| 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 | 625 | 1999 |
| 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 | 564 | 2014 |
| 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 | 553 | 2015 |
| 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 | 438 | 2012 |
| 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 | 426 | 2015 |
| 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 | 361 | 2014 |
| 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 | 351 | 2016 |
| 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 | 297 | 2014 |
| 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 | 283 | 2014 |
| 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 | 270 | 2017 |
| 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 | 259 | 2016 |
| 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 | 236 | 2017 |
| 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 | 194 | 2017 |
| 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 | 166 | 2013 |
| 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 | 157 | 2016 |
| Computational and statistical approaches to analyzing variants identified by exome sequencing NO Stitziel, A Kiezun, S Sunyaev Genome biology 12 (9), 1-10, 2011 | 157 | 2011 |
| 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 | 150 | 2017 |
| 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 | 146 | 2018 |
| 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 | 117 | 2004 |
| 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 | 109 | 2016 |
