(Q36955087)

English

Evaluation of BRCA1 and BRCA2 mutations and risk-prediction models in a typical Asian country (Malaysia) with a relatively low incidence of breast cancer

scientific article published on 16 July 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Evaluation of BRCA1 and BRCA2 mutations and risk-prediction models in a typical Asian country (Malaysia) with a relatively low incidence of breast cancer (English)

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

0 references

author name string

E Thirthagiri

1

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

S Y Lee

2

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

P Kang

3

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

D S Lee

4

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

G T Toh

5

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

S Selamat

6

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

S-Y Yoon

7

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

N A Mohd Taib

8

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

M K Thong

9

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

C H Yip

10

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

S H Teo

11

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

publication date

16 July 2008

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Breast Cancer Research

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

10

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

R59

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

https://scigraph.springernature.com/pub.10.1186/bcr2118

0 references

Establishing a cancer genetics programme in Asia - the singapore experience

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

BRCA1 and BRCA2 germline mutations in Malaysian women with early-onset breast cancer without a family history

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

BRCA1 and BRCA2 germline mutation analysis in the Indonesian population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

Contribution of germline BRCA1 and BRCA2 sequence alterations to breast cancer in Northern India

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

The roles of BRCA1 and BRCA2 and associated proteins in the maintenance of genomic stability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

Clinical management of BRCA1 and BRCA2 mutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

Disparities in genetic testing: thinking outside the BRCA box.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

Optimal selection of individuals for BRCA mutation testing: a comparison of available methods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of eight recurrent substitutions as neutral

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

The BOADICEA model of genetic susceptibility to breast and ovarian cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

BRCA1 c.2845insA is a recurring mutation with a founder effect in Singapore Malay women with early onset breast/ovarian cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

Hereditary breast and ovarian cancer in Asia: genetic epidemiology of BRCA1 and BRCA2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

The prevalence of BRCA1 mutations in Chinese patients with early onset breast cancer and affected relatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

29 September 2017

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=2575532

29 September 2017

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=2575532

29 September 2017

Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575532

27 June 2018

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

1 reference

https://api.crossref.org/works/10.1186%2FBCR2118

21 January 2018

BRCA1 and BRCA2 mutations in women from Shanghai China

1 reference

https://api.crossref.org/works/10.1186%2FBCR2118

21 January 2018

The prevalence of BRCA1 and BRCA2 mutations in eastern Chinese women with breast cancer.

1 reference

https://api.crossref.org/works/10.1186%2FBCR2118

21 January 2018

Mutational screening of breast cancer susceptibility gene 1 from early onset, bi-lateral, and familial breast cancer patients in Taiwan.

1 reference

https://api.crossref.org/works/10.1186%2FBCR2118

21 January 2018

Novel germline mutations in BRCA2 gene among 96 hereditary breast and breast-ovarian cancer families from Kerala, South India

1 reference

https://api.crossref.org/works/10.1186%2FBCR2118

21 January 2018

Update on the Manchester Scoring System for BRCA1 and BRCA2 testing

1 reference

https://api.crossref.org/works/10.1186%2FBCR2118

21 January 2018

BRCA1 disease-associated haplotypes in Singapore Malay women with early-onset breast/ovarian cancer.

1 reference

https://api.crossref.org/works/10.1186%2FBCR2118

21 January 2018

Evaluation of two different models to predict BRCA1 and BRCA2 mutations in a cohort of Danish hereditary breast and/or ovarian cancer families.

1 reference

https://api.crossref.org/works/10.1186%2FBCR2118

21 January 2018

Assessing BRCA carrier probabilities in extended families.

1 reference

https://api.crossref.org/works/10.1186%2FBCR2118

21 January 2018

Classification of IVS1-10T-->C as a polymorphism of BRCA1.

1 reference

https://api.crossref.org/works/10.1186%2FBCR2118

21 January 2018

Genetic testing in diverse populations: are researchers doing enough to get out the correct message?

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel germline BRCA1 mutations detected in women in singapore who developed breast carcinoma before the age of 36 years

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of Mutations in the BRCA1 Gene Among Chinese Patients With Breast Cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 and BRCA2 mutations in an Asian clinic-based population detected using a comprehensive strategy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 and BRCA2 mutations among breast cancer patients from the Philippines

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prevalence of BRCA1 and BRCA2 germline mutations in high-risk breast cancer patients of Chinese Han nationality: two recurrent mutations were identified

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An analysis of unclassified missense substitutions in human BRCA1

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 c.2845insA is a founder mutation in Singaporean Malay women with early onset breast/ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline BRCA1 mutation and survival analysis in familial breast cancer patients in Kerala; South India

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The analysis of BRCA1 mutations in eastern Chinese patients with early onset breast cancer and affected relatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of BRCA1 and BRCA2 germline mutations in Japanese breast cancer families

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation analysis of the BRCA1 gene in Malaysian breast cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Founder mutation in the BRCA1 gene in Malay breast cancer patients from Singapore

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution ofBRCA1andBRCA2mutations to inherited ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/18627636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/BCR2118

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

ResearchGate publication ID

0 references

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