(Q73108544)

English

Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Anglian Breast Cancer Study Group

scientific article published on 01 November 2000

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scholarly article

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Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11044354%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Anglian Breast Cancer Study Group (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11044354%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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1 November 2000

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Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11044354%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

British Journal of Cancer

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11044354%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

83

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11044354%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

10

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11044354%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1301-1308

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11044354%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cohort study analysis with a FORTRAN computer program.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the breast cancer susceptibility gene BRCA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1Mutations in a Population-Based Sample of Young Women with Breast Cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline BRCA1 185delAG mutations in Jewish women with breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

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/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential Contributions ofBRCA1andBRCA2to Early-Onset Breast Cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Study of a single BRCA2 mutation with high carrier frequency in a small population

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer Risks in Two Large Breast Cancer Families Linked to BRCA2 on Chromosome 13q12‐13

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ovarian cancer family

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of breast cancer attributable to BRCA1 in a population-based series of American women

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 mutations and breast cancer in the general population: analyses in women before age 35 years and in women before age 45 years with first-degree family history

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prognosis of BRCA1 hereditary breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Survival in early-onset BRCA1 breast-cancer patients. Institut Curie Breast Cancer Group.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population-based study of risk of breast cancer in carriers of BRCA2 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2. Australian Breast Cancer Family Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk models for familial ovarian and breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of inherited breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11044354

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1054/BJOC.2000.1407

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11044354%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11044354%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11044354%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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