(Q36611675)

15 August 2017

Optimal selection for BRCA1 and BRCA2 mutation testing using a combination of 'easy to apply' probability models (English)

1 reference

15 August 2017

1 reference

1 reference

1 reference

Nicoline Hoogerbrugge

7

object named as

Hoogerbrugge N

1 reference

15 August 2017

Bodmer D

1

1 reference

15 August 2017

Ligtenberg MJ

2

1 reference

15 August 2017

van der Hout AH

3

1 reference

15 August 2017

Gloudemans S

4

1 reference

15 August 2017

Ansink K

5

1 reference

15 August 2017

Oosterwijk JC

6

1 reference

15 August 2017

language of work or name

English

0 references

publication date

15 August 2006

1 reference

British Journal of Cancer

15 August 2017

1 reference

15 August 2017

95

1 reference

15 August 2017

6

1 reference

15 August 2017

757-762

1 reference

A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

Pre-test prediction models of BRCA1 or BRCA2 mutation in breast/ovarian families attending familial cancer clinics

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

Application of breast cancer risk prediction models in clinical practice

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

Cancer risks in BRCA2 families: estimates for sites other than breast and ovary.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

Update on the Manchester Scoring System for BRCA1 and BRCA2 testing

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

Evaluation of widely used models for predicting BRCA1 and BRCA2 mutations

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

Prevalence of BRCA1 and BRCA2 germline mutations in young breast cancer patients: a population-based study.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360521

BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes

20 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSJ.BJC.6603306

Population-Based Study of BRCA1 and BRCA2 Mutations in 1035 Unselected Finnish Breast Cancer Patients

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSJ.BJC.6603306

A preliminary validation of a family history assessment form to select women at risk for breast or ovarian cancer for referral to a genetics center

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Effect of BRCA1 and BRCA2 on the association between breast cancer risk and family history

1 reference

12 December 2020

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

1 reference

12 December 2020

Risk of cancer at sites other than the breast in Swedish families eligible for BRCA1 or BRCA2 mutation testing

1 reference

12 December 2020

Prevalence of BRCA1 and BRCA2 mutations in women diagnosed with ductal carcinoma in situ

1 reference

12 December 2020

Identifiers

DOI

10.1038/SJ.BJC.6603306

1 reference

Dimensions Publication ID

15 August 2017

0 references

1 reference

15 August 2017

PubMed publication ID

16909138

1 reference