(Q35238946)

English

The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women

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scholarly article

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Europe PubMed Central

PubMed publication ID

7 August 2017

The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Abeliovich D

1

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Kaduri L

2

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Lerer I

3

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Weinberg N

4

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Amir G

5

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Sagi M

6

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Zlotogora J

7

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Heching N

8

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Peretz T

9

1 reference

Europe PubMed Central

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7 August 2017

language of work or name

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publication date

1 March 1997

1 reference

Europe PubMed Central

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7 August 2017

American Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

7 August 2017

60

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Europe PubMed Central

PubMed publication ID

7 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

505-514

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 2018

Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 2018

Two distinct origins of a common BRCA1 mutation in breast-ovarian cancer families: a genetic study of 15 185delAG-mutation kindreds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 2018

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 2018

Estimates of the gene frequency of BRCA1 and its contribution to breast and ovarian cancer incidence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 2018

Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 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=1712523

13 July 2018

Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 2018

Neoplastic diseases in families of breast cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 2018

BRCA1 mutations in Ashkenazi Jewish women

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 2018

Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 2018

Mutation analysis of the BRCA1 gene in ovarian cancers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 2018

The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 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=1712523

13 July 2018

Development, multiplexing, and application of ARMS tests for common mutations in the CFTR gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

13 July 2018

One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

26 September 2018

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

8 December 2018

Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712523

8 December 2018

Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9042909

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breast cancer and BRCA1 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/9042909

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of the BRCA1 185delAG mutation among Jewish women with ovarian cancer and matched population controls

1 reference

https://pubmed.ncbi.nlm.nih.gov/9042909

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/9042909

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular diagnosis of Prader-Willi syndrome: parent-of-origin dependent methylation sites and non-isotopic detection of (CA)n dinucleotide repeat polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/9042909

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline BRCA1 185delAG mutations in Jewish women with breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9042909

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/9042909

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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