(Q34385784)

1 August 2017

title

Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study (English)

1 reference

1 August 2017

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Dominique Stoppa-Lyonnet

6

D Stoppa-Lyonnet

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Ana Osorio

11

A Osorio

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1 August 2017

T Bishop

21

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Susan L Neuhausen

1

S L Neuhausen

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1 August 2017

22

D Easton

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1 August 2017

27

P Devilee

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1 August 2017

23

J Benitez

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1 August 2017

12

M Stratton

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1 August 2017

Maria Adelaide Caligo

15

M A Caligo

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1 August 2017

29

S A Narod

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1 August 2017

13

K Offit

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1 August 2017

20

L Cannon-Albright

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1 August 2017

5

J Garber

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1 August 2017

A K Godwin

2

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1 August 2017

R Gershoni-Baruch

3

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1 August 2017

E Schubert

4

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1 August 2017

E Olah

7

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1 August 2017

B Csokay

8

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1 August 2017

O Serova

9

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1 August 2017

F Lalloo

10

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1 August 2017

J Boyd

14

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1 August 2017

R J Scott

16

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1 August 2017

A Schofield

17

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1 August 2017

E Teugels

18

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1 August 2017

M Schwab

19

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1 August 2017

M C King

24

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1 August 2017

B A Ponder

25

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1 August 2017

B Weber

26

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1 August 2017

A Borg

28

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1 August 2017

D Goldgar

30

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1 August 2017

language of work or name

English

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publication date

1 June 1998

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American Journal of Human Genetics

1 August 2017

published in

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1 August 2017

volume

62

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1 August 2017

issue

6

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1 August 2017

page(s)

1381-1388

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

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

Population genetics of BRCA1 and 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=1377164

The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi 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=1377164

Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast 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=1377164

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=1377164

Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by 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=1377164

A comprehensive genetic map of the human genome based on 5,264 microsatellites

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

The complete BRCA2 gene and mutations in chromosome 13q-linked 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=1377164

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

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=1377164

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=1377164

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=1377164

Could the 185delAG BRCA1 mutation be an ancient Jewish mutation?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

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=1377164

Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

9 December 2018

1 reference

12 December 2020

Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene

1 reference

12 December 2020

Breast cancer and BRCA1 mutations

1 reference

12 December 2020

Germline BRCA1 185delAG mutations in Jewish women with breast cancer

1 reference

12 December 2020

Identifiers

DOI

10.1086/301885

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1 August 2017

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1 August 2017

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