Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families (Q34387715)

1 August 2017

title

Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families (English)

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1 August 2017

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Morgan K

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1 August 2017

William David Foulkes

Foulkes WD

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Narod SA

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1 August 2017

Futreal PA

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1 August 2017

Tonin PN

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1 August 2017

Mes-Masson AM

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1 August 2017

Mahon M

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1 August 2017

Cole DE

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1 August 2017

Provencher D

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1 August 2017

Ghadirian P

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1 August 2017

language of work or name

English

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publication date

1 November 1998

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American Journal of Human Genetics

1 August 2017

published in

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1 August 2017

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1 August 2017

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1 August 2017

page(s)

1341-1351

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Analysis of BRCA1 and BRCA2 mutations in Hungarian families with breast or breast-ovarian cancer

1 August 2017

cites work

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6 July 2018

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Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families

6 July 2018

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Generation of an integrated transcription map of the BRCA2 region on chromosome 13q12-q13

6 July 2018

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6 July 2018

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Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer

6 July 2018

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Two distinct origins of a common BRCA1 mutation in breast-ovarian cancer families: a genetic study of 15 185delAG-mutation kindreds

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families

6 July 2018

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6 July 2018

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The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13

6 July 2018

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Variability of the genetic contribution of Quebec population founders associated to some deleterious genes.

6 July 2018

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BRCA1 mutations in Ashkenazi Jewish women

6 July 2018

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Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer

6 July 2018

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The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals

6 July 2018

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A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

6 July 2018

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Cystic fibrosis mutations in French Canadians: three CFTR mutations are relatively frequent in a Quebec population with an elevated incidence of cystic fibrosis

6 July 2018

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6 July 2018

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BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.

27 October 2018

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The genetic clock and the age of the founder effect in growing populations: a lesson from French Canadians and Ashkenazim

27 October 2018

1 reference

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High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377544

Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377544

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377544

Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation

9 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377544

Founder effect in beta-thalassaemia in Portneuf, Québec

9 December 2018

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12 December 2020

A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening

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12 December 2020

Rapid detection of BRCA1 mutations by the protein truncation test

1 reference

12 December 2020

Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer

1 reference

12 December 2020

New Austrian mutation in BRCA1 gene detected in three unrelated HBOC families

1 reference

12 December 2020

A common mutation in BRCA2 that predisposes to a variety of cancers is found in both Jewish Ashkenazi and non-Jewish individuals

1 reference

12 December 2020

Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

1 reference

12 December 2020

A polymorphic stop codon in BRCA2

1 reference

12 December 2020

Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13

1 reference

12 December 2020

Contribution of BRCA1 mutations to ovarian cancer

1 reference

12 December 2020

Primary carcinoma of the fallopian tube

1 reference

12 December 2020

Identifiers

DOI

10.1086/302099

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1 August 2017

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1 August 2017

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