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Praveen Surendran
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Genomic atlas of the human plasma proteome
BB Sun, JC Maranville, JE Peters, D Stacey, JR Staley, J Blackshaw, ...
Nature 558 (7708), 73-79, 2018
13502018
PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations
MA Kamat, JA Blackshaw, R Young, P Surendran, S Burgess, J Danesh, ...
Bioinformatics 35 (22), 4851-4853, 2019
11732019
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
E Evangelou, HR Warren, D Mosen-Ansorena, B Mifsud, R Pazoki, H Gao, ...
Nature genetics 50 (10), 1412-1425, 2018
11462018
PhenoScanner: a database of human genotype–phenotype associations
JR Staley, J Blackshaw, MA Kamat, S Ellis, P Surendran, BB Sun, ...
Bioinformatics 32 (20), 3207-3209, 2016
11212016
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), 186-190, 2017
6342017
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), 403-415, 2017
5752017
Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease
P Zanoni, SA Khetarpal, DB Larach, WF Hancock-Cerutti, JS Millar, ...
Science 351 (6278), 1166-1171, 2016
5602016
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), 1758-1766, 2017
5312017
Association of LPA variants with risk of coronary disease and the implications for lipoprotein (a)-lowering therapies: a Mendelian randomization analysis
S Burgess, BA Ference, JR Staley, DF Freitag, AM Mason, SF Nielsen, ...
JAMA cardiology 3 (7), 619-627, 2018
4682018
The polygenic and monogenic basis of blood traits and diseases
D Vuckovic, EL Bao, P Akbari, CA Lareau, A Mousas, T Jiang, MH Chen, ...
Cell 182 (5), 1214-1231. e11, 2020
4242020
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
A Mahajan, J Wessel, SM Willems, W Zhao, NR Robertson, AY Chu, ...
Nature genetics 50 (4), 559-571, 2018
4142018
Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations
MH Chen, LM Raffield, A Mousas, S Sakaue, JE Huffman, A Moscati, ...
Cell 182 (5), 1198-1213. e14, 2020
4012020
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators
New England Journal of Medicine 374 (12), 1134-1144, 2016
3982016
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
A Giri, JN Hellwege, JM Keaton, J Park, C Qiu, HR Warren, ES Torstenson, ...
Nature genetics 51 (1), 51-62, 2019
3632019
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
L Folkersen, S Gustafsson, Q Wang, DH Hansen, ÅK Hedman, A Schork, ...
Nature metabolism 2 (10), 1135-1148, 2020
3552020
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
3262018
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
P Surendran, F Drenos, R Young, H Warren, JP Cook, AK Manning, ...
Nature genetics 48 (10), 1151-1161, 2016
3152016
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms
JMM Howson, W Zhao, DR Barnes, WK Ho, R Young, DS Paul, LL Waite, ...
Nature genetics 49 (7), 1113-1119, 2017
2992017
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), 1162-1170, 2016
2612016
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
W Zhao, A Rasheed, E Tikkanen, JJ Lee, AS Butterworth, JMM Howson, ...
Nature genetics 49 (10), 1450-1457, 2017
2592017
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