gorski, AY Chu, M Li, V Mijatovic, M Garnaas, ...
Nature communications 7, 10023, 2016
5072016
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
LV Wain, GC Verwoert, PF O'Reilly, G Shi, T Johnson, AD Johnson, ...
Nature genetics 43 (10), 1005, 2011
5072011
New gene functions in megakaryopoiesis and platelet formation
C Gieger, A Radhakrishnan, A Cvejic, W Tang, E Porcu, G Pistis, ...
Nature 480 (7376), 201, 2011
4902011
Genome-wide associations for birth weight and correlations with adult disease
M Horikoshi, RN Beaumont, FR Day, NM Warrington, MN Kooijman, ...
Nature 538 (7624), 248, 2016
4782016
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
GB Ehret, T Ferreira, DI Chasman, AU Jackson, EM Schmidt, T Johnson, ...
Nature genetics 48 (10), 1171, 2016
4512016
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
SK Ganesh, NA Zakai, FJA Van Rooij, N Soranzo, AV Smith, MA Nalls, ...
Nature genetics 41 (11), 1191, 2009
4242009
Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk
OL Holmen, H Zhang, Y Fan, DH Hovelson, EM Schmidt, W Zhou, Y Guo, ...
Nature genetics 46 (4), 345, 2014
3322014
Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson–Gilford progeria syndrome
R Varga, M Eriksson, MR Erdos, M Olive, I Harten, F Kolodgie, BC Capell, ...
Proceedings of the National Academy of Sciences of the United States of …, 2006
3072006
Mortality differences by dialysis modality among incident ESRD patients with and without coronary artery disease
SK Ganesh, T Hulbert-Shearon, FK Port, K Eagle, AG Stack
Journal of the American Society of Nephrology 14 (2), 415-424, 2003
2982003
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
C Liu, AT Kraja, JA Smith, JA Brody, N Franceschini, JC Bis, K Rice, ...
Nature genetics 48 (10), 1162, 2016
2752016
Relevance of genetics and genomics for prevention and treatment of cardiovascular disease: a scientific statement from the American Heart Association Council on Epidemiology …
DK Arnett, AE Baird, RA Barkley, CT Basson, E Boerwinkle, SK Ganesh, ...
Circulation 115 (22), 2878-2901, 2007
2712007
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
2442014
A farnesyltransferase inhibitor prevents both the onset and late progression of cardiovascular disease in a progeria mouse model
BC Capell, M Olive, MR Erdos, K Cao, DA Faddah, UL Tavarez, ...
Proceedings of the National Academy of Sciences 105 (41), 15902-15907, 2008
2372008
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
ER Fox, JH Young, Y Li, AW Dreisbach, BJ Keating, SK Musani, K Liu, ...
Human molecular genetics 20 (11), 2273-2284, 2011
2102011
PHACTR1 is a genetic susceptibility locus for fibromuscular dysplasia supporting its complex genetic pattern of inheritance
SR Kiando, NR Tucker, LJ Castro-Vega, A Katz, V D’Escamard, C Tréard, ...
PLoS genetics 12 (10), e1006367, 2016
1892016
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci
V Tragante, MR Barnes, SK Ganesh, MB Lanktree, W Guo, ...
The American Journal of Human Genetics 94 (3), 349-360, 2014
1792014
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