(Q34705352)

4 August 2017

title

On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European populations (English)

1 reference

4 August 2017

author

Dominique Stoppa-Lyonnet

4

Dominique Stoppa-Lyonnet

0 references

Drakoulis Yannoukakos

15

Drakoulis Yannoukakos

0 references

Irene Konstantopoulou

16

Irene Konstantopoulou

0 references

William David Foulkes

William D Foulkes

22

0 references

Jan Lubiński

9

Jan Lubinski

1 reference

4 August 2017

19

Fergus J Couch

1 reference

4 August 2017

3

Lenka Foretova

1 reference

4 August 2017

5

Steven A Narod

1 reference

4 August 2017

10

Jacek Gronwald

1 reference

4 August 2017

11

Bohdan Gorski

1 reference

4 August 2017

13

Finn C Nielsen

1 reference

4 August 2017

21

David E Goldgar

1 reference

4 August 2017

12

Thomas v O Hansen

1 reference

4 August 2017

6

Evgeny Imyanitov

1 reference

4 August 2017

1

Nancy Hamel

1 reference

4 August 2017

14

Mads Thomassen

1 reference

4 August 2017

7

Olga Sinilnikova

1 reference

4 August 2017

8

Laima Tihomirova

1 reference

4 August 2017

Bing-Jian Feng

2

1 reference

4 August 2017

Vladimir Zajac

17

1 reference

4 August 2017

Sona Ciernikova

18

1 reference

4 August 2017

Celia M T Greenwood

20

1 reference

4 August 2017

language of work or name

1 reference

1 December 2010

1 reference

European Journal of Human Genetics

4 August 2017

published in

1 reference

4 August 2017

volume

19

1 reference

4 August 2017

issue

3

1 reference

4 August 2017

page(s)

300-306

1 reference

How old is this mutation? - a study of three Ashkenazi Jewish founder mutations.

4 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=3062007

Contribution of BRCA1 germ-line mutations to breast cancer in Greece: a hospital-based study of 987 unselected breast cancer cases

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

The limited spectrum of pathogenic BRCA1 and BRCA2 mutations in the French Canadian breast and breast-ovarian cancer families, a founder population of Quebec, Canada

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

Identification of germline BRCA1 and BRCA2 genetic alterations in Greek breast cancer moderate-risk and low-risk individuals--correlation with clinicopathological data

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

BRCA1 and BRCA2: 1994 and beyond

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

A high-resolution recombination map of the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

Prevalence of BRCA1 in a hospital-based population of Dutch breast cancer patients

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

Prevalence of founder BRCA1 and BRCA2 mutations among breast and ovarian cancer patients in Hungary

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

Frequency of BRCA1 mutation 5382insC in German breast cancer patients.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

Mutation of human short tandem repeats

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

BRCA1 and BRCA2 mutation prevalence and clinical characteristics of a population-based series of ovarian cancer cases from Denmark.

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2010.203

Hereditary ovarian cancer in Poland.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2010.203

Frequency of 5382insC mutation of the BRCA1 gene

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062007

Haplotype analysis of a BRCA1 : 185delAG mutation in a Chilean family supports its Ashkenazi origins

26 October 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2010.203

One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations: results of a prospective study in Southern Sweden

21 January 2018

1 reference

12 December 2020

Breast cancer predisposing alleles in Poland

1 reference

12 December 2020

Novel and common BRCA1 mutations in familial breast/ovarian cancer patients from Lithuania

1 reference

12 December 2020

Mutational analysis of theBRCA1 gene in 30 Czech ovarian cancer patients

1 reference

12 December 2020

Mutation screening of BRCA1 using PTT and LOH analysis at 17q21 in breast carcinomas from familial and non-familial cases

1 reference

12 December 2020

Prevalence of BRCA1 founder mutations in western Poland

1 reference

12 December 2020

Strong founder effects in BRCA1 mutation carrier breast cancer patients from Latvia. Mutation in brief no. 258. Online

1 reference

12 December 2020

Analysis of RAD51 polymorphism and BRCA1 mutations in Polish women with breast cancer

1 reference

12 December 2020

High incidence of mutations in BRCA1 and BRCA2 genes in ovarian cancer

1 reference

12 December 2020

BRCA1 and BRCA2 mutations in Turkish familial and non-familial ovarian cancer patients: a high incidence of mutations in non-familial cases

1 reference

12 December 2020

Germline mutations in the BRCA1 and BRCA2 genes in Turkish breast/ovarian cancer patients

1 reference

12 December 2020

Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

1 reference

12 December 2020

Identifiers

DOI

10.1038/EJHG.2010.203

1 reference

Dimensions Publication ID

4 August 2017

0 references

1 reference

4 August 2017

1 reference