Area of research
Surgery · Endocrinology, Diabetes and Metabolism
Research interest
Research interests include Paraganglioma, SDHB, SDHD, Medicine, SDHA, and Biology.
A Review of Genomic Testing and <scp>SDH</scp>‐ Deficiency in Gastrointestinal Stromal Tumors: Getting to the <scp>GIST</scp>
In vivo gastrin releasing peptide receptor expression in SDH deficient wild-type gastrointestinal stromal tumours (GIST): potential for theranostic applications
Knowledge-Based Therapeutics for Tricarboxylic Acid (TCA) Cycle-Deficient Cancers
Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants
Hyperpolarized 13C-Pyruvate Metabolism as a Surrogate for Tumor Grade and Poor Outcome in Renal Cell Carcinoma—A Proof of Principle Study
GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements
Succinate dehydrogenase and MYC-associated factor X mutations in pituitary neuroendocrine tumours
The role of [68 Ga]Ga-DOTATATE PET/CT in wild-type KIT/PDGFRA gastrointestinal stromal tumours (GIST)
Investigating the role of somatic sequencing platforms for phaeochromocytoma and paraganglioma in a large UK cohort
Familial wild-type gastrointestinal stromal tumour in association with germline truncating variants in both SDHA and PALB2
A review of the tumour spectrum of germline succinate dehydrogenase gene mutations: Beyond phaeochromocytoma and paraganglioma
The emerging role of cell surface receptor and protein binding radiopharmaceuticals in cancer diagnostics and therapy
SDHC epi-mutation testing in gastrointestinal stromal tumours and related tumours in clinical practice
Fumarate Metabolic Signature for the Detection of Reed Syndrome in Humans
Tumour risks and genotype–phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes <i>SDHB</i>, <i>SDHC</i> and <i>SDHD</i>
Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes
Clinical Practice Guidance: Surveillance for phaeochromocytoma and paraganglioma in paediatric succinate dehydrogenase gene mutation carriers
Adult female with symptomatic AVPR2-related nephrogenic syndrome of inappropriate antidiuresis (NSIAD)
Clinical and Molecular Features of Renal and Pheochromocytoma/Paraganglioma Tumor Association Syndrome (RAPTAS): Case Series and Literature Review
A case of a metastatic SDHA mutated paraganglioma re-presenting twenty-three years after initial surgery