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Volumn 29, Issue 9, 2014, Pages 560-566

Exploring the genetic basis of stroke. Spanish stroke genetics consortium;Aproximación al conocimiento de las bases genéticas del ictus. Consorcio español de genética del ictus

Author keywords

Association; Consortium; Genetic risk factors; Genetics; Prediction; Stroke

Indexed keywords

CEREBROVASCULAR ACCIDENT; GENETIC ASSOCIATION; GENETIC RISK; GENETICS; HUMAN; SCIENTIFIC LITERATURE; SHORT SURVEY; SPAIN; GENETIC EPIGENESIS; GENETIC PREDISPOSITION; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84922514932     PISSN: 02134853     EISSN: 15781968     Source Type: Journal    
DOI: 10.1016/j.nrl.2013.04.005     Document Type: Short Survey
Times cited : (6)

References (49)
  • 1
    • 55549131511 scopus 로고    scopus 로고
    • In-hospital mortality in stroke patients
    • Alvarez Sabin J. In-hospital mortality in stroke patients. Rev Esp Cardiol 2008, 61:1007-1009.
    • (2008) Rev Esp Cardiol , vol.61 , pp. 1007-1009
    • Alvarez Sabin, J.1
  • 3
    • 0035164329 scopus 로고    scopus 로고
    • Risk factors, outcome, and treatment in subtypes of ischemic stroke: The german stroke data bank
    • Grau A.J., Weimar C., Buggle F., Heinrich A., Goertler M., Neumaier S., et al. Risk factors, outcome, and treatment in subtypes of ischemic stroke: The german stroke data bank. Stroke 2001, 32:2559-2566.
    • (2001) Stroke , vol.32 , pp. 2559-2566
    • Grau, A.J.1    Weimar, C.2    Buggle, F.3    Heinrich, A.4    Goertler, M.5    Neumaier, S.6
  • 4
    • 84870931409 scopus 로고    scopus 로고
    • Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations
    • Bevan S., Traylor M., Adib-Samii P., Malik R., Paul N.L., Jackson C., et al. Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations. Stroke 2012, 43:3161-3167.
    • (2012) Stroke , vol.43 , pp. 3161-3167
    • Bevan, S.1    Traylor, M.2    Adib-Samii, P.3    Malik, R.4    Paul, N.L.5    Jackson, C.6
  • 5
    • 79959524146 scopus 로고    scopus 로고
    • A haplotype map of the human genome
    • International HapMap Consortium
    • A haplotype map of the human genome. Nature 2005, 437:1299-1320. International HapMap Consortium.
    • (2005) Nature , vol.437 , pp. 1299-1320
  • 6
    • 0029741063 scopus 로고    scopus 로고
    • The future of genetic studies of complex human diseases
    • Risch N., Merikangas K. The future of genetic studies of complex human diseases. Science 1996, 273:1516-1517.
    • (1996) Science , vol.273 , pp. 1516-1517
    • Risch, N.1    Merikangas, K.2
  • 7
    • 0037534908 scopus 로고    scopus 로고
    • Evaluating the genetic component of ischemic stroke subtypes: A family history study
    • Jerrard-Dunne P., Cloud G., Hassan A., Markus H.S. Evaluating the genetic component of ischemic stroke subtypes: A family history study. Stroke 2003, 34:1364-1369.
    • (2003) Stroke , vol.34 , pp. 1364-1369
    • Jerrard-Dunne, P.1    Cloud, G.2    Hassan, A.3    Markus, H.S.4
  • 8
    • 84867645825 scopus 로고    scopus 로고
    • Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): A meta-analysis of genome-wide association studies
    • Traylor M., Farrall M., Holliday E.G., Sudlow C., Hopewell J.C., Cheng Y.C., et al. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): A meta-analysis of genome-wide association studies. Lancet Neurol 2012, 11:951-962.
    • (2012) Lancet Neurol , vol.11 , pp. 951-962
    • Traylor, M.1    Farrall, M.2    Holliday, E.G.3    Sudlow, C.4    Hopewell, J.C.5    Cheng, Y.C.6
  • 9
    • 0026593463 scopus 로고
    • Intracerebral haemorrhage
    • Caplan L.R. Intracerebral haemorrhage. Lancet 1992, 339:656-658.
    • (1992) Lancet , vol.339 , pp. 656-658
    • Caplan, L.R.1
  • 10
    • 33645836496 scopus 로고    scopus 로고
    • The incidence of deep and lobar intracerebral hemorrhage in whites, blacks, and hispanics
    • author reply 956-957
    • Flaherty M.L., Woo D., Broderick J. The incidence of deep and lobar intracerebral hemorrhage in whites, blacks, and hispanics. Neurology 2006, 66:956-957. author reply 956-957.
    • (2006) Neurology , vol.66 , pp. 956-957
    • Flaherty, M.L.1    Woo, D.2    Broderick, J.3
  • 11
    • 0036255811 scopus 로고    scopus 로고
    • Candidate-gene approaches for studying complex genetic traits: Practical considerations
    • Tabor H.K., Risch N.J., Myers R.M. Candidate-gene approaches for studying complex genetic traits: Practical considerations. Nat Rev Genet 2002, 3:391-397.
    • (2002) Nat Rev Genet , vol.3 , pp. 391-397
    • Tabor, H.K.1    Risch, N.J.2    Myers, R.M.3
  • 12
    • 24644436338 scopus 로고    scopus 로고
    • Genetic association studies in stroke: Methodological issues and proposed standard criteria
    • Dichgans M., Markus H.S. Genetic association studies in stroke: Methodological issues and proposed standard criteria. Stroke 2005, 36:2027-2031.
    • (2005) Stroke , vol.36 , pp. 2027-2031
    • Dichgans, M.1    Markus, H.S.2
  • 13
    • 84867124426 scopus 로고    scopus 로고
    • COL4A1 and COL4A2 mutations and disease: Insights into pathogenic mechanisms and potential therapeutic targets
    • Kuo D.S., Labelle-Dumais C., Gould D.B. COL4A1 and COL4A2 mutations and disease: Insights into pathogenic mechanisms and potential therapeutic targets. Hum Mol Genet 2012, 21(R1):R97-R110.
    • (2012) Hum Mol Genet , vol.21 , Issue.R1 , pp. R97-R110
    • Kuo, D.S.1    Labelle-Dumais, C.2    Gould, D.B.3
  • 14
    • 33745261734 scopus 로고    scopus 로고
    • Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly
    • Breedveld G., de Coo I.F., Lequin M.H., Arts W.F., Heutink P., Gould D.B., et al. Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly. J Med Genet 2006, 43:490-495.
    • (2006) J Med Genet , vol.43 , pp. 490-495
    • Breedveld, G.1    de Coo, I.F.2    Lequin, M.H.3    Arts, W.F.4    Heutink, P.5    Gould, D.B.6
  • 18
    • 79960341939 scopus 로고    scopus 로고
    • APOE genotype and extent of bleeding and outcome in lobar intracerebral haemorrhage: A genetic association study
    • Biffi A., Anderson C.D., Jagiella J.M., Schmidt H., Kissela B., Hansen B.M., et al. APOE genotype and extent of bleeding and outcome in lobar intracerebral haemorrhage: A genetic association study. Lancet Neurol 2011, 10:702-709.
    • (2011) Lancet Neurol , vol.10 , pp. 702-709
    • Biffi, A.1    Anderson, C.D.2    Jagiella, J.M.3    Schmidt, H.4    Kissela, B.5    Hansen, B.M.6
  • 19
    • 35348983887 scopus 로고    scopus 로고
    • A second generation human haplotype map of over 3.1 million SNPs
    • International HapMap Consortium
    • Frazer K.A., Ballinger D.G., Cox D.R., Hinds D.A., Stuve L.L., Gibbs R.A., et al. A second generation human haplotype map of over 3.1 million SNPs. Nature 2007, 449:851-861. International HapMap Consortium.
    • (2007) Nature , vol.449 , pp. 851-861
    • Frazer, K.A.1    Ballinger, D.G.2    Cox, D.R.3    Hinds, D.A.4    Stuve, L.L.5    Gibbs, R.A.6
  • 20
    • 40849097776 scopus 로고    scopus 로고
    • Heritability in the genomics era--concepts and misconceptions
    • Visscher P.M., Hill W.G., Wray N.R. Heritability in the genomics era--concepts and misconceptions. Nat Rev Genet 2008, 9:255-266.
    • (2008) Nat Rev Genet , vol.9 , pp. 255-266
    • Visscher, P.M.1    Hill, W.G.2    Wray, N.R.3
  • 22
    • 2442585696 scopus 로고    scopus 로고
    • The effects of human population structure on large genetic association studies
    • Marchini J., Cardon L.R., Phillips M.S., Donnelly P. The effects of human population structure on large genetic association studies. Nat Genet 2004, 36:512-517.
    • (2004) Nat Genet , vol.36 , pp. 512-517
    • Marchini, J.1    Cardon, L.R.2    Phillips, M.S.3    Donnelly, P.4
  • 23
    • 55349099184 scopus 로고    scopus 로고
    • The positives, protocols, and perils of genome-wide association
    • Neale B.M., Purcell S. The positives, protocols, and perils of genome-wide association. Am J Med Genet B Neuropsychiatr Genet 2008, 147B:1288-1294.
    • (2008) Am J Med Genet B Neuropsychiatr Genet , vol.147 B , pp. 1288-1294
    • Neale, B.M.1    Purcell, S.2
  • 24
    • 20244380171 scopus 로고    scopus 로고
    • Complement factor H polymorphism in age-related macular degeneration
    • Klein R.J., Zeiss C., Chew E.Y., Tsai J.Y., Sackler R.S., Haynes C., et al. Complement factor H polymorphism in age-related macular degeneration. Science 2005, 308:385-389.
    • (2005) Science , vol.308 , pp. 385-389
    • Klein, R.J.1    Zeiss, C.2    Chew, E.Y.3    Tsai, J.Y.4    Sackler, R.S.5    Haynes, C.6
  • 25
    • 0033624575 scopus 로고    scopus 로고
    • The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
    • Altshuler D., Hirschhorn J.N., Klannemark M., Lindgren C.M., Vohl M.C., Nemesh J., et al. The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. Nat Genet 2000, 26:76-80.
    • (2000) Nat Genet , vol.26 , pp. 76-80
    • Altshuler, D.1    Hirschhorn, J.N.2    Klannemark, M.3    Lindgren, C.M.4    Vohl, M.C.5    Nemesh, J.6
  • 26
    • 0242524453 scopus 로고    scopus 로고
    • The inherited basis of diabetes mellitus: Implications for the genetic analysis of complex traits
    • Florez J.C., Hirschhorn J., Altshuler D. The inherited basis of diabetes mellitus: Implications for the genetic analysis of complex traits. Annu Rev Genomics Hum Genet 2003, 4:257-291.
    • (2003) Annu Rev Genomics Hum Genet , vol.4 , pp. 257-291
    • Florez, J.C.1    Hirschhorn, J.2    Altshuler, D.3
  • 27
    • 34249895023 scopus 로고    scopus 로고
    • Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
    • Zeggini E., Weedon M.N., Lindgren C.M., Frayling T.M., Elliott K.S., Lango H., et al. Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Science 2007, 316:1336-1341.
    • (2007) Science , vol.316 , pp. 1336-1341
    • Zeggini, E.1    Weedon, M.N.2    Lindgren, C.M.3    Frayling, T.M.4    Elliott, K.S.5    Lango, H.6
  • 28
    • 3242713277 scopus 로고    scopus 로고
    • A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis
    • Begovich A.B., Carlton V.E., Honigberg L.A., Schrodi S.J., Chokkalingam A.P., Alexander H.C., et al. A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. Am J Hum Genet 2004, 75:330-337.
    • (2004) Am J Hum Genet , vol.75 , pp. 330-337
    • Begovich, A.B.1    Carlton, V.E.2    Honigberg, L.A.3    Schrodi, S.J.4    Chokkalingam, A.P.5    Alexander, H.C.6
  • 29
    • 12144291502 scopus 로고    scopus 로고
    • A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes
    • Bottini N., Musumeci L., Alonso A., Rahmouni S., Nika K., Rostamkhani M., et al. A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes. Nat Genet 2004, 36:337-338.
    • (2004) Nat Genet , vol.36 , pp. 337-338
    • Bottini, N.1    Musumeci, L.2    Alonso, A.3    Rahmouni, S.4    Nika, K.5    Rostamkhani, M.6
  • 30
    • 0035978533 scopus 로고    scopus 로고
    • A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
    • Ogura Y., Bonen D.K., Inohara N., Nicolae D.L., Chen F.F., Ramos R., et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 2001, 411:603-606.
    • (2001) Nature , vol.411 , pp. 603-606
    • Ogura, Y.1    Bonen, D.K.2    Inohara, N.3    Nicolae, D.L.4    Chen, F.F.5    Ramos, R.6
  • 31
    • 84856036754 scopus 로고    scopus 로고
    • Stroke genetics
    • Markus H.S. Stroke genetics. Hum Mol Genet 2011, 20(R2):R124-R131.
    • (2011) Hum Mol Genet , vol.20 , Issue.R2 , pp. R124-R131
    • Markus, H.S.1
  • 32
    • 77956419347 scopus 로고    scopus 로고
    • The association of the 4q25 susceptibility variant for atrial fibrillation with stroke is limited to stroke of cardioembolic etiology
    • Lemmens R., Buysschaert I., Geelen V., Fernandez-Cadenas I., Montaner J., Schmidt H., et al. The association of the 4q25 susceptibility variant for atrial fibrillation with stroke is limited to stroke of cardioembolic etiology. Stroke 2010, 41:1850-1857.
    • (2010) Stroke , vol.41 , pp. 1850-1857
    • Lemmens, R.1    Buysschaert, I.2    Geelen, V.3    Fernandez-Cadenas, I.4    Montaner, J.5    Schmidt, H.6
  • 35
    • 84863393715 scopus 로고    scopus 로고
    • Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
    • International Stroke Genetics Consortium (ISGC), Wellcome Trust Case Control Consortium 2 (WTCCC2)
    • Bellenguez C., Bevan S., Gschwendtner A., Spencer C.C., Burgess A.I., Pirinen M., et al. Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nat Genet 2012, 44:328-333. International Stroke Genetics Consortium (ISGC), Wellcome Trust Case Control Consortium 2 (WTCCC2).
    • (2012) Nat Genet , vol.44 , pp. 328-333
    • Bellenguez, C.1    Bevan, S.2    Gschwendtner, A.3    Spencer, C.C.4    Burgess, A.I.5    Pirinen, M.6
  • 36
    • 33846587067 scopus 로고    scopus 로고
    • A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction
    • Kubo M., Hata J., Ninomiya T., Matsuda K., Yonemoto K., Nakano T., et al. A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction. Nat Genet 2007, 39:212-217.
    • (2007) Nat Genet , vol.39 , pp. 212-217
    • Kubo, M.1    Hata, J.2    Ninomiya, T.3    Matsuda, K.4    Yonemoto, K.5    Nakano, T.6
  • 40
    • 34250735539 scopus 로고    scopus 로고
    • Copy number variation in the human genome and its implications for cardiovascular disease
    • Pollex R.L., Hegele R.A. Copy number variation in the human genome and its implications for cardiovascular disease. Circulation 2007, 115:3130-3138.
    • (2007) Circulation , vol.115 , pp. 3130-3138
    • Pollex, R.L.1    Hegele, R.A.2
  • 42
    • 78149491805 scopus 로고    scopus 로고
    • Emerging role of epigenetics in stroke: Part 1: DNA methylation and chromatin modifications
    • Qureshi I.A., Mehler M.F. Emerging role of epigenetics in stroke: Part 1: DNA methylation and chromatin modifications. Arch Neurol 2010, 67:1316-1322.
    • (2010) Arch Neurol , vol.67 , pp. 1316-1322
    • Qureshi, I.A.1    Mehler, M.F.2
  • 46
    • 84870384401 scopus 로고    scopus 로고
    • SigCS base: An integrated genetic information resource for human cerebral stroke
    • S10.0509-5-S2-S10. Epub 2011 Dec 14
    • Park Y.K., Bang O.S., Cha M.H., Kim J., Cole J.W., Lee D., et al. SigCS base: An integrated genetic information resource for human cerebral stroke. BMC Syst Biol. 2011, 14(5 Suppl 2.). S10.0509-5-S2-S10. Epub 2011 Dec 14.
    • (2011) BMC Syst Biol. , vol.14 , Issue.5
    • Park, Y.K.1    Bang, O.S.2    Cha, M.H.3    Kim, J.4    Cole, J.W.5    Lee, D.6
  • 48
    • 78649506925 scopus 로고    scopus 로고
    • Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus
    • Bell C.G., Finer S., Lindgren C.M., Wilson G.A., Rakyan V.K., Teschendorff A.E., et al. Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus. PLoS One 2010, 5:e14040.
    • (2010) PLoS One , vol.5 , pp. e14040
    • Bell, C.G.1    Finer, S.2    Lindgren, C.M.3    Wilson, G.A.4    Rakyan, V.K.5    Teschendorff, A.E.6


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