Found: 13
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Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients.
- Published in:
- Cancers, 2020, v. 12, n. 4, p. 829, doi. 10.3390/cancers12040829
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- Publication type:
- Article
Comprehensive analysis and ACMG‐based classification of CHEK2 variants in hereditary cancer patients.
- Published in:
- Human Mutation, 2020, v. 41, n. 12, p. 2128, doi. 10.1002/humu.24110
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- Publication type:
- Article
Comprehensive establishment and characterization of orthoxenograft mouse models of malignant peripheral nerve sheath tumors for personalized medicine.
- Published in:
- EMBO Molecular Medicine, 2015, v. 7, n. 5, p. 608, doi. 10.15252/emmm.201404430
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- Publication type:
- Article
Next-generation sequencing meets genetic diagnostics: development of a comprehensive workflow for the analysis of BRCA1 and BRCA2 genes.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 8, p. 864, doi. 10.1038/ejhg.2012.270
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- Publication type:
- Article
BARD1 Pathogenic Variants Are Associated with Triple-Negative Breast Cancer in a Spanish Hereditary Breast and Ovarian Cancer Cohort.
- Published in:
- Genes, 2021, v. 12, n. 2, p. 150, doi. 10.3390/genes12020150
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- Publication type:
- Article
Colon-specific eQTL analysis to inform on functional SNPs.
- Published in:
- 2018
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- Publication type:
- journal article
Comprehensive analysis of copy number aberrations in microsatellite stable colon cancer in view of stromal component.
- Published in:
- 2017
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- Publication type:
- journal article
Impact of COVID-19 lockdown on physical activity, insomnia, and loneliness among Spanish women and men.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-30173-2
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- Publication type:
- Article
ICO Amplicon NGS Data Analysis: A Web Tool for Variant Detection in Common High-Risk Hereditary Cancer Genes Analyzed by Amplicon GS Junior Next-Generation Sequencing.
- Published in:
- Human Mutation, 2014, v. 35, n. 3, p. 271, doi. 10.1002/humu.22484
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- Publication type:
- Article
Author Correction: COLONOMICS - integrative omics data of one hundred paired normal-tumoral samples from colon cancer patients.
- Published in:
- 2022
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- Publication type:
- Correction Notice
COLONOMICS - integrative omics data of one hundred paired normal-tumoral samples from colon cancer patients.
- Published in:
- Scientific Data, 2022, v. 9, n. 1, p. 1, doi. 10.1038/s41597-022-01697-5
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- Publication type:
- Article
Identification of candidate susceptibility genes for colorectal cancer through eQTL analysis.
- Published in:
- Carcinogenesis, 2014, v. 35, n. 9, p. 2039, doi. 10.1093/carcin/bgu092
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- Publication type:
- Article
Susceptibility genetic variants associated with early-onset colorectal cancer.
- Published in:
- Carcinogenesis, 2012, v. 33, n. 3, p. 613
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- Publication type:
- Article