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(1 - 20 of 29)

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The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position?
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
Outcome of ovarian cancer after breast cancer in BRCA1 and BRCA2 mutation carriers
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
Sensitivity to systemic therapy for metastatic breast cancer in CHEK2 1100delC mutation carriers
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2
Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer
Timing of risk reducing mastectomy in breast cancer patients carrying a BRCA1/2 mutation: retrospective data from the Dutch HEBON study
Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade
Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium
Survival and contralateral breast cancer in CHEK2 1100delC breast cancer patients: impact of adjuvant chemotherapy
2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy
Genetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast
Sensitivity to first-line chemotherapy for metastatic breast cancer in CHEK2 1100delC mutation carriers is not different compared with sporadic breast cancer patients
FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium
Survival and contralateral breast cancer in CHEK2 1100deIC breast cancer patients: Impact of adjuvant chemotherapy
Outcome of BRCA1- compared with BRCA2-associated ovarian cancer: a nationwide study in the Netherlands
Genome-wide association studies identify four ER negative-specific breast cancer risk loci
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

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