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Nathan Stitziel
Nathan Stitziel
Verified email at wustl.edu - Homepage
Title
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Cited by
Year
Genome Sequence of the Nematode C. elegans: A Platform for Investigating Biology
C. elegans Sequencing Consortium*
Science 282 (5396), 2012-2018, 1998
16601998
Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
TG and HDL Working Group of the Exome Sequencing Project, National Heart ...
New England Journal of Medicine 371 (1), 22-31, 2014
8242014
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
7692015
Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials
JL Mega, NO Stitziel, JG Smith, DI Chasman, MJ Caulfield, JJ Devlin, ...
The Lancet 385 (9984), 2264-2271, 2015
7142015
A general approach to single-nucleotide polymorphism discovery
GT Marth, I Korf, MD Yandell, RT Yeh, Z Gu, H Zakeri, NO Stitziel, ...
Nature genetics 23 (4), 452-456, 1999
7021999
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
Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel
AC Sturm, JW Knowles, SS Gidding, ZS Ahmad, CD Ahmed, ...
Journal of the American College of Cardiology 72 (6), 662-680, 2018
528*2018
Polygenic risk score identifies subgroup with higher burden of atherosclerosis and greater relative benefit from statin therapy in the primary prevention setting
P Natarajan, R Young, NO Stitziel, S Padmanabhan, U Baber, R Mehran, ...
Circulation 135 (22), 2091-2101, 2017
5012017
Exome sequencing and the genetic basis of complex traits
A Kiezun, K Garimella, R Do, NO Stitziel, BM Neale, PJ McLaren, N Gupta, ...
Nature genetics 44 (6), 623-630, 2012
4962012
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
470*2016
Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease
Myocardial Infarction Genetics Consortium Investigators
New England Journal of Medicine 371 (22), 2072-2082, 2014
4642014
Distribution and medical impact of loss-of-function variants in the Finnish founder population
ET Lim, P Würtz, AS Havulinna, P Palta, T Tukiainen, K Rehnström, ...
PLoS genetics 10 (7), e1004494, 2014
4442014
ANGPTL3 deficiency and protection against coronary artery disease
NO Stitziel, AV Khera, X Wang, AJ Bierhals, AC Vourakis, AE Sperry, ...
Journal of the American College of Cardiology 69 (16), 2054-2063, 2017
4292017
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks
GM Peloso, PL Auer, JC Bis, A Voorman, AC Morrison, NO Stitziel, ...
The American Journal of Human Genetics 94 (2), 223-232, 2014
3782014
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
Systematic evaluation of pleiotropy identifies 6 further loci associated with coronary artery disease
TR Webb, J Erdmann, KE Stirrups, NO Stitziel, NGD Masca, H Jansen, ...
Journal of the American College of Cardiology 69 (7), 823-836, 2017
2472017
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis
B Coste, G Houge, MF Murray, N Stitziel, M Bandell, MA Giovanni, ...
Proceedings of the National Academy of Sciences 110 (12), 4667-4672, 2013
2402013
Mapping and characterization of structural variation in 17,795 human genomes
HJ Abel, DE Larson, AA Regier, C Chiang, I Das, KL Kanchi, RM Layer, ...
Nature 583 (7814), 83-89, 2020
2302020
Phenotypic characterization of genetically lowered human lipoprotein (a) levels
CA Emdin, AV Khera, P Natarajan, D Klarin, HH Won, GM Peloso, ...
Journal of the American College of Cardiology 68 (25), 2761-2772, 2016
2162016
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