Area of research
Genetics · Pulmonary and Respiratory Medicine
Research interest
Research interests include Glioma Diagnosis and Treatment, Virus-based gene therapy research, Brain Metastases and Treatment, and Cancer Research and Treatments.
Glioneuronal tumors PATZ1-fused: clinico-molecular and DNA methylation signatures for a variety of morphological and radiological profiles
Survival Outcomes Associated With First-Line Procarbazine, CCNU, and Vincristine or Temozolomide in Combination With Radiotherapy in IDH-Mutant 1p/19q-Codeleted Grade 3 Oligodendroglioma
Clinico-pathological and epigenetic heterogeneity of diffuse gliomas with FGFR3::TACC3 fusion
Molecular and clinical diversity in primary central nervous system lymphoma
Rosette‐forming glioneuronal tumours are midline, <i>FGFR1</i>‐mutated tumours
Molecular and clinical diversity in primary central nervous system lymphoma: a LOC Network study
An integrative histopathological and epigenetic characterization of primary intracranial mesenchymal tumors, FET:CREB‐fused broadening the spectrum of tumor entities in comparison with their soft tissue counterparts
Pineoblastoma segregates into molecular sub-groups with distinct clinico-pathologic features: a Rare Brain Tumor Consortium registry study
Molecular Profiling Reclassifies Adult Astroblastoma into Known and Clinically Distinct Tumor Entities with Frequent Mitogen-Activated Protein Kinase Pathway Alterations
A genome-wide association study identifies susceptibility loci for primary central nervous system lymphoma at 6p25.3 and 3p22.1: a LOC Network study
<i>EWSR1‐PATZ1</i> gene fusion may define a new glioneuronal tumor entity
Diffuse gliomas with <i>FGFR3‐TACC3</i> fusion have characteristic histopathological and molecular features
Integrated multi-omics analysis of oligodendroglial tumours identifies three subgroups of 1p/19q co-deleted gliomas
Natural course and prognosis of anaplastic gangliogliomas: a multicenter retrospective study of 43 cases from the French Brain Tumor Database
Histopathologic and Ultrastructural Features and Claudin Expression in Papillary Tumors of the Pineal Region