Author details

Full Name

Praveen Surendran

Affiliation

ORCID

Career Start Year

2010

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36720882	Quality control and removal of technical variation of NMR metabolic biomarker data in ~120,000 UK Biobank participants.	Sci Data	2023
37679551	Author Correction: Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets.	Nat Immunol	2023
37563310	Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets.	Nat Immunol	2023
37622920	Identification of blood protein biomarkers associated with prostate cancer risk using genetic prediction models: analysis of over 140,000 subjects.	Hum Mol Genet	2023
36991119	An atlas of genetic scores to predict multi-omic traits.	Nature	2023
34553764	Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.	Hum Mol Genet	2022
36357675	Rare and common genetic determinants of metabolic individuality and their effects on human health.	Nat Med	2022
35568032	Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites.	Am J Hum Genet	2022
36253349	Systematic Mendelian randomization using the human plasma proteome to discover potential therapeutic targets for stroke.	Nat Commun	2022
34582791	Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.	Am J Hum Genet	2021
33837377	Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19.	Nat Med	2021
33887194	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.	Am J Hum Genet	2021
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2021
34087167	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.	Am J Hum Genet	2021
33414548	A cross-platform approach identifies genetic regulators of human metabolism and health.	Nat Genet	2021
34836419	Salicylic Acid and Risk of Colorectal Cancer: A Two-Sample Mendelian Randomization Study.	Nutrients	2021
34543281	The blood metabolome of incident kidney cancer: A case-control study nested within the MetKid consortium.	PLoS Med	2021
30617275	Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci.	Mol Psychiatry	2020
33067605	Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.	Nat Metab	2020
33230300	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2020
32888494	The Polygenic and Monogenic Basis of Blood Traits and Diseases.	Cell	2020
32888493	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Cell	2020
30837465	Assessing the causal association of glycine with risk of cardio-metabolic diseases.	Nat Commun	2019
31233103	PhenoScanner V2: an expanded tool for searching human genotype-phenotype associations.	Bioinformatics	2019
31160809	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2019
29273807	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29926099	Association of LPA Variants With Risk of Coronary Disease and the Implications for Lipoprotein(a)-Lowering Therapies: A Mendelian Randomization Analysis.	JAMA Cardiol	2018
29875488	Genomic atlas of the human plasma proteome.	Nature	2018
30429575	Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.	Nat Genet	2018
30224653	Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.	Nat Genet	2018
29258006	Genetic variants in PPARGC1B and CNTN4 are associated with thromboxane A<sub>2</sub> formation and with cardiovascular event free survival in the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT).	Atherosclerosis	2018
29549330	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29549329	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29632382	Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.	Nat Genet	2018
28209224	Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated WithÂ Coronary ArteryÂ Disease.	J Am Coll Cardiol	2017
28869590	Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease.	Nat Genet	2017
28951623	Corrigendum: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.	Nat Genet	2017
28663568	Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity.	Sci Rep	2017
28530674	Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.	Nat Genet	2017
29030403	New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475â¿¿000 Individuals.	Circ Cardiovasc Genet	2017
28394258	Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.	J Clin Invest	2017
29083408	Exome-wide association study of plasma lipids in >300,000 individuals.	Nat Genet	2017
27940953	Genetic invalidation of Lp-PLA<sub>2</sub> as a therapeutic target: Large-scale study of five functional Lp-PLA<sub>2</sub>-lowering alleles.	Eur J Prev Cardiol	2017
28146470	Rare and low-frequency coding variants alter human adult height.	Nature	2017
28135244	Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.	Nat Genet	2017
27618447	Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.	Nat Genet	2016
27252175	A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease.	Sci Transl Med	2016
26934567	Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.	N Engl J Med	2016
26965621	Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease.	Science	2016
27318201	PhenoScanner: a database of human genotype-phenotype associations.	Bioinformatics	2016