(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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4

Morgan K

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1 August 2017

William David Foulkes

object named as

Foulkes WD

6

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Steven A. Narod

10

object named as

Narod SA

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1 August 2017

3

Futreal PA

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1 August 2017

Tonin PN

1

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1 August 2017

Mes-Masson AM

2

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1 August 2017

Mahon M

5

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1 August 2017

Cole DE

7

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1 August 2017

Provencher D

8

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1 August 2017

Ghadirian P

9

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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

volume

63

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1 August 2017

issue

5

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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

1 reference

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Frequently occurring germ-line mutations of the BRCA1 gene in ovarian cancer families from Russia

6 July 2018

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BRCA2 mutations in hereditary breast and ovarian cancer in France

6 July 2018

1 reference

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Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer

6 July 2018

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Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families

6 July 2018

1 reference

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A low proportion of BRCA2 mutations in Finnish breast cancer families.

6 July 2018

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A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

6 July 2018

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BRCA2 in American families with four or more cases of breast or ovarian cancer: recurrent and novel mutations, variable expression, penetrance, and the possibility of families whose cancer is not attributable to BRCA1 or BRCA2.

6 July 2018

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

6 July 2018

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Population genetics of BRCA1 and BRCA2.

6 July 2018

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Mutation analysis of the BRCA1 gene in 23 families with cases of cancer of the breast, ovary, and multiple other sites

6 July 2018

1 reference

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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

1 reference

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

Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians

6 July 2018

1 reference

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

6 July 2018

1 reference

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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

1 reference

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

Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden

6 July 2018

1 reference

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The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds

6 July 2018

1 reference

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Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study

6 July 2018

1 reference

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A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families

6 July 2018

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The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q

6 July 2018

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Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families

6 July 2018

1 reference

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Identification of the breast cancer susceptibility gene BRCA2

6 July 2018

1 reference

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

Clinical, metabolic, and genetic aspects of cytochrome C oxidase deficiency in Saguenay-Lac-Saint-Jean.

6 July 2018

1 reference

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Familial hypercholesterolemia in French-Canadians: taking advantage of the presence of a "founder effect".

6 July 2018

1 reference

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

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

6 July 2018

1 reference

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

An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Breast Cancer Linkage Consortium.

6 July 2018

1 reference

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

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

1 reference

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

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

6 July 2018

1 reference

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

BRCA1 mutations in Ashkenazi Jewish women

6 July 2018

1 reference

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

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

6 July 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 BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals

6 July 2018

1 reference

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

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

6 July 2018

1 reference

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

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

1 reference

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

Reproduction démographique et transmission génétique dans le nord-est de la province de Québec (XVIIIe-XXe siècles)

6 July 2018

1 reference

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

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

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

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

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

1 reference

12 December 2020

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

1 reference

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

1 reference

1 August 2017

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1 August 2017

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