(Q36543070)

14 August 2017

Haplotype analysis of the 185delAG BRCA1 mutation in ethnically diverse populations (English)

1 reference

14 August 2017

1 reference

9

1 reference

14 August 2017

Danielle Port

6

0 references

William G. Newman

object named as

William G Newman

11

0 references

Jeffrey N Weitzel

4

object named as

Jeffrey N Weitzel

1 reference

14 August 2017

1

Yael Laitman

1 reference

14 August 2017

15

David Goldgar

1 reference

14 August 2017

10

Ayse Latif

1 reference

14 August 2017

Bing-Jian Feng

2

1 reference

14 August 2017

Itay M Zamir

3

1 reference

14 August 2017

Paul Duncan

5

1 reference

14 August 2017

Eswary Thirthagiri

7

1 reference

14 August 2017

Soo-Hwang Teo

8

1 reference

14 August 2017

Ruth Gershoni-Baruch

12

1 reference

14 August 2017

Jamal Zidan

13

1 reference

14 August 2017

Shani Shimon-Paluch

14

1 reference

14 August 2017

Eitan Friedman

16

1 reference

14 August 2017

4 July 2012

1 reference

European Journal of Human Genetics

14 August 2017

1 reference

14 August 2017

21

1 reference

14 August 2017

2

1 reference

14 August 2017

212-216

1 reference

The impact of Converso Jews on the genomes of modern Latin Americans

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Ingredients for success: a familial cancer clinic in an oncology practice setting

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European populations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Presymptomatic breast cancer in Egypt: role of BRCA1 and BRCA2 tumor suppressor genes mutations detection

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian Peninsula

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Penetrance estimates for BRCA1 and BRCA2 based on genetic testing in a Clinical Cancer Genetics service setting: risks of breast/ovarian cancer quoted should reflect the cancer burden in the family

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-control association 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=3548269

Prevalence of BRCA1 and BRCA2 mutations in Pakistani breast and ovarian cancer patients

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Prevalence of BRCA mutations and founder effect in high-risk Hispanic families

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

BRCA1:185delAG found in the San Luis Valley probably originated in a Jewish founder

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

The Norwegian founder mutations in BRCA1: high penetrance confirmed in an incident cancer series and differences observed in the risk of ovarian cancer

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Identification of germline 185delAG BRCA1 mutations in non-Jewish Americans of Spanish ancestry from the San Luis Valley, Colorado

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

A high-resolution recombination map of the human genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Estimate of the mutation rate per nucleotide in humans

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Prevalence of BRCA1 and BRCA2 Jewish mutations in Spanish breast cancer patients.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

The 185delAG BRCA1 mutation originated before the dispersion of Jews in the diaspora and is not limited to Ashkenazim

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Mutation of human short tandem repeats

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Independent origin of 185delAG BRCA1 mutation in an Indian family.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

High frequency of BRCA1 5382insC mutation in Russian breast cancer patients.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

A genetic profile of contemporary Jewish populations

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

An update on DNA-based BRCA1/BRCA2 genetic counseling in hereditary breast cancer.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3548269

Population-based study of risk of breast cancer in carriers of BRCA2 mutation

21 September 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.124

Addition of pathology and biomarker information significantly improves the performance of the Manchester scoring system for BRCA1 and BRCA2 testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.124

Haplotype analysis of a BRCA1 : 185delAG mutation in a Chilean family supports its Ashkenazi origins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.124

Identification of the 185delAG BRCA1 mutation in a Spanish Gypsy population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.124

Breast cancer predisposing alleles in Poland

21 January 2018

1 reference

12 December 2020

Ashkenazi founder BRCA1/BRCA2 mutations in Slovak hereditary breast and/or ovarian cancer families

1 reference

12 December 2020

Mutational analyses ofBRCA1 andBRCA2 in Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer

2 references

12 December 2020

https://api.crossref.org/works/10.1038%2FEJHG.2012.124

7 January 2021

inferred from DOI database lookup

Germline BRCA1 mutation analysis in Indian breast/ovarian cancer families

1 reference

12 December 2020

Identifiers

DOI

10.1038/EJHG.2012.124

1 reference

Dimensions Publication ID

14 August 2017

0 references

1 reference

14 August 2017

PubMed publication ID

22763381

1 reference