Found: 17
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Genetic testing in Poland and Ukraine: should comprehensive germline testing of BRCA1 and BRCA2 be recommended for women with breast and ovarian cancer?
- Published in:
- Genetics Research, 2020, p. 1, doi. 10.1017/S0016672320000075
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- Publication type:
- Article
Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2.
- Published in:
- BMC Medical Genomics, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1755-8794-6-48
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- Publication type:
- Article
The use of DNA from archival dried blood spots with the Infinium HumanMethylation450 array.
- Published in:
- BMC Biotechnology, 2013, v. 12, n. 1, p. 1, doi. 10.1186/1472-6750-13-23
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- Publication type:
- Article
VTRNA2-1 : Genetic Variation, Heritable Methylation and Disease Association.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 5, p. 2535, doi. 10.3390/ijms22052535
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- Publication type:
- Article
FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine.
- Published in:
- BMC Medical Genetics, 2018, v. 19, p. 1, doi. 10.1186/s12881-018-0524-x
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- Publication type:
- Article
Saliva-derived DNA is suitable for the detection of clonal haematopoiesis of indeterminate potential.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-69398-0
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- Publication type:
- Article
Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations?
- Published in:
- 2018
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- Publication type:
- journal article
Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry.
- Published in:
- 2015
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- Publication type:
- Report
Epigenome-wide methylation in DNA from peripheral blood as a marker of risk for breast cancer.
- Published in:
- Breast Cancer Research & Treatment, 2014, v. 148, n. 3, p. 665, doi. 10.1007/s10549-014-3209-y
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- Publication type:
- Article
Mismatch repair gene pathogenic germline variants in a population-based cohort of breast cancer.
- Published in:
- Familial Cancer, 2020, v. 19, n. 3, p. 197, doi. 10.1007/s10689-020-00164-7
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- Publication type:
- Article
Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and Ukraine.
- Published in:
- Familial Cancer, 2018, v. 17, n. 3, p. 345, doi. 10.1007/s10689-017-0050-6
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- Publication type:
- Article
1322A pilot study of faecal sample collection from prospective cohort study participants.
- Published in:
- International Journal of Epidemiology, 2021, v. 50, p. 1, doi. 10.1093/ije/dyab168.100
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- Publication type:
- Article
Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer.
- Published in:
- Cancers, 2021, v. 13, n. 7, p. 1495, doi. 10.3390/cancers13071495
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- Publication type:
- Article
Population-Based Estimates of the Age-Specific Cumulative Risk of Breast Cancer for Pathogenic Variants in CHEK2 : Findings from the Australian Breast Cancer Family Registry.
- Published in:
- Cancers, 2021, v. 13, n. 6, p. 1378, doi. 10.3390/cancers13061378
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- Publication type:
- Article
Using SNP genotypes to improve the discrimination of a simple breast cancer risk prediction model.
- Published in:
- Breast Cancer Research & Treatment, 2013, v. 139, n. 3, p. 887, doi. 10.1007/s10549-013-2610-2
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- Publication type:
- Article
Rare germline genetic variants and risk of aggressive prostate cancer.
- Published in:
- International Journal of Cancer, 2020, v. 147, n. 8, p. 2142, doi. 10.1002/ijc.33024
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- Publication type:
- Article
Population-based estimates of breast cancer risk for carriers of pathogenic variants identified by gene-panel testing.
- Published in:
- NPJ Breast Cancer, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41523-021-00360-3
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- Publication type:
- Article