Publicacións nas que colabora con Ángel Carracedo Álvarez (69)
2023
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BMPR2 as a Novel Predisposition Gene for Hereditary Colorectal Polyposis
Gastroenterology, Vol. 165, Núm. 1, pp. 162-172.e5
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NAD pool as an antitumor target against cancer stem cells in head and neck cancer
Journal of Experimental and Clinical Cancer Research, Vol. 42, Núm. 1
2022
2021
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Exome sequencing of early-onset patients supports genetic heterogeneity in colorectal cancer
Scientific Reports, Vol. 11, Núm. 1
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Genetic susceptibility to CRC
Foundations of Colorectal Cancer (Elsevier), pp. 513-518
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Liquid biopsy biomarkers for immunotherapy in non-small cell lung carcinoma: Lessons learned and the road ahead
Journal of Personalized Medicine, Vol. 11, Núm. 10
2020
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Systematic meta-analyses, field synopsis and global assessment of the evidence of genetic association studies in colorectal cancer
Gut, Vol. 69, Núm. 8, pp. 1460-1471
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The road so far in colorectal cancer pharmacogenomics: Are we closer to individualised treatment?
Journal of Personalized Medicine, Vol. 10, Núm. 4, pp. 1-40
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Tumor Profiling at the Service of Cancer Therapy
Frontiers in Oncology, Vol. 10
2019
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Early colorectal cancers provide new evidence for a lynch syndrome-to-CMMRD phenotypic continuum
Cancers, Vol. 11, Núm. 8
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Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula
Nature Communications, Vol. 10, Núm. 1
2017
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Candidate predisposing germline copy number variants in early onset colorectal cancer patients
Clinical and Translational Oncology, Vol. 19, Núm. 5, pp. 625-632
2016
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Association of a let-7 miRNA binding region of TGFBR1 with hereditary mismatch repair proficient colorectal cancer (MSS HNPCC)
Carcinogenesis, Vol. 37, Núm. 8, pp. 751-758
2015
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A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS
Gut, Vol. 64, Núm. 1, pp. 111-120
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Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer
Journal of Medical Genetics, Vol. 52, Núm. 7, pp. 498-502
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Recurrent Coding Sequence Variation Explains only A Small Fraction of the Genetic Architecture of Colorectal Cancer
Scientific Reports, Vol. 5
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Susceptibilidad genética al cáncer colorrectal y a la respuesta al tratamiento quimioterápico
Abordaje multidisciplinar de cáncer colorrectal (Andavira), pp. 411-424
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Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations
International Journal of Cancer, Vol. 137, Núm. 8, pp. 1870-1878
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Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer
Genetics in Medicine, Vol. 17, Núm. 2, pp. 131-142