(Q34773464)

English

BRCA1/2 mutation screening in high-risk breast/ovarian cancer families and sporadic cancer patient surveilling for hidden high-risk families

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

BRCA1/2 mutation screening in high-risk breast/ovarian cancer families and sporadic cancer patient surveilling for hidden high-risk families (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Dace Berzina

1

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Miki Nakazawa-Miklasevica

2

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Jekaterina Zestkova

3

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Karina Aksenoka

4

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Arvids Irmejs

5

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Andris Gardovskis

6

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Dagnija Kalniete

7

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Janis Gardovskis

8

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Edvins Miklasevics

9

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

publication date

14 June 2013

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

BMC Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

14

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

61

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Genotype-phenotype correlations among BRCA1 4153delA and 5382insC mutation carriers from Latvia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3686592

7 July 2018

Genetic variants associated with breast-cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3686592

7 July 2018

Population screening for hereditary and familial cancer syndromes in Valka district of Latvia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3686592

7 July 2018

Clinical, molecular and geographical features of hereditary breast/ovarian cancer in latvia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3686592

7 July 2018

Genotyping of frequent BRCA1/2 SNPs with unlabeled probes: a supplement to HRMCA mutation scanning, allowing the strong reduction of sequencing burden

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3686592

7 July 2018

The contribution of BRCA1 and BRCA2 to ovarian cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3686592

7 July 2018

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=3686592

7 July 2018

Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3686592

7 July 2018

Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3686592

7 July 2018

High prevalence of two BRCA1 mutations, 4154delA and 5382insC, in Latvia

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-61

21 January 2018

Cancer variation associated with the position of the mutation in the BRCA2 gene

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-61

21 January 2018

Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-61

21 January 2018

Screening for a BRCA2 rearrangement in high-risk breast/ovarian cancer families: evidence for a founder effect and analysis of the associated phenotypes.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-61

21 January 2018

Counting potentially functional variants in BRCA1, BRCA2 and ATM predicts breast cancer susceptibility

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-61

21 January 2018

Prevalence and Predictors ofBRCA1andBRCA2Mutations in a Population-Based Study of Breast Cancer in White and Black American Women Ages 35 to 64 Years

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-61

21 January 2018

A high frequency of BRCA2 gene mutations in Polish families with ovarian and stomach cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/23767878

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/23767878

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic attributable risk of breast and ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/23767878

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of Common BRCA1 and BRCA2 Variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/23767878

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2350-14-61

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

ResearchGate publication ID

0 references

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