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Volumn 3, Issue 4, 2018, Pages 341-345

Association of racial/ethnic categories with the ability of genetic tests to detect a cause of cardiomyopathy

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ALASKA NATIVE; AMERICAN INDIAN; ARTICLE; ASIAN; BLACK PERSON; CARDIOMYOPATHY; CAUCASIAN; CHILD; COMPARATIVE STUDY; CONTROLLED STUDY; CROSS-SECTIONAL STUDY; DISEASE ASSOCIATION; ETHNIC DIFFERENCE; FAMILY HISTORY; FEMALE; GENETIC SCREENING; HEALTH CARE ACCESS; HEALTH CARE DISPARITY; HIGH RISK POPULATION; HISPANIC; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MASSACHUSETTS; NEWBORN; OUTCOME ASSESSMENT; PACIFIC ISLANDER; PREVALENCE; PRIORITY JOURNAL; RACE DIFFERENCE; SEX DIFFERENCE; ANCESTRY GROUP; ETHNIC GROUP; ETHNOLOGY; GENETICS; HEALTH CARE DELIVERY; MIDDLE AGED; PRESCHOOL CHILD; STANDARDS; STATISTICS AND NUMERICAL DATA; VERY ELDERLY; YOUNG ADULT;

EID: 85046040719     PISSN: 23806583     EISSN: 23806591     Source Type: Journal    
DOI: 10.1001/jamacardio.2017.5333     Document Type: Article
Times cited : (77)

References (9)
  • 1
    • 85030618497 scopus 로고    scopus 로고
    • Classification, epidemiology, and global burden of cardiomyopathies
    • McKenna WJ, Maron BJ, Thiene G. Classification, epidemiology, and global burden of cardiomyopathies. Circ Res. 2017;121(7):722-730.
    • (2017) Circ Res , vol.121 , Issue.7 , pp. 722-730
    • McKenna, W.J.1    Maron, B.J.2    Thiene, G.3
  • 3
    • 63149159240 scopus 로고    scopus 로고
    • The genetic bases for non-syndromic hearing loss among Chinese
    • Ouyang XM, Yan D, Yuan HJ, et al. The genetic bases for non-syndromic hearing loss among Chinese. J Hum Genet. 2009;54(3):131-140.
    • (2009) J Hum Genet , vol.54 , Issue.3 , pp. 131-140
    • Ouyang, X.M.1    Yan, D.2    Yuan, H.J.3
  • 4
    • 84881659773 scopus 로고    scopus 로고
    • Homozygosity for the V37I GJB2 mutation in fifteen probands with mild to moderate sensorineural hearing impairment: Further confirmation of pathogenicity and haplotype analysis in Asian populations
    • Gallant E, Francey L, Tsai EA, et al. Homozygosity for the V37I GJB2 mutation in fifteen probands with mild to moderate sensorineural hearing impairment: further confirmation of pathogenicity and haplotype analysis in Asian populations. Am J Med Genet A. 2013;161A(9): 2148-2157.
    • (2013) Am J Med Genet A , vol.161 A , Issue.9 , pp. 2148-2157
    • Gallant, E.1    Francey, L.2    Tsai, E.A.3
  • 5
    • 84992052837 scopus 로고    scopus 로고
    • Concurrent genetic and standard screening for hearing impairment in 9317 southern Chinese newborns
    • Peng Q, Huang S, Liang Y, et al. Concurrent genetic and standard screening for hearing impairment in 9317 southern Chinese newborns. Genet Test Mol Biomarkers. 2016;20(10):603-608.
    • (2016) Genet Test Mol Biomarkers , vol.20 , Issue.10 , pp. 603-608
    • Peng, Q.1    Huang, S.2    Liang, Y.3
  • 6
    • 84924035294 scopus 로고    scopus 로고
    • Government-funded universal newborn hearing screening and genetic analyses of deafness predisposing genes in Taiwan
    • Chu CW, Chen YJ, Lee YH, Jaung SJ, Lee FP, Huang HM. Government-funded universal newborn hearing screening and genetic analyses of deafness predisposing genes in Taiwan. Int J Pediatr Otorhinolaryngol. 2015;79(4):584-590.
    • (2015) Int J Pediatr Otorhinolaryngol , vol.79 , Issue.4 , pp. 584-590
    • Chu, C.W.1    Chen, Y.J.2    Lee, Y.H.3    Jaung, S.J.4    Lee, F.P.5    Huang, H.M.6
  • 7
    • 84982187833 scopus 로고    scopus 로고
    • Genetic misdiagnoses and the potential for health disparities
    • Manrai AK, Funke BH, Rehm HL, et al. Genetic misdiagnoses and the potential for health disparities. N Engl J Med. 2016;375(7):655-665.
    • (2016) N Engl J Med , vol.375 , Issue.7 , pp. 655-665
    • Manrai, A.K.1    Funke, B.H.2    Rehm, H.L.3
  • 8
    • 48849115241 scopus 로고    scopus 로고
    • Differential use of available genetic tests among primary care physicians in the United States: Results of a national survey
    • Shields AE, Burke W, Levy DE. Differential use of available genetic tests among primary care physicians in the United States: results of a national survey. Genet Med. 2008;10(6):404-414.
    • (2008) Genet Med , vol.10 , Issue.6 , pp. 404-414
    • Shields, A.E.1    Burke, W.2    Levy, D.E.3
  • 9
    • 85013459725 scopus 로고    scopus 로고
    • Racial disparities in BRCA testing and cancer risk management across a population-based sample of young breast cancer survivors
    • Cragun D, Weidner A, Lewis C, et al. Racial disparities in BRCA testing and cancer risk management across a population-based sample of young breast cancer survivors. Cancer. 2017;123 (13):2497-2505.
    • (2017) Cancer , vol.123 , Issue.13 , pp. 2497-2505
    • Cragun, D.1    Weidner, A.2    Lewis, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.