(Q51922489)

English

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

scientific article published on 13 February 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

Bayesian risk assessment in genetic testing for autosomal dominant disorders with age-dependent penetrance. (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

author name string

Shuji Ogino

1

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

Robert B Wilson

2

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

Bert Gold

3

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

Pamela Flodman

4

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

publication date

13 February 2007

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

Journal of Genetic Counseling

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

16

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

1

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

29-39

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

Accuracy and precision in Bayesian analysis.

1 reference

https://api.crossref.org/works/10.1007%2FS10897-006-9040-9

21 January 2018

Bayesian analysis and risk assessment in genetic counseling and testing.

1 reference

https://api.crossref.org/works/10.1007%2FS10897-006-9040-9

21 January 2018

Genetic testing and risk assessment for spinal muscular atrophy (SMA).

1 reference

https://pubmed.ncbi.nlm.nih.gov/17295057

12 December 2020

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Bayesian analysis for cystic fibrosis risks in prenatal and carrier screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/17295057

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic risk assessment in carrier testing for spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17295057

12 December 2020

based on heuristic

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Favourable mutation test outcomes for individuals at risk for Huntington disease change the perspectives of first-degree relatives.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17295057

12 December 2020

based on heuristic

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Calculating risk changes after negative mutation test outcomes for autosomal dominant hereditary late-onset disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/17295057

12 December 2020

based on heuristic

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Risk calculations: still essential in the molecular age.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17295057

12 December 2020

based on heuristic

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A Simple, Unified Approach to Bayesian Risk Calculations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17295057

12 December 2020

based on heuristic

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A genetic risk calculation surprise

1 reference

https://pubmed.ncbi.nlm.nih.gov/17295057

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk calculations for cystic fibrosis in neonatal screening by immunoreactive trypsinogen and CFTR mutation tests.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17295057

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic risk estimation by healthcare professionals

1 reference

https://pubmed.ncbi.nlm.nih.gov/17295057

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bayesian risk assessment for autosomal recessive diseases: fetal echogenic bowel with one or no detectable CFTR mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17295057

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17295057

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10897-006-9040-9

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17295057

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