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Volumn 44, Issue 10, 2012, Pages 1147-1151

Common variants at 6p21.1 are associated with large artery atherosclerotic stroke

(59)  Holliday, Elizabeth G a,b   Maguire, Jane M b,c,d   Evans, Tiffany Jane b,c   Koblar, Simon A e,f   Jannes, Jim e,f   Sturm, Jonathan W a,d   Hankey, Graeme J g,h   Baker, Ross g,i   Golledge, Jonathan j,k   Parsons, Mark W b   Malik, Rainer l   McEvoy, Mark a,b   Biros, Erik j   Lewis, Martin D e   Lincz, Lisa F b,c,m   Peel, Roseanne a,b   Oldmeadow, Christopher a,b   Smith, Wayne a,b   Moscato, Pablo b,n   Barlera, Simona o   more..


Author keywords

[No Author keywords available]

Indexed keywords

APOL1 GENE; APOL4 GENE; ARTERY DIAMETER; ARTICLE; AUSTRALIA; BRAIN ATHEROSCLEROSIS; BRAIN ISCHEMIA; CHROMOSOME 22Q; CHROMOSOME 6P; COHORT ANALYSIS; CONTROLLED STUDY; GENE; GENE CLUSTER; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; LARGE ARTERY ATHEROSCLEROTIC STROKE; MAJOR CLINICAL STUDY; PHENOTYPE; PRIORITY JOURNAL; REPLICATION STUDY; SLC5A4 GENE;

EID: 84866930896     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.2397     Document Type: Article
Times cited : (157)

References (37)
  • 1
    • 14844337377 scopus 로고    scopus 로고
    • World Health Organization World Health Organization Geneva
    • World Health Organization. Atlas of Heart Disease and Stroke. (World Health Organization, Geneva, 2004).
    • (2004) Atlas of Heart Disease and Stroke
  • 2
    • 62149099593 scopus 로고    scopus 로고
    • Worldwide stroke incidence and early case fatality reported in 56 population-based studies: A systematic review
    • Feigin, V.L., Lawes, C.M., Bennett, D.A., Barker-Collo, S.L. & Parag, V. Worldwide stroke incidence and early case fatality reported in 56 population-based studies: a systematic review. Lancet Neurol. 8, 355-369 (2009).
    • (2009) Lancet Neurol. , vol.8 , pp. 355-369
    • Feigin, V.L.1    Lawes, C.M.2    Bennett, D.A.3    Barker-Collo, S.L.4    Parag, V.5
  • 3
    • 33846245504 scopus 로고    scopus 로고
    • Preventing stroke: Saving lives around the world
    • Strong, K., Mathers, C. & Bonita, R. Preventing stroke: saving lives around the world. Lancet Neurol. 6, 182-187 (2007).
    • (2007) Lancet Neurol. , vol.6 , pp. 182-187
    • Strong, K.1    Mathers, C.2    Bonita, R.3
  • 4
    • 77955014011 scopus 로고    scopus 로고
    • Risk factors for ischaemic and intracerebral haemorrhagic stroke in 22 countries (the INTERSTROKE study): A case-control study
    • O'Donnell, M.J. et al. Risk factors for ischaemic and intracerebral haemorrhagic stroke in 22 countries (the INTERSTROKE study): a case-control study. Lancet 376, 112-123 (2010).
    • (2010) Lancet , vol.376 , pp. 112-123
    • O'Donnell, M.J.1
  • 5
    • 0346726097 scopus 로고    scopus 로고
    • Systematic review of methods and results of studies of the genetic epidemiology of ischemic stroke
    • Flossmann, E., Schulz, U.G. & Rothwell, P.M. Systematic review of methods and results of studies of the genetic epidemiology of ischemic stroke. Stroke 35, 212-227 (2004).
    • (2004) Stroke , vol.35 , pp. 212-227
    • Flossmann, E.1    Schulz, U.G.2    Rothwell, P.M.3
  • 6
    • 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 34, 1364-1369 (2003).
    • (2003) Stroke , vol.34 , pp. 1364-1369
    • Jerrard-Dunne, P.1    Cloud, G.2    Hassan, A.3    Markus, H.S.4
  • 7
    • 0037319447 scopus 로고    scopus 로고
    • Genetic and environmental contributions to atherosclerosis phenotypes in men and women: Heritability of carotid intima-media thickness in the Framingham Heart Study
    • Fox, C.S. et al. Genetic and environmental contributions to atherosclerosis phenotypes in men and women: heritability of carotid intima-media thickness in the Framingham Heart Study. Stroke 34, 397-401 (2003).
    • (2003) Stroke , vol.34 , pp. 397-401
    • Fox, C.S.1
  • 8
    • 11144242572 scopus 로고    scopus 로고
    • Heritability of carotid artery atherosclerotic lesions: An ultrasound study in 154 families
    • Moskau, S. et al. Heritability of carotid artery atherosclerotic lesions: an ultrasound study in 154 families. Stroke 36, 5-8 (2005).
    • (2005) Stroke , vol.36 , pp. 5-8
    • Moskau, S.1
  • 9
    • 0842289489 scopus 로고    scopus 로고
    • Heritability of leukoaraiosis in hypertensive sibships
    • Turner, S.T. et al. Heritability of leukoaraiosis in hypertensive sibships. Hypertension 43, 483-487 (2004).
    • (2004) Hypertension , vol.43 , pp. 483-487
    • Turner, S.T.1
  • 10
    • 0031778072 scopus 로고    scopus 로고
    • Evidence for genetic variance in white matter hyperintensity volume in normal elderly male twins
    • Carmelli, D. et al. Evidence for genetic variance in white matter hyperintensity volume in normal elderly male twins. Stroke 29, 1177-1181 (1998).
    • (1998) Stroke , vol.29 , pp. 1177-1181
    • Carmelli, D.1
  • 11
    • 64849095095 scopus 로고    scopus 로고
    • Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation
    • Kääb, S. et al. Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation. Eur. Heart J. 30, 813-819 (2009).
    • (2009) Eur. Heart J. , vol.30 , pp. 813-819
    • Kääb, S.1
  • 12
    • 55849100349 scopus 로고    scopus 로고
    • Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke
    • Gretarsdottir, S. et al. Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. Ann. Neurol. 64, 402-409 (2008).
    • (2008) Ann. Neurol. , vol.64 , pp. 402-409
    • Gretarsdottir, S.1
  • 13
    • 77149160077 scopus 로고    scopus 로고
    • Association between 9p21 genomic markers and heart disease: A meta-analysis
    • Palomaki, G.E., Melillo, S. & Bradley, L.A. Association between 9p21 genomic markers and heart disease: a meta-analysis. J. Am. Med. Assoc. 303, 648-656 (2010).
    • (2010) J. Am. Med. Assoc. , vol.303 , pp. 648-656
    • Palomaki, G.E.1    Melillo, S.2    Bradley, L.A.3
  • 14
    • 70449110469 scopus 로고    scopus 로고
    • Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: A large-scale genetic association study
    • Smith, J.G. et al. Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study. Circ. Cardiovasc. Genet. 2, 159-164 (2009).
    • (2009) Circ. Cardiovasc. Genet. , vol.2 , pp. 159-164
    • Smith, J.G.1
  • 15
    • 84863393715 scopus 로고    scopus 로고
    • Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
    • Bellenguez, C. et al. Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nat. Genet. 44, 328-333 (2012).
    • (2012) Nat. Genet. , vol.44 , pp. 328-333
    • Bellenguez, C.1
  • 16
    • 0027514354 scopus 로고
    • Classification of subtype of acute ischemic stroke Definitions for use in a multicenter clinical trial TOAST Trial of Org 10172 in Acute Stroke Treatment
    • Adams, H.P. Jr. et al. Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment. Stroke 24, 35-41 (1993).
    • (1993) Stroke , vol.24 , pp. 35-41
    • Adams Jr., H.P.1
  • 17
    • 11444269309 scopus 로고    scopus 로고
    • Potential confounding by intermediate phenotypes in studies of the genetics of ischaemic stroke
    • Flossmann, E., Schulz, U.G. & Rothwell, P.M. Potential confounding by intermediate phenotypes in studies of the genetics of ischaemic stroke. Cerebrovasc. Dis. 19, 1-10 (2005).
    • (2005) Cerebrovasc. Dis. , vol.19 , pp. 1-10
    • Flossmann, E.1    Schulz, U.G.2    Rothwell, P.M.3
  • 19
    • 65549104157 scopus 로고    scopus 로고
    • Histone modifications at human enhancers reflect global cell-type-specific gene expression
    • Heintzman, N.D. et al. Histone modifications at human enhancers reflect global cell-type-specific gene expression. Nature 459, 108-112 (2009).
    • (2009) Nature , vol.459 , pp. 108-112
    • Heintzman, N.D.1
  • 20
    • 0035872826 scopus 로고    scopus 로고
    • The human apolipoprotein L gene cluster: Identification, classification, and sites of distribution
    • Page, N.M., Butlin, D.J., Lomthaisong, K. & Lowry, P.J. The human apolipoprotein L gene cluster: identification, classification, and sites of distribution. Genomics 74, 71-78 (2001).
    • (2001) Genomics , vol.74 , pp. 71-78
    • Page, N.M.1    Butlin, D.J.2    Lomthaisong, K.3    Lowry, P.J.4
  • 21
    • 0033846760 scopus 로고    scopus 로고
    • Plasma apolipoprotein L concentrations correlate with plasma triglycerides and cholesterol levels in normolipidemic, hyperlipidemic, and diabetic subjects
    • Duchateau, P.N. et al. Plasma apolipoprotein L concentrations correlate with plasma triglycerides and cholesterol levels in normolipidemic, hyperlipidemic, and diabetic subjects. J. Lipid Res. 41, 1231-1236 (2000).
    • (2000) J. Lipid Res. , vol.41 , pp. 1231-1236
    • Duchateau, P.N.1
  • 22
    • 0033562558 scopus 로고    scopus 로고
    • Vascular endothelial genes that are responsive to tumor necrosis factor-α in vitro are expressed in atherosclerotic lesions, including inhibitor of apoptosis protein-1, stannin, and two novel genes
    • Horrevoets, A.J. et al. Vascular endothelial genes that are responsive to tumor necrosis factor-α in vitro are expressed in atherosclerotic lesions, including inhibitor of apoptosis protein-1, stannin, and two novel genes. Blood 93, 3418-3431 (1999).
    • (1999) Blood , vol.93 , pp. 3418-3431
    • Horrevoets, A.J.1
  • 23
    • 0036212122 scopus 로고    scopus 로고
    • The apolipoprotein L gene cluster has emerged recently in evolution and is expressed in human vascular tissue
    • Monajemi, H., Fontijn, R.D., Pannekoek, H. & Horrevoets, A.J. The apolipoprotein L gene cluster has emerged recently in evolution and is expressed in human vascular tissue. Genomics 79, 539-546 (2002).
    • (2002) Genomics , vol.79 , pp. 539-546
    • Monajemi, H.1    Fontijn, R.D.2    Pannekoek, H.3    Horrevoets, A.J.4
  • 24
    • 14644402496 scopus 로고    scopus 로고
    • Microarray analysis of primary endothelial cells challenged with different inflammatory and immune cytokines
    • Sana, T.R., Janatpour, M.J., Sathe, M., McEvoy, L.M. & McClanahan, T.K. Microarray analysis of primary endothelial cells challenged with different inflammatory and immune cytokines. Cytokine 29, 256-269 (2005).
    • (2005) Cytokine , vol.29 , pp. 256-269
    • Sana, T.R.1    Janatpour, M.J.2    Sathe, M.3    McEvoy, L.M.4    McClanahan, T.K.5
  • 25
    • 77956410251 scopus 로고    scopus 로고
    • Cohort profile: The Hunter Community Study
    • McEvoy, M. et al. Cohort profile: The Hunter Community Study. Int. J. Epidemiol. 39, 1452-1463 (2010).
    • (2010) Int. J. Epidemiol. , vol.39 , pp. 1452-1463
    • McEvoy, M.1
  • 26
    • 77954140531 scopus 로고    scopus 로고
    • Common SNPs explain a large proportion of the heritability for human height
    • Yang, J. et al. Common SNPs explain a large proportion of the heritability for human height. Nat. Genet. 42, 565-569 (2010).
    • (2010) Nat. Genet. , vol.42 , pp. 565-569
    • Yang, J.1
  • 27
    • 79952489475 scopus 로고    scopus 로고
    • Estimating missing heritability for disease from genome-wide association studies
    • Lee, S.H., Wray, N.R., Goddard, M.E. & Visscher, P.M. Estimating missing heritability for disease from genome-wide association studies. Am. J. Hum. Genet. 88, 294-305 (2011).
    • (2011) Am. J. Hum. Genet. , vol.88 , pp. 294-305
    • Lee, S.H.1    Wray, N.R.2    Goddard, M.E.3    Visscher, P.M.4
  • 28
    • 78651226264 scopus 로고    scopus 로고
    • Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis
    • Painter, J.N. et al. Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nat. Genet. 43, 51-54 (2011).
    • (2011) Nat. Genet. , vol.43 , pp. 51-54
    • Painter, J.N.1
  • 29
    • 58149345887 scopus 로고    scopus 로고
    • Practical aspects of imputation-driven meta-analysis of genome-wide association studies
    • de Bakker, P.I. et al. Practical aspects of imputation-driven meta-analysis of genome-wide association studies. Hum. Mol. Genet. 17, R122-R128 (2008).
    • (2008) Hum. Mol. Genet. , vol.17
    • De Bakker, P.I.1
  • 31
    • 78649508578 scopus 로고    scopus 로고
    • MaCH: Using sequence and genotype data to estimate haplotypes and unobserved genotypes
    • Li, Y., Willer, C.J., Ding, J., Scheet, P. & Abecasis, G.R. MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet. Epidemiol. 34, 816-834 (2010).
    • (2010) Genet. Epidemiol. , vol.34 , pp. 816-834
    • Li, Y.1    Willer, C.J.2    Ding, J.3    Scheet, P.4    Abecasis, G.R.5
  • 32
    • 13444269543 scopus 로고    scopus 로고
    • Haploview: Analysis and visualization of LD and haplotype maps
    • Barrett, J.C., Fry, B., Maller, J. & Daly, M.J. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 21, 263-265 (2005).
    • (2005) Bioinformatics , vol.21 , pp. 263-265
    • Barrett, J.C.1    Fry, B.2    Maller, J.3    Daly, M.J.4
  • 33
    • 41649094148 scopus 로고    scopus 로고
    • Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data
    • Dudbridge, F. Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data. Hum. Hered. 66, 87-98 (2008).
    • (2008) Hum. Hered. , vol.66 , pp. 87-98
    • Dudbridge, F.1
  • 34
    • 77956586071 scopus 로고    scopus 로고
    • LocusZoom: Regional visualization of genome-wide association scan results
    • Pruim, R.J. et al. LocusZoom: regional visualization of genome-wide association scan results. Bioinformatics 26, 2336-2337 (2010).
    • (2010) Bioinformatics , vol.26 , pp. 2336-2337
    • Pruim, R.J.1
  • 35
    • 40049098166 scopus 로고    scopus 로고
    • Cumulative association of five genetic variants with prostate cancer
    • Zheng, S.L. et al. Cumulative association of five genetic variants with prostate cancer. N. Engl. J. Med. 358, 910-919 (2008).
    • (2008) N. Engl. J. Med. , vol.358 , pp. 910-919
    • Zheng, S.L.1
  • 36
    • 77949558576 scopus 로고    scopus 로고
    • Stata Corp StataCorp LP, College Station, Texas
    • StataCorp. Stata: Release 11. Statistical Software. (StataCorp LP, College Station, Texas, 2009).
    • (2009) Stata: Release 11. Statistical Software
  • 37
    • 64149105182 scopus 로고    scopus 로고
    • Genetic control of human brain transcript expression in Alzheimer disease
    • Webster, J.A. et al. Genetic control of human brain transcript expression in Alzheimer disease. Am. J. Hum. Genet. 84, 445-458 (2009).
    • (2009) Am. J. Hum. Genet. , vol.84 , pp. 445-458
    • Webster, J.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.