Center-Authored Papers

Filters: Author is Rich, Stephen S  [Clear All Filters]
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Zubair N, Graff M, Ambite JL, Bush WS, Kichaev G, Lu Y, Manichaikul A, Sheu WH-H, Absher D, Assimes TL et al..  2016.  Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci.. Human molecular genetics. 25(24):5500-5512. Abstract
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Wu JHY, Lemaitre RN, Manichaikul A, Guan W, Tanaka T, Foy M, Kabagambe EK, Djousse L, Siscovick D, Fretts AM et al..  2013.  Genome-Wide Association Study Identifies Novel Loci Associated With Concentrations of Four Plasma Phospholipid Fatty Acids in the De Novo Lipogenesis Pathway: Results from the CHARGE Consortium.. Circulation. Cardiovascular genetics. Abstract
Weng L-C, Tang W, Rich SS, Smith NL, Redline S, O'Donnell CJ, Basu S, Reiner AP, Delaney JA, Tracy RP et al..  2014.  A genetic association study of D-dimer levels with 50K SNPs from a candidate gene chip in four ethnic groups.. Thrombosis research. 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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Tajuddin SM, Schick UM, Eicher JD, Chami N, Giri A, Brody JA, Hill DW, Kacprowski T, Li J, Lyytikäinen L-P et al..  2016.  Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.. American journal of human genetics. Abstract
Tabor HK, Auer PL, Jamal SM, Chong JX, Yu J-H, Gordon AS, Graubert TA, O'Donnell CJ, Rich SS, Nickerson DA et al..  2014.  Pathogenic variants for mendelian and complex traits in exomes of 6,517 European and african americans: implications for the return of incidental results.. American journal of human genetics. 95(2):183-93. Abstract
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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
Smith CE, Follis JL, Nettleton JA, Foy M, Wu JHY, Ma Y, Tanaka T, Manichakul AW, Wu H, Chu AY et al..  2015.  Dietary fatty acids modulate associations between genetic variants and circulating fatty acids in plasma and erythrocyte membranes: Meta-analysis of nine studies in the CHARGE consortium.. Molecular nutrition & food research. Abstract
Schick UM, Jain D, Hodonsky CJ, Morrison JV, Davis JP, Brown L, Sofer T, Conomos MP, Schurmann C, McHugh CP et al..  2016.  Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.. American journal of human genetics. Abstract
Schick UM, Auer PL, Bis JC, Lin H, Wei P, Pankratz N, Lange LA, Brody J, Stitziel NO, Kim DS et al..  2015.  Association of exome sequences with plasma C-reactive protein levels in >9000 participants.. Human molecular genetics. 24(2):559-71. Abstract
Saxena R, Elbers CC, Guo Y, Peter I, Gaunt TR, Mega JL, Lanktree MB, Tare A, Castillo BA, Li YR et al..  2012.  Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci.. American journal of human genetics. 90(3):410-25. Abstract
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Rosenthal EA, Makaryan V, Burt AA, Crosslin DR, Kim DS, Smith JD, Nickerson DA, Reiner AP, Rich SS, Jackson RD et al..  2016.  Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project.. Genetic epidemiology. 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
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
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Ng MCY, Shriner D, Chen BH, Li J, Chen W-M, Guo X, Liu J, Bielinski SJ, Yanek LR, Nalls MA et al..  2014.  Meta-analysis of genome-wide association studies in african americans provides insights into the genetic architecture of type 2 diabetes.. PLoS genetics. 10(8):e1004517. 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, 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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Mozaffarian D, Kabagambe EK, Johnson CO, Lemaitre RN, Manichaikul A, Sun Q, Foy M, Wang L, Wiener H, Irvin MR et al..  2015.  Genetic loci associated with circulating phospholipid trans fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.. The American journal of clinical nutrition. 101(2):398-406. Abstract
Manichaikul A, Wang X-Q, Zhao W, Wojczynski MK, Siebenthall K, Stamatoyannopoulos JA, Saleheen D, Borecki IB, Reilly MP, Rich SS et al..  2016.  Genetic association of long-chain acyl-CoA synthetase 1 variants with fasting glucose, diabetes, and subclinical atherosclerosis.. Journal of lipid research. 57(3):433-42. Abstract
Ma Y, Follis JL, Smith CE, Tanaka T, Manichaikul AW, Chu AY, Samieri C, Zhou X, Guan W, Wang L et al..  2016.  Interaction of methylation-related genetic variants with circulating fatty acids on plasma lipids: a meta-analysis of 7 studies and methylation analysis of 3 studies in the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium.. The American journal of clinical nutrition. Abstract
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Logsdon BA, Dai JY, Auer PL, Johnsen JM, Ganesh SK, Smith NL, Wilson JG, Tracy RP, Lange LA, Jiao S et al..  2014.  A variational Bayes discrete mixture test for rare variant association.. Genetic epidemiology. 38(1):21-30. Abstract
Liu C-T, Raghavan S, Maruthur N, Kabagambe EK, Hong J, Ng MCY, Hivert M-F, Lu Y, An P, Bentley AR et al..  2016.  Trans-ethnic Meta-Analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.. American journal of human genetics. 99(1):56-75. Abstract
Lemaitre RN, King IB, Kabagambe EK, Wu JHY, McKnight B, Manichaikul A, Guan W, Sun Q, Chasman DI, Foy M et al..  2015.  Genetic loci associated with circulating levels of very long-chain saturated fatty acids.. Journal of lipid research. 56(1):176-84. Abstract
Lange LA, Hu Y, Zhang H, Xue C, Schmidt EM, Tang Z-Z, Bizon C, Lange EM, Smith JD, Turner EH et al..  2014.  Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.. American journal of human genetics. 94(2):233-45. Abstract
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Kim DS, Crosslin DR, Auer PL, Suzuki SM, Marsillach J, Burt AA, Gordon AS, Meschia JF, Nalls MA, Worrall BB et al..  2014.  Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project.. Journal of lipid research. 55(6):1173-8. Abstract