Search Results - "Kroeze, Karin"
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Clinical correlates of low-risk variants in FGFR2, TNRC9, MAP3K1, LSP1 and 8q24 in a Dutch cohort of incident breast cancer cases
Published in Breast cancer research : BCR (01-01-2007)“…Seven SNPs in five genomic loci were recently found to confer a mildly increased risk of breast cancer. We have investigated the correlations between disease…”
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2
Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locus
Published in Genes chromosomes & cancer (01-11-2008)“…Breast cancer accounts for over 20% of all female cancers. A positive family history remains one of the most important risk factors for the disease, with…”
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Characterization of Familial Non-BRCA1/2 Breast Tumors by Loss of Heterozygosity and Immunophenotyping
Published in Clinical cancer research (15-03-2006)“…Purpose: Since the identification of BRCA1 and BRCA2 , there has been no major breast cancer susceptibility gene discovered by linkage analysis in breast…”
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Non-founder BRCA1 mutations in Russian breast cancer patients
Published in Cancer letters (08-12-2010)“…Abstract A few founder BRCA1 mutations (5382insC, 4154delA, 185delAG) account for up to 15% of high-risk (young-onset or familial or bilateral) breast cancer…”
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Evaluation of Linkage of Breast Cancer to the Putative BRCA3 Locus on Chromosome 13q21 in 128 Multiple Case Families from the Breast Cancer Linkage Consortium
Published in Proceedings of the National Academy of Sciences - PNAS (22-01-2002)“…The known susceptibility genes for breast cancer, including BRCA1 and BRCA2, only account for a minority of the familial aggregation of the disease. A recent…”
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A genome wide linkage search for breast cancer susceptibility genes
Published in Genes chromosomes & cancer (01-07-2006)“…Mutations in known breast cancer susceptibility genes account for a minority of the familial aggregation of the disease. To search for further breast cancer…”
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The CHEK21100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families
Published in Cancer research (Chicago, Ill.) (01-12-2003)“…The frame-shifting mutation 1100delC in the cell-cycle-checkpoint kinase 2 gene (CHEK2) has been reported to be associated with familial breast cancer in…”
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