-
1
-
-
15744389581
-
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
-
2
-
-
13944252940
-
Genetic risk estimation by healthcare professionals
-
Bonke, B., Tibben, A., Lindhout, D., Clarke, A. J., & Stijnen, T. (2005). Genetic risk estimation by healthcare professionals. Med J Aust, 182, 116-118.
-
(2005)
Med J Aust
, vol.182
, pp. 116-118
-
-
Bonke, B.1
Tibben, A.2
Lindhout, D.3
Clarke, A.J.4
Stijnen, T.5
-
3
-
-
0036765886
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
|