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Molecular comparison of interval and screen‐detected breast cancers.
- Published in:
- Journal of Pathology, 2019, v. 248, n. 2, p. 243, doi. 10.1002/path.5251
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- Article
Molecular analysis of PALB2‐associated breast cancers.
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- Journal of Pathology, 2018, v. 245, n. 1, p. 53, doi. 10.1002/path.5055
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- Article
RNF43 is a tumour suppressor gene mutated in mucinous tumours of the ovary.
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- Journal of Pathology, 2013, v. 229, n. 3, p. 469, doi. 10.1002/path.4134
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- Article
Reevaluation of the BRCA2 truncating allele c.9976A >T (p.Lys3326Ter) in a familial breast cancer context.
- Published in:
- Scientific Reports, 2015, p. 1, doi. 10.1038/srep14800
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- Article
Analysis of RAD51D in Ovarian Cancer Patients and Families with a History of Ovarian or Breast Cancer.
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- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0054772
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- Article
MicroRNA Genes and Their Target 39-Untranslated Regions Are Infrequently Somatically Mutated in Ovarian Cancers.
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- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0035805
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- Article
Long Range Regulation of Human FXN Gene Expression.
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- PLoS ONE, 2011, v. 6, n. 7, p. 1, doi. 10.1371/journal.pone.0022001
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- Article
Wolbachia pipientis in Australian Spiders.
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- Current Microbiology, 2004, v. 49, n. 3, p. 208, doi. 10.1007/s00284-004-4346-z
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- Article
Integration of tumour sequencing and case–control data to assess pathogenicity of RAD51C missense variants in familial breast cancer.
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- NPJ Breast Cancer, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41523-021-00373-y
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- Publication type:
- Article
Investigation of monogenic causes of familial breast cancer: data from the BEACCON case-control study.
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- NPJ Breast Cancer, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41523-021-00279-9
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- Article
The TP53 mutation rate differs in breast cancers that arise in women with high or low mammographic density.
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- NPJ Breast Cancer, 2020, v. 6, n. 1, p. 1, doi. 10.1038/s41523-020-00176-7
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- Article
The genetic architecture of breast papillary lesions as a predictor of progression to carcinoma.
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- NPJ Breast Cancer, 2020, v. 6, n. 1, p. 1, doi. 10.1038/s41523-020-0150-6
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- Publication type:
- Article
Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs.
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- 2018
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- Publication type:
- journal article
Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls.
- Published in:
- Breast Cancer Research, 2015, v. 17, n. 1, p. 1, doi. 10.1186/s13058-015-0627-7
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- Article
Loss of heterozygosity: what is it good for?
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- BMC Medical Genomics, 2015, v. 8, n. 1, p. 1, doi. 10.1186/s12920-015-0123-z
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- Article
Molecular comparison of pure ovarian fibroma with serous benign ovarian tumours.
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- BMC Research Notes, 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13104-020-05194-z
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- Article
FXN methylation predicts expression and clinical outcome in Friedreich ataxia.
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- Annals of Neurology, 2012, v. 71, n. 4, p. 487, doi. 10.1002/ana.22671
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- Publication type:
- Article
Exome Sequencing Identifies Rare Deleterious Mutations in DNA Repair Genes FANCC and BLM as Potential Breast Cancer Susceptibility Alleles.
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- PLoS Genetics, 2012, v. 8, n. 9, p. 1, doi. 10.1371/journal.pgen.1002894
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- Article
Mutational landscape of mucinous ovarian carcinoma and its neoplastic precursors.
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- Genome Medicine, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13073-015-0210-y
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- Article
A simple consensus approach improves somatic mutation prediction accuracy.
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- Genome Medicine, 2013, v. 5, n. 9, p. 1, doi. 10.1186/gm494
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- Article
Somatic Inactivation of Breast Cancer Predisposition Genes in Tumours Associated with Pathogenic Germline Variants.
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- JNCI: Journal of the National Cancer Institute, 2023, v. 115, n. 2, p. 181, doi. 10.1093/jnci/djac196
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- Article
Combined Tumor Sequencing and Case-Control Analyses of RAD51C in Breast Cancer.
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- 2019
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- Publication type:
- journal article
Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15461-z
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- Publication type:
- Article
Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0375-z
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- Publication type:
- Article