Mieke Kriege

Rotterdam, ZH, Netherlands

Last Updated: 09/26/2026

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Found 24 publications

Improving the diagnostic accuracy of a stratified screening strategy by identifying the optimal risk cutoff.

Improving the diagnostic accuracy of a stratified screening strategy by identifying the optimal risk cutoff.

Journal: Cancer causes & control : CCC

Published: August 10, 2018

The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations.

The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations.

Journal: JNCI cancer spectrum

Published: August 02, 2018

The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position?

The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position?

Journal: European journal of human genetics : EJHG

Published: May 24, 2017

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

Journal: Breast cancer research and treatment

Published: October 05, 2016

Outcome of ovarian cancer after breast cancer in BRCA1 and BRCA2 mutation carriers.

Outcome of ovarian cancer after breast cancer in BRCA1 and BRCA2 mutation carriers.

Journal: British journal of cancer

Published: April 23, 2016

Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).

Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).

Journal: Scientific reports

Published: April 21, 2016

Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry.

Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry.

Journal: Cancer causes & control : CCC

Published: June 22, 2015

Sensitivity to systemic therapy for metastatic breast cancer in CHEK2 1100delC mutation carriers.

Sensitivity to systemic therapy for metastatic breast cancer in CHEK2 1100delC mutation carriers.

Journal: Journal of cancer research and clinical oncology

Published: March 26, 2015

Timing of risk reducing mastectomy in breast cancer patients carrying a BRCA1/2 mutation: retrospective data from the Dutch HEBON study.

Timing of risk reducing mastectomy in breast cancer patients carrying a BRCA1/2 mutation: retrospective data from the Dutch HEBON study.

Journal: Familial cancer

Published: February 22, 2015

Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer.

Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer.

Journal: Carcinogenesis

Published: January 15, 2015

Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.

Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.

Journal: Human molecular genetics

Published: December 22, 2014

Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium.

Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium.

Journal: Human molecular genetics

Published: June 20, 2014

Showing 1-12 of 24

Last Updated: 09/26/2026