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REPAIR-POL: Advancing knowledge and diagnostics of DNA repair-deficient hereditary gastrointestinal polyposes through functional genomics, AI pathology, and syndrome discovery
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Cuidal'HFutur Diagnostic: Implementation of Precision Genomics for the Diagnosis of Unresolved Hereditary Cancer and Adult Rare Diseases
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Global Projects
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Underpining the effects of defective miRNA biogenesis in the formation of thyroid tumors
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DNA MisMatch Repair Lab
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SpadaHC: Spanish DataBase for Hereditary Cancer
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IMPaCT-VUScan: Development and implementation of a functional genomics platform for undiagnosed hereditary cancer
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Clinical Genetics Lab
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Role of immune system inborn errors as determinants of the COVID-19 severity in hospitalized patients
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Hereditary Cancer Research Group - AGAUR
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NF1 nonsense suppression by targeted pseudouridylation
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Clarifying the phenotypic spectrum associated with RAD51 partners and the proteomic interplay of RAD51 paralogs.
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Rare TumorS Lab
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MedPerCan: Personalised Medicine in Cancer - Catalonia: A pilot study on the impact of genomic testing in the decision-making process in Oncology
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INGENIO: Integrative genomic, digital imaging and clinical information towards precision oncology optimization
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IMPaCT Genómica: Implementation of Precision Medicine in the Spanish National Health System.
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CRISPR/Cas9-edited organoids for the functional evaluation of gene variants in colorectal cancer
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ProofREAD4MED: Polymerase proofreading-deficient tumors: genetics and immune biology insights for improved predictive medicine
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Comprehensive research in colorectal cancer and polyposis predisposition: searching for genetic and epigenetic causes of the disease
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MicroRNAs in sporadic and familial colorectal cancer
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SOLVE-RD: Solving the unsolved rare diseases
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Colorectal Cancer Predisposition Lab
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