Christopher Previti
Heidelberg, BW, Germany
Last Updated: 09/26/2026
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Found 16 publications
Molecular characterization of mismatch repair deficient tumors in young Jordanian patients.
Journal: Discover oncology
Published: March 03, 2026
Circulating tumor DNA precision oncology enables effective and sensitive molecular diagnostics and actionable target detection in pediatric solid tumors - the INFORM experience.
Journal: Genome medicine
Published: February 17, 2026
The ITCC-P4 PDX Platform Enables Preclinical Testing of Pediatric Cancers.
Journal: Cancer research
Published: November 19, 2025
Investigation of DNA Damage Response Genes Validates the Role of DNA Repair in Pediatric Cancer Risk and Identifies SMARCAL1 as a Novel Osteosarcoma Predisposition Gene.
Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Published: October 09, 2025
Comprehensive investigation of DNA damage repair genes in children with cancer identifies SMARCAL1 as novel osteosarcoma predisposition gene.
Journal: medRxiv : the preprint server for health sciences
Published: June 04, 2025
Molecular characterization and clinical features of diffuse midline glioma in the pediatric precision oncology registry INFORM.
Journal: Acta neuropathologica
Published: May 29, 2025
Pediatric spinal high-grade glioma in the pediatric precision oncology registry INFORM: Identification of potential therapeutic targets.
Journal: Neuro-oncology advances
Published: February 03, 2025
Integrative Multiomics and Drug Sensitivity Profiling Reveal Potential Biomarkers and Therapeutic Strategies in Pediatric Solid Tumors.
Journal: Cancer research
Published: June 16, 2024
Author Correction: Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology.
Journal: Nature medicine
Published: October 24, 2023
Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology.
Journal: Nature medicine
Published: August 04, 2022
Drug sensitivity profiling of 3D tumor tissue cultures in the pediatric precision oncology program INFORM.
Journal: NPJ precision oncology
Published: May 05, 2022
Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin.
Journal: Acta neuropathologica
Published: January 26, 2021
Last Updated: 09/26/2026