BIOCIENCIAS: Bª Y CLÍNICA DEL CÁNCER Y MEDIC. TRASLACIONAL
Escuela de doctorado
Javier
Benítez Ortiz
Publicaciones en las que colabora con Javier Benítez Ortiz (18)
2023
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Clinical parameters affecting survival outcomes in patients with low-grade serous ovarian carcinoma: An international multicentre analysis
CMAJ. Canadian Medical Association Journal, Vol. 66, Núm. 3, pp. E310-E320
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p53 and ovarian carcinoma survival: an Ovarian Tumor Tissue Analysis consortium study
Journal of Pathology: Clinical Research, Vol. 9, Núm. 3, pp. 208-222
2022
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CDK5RAP3, a New BRCA2 Partner That Regulates DNA Repair, Is Associated with Breast Cancer Survival
Cancers, Vol. 14, Núm. 2
2021
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Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer
Cancer Epidemiology Biomarkers and Prevention, Vol. 30, Núm. 9, pp. 1669-1680
2020
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Prognostic gene expression signature for high-grade serous ovarian cancer
Annals of Oncology, Vol. 31, Núm. 9, pp. 1240-1250
2018
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Assessment of moderate coffee consumption and risk of epithelial ovarian cancer: A Mendelian randomization study
International Journal of Epidemiology, Vol. 47, Núm. 2, pp. 450-459
2017
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Analyses of germline variants associated with ovarian cancer survival identify functional candidates at the 1q22 and 19p12 outcome loci
Oncotarget, Vol. 8, Núm. 39, pp. 64670-64684
2016
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DNA copy number profiling reveals different patterns of chromosomal instability within colorectal cancer according to the age of onset
Molecular Carcinogenesis, Vol. 55, Núm. 5, pp. 705-716
2015
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Classifying early-onset colorectal cancer according to tumor location: New potential subcategories to explore
American Journal of Cancer Research, Vol. 5, Núm. 7, pp. 2308-2313
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Germline mutation in BRCA1 or BRCA2 and ten-year survival for women diagnosed with epithelial ovarian cancer
Clinical Cancer Research, Vol. 21, Núm. 3, pp. 652-657
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Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Nature Genetics, Vol. 47, Núm. 2, pp. 164-171
2013
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Evaluation of Rare Variants in the New Fanconi Anemia Gene ERCC4 (FANCQ) as Familial Breast/Ovarian Cancer Susceptibility Alleles
Human Mutation, Vol. 34, Núm. 12, pp. 1615-1618
2012
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Shorter telomere length is associated with increased: Ovarian cancer risk in both familial and sporadic cases
Journal of Medical Genetics, Vol. 49, Núm. 5, pp. 341-344
2009
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The SRY-HMG box gene, SOX4, is a target of gene amplification at chromosome 6p in lung cancer
Human Molecular Genetics, Vol. 18, Núm. 7, pp. 1343-1352
2006
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A haplotype containing the p53 polymorphisms Ins16bp and Arg72Pro modifies cancer risk in BRCA2 mutation carriers
Human Mutation, Vol. 27, Núm. 3, pp. 242-248
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Genomic rearrangements at the BRCA1 locus in Spanish families with breast/ovarian cancer
Clinical Chemistry, Vol. 52, Núm. 8, pp. 1480-1485
2004
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The variant E233G of the rad51d gene could be a low-penetrance allele in high-risk breast cancer families without BRCA1/2 mutations
International Journal of Cancer, Vol. 110, Núm. 6, pp. 845-849
2003
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Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: A high proportion of mutations unique to Spain and evidence of founder effects
Human Mutation, Vol. 22, Núm. 4, pp. 301-312