(Q33355677)

English

Novel sequence variants and a high frequency of recurrent polymorphisms in BRCA1 gene in Sri Lankan breast cancer patients and at risk individuals

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Novel sequence variants and a high frequency of recurrent polymorphisms in BRCA1 gene in Sri Lankan breast cancer patients and at risk individuals (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

author name string

Wasanthi De Silva

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Eric H Karunanayake

2

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Kamani H Tennekoon

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Marie Allen

4

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Indrani Amarasinghe

5

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Preethika Angunawala

6

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Mohamed H Ziard

7

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

language of work or name

0 references

publication date

29 July 2008

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

214

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

A novel BRCA-1 mutation in Arab kindred from east Jerusalem with 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=2519088

21 June 2018

Cancer risks among 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=2519088

21 June 2018

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=2519088

21 June 2018

Intronic alterations in BRCA1 and BRCA2: effect on mRNA splicing fidelity and expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

Global cancer statistics, 2002

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

Characterization of a novel large deletion and single point mutations in the BRCA1 gene in a Greek cohort of families with suspected hereditary breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

BRCA1 and BRCA2: 1994 and beyond

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

The multiple nuclear functions of BRCA1: transcription, ubiquitination and DNA repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

Differentiating pathogenic mutations from polymorphic alterations in the splice sites 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=2519088

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

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=2519088

21 June 2018

Structural consequences of a cancer-causing BRCA1-BRCT missense mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

Germ line BRCA1 & BRCA2 mutations in Greek breast/ovarian cancer families: 5382insC is the most frequent mutation observed

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

The lifetime risks of breast cancer in Ashkenazi Jewish carriers of 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=2519088

21 June 2018

BRCA1 and BRCA2 are necessary for the transcription-coupled repair of the oxidative 8-oxoguanine lesion in human cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

Ethnic differences in cancer risk resulting from genetic variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 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=2519088

21 June 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=2519088

21 June 2018

Risks of cancer in BRCA1-mutation carriers. 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=2519088

21 June 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

21 June 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-8-214

21 January 2018

Incidence of BRCA1 and BRCA2 mutations in young Korean breast cancer patients.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-8-214

21 January 2018

Complete allelic analysis of BRCA1 and BRCA2 variants in young Nigerian breast cancer patients

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-8-214

21 January 2018

Germline mutations of BRCA1 and BRCA2 in Korean breast and/or ovarian cancer families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2519088

31 October 2018

BRCA1 and BRCA2 mutations among breast cancer patients from the Philippines

1 reference

https://pubmed.ncbi.nlm.nih.gov/18662409

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 and BRCA2 sequence variants in Chinese breast cancer families

1 reference

https://pubmed.ncbi.nlm.nih.gov/18662409

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Biochemical analysis demonstrates that the BRCA1 intronic variant IVS10-2A→C is a mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18662409

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel germline mutations in the BRCA1 and BRCA2 genes in Indian breast and breast-ovarian cancer families

1 reference

https://pubmed.ncbi.nlm.nih.gov/18662409

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of BRCA1 and BRCA2 germ-line mutations to the incidence of breast cancer in young women: results from a prospective population-based study in France

1 reference

https://pubmed.ncbi.nlm.nih.gov/18662409

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 mutations and polymorphisms in a hospital-based consecutive series of breast cancer patients from Apulia, Italy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18662409

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of 2 novel and 2 recurring BRCA1 germline mutations in breast and/or ovarian carcinoma patients from the area of Naples

1 reference

https://pubmed.ncbi.nlm.nih.gov/18662409

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2407-8-214

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

ResearchGate publication ID

0 references

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