(Q35207476)

7 August 2017

title

Modification of BRCA1-Associated Breast and Ovarian Cancer Risk by BRCA1-Interacting Genes (English)

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7 August 2017

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18

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28

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Katherine L Nathanson

object named as

Katherine L Nathanson

39

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Susan M Domchek

3

object named as

Susan M Domchek

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35

Susan L Neuhausen

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11

Olufunmilayo I Olopade

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23

Douglas F Easton

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29

Fergus J Couch

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30

Irene L Andrulis

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12

Jeffrey N Weitzel

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36

Steven A Narod

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27

Claudine Isaacs

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16

Antonis C Antoniou

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37

Catherine M Phelan

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Mary B Daly

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Patricia A Ganz

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7 August 2017

9

Joanne L Blum

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7 August 2017

15

Judy E Garber

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7 August 2017

Timothy R Rebbeck

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7 August 2017

Nandita Mitra

2

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7 August 2017

Fei Wan

4

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7 August 2017

Tara M Friebel

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7 August 2017

Teo V Tran

6

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7 August 2017

Christian F Singer

7

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7 August 2017

Muy-Kheng Maria Tea

8

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7 August 2017

Nadine Tung

10

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7 August 2017

Henry T Lynch

13

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7 August 2017

Carrie L Snyder

14

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7 August 2017

Susan Peock

17

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7 August 2017

Joan Paterson

19

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7 August 2017

M John Kennedy

20

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7 August 2017

Alan Donaldson

21

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7 August 2017

Huw Dorkins

22

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7 August 2017

Epidemiological Study of BRCA1 and BRCA2 Mutation Carriers (EMBRACE)

24

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7 August 2017

Wendy S Rubinstein

25

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7 August 2017

Eitan Freidman

31

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7 August 2017

Yael Laitman

32

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7 August 2017

Gail E Tomlinson

34

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7 August 2017

Roger Greenberg

38

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7 August 2017

language of work or name

English

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publication date

28 July 2011

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7 August 2017

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7 August 2017

volume

71

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7 August 2017

issue

17

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7 August 2017

page(s)

5792-5805

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Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

NBA1/MERIT40 and BRE interaction is required for the integrity of two distinct deubiquitinating enzyme BRCC36-containing complexes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

Modification of ovarian cancer risk by BRCA1/2-interacting genes in a multicenter cohort of BRCA1/2 mutation carriers

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

NBA1, a new player in the Brca1 A complex, is required for DNA damage resistance and checkpoint control

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

Mutational analysis of the breast cancer susceptibility gene BRIP1 /BACH1/FANCJ in high-risk non-BRCA1/BRCA2 breast cancer families

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

Analysis of the gene coding for the BRCA2-interacting protein PALB2 in hereditary prostate cancer

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

A single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

Genetic and Histopathologic Evaluation ofBRCA1andBRCA2DNA Sequence Variants of Unknown Clinical Significance

8 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170727

A weighted cohort approach for analysing factors modifying disease risks in carriers of high-risk susceptibility genes

8 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21799032

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21799032

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1158/0008-5472.CAN-11-0773

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7 August 2017

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7 August 2017

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