The independent association between age at diagnosis and chromosomal copy number variation (CNV) events. (DOCX 15 kb
Additional file 1: Fig. S1. Detailed distribution of age at breast cancer diagnosis and family histo...
Figure S1. Copy number variation profiles of ATM-associated tumours analysed with the OncoScan array...
Breast cancer (BC) predisposition in populations arises from both genetic and nongenetic risk factor...
The independent association between age at diagnosis and gene expression signatures (>10,000) in a l...
CNV data for cases and controls. Chromosome coordinates given according to Hg18. (XLSX 819 kb
Frequency of variants of unknown significance and DCIS in women <â50Â years of age by gene. (DOCX ...
Taqman assays used for CNV assessment at 7 gene loci. Table S3. Cancer-predisposing genes disrupted ...
Age of onset of DCIS and family history details of women with two pathogenic variants in different g...
Performance of cytogenetic combinations as predictors of invasive cancer. (DOC 55 kb
Results from a genome-wide association analysis of CNVs overlapping gene loci. (XLSX 205 kb
Breast cancer (BC) patients considered for the study, their age at diagnosis and the number of affec...
Treatments and outcomes of patients with ductal carcinoma in situ (DCIS), with and without invasive ...
Copy number variation (CNV) GISTIC The Cancer Genome Atlas (TCGA). List of significant (q <0.25) amp...
Age at breast cancer diagnosis is a known prognostic factor. Previously, several groups including ou...
Correlation coefficients and measures of significance for each gene pair in our analysis of breast c...
Additional file 1: Fig. S1. Detailed distribution of age at breast cancer diagnosis and family histo...
Figure S1. Copy number variation profiles of ATM-associated tumours analysed with the OncoScan array...
Breast cancer (BC) predisposition in populations arises from both genetic and nongenetic risk factor...
The independent association between age at diagnosis and gene expression signatures (>10,000) in a l...
CNV data for cases and controls. Chromosome coordinates given according to Hg18. (XLSX 819 kb
Frequency of variants of unknown significance and DCIS in women <â50Â years of age by gene. (DOCX ...
Taqman assays used for CNV assessment at 7 gene loci. Table S3. Cancer-predisposing genes disrupted ...
Age of onset of DCIS and family history details of women with two pathogenic variants in different g...
Performance of cytogenetic combinations as predictors of invasive cancer. (DOC 55 kb
Results from a genome-wide association analysis of CNVs overlapping gene loci. (XLSX 205 kb
Breast cancer (BC) patients considered for the study, their age at diagnosis and the number of affec...
Treatments and outcomes of patients with ductal carcinoma in situ (DCIS), with and without invasive ...
Copy number variation (CNV) GISTIC The Cancer Genome Atlas (TCGA). List of significant (q <0.25) amp...
Age at breast cancer diagnosis is a known prognostic factor. Previously, several groups including ou...
Correlation coefficients and measures of significance for each gene pair in our analysis of breast c...
Additional file 1: Fig. S1. Detailed distribution of age at breast cancer diagnosis and family histo...
Figure S1. Copy number variation profiles of ATM-associated tumours analysed with the OncoScan array...
Breast cancer (BC) predisposition in populations arises from both genetic and nongenetic risk factor...
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