(Q41193996)

28 September 2017

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title

Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families (English)

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28 September 2017

15

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28 September 2017

William David Foulkes

24

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28 September 2017

6

Neuhausen S

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28 September 2017

4

Couch F

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28 September 2017

22

Norton L

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28 September 2017

3

Offit K

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28 September 2017

Tonin P

1

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28 September 2017

Weber B

2

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28 September 2017

Rebbeck TR

5

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28 September 2017

Godwin AK

7

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28 September 2017

Daly M

8

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28 September 2017

Wagner-Costalos J

9

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28 September 2017

Berman D

10

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28 September 2017

Grana G

11

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28 September 2017

Fox E

12

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28 September 2017

Kane MF

13

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28 September 2017

Kolodner RD

14

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28 September 2017

Haber DA

16

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28 September 2017

Struewing JP

17

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28 September 2017

Warner E

18

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28 September 2017

Rosen B

19

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28 September 2017

Lerman C

20

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28 September 2017

Peshkin B

21

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28 September 2017

Serova O

23

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28 September 2017

Garber JE

25

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28 September 2017

language of work or name

English

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publication date

1 November 1996

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28 September 2017

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28 September 2017

2

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28 September 2017

1179-1183

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28 September 2017

11

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https://scigraph.springernature.com/pub.10.1038/nm1196-1179

28 September 2017

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cites work

Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

Jewish religion and risk of breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

Identification of the breast cancer susceptibility gene BRCA2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

A large multisite cancer family is linked to BRCA2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

7 January 2021

The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

7 January 2021

Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

7 January 2021

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

7 January 2021

Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

7 January 2021

The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

7 January 2021

Germline BRCA1 185delAG mutations in Jewish women with breast cancer

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

7 January 2021

BRCA2 germline mutations in male breast cancer cases and breast cancer families

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

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/10.1038%2FNM1196-1179

7 January 2021

Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

7 January 2021

Growth retardation and tumour inhibition by BRCA1.

1 reference

https://api.crossref.org/works/10.1038%2FNM1196-1179

7 January 2021

Identifiers

DOI

10.1038/NM1196-1179

1 reference

28 September 2017

1 reference