메뉴 건너뛰기




Volumn 34, Issue 10, 2003, Pages 2512-2516

Human genome sequence variation and the search for genes influencing stroke

Author keywords

Genetics; Human genome project; Stroke

Indexed keywords

DNA;

EID: 0141819132     PISSN: 00392499     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.STR.0000091844.02111.07     Document Type: Review
Times cited : (29)

References (22)
  • 5
    • 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 HP Jr, Bendixen BH, Kappelle LJ, Biller J, Love BB, Gordon DL, Marsh EE III. 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. 1993;24:35-41.
    • (1993) Stroke , vol.24 , pp. 35-41
    • Adams H.P., Jr.1    Bendixen, B.H.2    Kappelle, L.J.3    Biller, J.4    Love, B.B.5    Gordon, D.L.6    Marsh E.E. III7
  • 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
  • 10
    • 0026053092 scopus 로고
    • Low nucleotide diversity in man
    • Li WH, Sadler LA. Low nucleotide diversity in man. Genetics. 1991;129:513-523.
    • (1991) Genetics , vol.129 , pp. 513-523
    • Li, W.H.1    Sadler, L.A.2
  • 14
    • 0037381234 scopus 로고    scopus 로고
    • Quality and completeness of SNP databases
    • Reich DE, Gabriel SB, Altshuler D. Quality and completeness of SNP databases. Nat Genet. 2003;33:457-458.
    • (2003) Nat Genet , vol.33 , pp. 457-458
    • Reich, D.E.1    Gabriel, S.B.2    Altshuler, D.3
  • 17
    • 0037312921 scopus 로고    scopus 로고
    • Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
    • Lohmueller KE, Pearce CL, Pike M, Lander ES, Hirschhorn JN. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Nat Genet. 2003;33:177-182.
    • (2003) Nat Genet , vol.33 , pp. 177-182
    • Lohmueller, K.E.1    Pearce, C.L.2    Pike, M.3    Lander, E.S.4    Hirschhorn, J.N.5
  • 18
    • 0037047021 scopus 로고    scopus 로고
    • Stroke in the young: Coming of age
    • Kittner SJ. Stroke in the young: coming of age. Neurology. 2002;59:6-7.
    • (2002) Neurology , vol.59 , pp. 6-7
    • Kittner, S.J.1
  • 19
    • 0036901345 scopus 로고    scopus 로고
    • Addressing the heterogeneity of the ischemic stroke phenotype in human genetics research
    • Meschia JF. Addressing the heterogeneity of the ischemic stroke phenotype in human genetics research. Stroke. 2002;33:2770-2774.
    • (2002) Stroke , vol.33 , pp. 2770-2774
    • Meschia, J.F.1
  • 20
    • 0038823525 scopus 로고    scopus 로고
    • The endophenotype concept in psychiatry: Etymology and strategic intentions
    • Gottesman II, Gould TD. The endophenotype concept in psychiatry: etymology and strategic intentions. Am J Psychiatry. 2003;160:636-645.
    • (2003) Am J Psychiatry , vol.160 , pp. 636-645
    • Gottesman, I.I.1    Gould, T.D.2
  • 21
    • 0034969437 scopus 로고    scopus 로고
    • Are rare variants responsible for susceptibility to complex diseases?
    • Pritchard JK. Are rare variants responsible for susceptibility to complex diseases? Am J Hum Genet. 2001;69:124-137.
    • (2001) Am J Hum Genet , vol.69 , pp. 124-137
    • Pritchard, J.K.1
  • 22
    • 0036360439 scopus 로고    scopus 로고
    • Progress in high throughput SNP genotyping methods
    • Tsuchihashi Z, Dracopoli NC. Progress in high throughput SNP genotyping methods. Pharmacogenomics J. 2002;2:103-110.
    • (2002) Pharmacogenomics J , vol.2 , pp. 103-110
    • Tsuchihashi, Z.1    Dracopoli, N.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.