Sandosh Padmanabhan
Sandosh Padmanabhan
Підтверджена електронна адреса в glasgow.ac.uk - Домашня сторінка
НазваПосиланняРік
Heart disease and stroke statistics-2017 update: a report from the American Heart Association.
EJ Benjamin, MJ Blaha, SE Chiuve, M Cushman, SR Das, R Deo, J Floyd, ...
circulation 135 (10), e146-e603, 2017
57612017
Genetically distinct subsets within ANCA-associated vasculitis
PA Lyons, TF Rayner, S Trivedi, JU Holle, RA Watts, DRW Jayne, ...
New England Journal of Medicine 367 (3), 214-223, 2012
6232012
Spironolactone versus placebo, bisoprolol, and doxazosin to determine the optimal treatment for drug-resistant hypertension (PATHWAY-2): a randomised, double-blind, crossover trial
B Williams, TM MacDonald, S Morant, DJ Webb, P Sever, G McInnes, ...
The Lancet 386 (10008), 2059-2068, 2015
4702015
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data
MV Holmes, CE Dale, L Zuccolo, RJ Silverwood, Y Guo, Z Ye, ...
Bmj 349, g4164, 2014
4042014
Risk HLA-DQA1 and PLA2R1 alleles in idiopathic membranous nephropathy
HC Stanescu, M Arcos-Burgos, A Medlar, D Bockenhauer, A Kottgen, ...
New England Journal of Medicine 364 (7), 616-626, 2011
3962011
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, 2014
3012014
Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension
S Padmanabhan, O Melander, T Johnson, AM Di Blasio, WK Lee, ...
PLoS genetics 6 (10), e1001177, 2010
2912010
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
N Sotoodehnia, A Isaacs, PIW De Bakker, M Dörr, C Newton-Cheh, ...
Nature genetics 42 (12), 1068, 2010
2752010
Seventy-five genetic loci influencing the human red blood cell
P Van Der Harst, W Zhang, IM Leach, A Rendon, N Verweij, J Sehmi, ...
Nature 492 (7429), 369, 2012
2732012
Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186, 2017
2582017
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci
R Saxena, CC Elbers, Y Guo, I Peter, TR Gaunt, JL Mega, MB Lanktree, ...
The American Journal of Human Genetics 90 (3), 410-425, 2012
2442012
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci
FW Asselbergs, Y Guo, S Sivapalaratnam, V Tragante, MB Lanktree, ...
The American Journal of Human Genetics 91 (5), 823-838, 2012
2242012
Should diabetes be considered a coronary heart disease risk equivalent?: results from 25 years of follow-up in the Renfrew and Paisley survey
L Whiteley, S Padmanabhan, D Hole, C Isles
Diabetes Care 28 (7), 1588-1593, 2005
2192005
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
HR Warren, E Evangelou, CP Cabrera, H Gao, M Ren, B Mifsud, I Ntalla, ...
Nature genetics 49 (3), 403, 2017
2172017
HLA has strongest association with IgA nephropathy in genome-wide analysis
J Feehally, M Farrall, A Boland, DP Gale, I Gut, S Heath, A Kumar, ...
Journal of the American Society of Nephrology 21 (10), 1791-1797, 2010
2052010
Obesity paradox in a cohort of 4880 consecutive patients undergoing percutaneous coronary intervention
CE Hastie, S Padmanabhan, R Slack, ACH Pell, KG Oldroyd, AD Flapan, ...
European heart journal 31 (2), 222-226, 2009
2042009
Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders
M Den Hoed, M Eijgelsheim, T Esko, BJJM Brundel, DS Peal, DM Evans, ...
Nature genetics 45 (6), 621, 2013
2032013
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
1712014
Blood pressure loci identified with a gene-centric array
T Johnson, TR Gaunt, SJ Newhouse, S Padmanabhan, M Tomaszewski, ...
The American Journal of Human Genetics 89 (6), 688-700, 2011
1712011
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study
AF Schmidt, DI Swerdlow, MV Holmes, RS Patel, Z Fairhurst-Hunter, ...
The lancet Diabetes & endocrinology 5 (2), 97-105, 2017
1672017
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