A/Prof Richard Tothill
Principal Res Fellow, Cancer Genomics Group Leader
Department of Clinical Pathology
113 Scholarly works
26 Projects
HIGHLIGHTS
2020
Research grants (ARC, NHMRC, MRFF)
Super-Next: Complete Genome Profiling for Cancer of Unknown Primary
2020
Research Grant
Super-Next: Complete Genome Profiling for Cancer of Unknown Primary
2020
Research grants (ARC, NHMRC, MRFF)
Evaluation of Fibroblastic Activation Protein Inhibitors (FAPI) as a Novel Radiopharmaceutical Targeting Cancer-Associated Fibroblasts for the Diagnosis and Treatment of Patients With Cancer of Unknown Primary: The FAPI-CUP Trial
2015
Journal article
Whole-genome characterization of chemoresistant ovarian cancer
DOI: 10.1038/nature144102014
Journal article
Bioinformatics pipelines for targeted resequencing and whole-exome sequencing of human and mouse genomes: A virtual appliance approach for instant deployment
DOI: 10.1371/journal.pone.00952172013
Journal article
Targeted-capture massively-parallel sequencing enables robust detection of clinically informative mutations from formalin-fixed tumours
DOI: 10.1038/srep034942013
Journal article
Massively-parallel sequencing assists the diagnosis and guided treatment of cancers of unknown primary
DOI: 10.1002/path.4251
RECENT SCHOLARLY WORKS
2025
Journal article
Duplex-Specific DNase Signal Amplification Allows Attomolar Electrochemical Detection of MicroRNAs
DOI: 10.1002/smll.2025079972025
Journal article
762MO Clinical whole genome and transcriptome sequencing for cancer of unknown primary: An Australian prospective observational study
DOI: 10.1016/j.annonc.2025.10.11772025
Journal article
Solving unknown primary cancer with earlier diagnosis - the SUPER-ED trial: study protocol for a stepped-wedge cluster randomised controlled trial to support earlier diagnosis for people presenting with malignancy of undefined primary origin
DOI: 10.1186/s12885-025-13506-42025
Journal article
Pathologist-initiated whole genome and transcriptome sequencing demonstrates diagnostic utility in resolving difficult-to-diagnose tumors
DOI: 10.1186/s13073-025-01534-52025
Journal article
Whole genome sequencing improves tissue-of-origin diagnosis and treatment options for cancer of unknown primary
DOI: 10.1038/s41467-025-59661-x2025
Journal article
Multi-omic analysis of SDHB-deficient pheochromocytomas and paragangliomas identifies metastasis and treatment-related molecular profiles
DOI: 10.1038/s41467-025-57595-y2024
Journal article
Disruption of metazoan gene regulatory networks in cancer alters the balance of co-expression between genes of unicellular and multicellular origins
DOI: 10.1186/s13059-024-03247-12024
Journal article
Recent progress in molecular classification of phaeochromocytoma and paraganglioma
DOI: 10.1016/j.beem.2024.101939