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36 projects
Ability of a polygenic risk score to refine cancer risk in Lynch syndrome
Assessment of a novel pan-cancer biomarker to improve immunotherapy response prediction
Autoantibodies against type I interferons continue to confer a higher risk of severe COVID-19 in fully vaccinated population
Understanding the risk factors behind the most severe cases of COVID-19
Understanding the risk factors behind the most severe cases of COVID-19Translational Medicine Area
Building the Network of Rare Ovarian Tumors (NRTO), an intercontinental initiative
Ovarian cancer susceptibility syndromes
Ovarian cancer susceptibility syndromesTranslational Medicine Area
Characterization of the novel DGCR8-microprocessor syndrome
miRNA biogenesis associated tumors
miRNA biogenesis associated tumors Translational Medicine Area
Characterizing early events driving carcinogenesis in Constitutional Mismatch Repair Deficiency (CMMRD) syndrome as a potential strategy for precision surveillance and prevention
Clarifying the phenotypic spectrum associated with RAD51 partners and the proteomic interplay of RAD51 paralogs.
Novel DNA repair associated tumor syndromes
Novel DNA repair associated tumor syndromesTranslational Medicine Area
Clinical and molecular characterization of novel subtypes of Sex Cord-Stromal Tumors of the ovary
Ovarian cancer susceptibility syndromes
Ovarian cancer susceptibility syndromesTranslational Medicine Area
Comprehensive research in colorectal cancer and polyposis predisposition: searching for genetic and epigenetic causes of the disease
Identification of new genes involved in the predisposition of colorectal cancer and polyposis
Identification of new genes involved in the predisposition of colorectal cancer and polyposisTranslational Medicine Area
CRISPR/Cas9-edited organoids for the functional evaluation of gene variants in colorectal cancer
Establishment, optimization and implementation of state-of-the-art models for the functional characterization of genetic variants in hereditary cancer genes
Establishment, optimization and implementation of state-of-the-art models for the functional characterization of genetic variants in hereditary cancer genesTranslational Medicine Area
Cuidal’HFutur Diagnostic: Implementation of Precision Genomics for the Diagnosis of Unresolved Hereditary Cancer and Adult Rare Diseases
Elucidating the molecular mechanisms driven by FGFR1 mutants in Low Grade Gliomas
Oncogenic mutations and pediatric cancer syndromes.
Oncogenic mutations and pediatric cancer syndromes. Translational Medicine Area
Hereditary Cancer Research Group – AGAUR
Participation in national and regional initiatives of genomic-based precision medicine in cancer
Participation in national and regional initiatives of genomic-based precision medicine in cancerTranslational Medicine Area
Hereditary forms and development of biomarkers in gastrointestinal cancer
IMPaCT Genómica: Implementation of Precision Medicine in the Spanish National Health System.
Participation in national and regional initiatives of genomic-based precision medicine in cancer
Participation in national and regional initiatives of genomic-based precision medicine in cancerTranslational Medicine Area
IMPaCT-VUScan: Development and implementation of a functional genomics platform for undiagnosed hereditary cancer
Participation in national and regional initiatives of genomic-based precision medicine in cancer
Participation in national and regional initiatives of genomic-based precision medicine in cancerTranslational Medicine Area
INGENIO: Integrative genomic, digital imaging and clinical information towards precision oncology optimization
Participation in the development of international guidelines for hereditary or early-onset colorectal cancer
Participation in the development of international guidelines for hereditary or early-onset colorectal cancerTranslational Medicine Area
MedPerCan: Personalised Medicine in Cancer – Catalonia: A pilot study on the impact of genomic testing in the decision-making process in Oncology
Participation in the development of international guidelines for hereditary or early-onset colorectal cancer
Participation in the development of international guidelines for hereditary or early-onset colorectal cancerTranslational Medicine Area
MicroRNAs in sporadic and familial colorectal cancer
Identification of new genes involved in the predisposition of colorectal cancer and polyposis
Identification of new genes involved in the predisposition of colorectal cancer and polyposisTranslational Medicine Area
Modeling precancer in germline mismatch repair deficiency for a personalized immune-based surveillance (MIsMatch4PERSON)
National collaborative strategy to improve the identification and clinical management of Constitutional Mismatch Repair Deficiency (CMMRD) syndrome
Neutralizing autoantibodies against type I interferons continue to confer a higher risk of severe COVID-19 in fully vaccinated population
Understanding the risk factors behind the most severe cases of COVID-19
Understanding the risk factors behind the most severe cases of COVID-19Translational Medicine Area
NF1 nonsense suppression by targeted pseudouridylation
Identification of new personalized therapeutic agents against Malignant peripheral nerve sheath tumors (MPNSTs)
Identification of new personalized therapeutic agents against Malignant peripheral nerve sheath tumors (MPNSTs)Translational Medicine Area
Non-conventional mechanisms of gene inactivation in hereditary colorectal cancer
Pancreatic orthotopic PDX mouse models as tools to test new therapeutic strategies for pancreatic cancer
ProofREAD4MED: Polymerase proofreading-deficient tumors: genetics and immune biology insights for improved predictive medicine
Clinical and molecular characterization of hereditary cancer syndromes and genes, with special focus on polyposis syndromes
Clinical and molecular characterization of hereditary cancer syndromes and genes, with special focus on polyposis syndromesTranslational Medicine Area
REPAIR-POL: Advancing knowledge and diagnostics of DNA repair-deficient hereditary gastrointestinal polyposes through functional genomics, AI pathology, and syndrome discovery
Role of immune system inborn errors as determinants of the COVID-19 severity in hospitalized patients
Understanding the risk factors behind the most severe cases of COVID-19
Understanding the risk factors behind the most severe cases of COVID-19Translational Medicine Area
SOLVE-RD: Solving the unsolved rare diseases
Identification of new genes involved in the predisposition of colorectal cancer and polyposis
Identification of new genes involved in the predisposition of colorectal cancer and polyposisTranslational Medicine Area
SpadaHC: Spanish DataBase for Hereditary Cancer
Participation in the development of international guidelines for hereditary or early-onset colorectal cancer
Participation in the development of international guidelines for hereditary or early-onset colorectal cancerTranslational Medicine Area
Tackling current challenges in the genetic diagnosis of hereditary cancer through integrative analysis of molecular, clinical and population data
Improving clinical applicability of multi-gene panels in the setting of hereditary cancer
Improving clinical applicability of multi-gene panels in the setting of hereditary cancerTranslational Medicine Area
Testing the Malignant Peripheral Nerve Sheath Tumor vulnerability to precision therapies directed to recurrent genomic alterations
Identification of new personalized therapeutic agents against Malignant peripheral nerve sheath tumors (MPNSTs)
Identification of new personalized therapeutic agents against Malignant peripheral nerve sheath tumors (MPNSTs)Translational Medicine Area
The mechanistic basis for constitutional MLH1 methylation
To uncover the genetic causes of Gorlin-like patients without an identified molecular cause.
Oncogenic mutations and pediatric cancer syndromes.
Oncogenic mutations and pediatric cancer syndromes. Translational Medicine Area
Underpining the effects of defective miRNA biogenesis in the formation of thyroid tumors
miRNA biogenesis associated tumors
miRNA biogenesis associated tumors Translational Medicine Area
Validation of the clinical use of high-sensitivity microsatellite instability assessment in improving early diagnosis of endometrial cancer and establishing personalized gynecological follow-up strategies in Lynch syndrome