A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families (Q24680760)

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English	A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families	scientific article

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scholarly article

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A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families (English)

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1 reference

based on heuristic

inferred from title

25

object named as

P Devilee

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author name string

T Peelen

1

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M van Vliet

2

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A Petrij-Bosch

3

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R Mieremet

4

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C Szabo

5

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A M van den Ouweland

6

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F Hogervorst

7

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R Brohet

8

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M J Ligtenberg

9

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E Teugels

10

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R van der Luijt

11

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A H van der Hout

12

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J J Gille

13

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G Pals

14

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I Jedema

15

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R Olmer

16

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I van Leeuwen

17

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B Newman

18

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M Plandsoen

19

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M van der Est

20

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G Brink

21

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S Hageman

22

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P J Arts

23

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M M Bakker

24

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language of work or name

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publication date

May 1997

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American Journal of Human Genetics

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60

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5

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1041-9

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Genetic linkage analysis in familial breast and ovarian cancer: results from 214 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=1712432

7 April 2017

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=1712432

7 April 2017

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

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712432

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712432

7 April 2017

High-density genetic map of the BRCA1 region of chromosome 17q12-q21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712432

7 April 2017

Linkage of early-onset familial breast cancer to chromosome 17q21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712432

7 April 2017

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=1712432

7 April 2017

Mutation nomenclature: nicknames, systematic names, and unique identifiers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712432

28 September 2017

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=1712432

28 September 2017

Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712432

28 September 2017

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=1712432

28 September 2017

A high incidence of BRCA1 mutations in 20 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=1712432

28 September 2017

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=1712432

28 September 2017

Mutation of human short tandem repeats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712432

28 September 2017

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=1712432

28 September 2017

Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712432

28 September 2017

Breast and ovarian cancer incidence 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=1712432

28 September 2017

Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712432

28 September 2017

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=1712432

28 September 2017

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=1712432

28 September 2017

The genetics 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=1712432

28 September 2017

A common BRCA1 mutation in Norwegian 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=1712432

30 May 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=1712432

30 May 2018

Rapid detection of translation-terminating mutations at the adenomatous polyposis coli (APC) gene by direct protein truncation test.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712432

28 November 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=1712432

28 November 2018

Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes

1 reference

https://pubmed.ncbi.nlm.nih.gov/9150151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/9150151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9150151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9150151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid detection of BRCA1 mutations by the protein truncation test

1 reference

https://pubmed.ncbi.nlm.nih.gov/9150151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New Austrian mutation in BRCA1 gene detected in three unrelated HBOC families

1 reference

https://pubmed.ncbi.nlm.nih.gov/9150151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene. Breast Cancer Information Core

1 reference

https://pubmed.ncbi.nlm.nih.gov/9150151

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/9150151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The majority of 22 Dutch high-risk breast cancer families are due to either BRCA1 or BRCA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/9150151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 germline mutational spectrum in Italian families from Tuscany: a high frequency of novel mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/9150151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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