Dr Marian Todaro
Honorary (Fellow)
Department of Medicine
58 Scholarly works
2 Projects
HIGHLIGHTS
2026
Journal article
Transcription Factor Binding and Individual Genetic Risk of Valproate Teratogenicity
DOI: 10.1212/WNL.00000000002145702025
Journal article
Characterisation of the expression of P2X7 receptor, cancer stem cell markers and immunological mediators in human high-grade gliomas
DOI: 10.1186/s12868-025-00973-52025
Journal article
The impact of CGRP monoclonal antibodies on cytokine expression in chronic migraine: a cohort study
DOI: 10.1007/s00415-025-13400-w2024
Journal article
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
DOI: 10.1038/s41593-024-01747-82024
Journal article
Elevated plasma neurofilament light and glial fibrillary acidic protein in epilepsy versus nonepileptic seizures and nonepileptic disorders
DOI: 10.1111/epi.180652023
Journal article
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
DOI: 10.1038/s41467-023-39539-62013
Journal article
MRI-identified pathology in adults with new-onset seizures
DOI: 10.1212/WNL.0b013e3182a35193
RECENT SCHOLARLY WORKS
2023
Journal article
P2X7 receptor antagonism by AZ10606120 significantly reduced in vitro tumour growth in human glioblastoma
DOI: 10.1038/s41598-023-35712-52023
Journal article
Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic Architecture
DOI: 10.1002/ana.267652023
Journal article
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
DOI: 10.1038/s41588-023-01485-w2022
Journal article
Somatic Mosaic Pathogenic Variant Gradient Detected in Trace Brain Tissue from Stereo-EEG Depth Electrodes
DOI: 10.1212/WNL.0000000000201469
RECENT PROJECTS
2014
Research Grant
Rapid Point-of-Care Detection of Genomic Variations for Personalised Medicine
2014
Research Grant
Rapid Point-of-Care Detection of Genomic Variations for Personalised Medicine