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Volumn 164, Issue 5, 2014, Pages 1192-1197

An economic analysis of prenatal cytogenetic technologies for sonographically detected fetal anomalies

Author keywords

Array comparative genomic hybridization (aCGH); Chromosomal microarray (CMA); Congenital anomalies; Cost effectiveness analysis; Ultrasonic prenatal diagnosis

Indexed keywords

ARTICLE; CHROMOSOMAL MICROARRAY; CLINICAL EFFECTIVENESS; COMPARATIVE EFFECTIVENESS; COST EFFECTIVENESS ANALYSIS; CYTOGENETICS; FETUS; FETUS ECHOGRAPHY; FETUS MALFORMATION; HUMAN; KARYOTYPING; MICROARRAY ANALYSIS; MONTE CARLO METHOD; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SENSITIVITY ANALYSIS; SYSTEMATIC REVIEW; CHROMOSOME ANALYSIS; CONGENITAL ABNORMALITIES; COST BENEFIT ANALYSIS; DECISION TREE; ECONOMICS; GENETICS; INCIDENCE; META ANALYSIS;

EID: 84898887023     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36435     Document Type: Article
Times cited : (13)

References (33)
  • 1
    • 73549121749 scopus 로고    scopus 로고
    • ACOG Committee Opinion no. 446: Array comparative genomic hybridization in prenatal diagnosis
    • American College of Obstetricians and Gynecologists
    • American College of Obstetricians and Gynecologists. 2009. ACOG Committee Opinion no. 446: Array comparative genomic hybridization in prenatal diagnosis. Obstet Gynecol 114:1161-1163.
    • (2009) Obstet Gynecol , vol.114 , pp. 1161-1163
  • 2
    • 43649098567 scopus 로고    scopus 로고
    • Comparison of targeted and whole genome analysis of postnatal specimens using a commercially available array based comparative genomic hybridisation (aCGH) microarray platform
    • Aston E, Whitby H, Maxwell T, Glaus N, Cowley B, Lowry D, Zhu XL, Issa B, South ST, Brothman AR. 2008. Comparison of targeted and whole genome analysis of postnatal specimens using a commercially available array based comparative genomic hybridisation (aCGH) microarray platform. J Med Genet 45:268-274.
    • (2008) J Med Genet , vol.45 , pp. 268-274
    • Aston, E.1    Whitby, H.2    Maxwell, T.3    Glaus, N.4    Cowley, B.5    Lowry, D.6    Zhu, X.L.7    Issa, B.8    South, S.T.9    Brothman, A.R.10
  • 3
    • 1642423677 scopus 로고    scopus 로고
    • An outcomes analysis of five prenatal screening strategies for trisomy 21 in women younger than 35 years
    • Biggio JR Jr, Morris TC, Owen J, Stringer JS. 2004. An outcomes analysis of five prenatal screening strategies for trisomy 21 in women younger than 35 years. Am J Obstet Gynecol 190:721-729.
    • (2004) Am J Obstet Gynecol , vol.190 , pp. 721-729
    • Biggio Jr., J.R.1    Morris, T.C.2    Owen, J.3    Stringer, J.S.4
  • 4
    • 84859141764 scopus 로고    scopus 로고
    • Genomic microarrays: A technology overview
    • Brady PD, Vermeesch JR. 2012. Genomic microarrays: A technology overview. Prenat Diagn 32:336-343.
    • (2012) Prenat Diagn , vol.32 , pp. 336-343
    • Brady, P.D.1    Vermeesch, J.R.2
  • 5
    • 72149094033 scopus 로고    scopus 로고
    • Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray
    • Coppinger J, Alliman S, Lamb AN, Torchia BS, Bejjani BA, Shaffer LG. 2009. Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray. Prenat Diagn 29:1156-1166.
    • (2009) Prenat Diagn , vol.29 , pp. 1156-1166
    • Coppinger, J.1    Alliman, S.2    Lamb, A.N.3    Torchia, B.S.4    Bejjani, B.A.5    Shaffer, L.G.6
  • 6
    • 77956117452 scopus 로고    scopus 로고
    • Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis
    • Faas BH, van der Burgt I, Kooper AJ, Pfundt R, Hehir-Kwa JY, Smits AP, de Leeuw N. 2010. Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis. J Med Genet 47:586-594.
    • (2010) J Med Genet , vol.47 , pp. 586-594
    • Faas, B.H.1    van der Burgt, I.2    Kooper, A.J.3    Pfundt, R.4    Hehir-Kwa, J.Y.5    Smits, A.P.6    de Leeuw, N.7
  • 8
    • 78650632807 scopus 로고    scopus 로고
    • Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: A systematic review and meta-analysis
    • Hillman SC, Pretlove S, Coomarasamy A, McMullan DJ, Davison EV, Maher ER, Kilby MD. 2011. Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: A systematic review and meta-analysis. Ultrasound Obstet Gynecol 37:6-14.
    • (2011) Ultrasound Obstet Gynecol , vol.37 , pp. 6-14
    • Hillman, S.C.1    Pretlove, S.2    Coomarasamy, A.3    McMullan, D.J.4    Davison, E.V.5    Maher, E.R.6    Kilby, M.D.7
  • 9
    • 73449106142 scopus 로고    scopus 로고
    • Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype
    • Kleeman L, Bianchi DW, Shaffer LG, Rorem E, Cowan J, Craigo SD, Tighiouart H, Wilkins-Haug LE. 2009. Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype. Prenat Diagn 29:1213-1217.
    • (2009) Prenat Diagn , vol.29 , pp. 1213-1217
    • Kleeman, L.1    Bianchi, D.W.2    Shaffer, L.G.3    Rorem, E.4    Cowan, J.5    Craigo, S.D.6    Tighiouart, H.7    Wilkins-Haug, L.E.8
  • 10
    • 0033974777 scopus 로고    scopus 로고
    • Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study
    • Lapierre JM, Cacheux V, Luton D, Collot N, Oury JF, Aurias A, Tachdjian G. 2000. Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study. Prenat Diagn 20:123-131.
    • (2000) Prenat Diagn , vol.20 , pp. 123-131
    • Lapierre, J.M.1    Cacheux, V.2    Luton, D.3    Collot, N.4    Oury, J.F.5    Aurias, A.6    Tachdjian, G.7
  • 16
    • 77951977961 scopus 로고    scopus 로고
    • Value for money? Array genomic hybridization for diagnostic testing for genetic causes of intellectual disability
    • Regier DA, Friedman JM, Marra CA. 2010. Value for money? Array genomic hybridization for diagnostic testing for genetic causes of intellectual disability. Am J Hum Genet 86:765-772.
    • (2010) Am J Hum Genet , vol.86 , pp. 765-772
    • Regier, D.A.1    Friedman, J.M.2    Marra, C.A.3
  • 18
    • 0030020467 scopus 로고    scopus 로고
    • Distribution of abnormal karyotypes among malformed fetuses detected by ultrasound throughout gestation
    • Rizzo N, Pittalis MC, Pilu G, Perolo A, Banzi C, Visentin A, Bovicelli L. 1996. Distribution of abnormal karyotypes among malformed fetuses detected by ultrasound throughout gestation. Prenat Diagn 16:159-163.
    • (1996) Prenat Diagn , vol.16 , pp. 159-163
    • Rizzo, N.1    Pittalis, M.C.2    Pilu, G.3    Perolo, A.4    Banzi, C.5    Visentin, A.6    Bovicelli, L.7
  • 20
    • 79953161375 scopus 로고    scopus 로고
    • Evolving applications of microarray analysis in prenatal diagnosis
    • Savage MS, Mourad MJ, Wapner RJ. 2011. Evolving applications of microarray analysis in prenatal diagnosis. Curr Opin Obstet Gynecol 23:103-108.
    • (2011) Curr Opin Obstet Gynecol , vol.23 , pp. 103-108
    • Savage, M.S.1    Mourad, M.J.2    Wapner, R.J.3
  • 23
    • 0034513406 scopus 로고    scopus 로고
    • Molecular mechanisms for constitutional chromosomal rearrangements in humans
    • Shaffer LG, Lupski JR. 2000. Molecular mechanisms for constitutional chromosomal rearrangements in humans. Annu Rev Genet 34:297-329.
    • (2000) Annu Rev Genet , vol.34 , pp. 297-329
    • Shaffer, L.G.1    Lupski, J.R.2
  • 28
    • 0041807885 scopus 로고    scopus 로고
    • What is the price of life and why doesn't it increase at the rate of inflation
    • Ubel PA, Hirth RA, Chernew ME, Fendrick AM. 2003. What is the price of life and why doesn't it increase at the rate of inflation? Arch Intern Med 163:1637-1641.
    • (2003) Arch Intern Med , vol.163 , pp. 1637-1641
    • Ubel, P.A.1    Hirth, R.A.2    Chernew, M.E.3    Fendrick, A.M.4
  • 30
    • 84859133651 scopus 로고    scopus 로고
    • Integration of microarray technology into prenatal diagnosis: Counselling issues generated during the NICHD clinical trial
    • Wapner RJ, Driscoll DA, Simpson JL. 2012a. Integration of microarray technology into prenatal diagnosis: Counselling issues generated during the NICHD clinical trial. Prenat Diagn 32:396-400.
    • (2012) Prenat Diagn , vol.32 , pp. 396-400
    • Wapner, R.J.1    Driscoll, D.A.2    Simpson, J.L.3
  • 32
    • 84873058081 scopus 로고    scopus 로고
    • Technology-driven and evidence-based genomic analysis for integrated pediatric and prenatal genetics evaluation
    • Wei Y, Xu F, Li P. 2013. Technology-driven and evidence-based genomic analysis for integrated pediatric and prenatal genetics evaluation. J Genet Genomics 40:1-14.
    • (2013) J Genet Genomics , vol.40 , pp. 1-14
    • Wei, Y.1    Xu, F.2    Li, P.3
  • 33
    • 0026457861 scopus 로고
    • Fetal ultrasound abnormalities: correlation with fetal karyotype, autopsy findings, and postnatal outcome--five-year prospective study
    • Wilson RD, Chitayat D, McGillivray BC. 1992. Fetal ultrasound abnormalities: correlation with fetal karyotype, autopsy findings, and postnatal outcome--five-year prospective study. Am J Med Genet 44:586-590.
    • (1992) Am J Med Genet , vol.44 , pp. 586-590
    • Wilson, R.D.1    Chitayat, D.2    McGillivray, B.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.