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Volumn 55, Issue 6, 2014, Pages 1173-1178

Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project

(17)  Kim, Daniel Seung a   Crosslin, David R a   Auer, Paul L b,c   Suzuki, Stephanie M a   Marsillach, Judit a   Burt, Amber A a   Gordon, Adam S a   Meschia, James F d   Nalls, Mike A e   Worrall, Bradford B f,g   Longstreth Jr , W T h   Gottesman, Rebecca F i   Furlong, Clement E a   Peters, Ulrike b,h   Rich, Stephen S f   Nickerson, Deborah A a   Jarvik, Gail P a  


Author keywords

Atherosclerosis; Genetics; Rare variation

Indexed keywords

ARYLDIALKYLPHOSPHATASE 1; ARYLDIALKYLPHOSPHATASE; PON1 PROTEIN, HUMAN;

EID: 84901675897     PISSN: 00222275     EISSN: 15397262     Source Type: Journal    
DOI: 10.1194/jlr.P049247     Document Type: Article
Times cited : (23)

References (20)
  • 8
    • 1542331537 scopus 로고    scopus 로고
    • Four paraoxonase gene polymorphisms in 11 212 cases of coronary heart disease and 12 786 controls: Meta-analysis of 43 studies
    • Wheeler, J. G., B. D. Keavney, H. Watkins, R. Collins, and J. Danesh. 2004. Four paraoxonase gene polymorphisms in 11 212 cases of coronary heart disease and 12 786 controls: meta-analysis of 43 studies. Lancet. 363: 689-695.
    • (2004) Lancet. , vol.363 , pp. 689-695
    • Wheeler, J.G.1    Keavney, B.D.2    Watkins, H.3    Collins, R.4    Danesh, J.5
  • 9
    • 79151474813 scopus 로고    scopus 로고
    • Four genetic polymorphisms of paraoxonase gene and risk of coronary heart disease: A meta-analysis based on 88 case-control studies
    • Wang, M., X. Lang, L. Zou, S. Huang, and Z. Xu. 2011. Four genetic polymorphisms of paraoxonase gene and risk of coronary heart disease: a meta-analysis based on 88 case-control studies. Atherosclerosis. 214: 377-385.
    • (2011) Atherosclerosis. , vol.214 , pp. 377-385
    • Wang, M.1    Lang, X.2    Zou, L.3    Huang, S.4    Xu, Z.5
  • 10
  • 11
    • 84863556835 scopus 로고    scopus 로고
    • Evolution and functional impa ct of rare coding variation from deep sequencing of human exomes
    • NHLBI Exome Sequencing Project.
    • Tennessen, J. A., A. W. Bigham, T. D. O Connor, W. Fu, E. E. Kenny, S. Gravel, S. McGee, R. Do, X. Liu, G. Jun, et al, NHLBI Exome Sequencing Project. 2012. Evolution and functional impa ct of rare coding variation from deep sequencing of human exomes. Science. 337: 64-69.
    • (2012) Science. , vol.337 , pp. 64-69
    • Tennessen, J.A.1    Bigham, A.W.2    Oconnor, T.D.3    Fu, W.4    Kenny, E.E.5    Gravel, S.6    McGee, S.7    Do, R.8    Liu, X.9    Jun, G.10
  • 12
    • 22244452677 scopus 로고    scopus 로고
    • Distribution and intensity of constraint in mammalian genomic sequence
    • NISC Comparative Sequencing Program E. D. Green S. Batzoglou A . Sidow
    • Cooper, G. M., E. A. Stone, G. Asimenos, NISC Comparative Sequencing Program, E. D. Green, S. Batzoglou, and A . Sidow. 2005. Distribution and intensity of constraint in mammalian genomic sequence. Genome Res. 15: 901-913.
    • (2005) Genome Res. , vol.15 , pp. 901-913
    • Cooper, G.M.1    Stone, E.A.2    Asimenos, G.3
  • 13
    • 84870820953 scopus 로고    scopus 로고
    • A high-performance computing toolset for relatedness and principal component analysis of SNP data
    • Zheng, X., D. Levine, J. Shen, S. M. Gogarten, C. Laurie, and B. S. Weir. 2012. A high-performance computing toolset for relatedness and principal component analysis of SNP data. Bioinformatics. 28: 3326-3328.
    • (2012) Bioinformatics. , vol.28 , pp. 3326-3328
    • Zheng, X.1    Levine, D.2    Shen, J.3    Gogarten, S.M.4    Laurie, C.5    Weir, B.S.6
  • 14
    • 80051499915 scopus 로고    scopus 로고
    • Rarevariant association testing for sequencing data with the sequence kernel association test
    • Wu, M. C., S. Lee, T. Cai, Y. Li, M. Boehnke, and X. Lin. 2011. Rarevariant association testing for sequencing data with the sequence kernel association test. Am. J. Hum. Genet. 89: 82-93.
    • (2011) Am. J. Hum. Genet. , vol.89 , pp. 82-93
    • Wu, M.C.1    Lee, S.2    Cai, T.3    Li, Y.4    Boehnke, M.5    Lin, X.6
  • 15
    • 31744435871 scopus 로고    scopus 로고
    • Joint analysis is more effi cient than replication-based analysis for twostage genome-wide association studies
    • Skol, A. D., L. J. Scott, G. R. Abecasis, and M. Boehnke. 2006. Joint analysis is more effi cient than replication-based analysis for twostage genome-wide association studies. Nat. Genet. 38: 209-213.
    • (2006) Nat. Genet. , vol.38 , pp. 209-213
    • Skol, A.D.1    Scott, L.J.2    Abecasis, G.R.3    Boehnke, M.4
  • 16
    • 84893651437 scopus 로고    scopus 로고
    • Heart disease and stroke statistics2014 update: A report from the american h eart association
    • American Heart Association Statistics Committee and Stroke Statistics Subcommittee. 2014
    • Go, A. S., D. Mozaffarian, V. L. Roger, E. J. Benjamin, J. D. Berry, M. J. Blaha, S. Dai, E. S. Ford, C. S. Fox, S. Franco, et al, American Heart Association Statistics Committee and Stroke Statistics Subcommittee. 2014. Heart disease and stroke statistics2014 update: a report from the American H eart Association. Circulation. 129: e28-e292.
    • Circulation. , vol.129
    • Go, A.S.1    Mozaffarian, D.2    Roger, V.L.3    Benjamin, E.J.4    Berry, J.D.5    Blaha, M.J.6    Dai, S.7    Ford, E.S.8    Fox, C.S.9    Franco, S.10
  • 18
    • 84856405512 scopus 로고    scopus 로고
    • The mystery of missing heritability: Genetic interactions create phantom heritability
    • Zuk, O., E. Hechter, S. R. Sunyaev, and E. S. Lander. 2012. The mystery of missing heritability: genetic interactions create phantom heritability. Proc. Natl. Acad. Sci. USA. 109: 1193-1198.
    • (2012) Proc. Natl. Acad. Sci. USA. , vol.109 , pp. 1193-1198
    • Zuk, O.1    Hechter, E.2    Sunyaev, S.R.3    Lander, E.S.4
  • 19
    • 84876795750 scopus 로고    scopus 로고
    • Novel geneby-environment interactions: APOB and NPC1L1 variants affect the relationship between dietary and total plasma cholesterol
    • Kim, D. S., A. A. Burt, J. E. Ranchalis, E. R. Jarvik, E. A. Rosenthal, T. S. Hatsukami, C. E. Furlong, and G. P. Jarvik. 2013. Novel geneby-environment interactions: APOB and NPC1L1 variants affect the relationship between dietary and total plasma cholesterol. J. Lipid Res. 54: 1512-1520.
    • (2013) J. Lipid Res. , vol.54 , pp. 1512-1520
    • Kim, D.S.1    Burt, A.A.2    Ranchalis, J.E.3    Jarvik, E.R.4    Rosenthal, E.A.5    Hatsukami, T.S.6    Furlong, C.E.7    Jarvik, G.P.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.