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Author Correction: Single-nuclei and bulk-tissue gene-expression analysis of pheochromocytoma and paraganglioma links disease subtypes with tumor microenvironment.
- Published in:
- 2023
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- Publication type:
- Correction Notice
Single-nuclei and bulk-tissue gene-expression analysis of pheochromocytoma and paraganglioma links disease subtypes with tumor microenvironment.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-34011-3
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- Article
Genomic analysis of low‐grade serous ovarian carcinoma to identify key drivers and therapeutic vulnerabilities.
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- Journal of Pathology, 2021, v. 253, n. 1, p. 41, doi. 10.1002/path.5545
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- Publication type:
- Article
Atypical ductal hyperplasia is a multipotent precursor of breast carcinoma.
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- Journal of Pathology, 2019, v. 248, n. 3, p. 326, doi. 10.1002/path.5262
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- Article
Molecular comparison of interval and screen‐detected breast cancers.
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- Journal of Pathology, 2019, v. 248, n. 2, p. 243, doi. 10.1002/path.5251
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- Publication type:
- 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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- Publication type:
- Article
MAIT cells regulate NK cell-mediated tumor immunity.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-25009-4
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- Publication type:
- Article
Distinct modulation of IFNγ-induced transcription by BET bromodomain and catalytic P300/CBP inhibition in breast cancer.
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- Clinical Epigenetics, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13148-022-01316-5
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- Publication type:
- Article
Distinct modulation of IFNγ-induced transcription by BET bromodomain and catalytic P300/CBP inhibition in breast cancer.
- Published in:
- Clinical Epigenetics, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13148-022-01316-5
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- Publication type:
- Article
Evaluating statistical approaches to define clonal origin of tumours using bulk DNA sequencing: context is everything.
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- Genome Biology, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s13059-022-02600-6
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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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- Publication type:
- Article
Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects.
- Published in:
- NPJ Breast Cancer, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41523-021-00255-3
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- Publication type:
- 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
Bcor loss perturbs myeloid differentiation and promotes leukaemogenesis.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-09250-6
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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.
- Published in:
- 2018
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- Publication type:
- journal article
Universal genetic testing for women with newly diagnosed breast cancer in the context of multidisciplinary team care.
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- Medical Journal of Australia, 2023, v. 218, n. 8, p. 368, doi. 10.5694/mja2.51906
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- Publication type:
- Article
A synonymous VHL variant in exon 2 confers susceptibility to familial pheochromocytoma and von Hippel-Lindau disease.
- Published in:
- 2019
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- Publication type:
- journal 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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- Publication type:
- Article
Combined Tumor Sequencing and Case-Control Analyses of RAD51C in Breast Cancer.
- Published in:
- 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.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15461-z
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- Publication type:
- Article