(Q59688934)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17688236%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

title

Contribution of BRCA1 and BRCA2 mutations to inherited ovarian cancer (English)

1 reference

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3 January 2020

1 reference

1

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3 January 2020

Ian Jacobs

8

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3 January 2020

10

Alice S Whittemore

1 reference

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3 January 2020

14

Simon A Gayther

1 reference

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3 January 2020

13

Paul D P Pharoah

1 reference

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3 January 2020

author name string

Carole Pye

3

1 reference

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3 January 2020

Kim Garlinghouse-Jones

6

1 reference

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3 January 2020

Ingrid Oakley-Girvan

7

1 reference

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3 January 2020

Patricia A Harrington

2

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3 January 2020

Richard A DiCioccio

4

1 reference

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3 January 2020

Mark J Cox

5

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3 January 2020

Richard M Hardy

9

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3 January 2020

Bruce A J Ponder

11

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3 January 2020

M Steven Piver

12

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3 January 2020

publication date

1 December 2007

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3 January 2020

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3 January 2020

volume

28

1 reference

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3 January 2020

issue

12

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3 January 2020

page(s)

1207-1215

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Risk models for familial ovarian and breast cancer

3 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

The Exon 13 Duplication in the BRCA1 Gene Is a Founder Mutation Present in Geographically Diverse Populations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

The contribution of germline rearrangements to the spectrum of BRCA2 mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Genomic rearrangements in the BRCA1 and BRCA2 genes.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

The nonsense-mediated mRNA decay pathway triggers degradation of most BRCA1 mRNAs bearing premature termination codons

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Polygenic susceptibility to breast cancer and implications for prevention

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Comparative study of ovarian cancer histopathology by registry pathologists and referral pathologists: a study by the Gilda Radner Familial Ovarian Cancer Registry

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Screening for theBRCA1-ins6kbEx13mutation: potential for misdiagnosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Association of BRCA1 with Rad51 in mitotic and meiotic cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

A systematic review and meta-analysis of family history and risk of ovarian cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Variation in cancer risks, by mutation position, in BRCA2 mutation carriers

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Significant contribution of germline BRCA2 rearrangements in male breast cancer families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Does nonsense-mediated mRNA decay explain the ovarian cancer cluster region of the BRCA2 gene?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Histopathology, FIGO stage, and BRCA mutation status of ovarian cancers from the Gilda Radner Familial Ovarian Cancer Registry

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Large genomic rearrangements of both BRCA2 and BRCA1 are a feature of the inherited breast/ovarian cancer phenotype in selected families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Identification of the breast cancer susceptibility gene BRCA2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20599

7 January 2021

Identifiers

DOI

10.1002/HUMU.20599

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17688236%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

1 reference