Nathan Stitziel
Nathan Stitziel
Associate Professor of Medicine and Genetics, Washington University
Verified email at wustl.edu
Title
Cited by
Cited by
Year
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
6281999
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
5742014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, PA Merlini, A Kiezun, ...
Nature 518 (7537), 102-106, 2015
5662015
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
4532015
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, 2012
4462012
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
3682014
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
3652016
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 Genet 10 (7), e1004494, 2014
3072014
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
2942014
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
2882017
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
2762016
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
2592017
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
2122017
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
1712013
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
1662016
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
1592017
Computational and statistical approaches to analyzing variants identified by exome sequencing
NO Stitziel, A Kiezun, S Sunyaev
Genome biology 12 (9), 1-10, 2011
1582011
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
1572018
topoSNP: a topographic database of non‐synonymous single nucleotide polymorphisms with and without known disease association
NO Stitziel, TA Binkowski, YY Tseng, S Kasif, J Liang
Nucleic acids research 32 (suppl_1), D520-D522, 2004
1192004
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
1162016
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