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Volumn 16, Issue 1, 2007, Pages 29-39

Bayesian risk assessment in genetic testing for autosomal dominant disorders with age-dependent penetrance

Author keywords

Autosomal dominant; Bayes; Bayesian; Genetic counseling; Genetic risk; Hereditary cancer; Penetrance; Risk assessment; Sensitivity

Indexed keywords

AGE DISTRIBUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BAYES THEOREM; CANCER RISK; DECISION MAKING; FAMILIAL CANCER; GENETIC ANALYSIS; GENETIC COUNSELING; HUMAN; RISK ASSESSMENT; SENSITIVITY ANALYSIS;

EID: 33847654632     PISSN: 10597700     EISSN: 15733599     Source Type: Journal    
DOI: 10.1007/s10897-006-9040-9     Document Type: Article
Times cited : (6)

References (16)
  • 1
    • 15744389581 scopus 로고    scopus 로고
    • Accuracy and precision in Bayesian analysis
    • Biesecker, L. (2005). Accuracy and precision in Bayesian analysis. Am J Med Genet A, 134, 111.
    • (2005) Am J Med Genet A , vol.134 , pp. 111
    • Biesecker, L.1
  • 3
    • 0036765886 scopus 로고    scopus 로고
    • Favourable mutation test outcomes for individuals at risk for Huntington disease change the perspectives of first-degree relatives
    • Bonke, B., Tibben, A., Lindhout, D., & Stijnen, T. (2002). Favourable mutation test outcomes for individuals at risk for Huntington disease change the perspectives of first-degree relatives. Hum Genet, 111, 297-298.
    • (2002) Hum Genet , vol.111 , pp. 297-298
    • Bonke, B.1    Tibben, A.2    Lindhout, D.3    Stijnen, T.4
  • 4
    • 33644586029 scopus 로고    scopus 로고
    • Calculating risk changes after negative mutation test outcomes for autosomal dominant hereditary late-onset disorders
    • Bonke, B., Tibben, A., Lindhout, D., & Stijnen, T. (2006). Calculating risk changes after negative mutation test outcomes for autosomal dominant hereditary late-onset disorders. Heredity, 96, 259-261.
    • (2006) Heredity , vol.96 , pp. 259-261
    • Bonke, B.1    Tibben, A.2    Lindhout, D.3    Stijnen, T.4
  • 6
    • 0035932782 scopus 로고    scopus 로고
    • A genetic risk calculation surprise
    • Flodman, P., & Hodge, S. E. (2001). A genetic risk calculation surprise. Am J Med Genet, 100, 169-171.
    • (2001) Am J Med Genet , vol.100 , pp. 169-171
    • Flodman, P.1    Hodge, S.E.2
  • 7
    • 0031802153 scopus 로고    scopus 로고
    • A simple, unified approach to Bayesian risk calculations
    • Hodge, S. E. (1998). A simple, unified approach to Bayesian risk calculations. J Genet Couns, 7, 235-261.
    • (1998) J Genet Couns , vol.7 , pp. 235-261
    • Hodge, S.E.1
  • 8
    • 4444242300 scopus 로고    scopus 로고
    • Risk calculations: Still essential in the molecular age
    • Hodge, S. E., & Flodman, P. L. (2004). Risk calculations: still essential in the molecular age. Am J Med Genet, 129A, 215-217.
    • (2004) Am J Med Genet , vol.129 A , pp. 215-217
    • Hodge, S.E.1    Flodman, P.L.2
  • 9
    • 20444449283 scopus 로고    scopus 로고
    • Risk calculations for cystic fibrosis in neonatal screening by immunoreactive trypsinogen and CFTR mutation tests
    • Ogino, S., Flodman, P., Wilson, R. B., Gold, B., & Grody, W. W. (2005). Risk calculations for cystic fibrosis in neonatal screening by immunoreactive trypsinogen and CFTR mutation tests. Genet Med, 7, 317-327.
    • (2005) Genet Med , vol.7 , pp. 317-327
    • Ogino, S.1    Flodman, P.2    Wilson, R.B.3    Gold, B.4    Grody, W.W.5
  • 10
    • 0037100098 scopus 로고    scopus 로고
    • Genetic risk assessment in carrier testing for spinal muscular atrophy
    • Ogino, S., Leonard, D. G., Rennert, H., Ewens, W. J., & Wilson, R. B. (2002). Genetic risk assessment in carrier testing for spinal muscular atrophy. Am J Med Genet, 110, 301-307.
    • (2002) Am J Med Genet , vol.110 , pp. 301-307
    • Ogino, S.1    Leonard, D.G.2    Rennert, H.3    Ewens, W.J.4    Wilson, R.B.5
  • 11
    • 0036942226 scopus 로고    scopus 로고
    • Genetic testing and risk assessment for spinal muscular atrophy (SMA)
    • Ogino, S., & Wilson, R. B. (2002). Genetic testing and risk assessment for spinal muscular atrophy (SMA). Hum Genet, 111, 477-500.
    • (2002) Hum Genet , vol.111 , pp. 477-500
    • Ogino, S.1    Wilson, R.B.2
  • 12
    • 1142275285 scopus 로고    scopus 로고
    • Bayesian Analysis and Risk Assessment in Genetic Counseling and Testing
    • Ogino, S., & Wilson, R. B. (2004). Bayesian Analysis and Risk Assessment in Genetic Counseling and Testing. J Mol Diagn, 6, 1-9.
    • (2004) J Mol Diagn , vol.6 , pp. 1-9
    • Ogino, S.1    Wilson, R.B.2
  • 13
    • 4644339181 scopus 로고    scopus 로고
    • Bayesian analysis for cystic fibrosis risks in prenatal and carrier screening
    • Ogino, S., Wilson, R. B., Gold, B., Hawley, P., & Grody, W. W. (2004a). Bayesian analysis for cystic fibrosis risks in prenatal and carrier screening. Genet Med, 6, 439-449.
    • (2004) Genet Med , vol.6 , pp. 439-449
    • Ogino, S.1    Wilson, R.B.2    Gold, B.3    Hawley, P.4    Grody, W.W.5
  • 14
    • 3042769509 scopus 로고    scopus 로고
    • Bayesian risk assessment for autosomal recessive diseases: Fetal echogenic bowel with one or no detectable CFTR mutation
    • Ogino, S., Wilson, R. B., & Grody, W. W. (2004b). Bayesian risk assessment for autosomal recessive diseases: fetal echogenic bowel with one or no detectable CFTR mutation. J Med Genet, 41, e70.
    • (2004) J Med Genet , vol.41
    • Ogino, S.1    Wilson, R.B.2    Grody, W.W.3
  • 15
    • 0034614010 scopus 로고    scopus 로고
    • Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant conditions and the calculation of recurrence risks for their offspring. I. Autosomal dominant genes
    • Otto, P. A., & Maestrelli, S. R. (2000). Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant conditions and the calculation of recurrence risks for their offspring. I. Autosomal dominant genes. Am J Med Genet, 95, 43-48.
    • (2000) Am J Med Genet , vol.95 , pp. 43-48
    • Otto, P.A.1    Maestrelli, S.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.