Center-Authored Papers

Filters: Author is Peloso, Gina M  [Clear All Filters]
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Peloso GM, Auer PL, Bis JC, Voorman A, Morrison AC, Stitziel NO, Brody JA, Khetarpal SA, Crosby JR, Fornage M et al..  2014.  Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.. American journal of human genetics. 94(2):223-32. Abstract
Naik RP, Derebail VK, Grams ME, Franceschini N, Auer PL, Peloso GM, Young BA, Lettre G, Peralta CA, Katz R et al..  2014.  Association of sickle cell trait with chronic kidney disease and albuminuria in African Americans.. JAMA. 312(20):2115-25. Abstract
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Stitziel NO, Fouchier SW, Sjouke B, Peloso GM, Moscoso AM, Auer PL, Goel A, Gigante B, Barnes TA, Melander O et al..  2013.  Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia.. Arteriosclerosis, thrombosis, and vascular biology. 33(12):2909-14. Abstract
Do R, Stitziel NO, Won H-H, Jørgensen AB, Duga S, Merlini PA, Kiezun A, Farrall M, Goel A, Zuk O et al..  2015.  Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.. Nature. 518(7537):102-6. Abstract
Stitziel NO, Peloso GM, Abifadel M, Cefalu AB, Fouchier S, Motazacker MM, Tada H, Larach DB, Awan Z, Haller JF et al..  2015.  Exome sequencing in suspected monogenic dyslipidemias.. Circulation. Cardiovascular genetics. 8(2):343-50. Abstract
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Stitziel NO, Won H-H, Morrison AC, Peloso GM, Do R, Lange LA, Fontanillas P, Gupta N, Duga S, Goel A et al..  2014.  Inactivating mutations in NPC1L1 and protection from coronary heart disease.. The New England journal of medicine. 371(22):2072-82. Abstract
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Crosby J, Peloso GM, Auer PL, Crosslin DR, Stitziel NO, Lange LA, Lu Y, Tang Z-Z, Zhang H, Hindy G et al..  2014.  Loss-of-function mutations in APOC3, triglycerides, and coronary disease.. The New England journal of medicine. 371(1):22-31. Abstract
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Liu DJ, Peloso GM, Zhan X, Holmen OL, Zawistowski M, Feng S, Nikpay M, Auer PL, Goel A, Zhang H et al..  2014.  Meta-analysis of gene-level tests for rare variant association.. Nature genetics. 46(2):200-4. Abstract
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Eicher JD, Chami N, Kacprowski T, Nomura A, Chen M-H, Yanek LR, Tajuddin SM, Schick UM, Slater AJ, Pankratz N et al..  2016.  Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.. American journal of human genetics. Abstract
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Marouli E, Graff M, Medina-Gomez C, Lo KS, Wood AR, Kjaer TR, Fine RS, Lu Y, Schurmann C, Highland HM et al..  2017.  Rare and low-frequency coding variants alter human adult height.. Nature. 542(7640):186-190. Abstract
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Webb TR, Erdmann J, Stirrups KE, Stitziel NO, Masca NGD, Jansen H, Kanoni S, Nelson CP, Ferrario PG, König IR et al..  2017.  Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.. Journal of the American College of Cardiology. 69(7):823-836. Abstract
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Polfus LM, Khajuria RK, Schick UM, Pankratz N, Pazoki R, Brody JA, Chen M-H, Auer PL, Floyd JS, Huang J et al..  2016.  Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.. American journal of human genetics. 99(2):481-8. Abstract