The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes (Q34145680)

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English	The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1 reference

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Douglas F. Easton

5

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Easton DF

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Antonis C Antoniou

4

object named as

Antoniou AC

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Simon A Gayther

1

object named as

Gayther SA

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

Russell P

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Harrington P

3

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Europe PubMed Central

PubMed publication ID

31 July 2017

Ponder BA

6

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Europe PubMed Central

PubMed publication ID

31 July 2017

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publication date

1 October 1999

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

American Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

31 July 2017

65

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Europe PubMed Central

PubMed publication ID

31 July 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1021-1029

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Clues to the function of the tumour susceptibility gene BRCA2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

The BRC repeats in BRCA2 are critical for RAD51 binding and resistance to methyl methanesulfonate treatment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

BRCA1, BRCA2, and DNA Damage Response: Collision or Collusion?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

RAD51 Interacts with the Evolutionarily Conserved BRC Motifs in the Human Breast Cancer Susceptibility Gene brca2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

Mutation analysis of BRCA1 and BRCA2 in a male breast cancer population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

Association of BRCA1 with Rad51 in mitotic and meiotic cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

Estimates of the gene frequency of BRCA1 and its contribution to breast and ovarian cancer incidence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

Identification of the breast cancer susceptibility gene BRCA2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

Mutation of a mutL homolog in hereditary colon cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

Familial site-specific ovarian cancer is linked to BRCA1 on 17q12-21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

Genetic analysis of breast cancer in the cancer and steroid hormone study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

5 July 2018

An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

28 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288234

28 October 2018

Surveillance and management of patients at high genetic risk for ovarian carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/10486320

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Programs for pedigree analysis: Mendel, Fisher, and dGene

1 reference

https://pubmed.ncbi.nlm.nih.gov/10486320

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10486320

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcriptional activation by BRCA1

1 reference

https://pubmed.ncbi.nlm.nih.gov/10486320

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10486320

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 1-kb Alu-mediated germ-line deletion removing BRCA1 exon 17

1 reference

https://pubmed.ncbi.nlm.nih.gov/10486320

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breast cancer genes--what are the real risks?

1 reference

https://pubmed.ncbi.nlm.nih.gov/10486320

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a 14 kb deletion involving the promoter region of BRCA1 in a breast cancer family

1 reference

https://pubmed.ncbi.nlm.nih.gov/10486320

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A systematic review and meta-analysis of family history and risk of ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/10486320

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Survival in familial, BRCA1-associated, and BRCA2-associated epithelial ovarian cancer. United Kingdom Coordinating Committee for Cancer Research (UKCCCR) Familial Ovarian Cancer Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/10486320

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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31 July 2017

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31 July 2017

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Europe PubMed Central

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31 July 2017

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