Center-Authored Papers

Filters: Author is Kathiresan, Sekar  [Clear All Filters]
A
Asselbergs FW, Guo Y, van Iperen EPA, Sivapalaratnam S, Tragante V, Lanktree MB, Lange LA, Almoguera B, Appelman YE, Barnard J et al..  2012.  Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci.. American journal of human genetics. 91(5):823-38. Abstract
Assimes TL, Hólm H, Kathiresan S, Reilly MP, Thorleifsson G, Voight BF, Erdmann J, Willenborg C, Vaidya D, Xie C et al..  2010.  Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.. Journal of the American College of Cardiology. 56(19):1552-63. Abstract
B
Berndt SI, Gustafsson S, Mägi R, Ganna A, Wheeler E, Feitosa MF, Justice AE, Monda KL, Croteau-Chonka DC, Day FR et al..  2013.  Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.. Nature genetics. 45(5):501-12. Abstract
C
Chami N, Chen M-H, Slater AJ, Eicher JD, Evangelou E, Tajuddin SM, Love-Gregory L, Kacprowski T, Schick UM, Nomura A et al..  2016.  Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.. American journal of human genetics. Abstract
Christophersen IE, Rienstra M, Roselli C, Yin X, Geelhoed B, Barnard J, Lin H, Arking DE, Smith AV, Albert CM et al..  2017.  Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.. Nature genetics. 49(6):946-952. Abstract
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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
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Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang S-J et al..  2011.  Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.. Nature. 478(7367):103-9. Abstract
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
Elbers CC, Guo Y, Tragante V, van Iperen EPA, Lanktree MB, Castillo BA, Chen F, Yanek LR, Wojczynski MK, Li YR et al..  2012.  Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations.. PloS one. 7(12):e50198. Abstract
Erdmann J, Grosshennig A, Braund PS, König IR, Hengstenberg C, Hall AS, Linsel-Nitschke P, Kathiresan S, Wright B, Trégouët D-A et al..  2009.  New susceptibility locus for coronary artery disease on chromosome 3q22.3.. Nature genetics. 41(3):280-2. Abstract
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Howson JMM, Zhao W, Barnes DR, Ho W-K, Young R, Paul DS, Waite LL, Freitag DF, Fauman EB, Salfati EL et al..  2017.  Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.. Nature genetics. Abstract
Huang J, Sabater-Lleal M, Asselbergs FW, Tregouet D, Shin S-Y, Ding J, Baumert J, Oudot-Mellakh T, Folkersen L, Johnson AD et al..  2012.  Genome-wide association study for circulating levels of plasminogen activator inhibitor-1 (PAI-1) provides novel insights into the regulation of PAI-1.. Blood. Abstract
Huang J, Huffman JE, Yamkauchi M, Trompet S, Asselbergs FW, Sabater-Lleal M, Trégouët D-A, Chen W-M, Smith NL, Kleber ME et al..  2014.  Genome-Wide Association Study for Circulating Tissue Plasminogen Activator Levels and Functional Follow-Up Implicates Endothelial STXBP5 and STX2.. Arteriosclerosis, thrombosis, and vascular biology. Abstract
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Ibrahim-Verbaas CA, Fornage M, Bis JC, Choi SH, Psaty BM, Meigs JB, Rao M, Nalls M, Fontes JD, O'Donnell CJ et al..  2014.  Predicting Stroke Through Genetic Risk Functions: The CHARGE Risk Score Project.. Stroke; a journal of cerebral circulation. 45(2):403-12. Abstract
J
Johansen CT, Wang J, Lanktree MB, McIntyre AD, Ban MR, Martins RA, Kennedy BA, Hassell RG, Visser ME, Schwartz SM et al..  2011.  An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemia.. Arteriosclerosis, thrombosis, and vascular biology. 31(8):1916-26. Abstract
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Kathiresan S, Voight BF, Purcell S, Musunuru K, Ardissino D, Mannucci PM, Anand S, Engert JC, Samani NJ, Schunkert H et al..  2009.  Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.. Nature genetics. 41(3):334-41. Abstract
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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
Lim ET, Würtz P, Havulinna AS, Palta P, Tukiainen T, Rehnström K, Esko T, Mägi R, Inouye M, Lappalainen T et al..  2014.  Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population.. PLoS genetics. 10(7):e1004494. Abstract
Liu C, Kraja AT, Smith JA, Brody JA, Franceschini N, Bis JC, Rice K, Morrison AC, Lu Y, Weiss S et al..  2016.  Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.. Nature genetics. 48(10):1162-1170. Abstract
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
Locke AE, Kahali B, Berndt SI, Justice AE, Pers TH, Day FR, Powell C, Vedantam S, Buchkovich ML, Yang J et al..  2015.  Genetic studies of body mass index yield new insights for obesity biology.. Nature. 518(7538):197-206. Abstract
Lubitz SA, Lunetta KL, Lin H, Arking DE, Trompet S, Li G, Krijthe BP, Chasman DI, Barnard J, Kleber ME et al..  2014.  Novel Genetic Markers Associate with Atrial Fibrillation Risk in Europeans and Japanese.. Journal of the American College of Cardiology. Abstract
Lucas G, Lluís-Ganella C, Subirana I, Musameh MD, Gonzalez JR, Nelson CP, Sentí M, Schwartz SM, Siscovick D, O'Donnell CJ et al..  2012.  Hypothesis-Based Analysis of Gene-Gene Interactions and Risk of Myocardial Infarction.. PloS one. 7(8):e41730. Abstract
M
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
van Meurs JBJ, Pare G, Schwartz SM, Hazra A, Tanaka T, Vermeulen SH, Cotlarciuc I, Yuan X, Mälarstig A, Bandinelli S et al..  2013.  Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.. The American journal of clinical nutrition. Abstract