Found: 18
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Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-99409-3
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- Publication type:
- Article
Rare germline copy number variants (CNVs) and breast cancer risk.
- Published in:
- Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-021-02990-6
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- Publication type:
- Article
Breast cancer risks associated with missense variants in breast cancer susceptibility genes.
- Published in:
- Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01052-8
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- Article
Common variants in breast cancer risk loci predispose to distinct tumor subtypes.
- Published in:
- 2022
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- Publication type:
- journal article
Mutation Analysis of the <i>ERCC4/FANCQ</i> Gene in Hereditary Breast Cancer.
- Published in:
- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0085334
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- Article
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-018-08053-5
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- Publication type:
- Article
Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases.
- Published in:
- Cancers, 2023, v. 15, n. 13, p. 3313, doi. 10.3390/cancers15133313
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- Publication type:
- Article
A counter-clockwise northern route of the Y-chromosome haplogroup N from Southeast Asia towards Europe.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 2, p. 204, doi. 10.1038/sj.ejhg.5201748
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- Publication type:
- Article
Nonsense mutation p.Q548X in BLM, the gene mutated in Bloom's syndrome, is associated with breast cancer in Slavic populations.
- Published in:
- Breast Cancer Research & Treatment, 2013, v. 137, n. 2, p. 533, doi. 10.1007/s10549-012-2357-1
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- Publication type:
- Article
A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer.
- Published in:
- 2010
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- Publication type:
- Report
Two truncating variants in FANCC and breast cancer risk.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-48804-y
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- Publication type:
- Article
Genome-wide association study of germline variants and breast cancer-specific mortality.
- Published in:
- 2019
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- Publication type:
- journal article
A Splice Site Variant of CDK12 and Breast Cancer in Three Eurasian Populations.
- Published in:
- Frontiers in Oncology, 2019, p. N.PAG, doi. 10.3389/fonc.2019.00493
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- Publication type:
- Article
Mendelian randomisation study of smoking exposure in relation to breast cancer risk.
- Published in:
- 2021
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- Publication type:
- journal article
Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe.
- Published in:
- Familial Cancer, 2015, v. 14, n. 1, p. 145, doi. 10.1007/s10689-014-9748-x
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- Publication type:
- Article
Prevalence of PALB2 mutation c.509_510delGA in unselected breast cancer patients from Central and Eastern Europe.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 137, doi. 10.1007/s10689-013-9684-1
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- Publication type:
- Article
Mitochondrial DNA Variations in Russian and Belorussian Populations.
- Published in:
- Human Biology, 2003, v. 75, n. 5, p. 647, doi. 10.1353/hub.2003.0069
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- Publication type:
- Article
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-019-14100-6
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- Publication type:
- Article