(Q30438623)

14 August 2017

Risk for contralateral breast cancer among carriers of the CHEK2*1100delC mutation in the WECARE Study (English)

1 reference

14 August 2017

L Mellemkjaer

1

0 references

Patrick Concannon

object named as

P Concannon

16

0 references

Anne-Lise Børresen-Dale

7

object named as

A-L Børresen-Dale

1 reference

14 August 2017

10

L Bernstein

1 reference

14 August 2017

12

K E Malone

1 reference

WECARE Study Collaborative Group

14 August 2017

19

object named as

WECARE Study Collaborative Group

1 reference

14 August 2017

C Dahl

2

1 reference

14 August 2017

J H Olsen

3

1 reference

14 August 2017

L Bertelsen

4

1 reference

14 August 2017

P Guldberg

5

1 reference

14 August 2017

J Christensen

6

1 reference

14 August 2017

M Stovall

8

1 reference

14 August 2017

B Langholz

9

1 reference

14 August 2017

C F Lynch

11

1 reference

14 August 2017

R W Haile

13

1 reference

14 August 2017

M Andersson

14

1 reference

14 August 2017

D C Thomas

15

1 reference

14 August 2017

M Capanu

17

1 reference

14 August 2017

J D Boice

18

1 reference

14 August 2017

J L Bernstein

20

1 reference

14 August 2017

language of work or name

English

0 references

publication date

5 February 2008

1 reference

British Journal of Cancer

14 August 2017

1 reference

14 August 2017

98

1 reference

14 August 2017

4

1 reference

14 August 2017

728-733

1 reference

Variation of breast cancer risk among BRCA1/2 carriers

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259175

Identification of women with an increased risk of developing radiation-induced breast cancer: a case only study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259175

The CHEK2 gene and inherited breast cancer susceptibility

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259175

Frequency of CHEK2 mutations in a population based, case-control study of breast cancer in young women

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259175

Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK2*1100delC variant

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259175

CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259175

Study design: evaluating gene-environment interactions in the etiology of breast cancer - the WECARE study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259175

A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259175

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259175

Characterization of tumor-associated Chk2 mutations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259175

Chromosomal radiosensitivity of breast cancer with a CHEK2 mutation.

20 June 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604228

The CHEK2*1100delC allelic variant and risk of breast cancer: screening results from the Breast Cancer Family Registry

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604228

Excess risk for contralateral breast cancer in CHEK2*1100delC germline mutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604228

CHEK2 1100delC mutation is frequent among Russian breast cancer patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604228

Correlation of CHEK2 protein expression and c.1100delC mutation status with tumor characteristics among unselected breast cancer patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604228

The breast cancer low-penetrance allele 1100delC in the CHEK2 gene is not present in Spanish familial breast cancer population

21 January 2018

1 reference

12 December 2020

The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families

1 reference

12 December 2020

Aberrations of the Chk2 tumour suppressor in advanced urinary bladder cancer

1 reference

12 December 2020

Pathology of breast cancer in women with constitutional CHEK2 mutations

1 reference

12 December 2020

Low frequency of the CHEK2*1100delC mutation among breast cancer probands from three regions of Poland

1 reference

12 December 2020

Increased risk of breast cancer associated with CHEK2*1100delC

1 reference

12 December 2020

Breast Cancer Survival and Tumor Characteristics in Premenopausal Women Carrying theCHEK2*1100delCGermline Mutation

1 reference

12 December 2020

Identifiers

DOI

10.1038/SJ.BJC.6604228

1 reference

Dimensions Publication ID

14 August 2017

0 references

1 reference

14 August 2017

PubMed publication ID

18253122

1 reference