Area of research
Pulmonary and Respiratory Medicine · Oncology
Research interest
Research focused on SMARCA4 and Fluorescence in situ hybridization, with related work in Cancer research, HRAS, Sarcoma. Notable publications include 'SMARCA4 inactivation defines a group of undifferentiated thoracic malignancies transcriptionally related to BAF-deficient sarcomas', 'SMARCA4-deficient Thoracic Sarcomas', and 'Molecular screening program to select molecular-based recommended therapies for metastatic cancer patients: analysis from the ProfiLER trial'.
Primary cutaneous <scp>NUT</scp> adnexal carcinoma: morphologic, genetic and methylation analysis of seven new cases with comparison to extracutaneous <scp>NUT</scp> carcinoma and <i>NUTM1</i>‐rearranged porocarcinoma
Clinical, Morphologic, and Genomic Findings in Spitz Tumors With RET Fusion: A Series of 31 Cases
Comprehensive Molecular Profiling of Cribriform Tumors: Identification of Recurrent 6q/9q Codeletion and CD38 Expression
Multi‐omics profiling identified two epithelioid sarcoma molecular subtypes with distinct signaling and immune characteristics
ACTB::ZMIZ2-rearranged adnexal carcinoma: a second case
Porocarcinomas with <i>PAK1/2/3</i> fusions: a series of 12 cases
SOX10-Internal Tandem Duplications and PLAG1 or HMGA2 Fusions Segregate Eccrine-Type and Apocrine-Type Cutaneous Mixed Tumors
Update on gene fusions and the emerging clinicopathological landscape of peritoneal and pleural mesotheliomas and other neoplasms
Recurrent <scp><i>GRHL</i></scp> fusions in a subset of sebaceoma: microscopic and molecular characterisation of eight cases
Sweat Gland Tumors Arising on Acral Sites
Gene fusions in poroma, porocarcinoma and related adnexal skin tumours: An update
Spectrum of Melanocytic Tumors Harboring BRAF Gene Fusions: 58 Cases With Histomorphologic and Genetic Correlations
Distinct regulations driving <scp>YAP1</scp> expression loss in poroma, porocarcinoma and <i>RB1</i>‐deficient skin carcinoma
Recurrent <i>PAK2</i> rearrangements in poroma with folliculo‐sebaceous differentiation
A comprehensive analysis of infantile central nervous system tumors to improve distinctive criteria for infant‐type hemispheric glioma versus desmoplastic infantile ganglioglioma/astrocytoma
Histologic and Genetic Features of 51 Melanocytic Neoplasms With Protein Kinase C Fusion Genes
GRM1 Gene Fusions as an Alternative Molecular Driver in Blue Nevi and Related Melanomas
Wholistic approach: Transcriptomic analysis and beyond using archival material for molecular diagnosis
Intra‐ and extra‐cranial <scp><i>BCOR‐</i>ITD</scp> tumours are separate entities within the <scp><i>BCOR</i></scp>‐rearranged family
Small-Cell Lung Cancer Transformation as a Mechanism of Resistance to Pralsetinib in RET-Rearranged Lung Adenocarcinoma: A Case Report
Attempting to Solve the Pigmented Epithelioid Melanocytoma (PEM) Conundrum
A Combination of MTAP and p16 Immunohistochemistry Can Substitute for <i>CDKN2A</i> Fluorescence In Situ Hybridization in Diagnosis and Prognosis of Pleural Mesotheliomas
Expanding the molecular spectrum of tenosynovial giant cell tumors
Superficial CD34‐positive fibroblastic tumor and <i>PRDM10</i>‐rearranged soft tissue tumor are overlapping entities: a comprehensive study of 20 cases
Morphologic features in a series of 352 Spitz melanocytic proliferations help predict their oncogenic drivers
NUT carcinoma of the lung
Spitz nevus with a novel <scp><i>TFG‐NTRK2</i></scp> fusion: The first case report of <scp><i>NTRK2</i></scp>‐rearranged Spitz/Reed nevus
Reply to: Expanding the Spectrum of Primary Cutaneous Carcinoma With BRD3-NUTM1 Fusion
RASGRF2 gene fusions identified in a variety of melanocytic lesions with distinct morphological features
Comprehensive Molecular and Pathologic Evaluation of Transitional Mesothelioma Assisted by Deep Learning Approach: A Multi-Institutional Study of the International Mesothelioma Panel from the MESOPATH Reference Center