메뉴 건너뛰기




Volumn 39, Issue 2, 2008, Pages 252-254

Update on the genetics of stroke and cerebrovascular disease 2007

Author keywords

Cerebrovascular disease; Genetics; Stroke

Indexed keywords

DNA MARKER;

EID: 39349090859     PISSN: 00392499     EISSN: None     Source Type: Journal    
DOI: 10.1161/STROKEAHA.107.510503     Document Type: Review
Times cited : (7)

References (30)
  • 2
    • 34250010480 scopus 로고    scopus 로고
    • Helgadottir A, Thorleifsson G, Manolescu A, Gretarsdottir S, Blondal T, Jonasdottir A, Jonasdottir A, Sigurdsson A, Baker A, Palsson A, Masson G, Gudbjartsson DF, Magnusson KP, Andersen K, Levey AI, Backman VM, Matthiasdottir S, Jonsdottir T, Palsson S, Einarsdottir H, Gunnarsdottir S, Gylfason A, Vaccarino V, Hooper WC, Reilly MP, Granger CB, Austin H, Rader DJ, Shah SH, Quyyumi AA, Gulcher JR, Thorgeirsson G, Thorsteinsdottir U, Kong A, Stefansson K. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science. 2007;316:1491-1493.
    • Helgadottir A, Thorleifsson G, Manolescu A, Gretarsdottir S, Blondal T, Jonasdottir A, Jonasdottir A, Sigurdsson A, Baker A, Palsson A, Masson G, Gudbjartsson DF, Magnusson KP, Andersen K, Levey AI, Backman VM, Matthiasdottir S, Jonsdottir T, Palsson S, Einarsdottir H, Gunnarsdottir S, Gylfason A, Vaccarino V, Hooper WC, Reilly MP, Granger CB, Austin H, Rader DJ, Shah SH, Quyyumi AA, Gulcher JR, Thorgeirsson G, Thorsteinsdottir U, Kong A, Stefansson K. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science. 2007;316:1491-1493.
  • 3
    • 84969213492 scopus 로고    scopus 로고
    • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
    • Wellcome Trust Case Control Consortium
    • Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007;447:661-678.
    • (2007) Nature , vol.447 , pp. 661-678
  • 4
    • 34547623750 scopus 로고    scopus 로고
    • Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, Dixon RJ, Meitinger T, Braund P, Wichmann HE, Barrett JH, Konig IR, Stevens SE, Szymczak S, Tregouet DA, Iles MM, Pahlke F, Pollard H, Lieb W, Cambien F, Fischer M, Ouwehand W, Blankenberg S, Balmforth AJ, Baessler A, Ball SG, Strom TM, Braenne I, Gieger C, Deloukas P, Tobin MD, Ziegler A, Thompson JR, Schunkert H; WTCCC and the Cardiogenics Consortium. Genomewide association analysis of coronary artery disease. N Engl J Med. 2007;357:443-453.
    • Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, Dixon RJ, Meitinger T, Braund P, Wichmann HE, Barrett JH, Konig IR, Stevens SE, Szymczak S, Tregouet DA, Iles MM, Pahlke F, Pollard H, Lieb W, Cambien F, Fischer M, Ouwehand W, Blankenberg S, Balmforth AJ, Baessler A, Ball SG, Strom TM, Braenne I, Gieger C, Deloukas P, Tobin MD, Ziegler A, Thompson JR, Schunkert H; WTCCC and the Cardiogenics Consortium. Genomewide association analysis of coronary artery disease. N Engl J Med. 2007;357:443-453.
  • 9
    • 34249888775 scopus 로고    scopus 로고
    • Diabetes Genetics Initiative of Broad Institute of Harvard and MIT, Lund University, and Novartis Institutes of BioMedical Research, Saxena R, Voight BF, Lyssenko V, Burtt NP, de Bakker PI, Chen H, Roix JJ, Kathiresan S, Hirschhorn JN, Daly MJ, Hughes TE, Groop L, Altshuler D, Almgren P, Florez JC, Meyer J, Ardlie K, Bengtsson Bostrom K, Isomaa B, Lettre G, Lindblad U, Lyon HN, Melander O, Newton-Cheh C, Nilsson P, Orho-Melander M, Rastam L, Speliotes EK, Taskinen MR, Tuomi T, Guiducci C, Berglund A, Carlson J, Gianniny L, Hackett R, Hall L, Holmkvist J, Laurila E, Sjogren M, Sterner M, Surti A, Svensson M, Tewhey R, Blumenstiel B, Parkin M, Defelice M, Barry R, Brodeur W, Camarata J, Chia N, Fava M, Gibbons J, Handsaker B, Healy C, Nguyen K, Gates C, Sougnez C, Gage D, Nizzari M, Gabriel SB, Chirn GW, Ma Q, Parikh H, Richardson D, Ricke D, Purcell S. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science. 2007;316:1331-1336
    • Diabetes Genetics Initiative of Broad Institute of Harvard and MIT, Lund University, and Novartis Institutes of BioMedical Research, Saxena R, Voight BF, Lyssenko V, Burtt NP, de Bakker PI, Chen H, Roix JJ, Kathiresan S, Hirschhorn JN, Daly MJ, Hughes TE, Groop L, Altshuler D, Almgren P, Florez JC, Meyer J, Ardlie K, Bengtsson Bostrom K, Isomaa B, Lettre G, Lindblad U, Lyon HN, Melander O, Newton-Cheh C, Nilsson P, Orho-Melander M, Rastam L, Speliotes EK, Taskinen MR, Tuomi T, Guiducci C, Berglund A, Carlson J, Gianniny L, Hackett R, Hall L, Holmkvist J, Laurila E, Sjogren M, Sterner M, Surti A, Svensson M, Tewhey R, Blumenstiel B, Parkin M, Defelice M, Barry R, Brodeur W, Camarata J, Chia N, Fava M, Gibbons J, Handsaker B, Healy C, Nguyen K, Gates C, Sougnez C, Gage D, Nizzari M, Gabriel SB, Chirn GW, Ma Q, Parikh H, Richardson D, Ricke D, Purcell S. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science. 2007;316:1331-1336.
  • 13
    • 34250019387 scopus 로고    scopus 로고
    • Genomics: Guilt by association
    • Bowcock AM. Genomics: guilt by association. Nature. 447, 645-646.
    • Nature , vol.447 , pp. 645-646
    • Bowcock, A.M.1
  • 14
    • 34547629039 scopus 로고    scopus 로고
    • Scanning the genome for coronary risk
    • Rosenzweig A. Scanning the genome for coronary risk. N Engl J Med. 2007;357:497-499.
    • (2007) N Engl J Med , vol.357 , pp. 497-499
    • Rosenzweig, A.1
  • 15
    • 37349059633 scopus 로고    scopus 로고
    • Biomarker and genetic data: Association studies in an era of too much information
    • Loscalzo J. Biomarker and genetic data: association studies in an era of too much information. Circulation. 2007;116:1866-1870.
    • (2007) Circulation , vol.116 , pp. 1866-1870
    • Loscalzo, J.1
  • 17
    • 0036065699 scopus 로고    scopus 로고
    • SNP judgments and freedom of association
    • Hegele RA. SNP judgments and freedom of association. Arterioscler Thromb Vasc Biol. 2002;22:1058-1061.
    • (2002) Arterioscler Thromb Vasc Biol , vol.22 , pp. 1058-1061
    • Hegele, R.A.1
  • 18
    • 24644436338 scopus 로고    scopus 로고
    • Genetic association studies in stroke: Methodological issues and proposed standard criteria
    • Dichgans M, Markus HS. 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
  • 20
    • 38449110694 scopus 로고    scopus 로고
    • Mutation of the p16/CDKN2 gene and loss of heterozygosity in malignant mucosal melanoma and adenoid cystic carcinoma of the head and neck
    • Suzuki N, Onda T, Yamamoto N, Katakura A, Mizoe JE, Shibahara T. Mutation of the p16/CDKN2 gene and loss of heterozygosity in malignant mucosal melanoma and adenoid cystic carcinoma of the head and neck. Int J Oncol. 2007;31:1061-1067.
    • (2007) Int J Oncol , vol.31 , pp. 1061-1067
    • Suzuki, N.1    Onda, T.2    Yamamoto, N.3    Katakura, A.4    Mizoe, J.E.5    Shibahara, T.6
  • 21
    • 34848886609 scopus 로고    scopus 로고
    • Two common gene variants on chromosome 9 and risk of atherothrombosis
    • Zee RY, Ridker PM. Two common gene variants on chromosome 9 and risk of atherothrombosis. Stroke. 2007;38:e111.
    • (2007) Stroke , vol.38
    • Zee, R.Y.1    Ridker, P.M.2
  • 22
    • 44449176689 scopus 로고    scopus 로고
    • Whole genome analysis suggests ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21
    • in press
    • Matarin M, Brown M, Singleton A, Hardy JA, Meschia JF. Whole genome analysis suggests ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21. Stroke. 2008; in press.
    • (2008) Stroke
    • Matarin, M.1    Brown, M.2    Singleton, A.3    Hardy, J.A.4    Meschia, J.F.5
  • 25
    • 35548976654 scopus 로고    scopus 로고
    • Hamshere ML, Holmans PA, Avramopoulos D, Bassett SS, Blacker D, Bertram L, Wiener H, Rochberg N, Tanzi RE, Myers A, Wavrant-De Vrieze F, Go R, Fallin D, Lovestone S, Hardy J, Goate A, O'donovan M, Williams J, Owen MJ Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's Disease. Hum Mol Genet. 2007;16:2703-2712.
    • Hamshere ML, Holmans PA, Avramopoulos D, Bassett SS, Blacker D, Bertram L, Wiener H, Rochberg N, Tanzi RE, Myers A, Wavrant-De Vrieze F, Go R, Fallin D, Lovestone S, Hardy J, Goate A, O'donovan M, Williams J, Owen MJ Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's Disease. Hum Mol Genet. 2007;16:2703-2712.
  • 26
    • 34249699119 scopus 로고    scopus 로고
    • Phenomics and lamins: From disease to therapy
    • Hegele RA, Oshima J. Phenomics and lamins: from disease to therapy. Exp Cell Res. 2007;313:2134-2143.
    • (2007) Exp Cell Res , vol.313 , pp. 2134-2143
    • Hegele, R.A.1    Oshima, J.2
  • 27
    • 34447515621 scopus 로고    scopus 로고
    • Gudbjartsson DF, Arnar DO, Helgadottir A, Gretarsdottir S, Holm H, Sigurdsson A, Jonasdottir A, Baker A, Thorleifsson G, Kristjansson K, Palsson A, BlondalT, Sulem P, Backman VM, Hardarson GA, Palsdottir E, Helgason A, Sigurjonsdottir R, Sverrisson JT, Kostulas K, Ng MC, Baum L, So WY, Wong KS, Chan JC, Furie KL, Greenberg SM, Sale M, Kelly P, MacRae CA, Smith EE, Rosand J, Hillert J, Ma RC, Ellinor PT, Thorgeirsson G, Gulcher JR, Kong A, Thorsteinsdottir U, Stefansson K. Variants conferring risk of atrial fibrillation on chromosome 4q25. Nature. 2007;448:353-357.
    • Gudbjartsson DF, Arnar DO, Helgadottir A, Gretarsdottir S, Holm H, Sigurdsson A, Jonasdottir A, Baker A, Thorleifsson G, Kristjansson K, Palsson A, BlondalT, Sulem P, Backman VM, Hardarson GA, Palsdottir E, Helgason A, Sigurjonsdottir R, Sverrisson JT, Kostulas K, Ng MC, Baum L, So WY, Wong KS, Chan JC, Furie KL, Greenberg SM, Sale M, Kelly P, MacRae CA, Smith EE, Rosand J, Hillert J, Ma RC, Ellinor PT, Thorgeirsson G, Gulcher JR, Kong A, Thorsteinsdottir U, Stefansson K. Variants conferring risk of atrial fibrillation on chromosome 4q25. Nature. 2007;448:353-357.
  • 28
    • 33751329250 scopus 로고    scopus 로고
    • Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, Chen W, Cho EK, Dallaire S, Freeman JL, Gonzalez JR, Gratacos M, Huang J, Kalaitzopoulos D, Komura D, MacDonald JR, Marshall CR, Mei R, Montgomery L, Nishimura K, Okamura K, Shen F, Somerville MJ, Tchinda J, Valsesia A, Woodwark C, Yang F, Zhang J, Zerjal T, Zhang J, Armengol L, Conrad DF, Estivill X, Tyler-Smith C, Carter NP, Aburatani H, Lee C, Jones KW, Scherer SW, Hurles ME. Global variation in copy number in the human genome. Nature. 2006;444:444-454.
    • Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, Chen W, Cho EK, Dallaire S, Freeman JL, Gonzalez JR, Gratacos M, Huang J, Kalaitzopoulos D, Komura D, MacDonald JR, Marshall CR, Mei R, Montgomery L, Nishimura K, Okamura K, Shen F, Somerville MJ, Tchinda J, Valsesia A, Woodwark C, Yang F, Zhang J, Zerjal T, Zhang J, Armengol L, Conrad DF, Estivill X, Tyler-Smith C, Carter NP, Aburatani H, Lee C, Jones KW, Scherer SW, Hurles ME. Global variation in copy number in the human genome. Nature. 2006;444:444-454.
  • 29
    • 34250735539 scopus 로고    scopus 로고
    • Copy number variation in the human genome and its implications for cardiovascular disease
    • Pollex RL, Hegele RA. 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.