Analysis of PALB2/FANCN-associated breast cancer families (Q24683771)

11

Atilla Omeroglu

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William David Foulkes

William D Foulkes

20

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Jorge Reis-Filho

4

Jorge S Reis-Filho

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Steven A. Narod

18

Steven A Narod

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Marc Tischkowitz

1

Marc Tischkowitz

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author name string

Bing Xia

2

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Nelly Sabbaghian

3

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Nancy Hamel

5

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Guilan Li

6

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Erik H van Beers

7

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Lili Li

8

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Tayma Khalil

9

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Louise A Quenneville

10

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Aletta Poll

12

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Pierre Lepage

13

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Nora Wong

14

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Petra M Nederlof

15

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Patricia N Tonin

17

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David M Livingston

Proceedings of the National Academy of Sciences of the United States of America

19

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language of work or name

English

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publication date

17 April 2007

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published in

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volume

104

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issue

16

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page(s)

6788-93

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cites work

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=1871863

Allelic imbalances of chromosomes 8p and 18q and their roles in distant relapse of early stage, node-negative breast cancer

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

Involvement of Brca2 in DNA repair

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

A genome wide linkage search for breast cancer susceptibility genes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

A multiplex PCR predictor for aCGH success of FFPE samples

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

Analysis of array CGH data: from signal ratio to gain and loss of DNA regions

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

Pooled analysis of loss of heterozygosity in breast cancer: a genome scan provides comparative evidence for multiple tumor suppressors and identifies novel candidate regions

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

Breast and ovarian cancer

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871863

A recurrent mutation in PALB2 in Finnish cancer families.

28 September 2017

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0701724104

Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0701724104

Genomic imbalances detected by comparative genomic hybridization are prognostic markers in invasive ductal breast carcinomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0701724104

Evaluation of Phi29-based whole-genome amplification for microarray-based comparative genomic hybridisation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0701724104

BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0701724104

Pleomorphic lobular carcinoma of the breast: role of comprehensive molecular pathology in characterization of an entity

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0701724104

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0701724104

Genetic changes in breast cancer detected by comparative genomic hybridisation

21 January 2018

1 reference

12 December 2020

DNA sequence losses on chromosomes 11p and 18q are associated with clinical outcome in lymph node-negative ductal breast cancer

1 reference

12 December 2020

Somatic genetic alterations inBRCA2-associated and sporadic male breast cancer

1 reference

12 December 2020

Comparative genomic hybridization profiles in human BRCA1 and BRCA2 breast tumors highlight differential sets of genomic aberrations

1 reference

12 December 2020