(Q33393743)

26 July 2017

title

PEL: an unbiased method for estimating age-dependent genetic disease risk from pedigree data unselected for family history (English)

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26 July 2017

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Dominique Stoppa-Lyonnet

5

object named as

D Stoppa-Lyonnet

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Catherine Bourgain

object named as

C Bourgain

2

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author name string

F Alarcon

1

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26 July 2017

M Gauthier-Villars

3

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26 July 2017

V Planté-Bordeneuve

4

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26 July 2017

C Bonaïti-Pellié

6

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26 July 2017

publication date

1 July 2009

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26 July 2017

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26 July 2017

volume

33

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26 July 2017

issue

5

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26 July 2017

page(s)

379-385

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Estimating penetrance from family data using a retrospective likelihood when ascertainment depends on genotype and age of onset

26 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

Genetic study of transthyretin amyloid neuropathies: carrier risks among French and Portuguese families.

21 June 2018

1 reference

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Genetic tests under incomplete ascertainment

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

Optimal designs for estimating penetrance of rare mutations of a disease-susceptibility gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

Sensitivity and predictive value of criteria for p53 germline mutation screening

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

Bias and efficiency in family-based gene-characterization studies: conditional, prospective, retrospective, and joint likelihoods

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

Inherent intractability of the ascertainment problem for pedigree data: a general likelihood framework

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

ARCAD: a method for estimating age-dependent disease risk associated with mutation carrier status from family data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

A General Model for the Genetic Analysis of Pedigree Data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

A time-dependent logistic hazard function for modeling variable age of onset in analysis of familial diseases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

Ascertainment in the sequential sampling of pedigrees

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

Estimating cancer risk in HNPCC by the GRL method.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

Hereditary non-polyposis colorectal cancer: current risks of colorectal cancer largely overestimated.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

Designing studies to estimate the penetrance of an identified autosomal dominant mutation: cohort, case-control, and genotyped-proband designs.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3108000

Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations

31 October 2018

1 reference

12 December 2020

Cancer risk associated with germline DNA mismatch repair gene mutations

1 reference

12 December 2020

The Kin-Cohort Study for Estimating Penetrance

1 reference

12 December 2020

Recommendations for medical management of hereditary breast and ovarian cancer: the French National Ad Hoc Committee

1 reference

12 December 2020

Contribution of BRCA1 and BRCA2 germ-line mutations to the incidence of breast cancer in young women: results from a prospective population-based study in France

1 reference

12 December 2020

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.20390

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1002/GEPI.20390

1 reference

26 July 2017

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26 July 2017

1 reference