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Volumn 27, Issue 1, 2009, Pages 73-94

Genomics: Implications for anesthesia, perioperative care and outcomes

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EID: 84861371524     PISSN: 07376146     EISSN: None     Source Type: Book Series    
DOI: 10.1016/j.aan.2009.07.006     Document Type: Review
Times cited : (2)

References (8)
  • 1
    • 0036255811 scopus 로고    scopus 로고
    • Opinion: Candidate-gene approaches for studying complex genetic traits: practical considerations
    • Tabor HK, Risch NJ, Myers RM. Opinion: Candidate-gene approaches for studying complex genetic traits: practical considerations. Nat Rev Genet 2002;3(5):391-7.
    • (2002) Nat Rev Genet , vol.3 , Issue.5 , pp. 391-397
    • Tabor, H.K.1    Risch, N.J.2    Myers, R.M.3
  • 2
    • 58749095297 scopus 로고    scopus 로고
    • Cost-effectiveness of using pharmacogenetic information in warfarin dosing for patients with nonvalvular atrial fibrillation
    • Eckman MH, Rosand J, Greenberg SM, et al. Cost-effectiveness of using pharmacogenetic information in warfarin dosing for patients with nonvalvular atrial fibrillation. Ann Intern Med 2009;150(2):73-83.
    • (2009) Ann Intern Med , vol.150 , Issue.2 , pp. 73-83
    • Eckman, M.H.1    Rosand, J.2    Greenberg, S.M.3
  • 4
    • 37549036689 scopus 로고    scopus 로고
    • Prevalence of pathogenic BRCA1 mutation carriers in 5 US racial/ethnic groups
    • John EM, Miron A, Gong G, et al. Prevalence of pathogenic BRCA1 mutation carriers in 5 US racial/ethnic groups. JAMA 2007;298(24):2869-76.
    • (2007) JAMA , vol.298 , Issue.24 , pp. 2869-2876
    • John, E.M.1    Miron, A.2    Gong, G.3
  • 5
    • 78649996861 scopus 로고    scopus 로고
    • National Cancer Institute. Accessed August 10
    • National Cancer Institute. BRCA1 and BRCA2: cancer risk and genetic testing. Available at: http://www.cancer.gov/cancertopics/factsheet/risk.brca. Accessed August 10, 2009.
    • (2009) BRCA1 and BRCA2: cancer risk and genetic testing
  • 6
    • 58749087343 scopus 로고    scopus 로고
    • Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3
    • Paynter NP, Chasman DI, Buring JE, et al. Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3. Ann Intern Med 2009;150(2):65-72.
    • (2009) Ann Intern Med , vol.150 , Issue.2 , pp. 65-72
    • Paynter, N.P.1    Chasman, D.I.2    Buring, J.E.3
  • 7
    • 34447515621 scopus 로고    scopus 로고
    • Variants conferring risk of atrial fibrillation on chromosome 4q25
    • Gudbjartsson DF, Arnar DO, Helgadottir A, et al. Variants conferring risk of atrial fibrillation on chromosome 4q25. Nature 2007;448(7151):353-7.
    • (2007) Nature , vol.448 , Issue.7151 , pp. 353-357
    • Gudbjartsson, D.F.1    Arnar, D.O.2    Helgadottir, A.3
  • 8
    • 70449730582 scopus 로고    scopus 로고
    • Variation in the 4q25 chromosomal locus predicts newonset atrial fibrillation after cardiac surgery [abstract]
    • Body S, Collard C, Shernan S, et al. Variation in the 4q25 chromosomal locus predicts newonset atrial fibrillation after cardiac surgery [abstract]. Circulation 2008;118:S882.
    • (2008) Circulation , vol.118
    • Body, S.1    Collard, C.2    Shernan, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.