(Q44953939)

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Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics

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scholarly article

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Europe PubMed Central

PubMed publication ID

7 December 2017

Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Douglas F. Easton

6

object named as

Douglas F Easton

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

8

object named as

John L Hopper

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Melissa C. Southey

3

object named as

Melissa C Southey

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Kelly-Anne Phillips

7

object named as

Kelly-Anne Phillips

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

author name string

Clare L Scott

1

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Mark A Jenkins

2

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Tracey A Davis

4

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Jennifer A Leary

5

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

publication date

25 February 2003

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

112

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

5-6

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

542-551

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

https://scigraph.springernature.com/pub.10.1007/s00439-003-0908-6

0 references

BRCA1 mutations and other sequence variants in a population-based sample of Australian women with breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

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/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutant BRCA1 genes antagonize phenotype of wild-type BRCA1

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

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/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the use of familial aggregation in population-based case probands for calculating penetrance.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

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/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intention to undergo prophylactic bilateral mastectomy in women at increased risk of developing hereditary breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation in cancer risks, by mutation position, in BRCA2 mutation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominant Negative ATM Mutations in Breast Cancer Families

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic epidemiology of female breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

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/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation in BRCA1 cancer risks by mutation position

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nomenclature for the description of human sequence variations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

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/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The BRCA2 372 HH genotype is associated with risk of breast cancer in Australian women under age 60 years.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 and BRCA2 and the genetics of breast and ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The HUGO Gene Nomenclature Committee (HGNC).

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth retardation and tumour inhibition by BRCA1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphic stop codon in BRCA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lessons learned from BRCA1 and BRCA2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

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/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a RING protein that can interact in vivo with the BRCA1 gene product

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

kConFab: a research resource of Australasian breast cancer families. Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Design and analysis issues in a population-based, case-control-family study of the genetic epidemiology of breast cancer and the Co-operative Family Registry for Breast Cancer Studies (CFRBCS).

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Australia takes two-step approach on genetic studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12601471

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-003-0908-6

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

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