(Q34542998)

English

Contribution of the PALB2 c.2323C>T [p.Q775X] founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Contribution of the PALB2 c.2323C>T [p.Q775X] founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

1 reference

based on heuristic

inferred from title

Anne-Marie Mes-Masson

object named as

Anne-Marie Mes-Masson

6

0 references

William David Foulkes

object named as

William D Foulkes

5

0 references

Marc Tischkowitz

1

object named as

Marc Tischkowitz

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

author name string

Nelly Sabbaghian

2

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Nancy Hamel

3

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Carly Pouchet

4

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Diane M Provencher

7

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Patricia N Tonin

8

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

publication date

9 January 2013

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

BMC Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

14

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

https://scigraph.springernature.com/pub.10.1186/1471-2350-14-5

0 references

Rare germline mutations in PALB2 and breast cancer risk: a population-based study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Chromosome 3 anomalies investigated by genome wide SNP analysis of benign, low malignant potential and low grade ovarian serous tumours

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

PALB2/FANCN: recombining cancer and Fanconi anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Discovering moderate-risk breast cancer susceptibility genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

A novel germline PALB2 deletion in Polish breast and ovarian cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Analysis of the gene coding for the BRCA2-interacting protein PALB2 in familial and sporadic pancreatic cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Inherited susceptibility to common cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Promoter hypermethylation of the PALB2 susceptibility gene in inherited and sporadic 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=3549741

7 July 2018

Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Analysis of PALB2/FANCN-associated breast cancer families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

The limited spectrum of pathogenic BRCA1 and BRCA2 mutations in the French Canadian breast and breast-ovarian cancer families, a founder population of Quebec, Canada

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Application of BRCA1 and BRCA2 mutation carrier prediction models in breast and/or ovarian cancer families of French Canadian descent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Haplotype analysis suggest common founders in carriers of the recurrent BRCA2mutation, 3398delAAAAG, in French Canadian hereditary 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=3549741

7 July 2018

Population history and its impact on medical genetics in Quebec

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Human genetics: lessons from Quebec populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Fragmentation of the Québec population genetic pool (Canada): evidence from the genetic contribution of founders per region in the 17th and 18th centuries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3549741

7 July 2018

Founder BRCA1 and BRCA2 mutations in French 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=3549741

7 July 2018

A recurrent mutation in PALB2 in Finnish cancer families.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-5

21 January 2018

PALB2 sequence variants in young South African breast cancer patients

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-5

21 January 2018

Evaluation of the contribution of the three breast cancer susceptibility genes CHEK2, STK11, and PALB2 in non-BRCA1/2 French Canadian families with high risk of breast cancer.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-5

21 January 2018

Rare occurrence of PALB2 mutations in ovarian cancer patients from the Volga-Ural region

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-5

21 January 2018

A PALB2 germline mutation associated with hereditary breast cancer in Italy

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-5

21 January 2018

Molecular and genealogical characterization of the R1443X BRCA1 mutation in high-risk French-Canadian breast/ovarian cancer families

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-5

21 January 2018

Analysis of FANCB and FANCN/PALB2 Fanconi Anemia genes in BRCA1/2-negative Spanish breast cancer families

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-5

21 January 2018

The BRCA2 c.9004G>A (E2003K) variant is likely pathogenic and recurs in breast and/or ovarian cancer families of French Canadian descent

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-5

21 January 2018

Significant proportion of breast and/or ovarian cancer families of French Canadian descent harbor 1 of 5BRCA1 andBRCA2 mutations

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-5

21 January 2018

Haplotype Analysis of BRCA2 8765delAG Mutation Carriers in French Canadian and Yemenite Jewish Hereditary Breast Cancer Families

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-5

21 January 2018

The prevalence of PALB2 germline mutations in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/23302520

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The contribution of founder mutations to early-onset breast cancer in French-Canadian women

1 reference

https://pubmed.ncbi.nlm.nih.gov/23302520

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1186/1471-2350-14-5

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

ResearchGate publication ID

0 references

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