Area of research
Psychiatry and Mental health · Genetics
Research interest
Research interests include Epilepsy research and treatment, Pharmacological Effects and Toxicity Studies, Genomics and Rare Diseases, and Genetics and Neurodevelopmental Disorders.
Evaluation of metformin for epilepsy prevention or seizure control in people without evidence of diabetes: retrospective cohort study
P16-2 Quantifying the proportion of incident epilepsy that is potentially preventable – a Welsh cohort study
P16-1 Determining the association between individual-level socioeconomic factors and incident epilepsy: a welsh population cohort study of 2.9 million people
Paediatric Idiopathic Intracranial Hypertension in Wales: A Retrospective Observational Study
Pathogenic ultra-rare variants in <i>SLC6A1, SLC6A11, GAD1 and GAD2</i> are new & recurrent GABAergic loci for GGE syndromes
A synonymous <i>SLC2A1</i> variant causes familial epilepsy and paroxysmal exercise-induced dyskinesia by creating aberrant mosaic splicing patterns
Rare Cholesterol Related Disorders – A Sterolomic Library for Diagnosis and Monitoring of Diseases
Pathogenic Ultra-Rare Variants in SLC6A1, SLC6A11, GAD1 and GAD2 are New &amp; Recurrent GABAergic Loci for Genetic Generalised Epilepsy
Educational attainment of children with self-limited epilepsy with CentroTemporal spikes (SELECTS), other epilepsies, and without epilepsy: A retrospective cohort study
Developing and validating a clinical prediction model to predict epilepsy-related emergency department attendance, hospital admission, or death: A cohort study protocol
Capability, opportunity and motivation for shared decision‐making about valproate as an antiseizure medication treatment for epilepsy in women with pregnancy potential: A qualitative study of patient perspectives
Assessing the extent and determinants of socioeconomic inequalities in epilepsy in the UK: a systematic review and meta-analysis of evidence
Natural language processing to automate a web-based model of care and modernize skin cancer multidisciplinary team meetings
Epidemiology of self-limited epilepsy with centrotemporal spikes (SeLECTS): A population study using primary care records
Epilepsy and the risk of <scp>COVID</scp>‐19‐related hospitalization and death: A population study
Health care utilization and mortality for people with epilepsy during <scp>COVID</scp>‐19: A population study
Annotation of epilepsy clinic letters for natural language processing
Improving surveillance of emergency department activity through natural language processing
Prevalence and temporal relationship of clinical co-morbidities in idiopathic dystonia: a UK linkage-based study
Comparing the Pathology, Clinical, and Demographic Characteristics of Younger and Older‐Onset Multiple Sclerosis
Validating a novel natural language processing pathway for automated quality assurance in surgical oncology: incomplete excision rates of 34 955 basal cell carcinomas
Revisiting basal cell carcinoma clinical margins: Leveraging natural language processing and multivariate analysis with updated Royal College of Pathologists histological reporting standards
COVID-19 vaccination uptake in people with epilepsy in wales
Epilepsy genetics: a practical guide for adult neurologists
Genetic influences on epilepsy outcomes: A whole‐exome sequencing and health care records data linkage study
Developing and validating a clinical prediction model to predict epilepsy-related hospital admission or death within the next year using administrative healthcare data: a population-based cohort study protocol
Gold standard annotation of epilepsy clinic letters for the development of information extraction tools
Gold standard annotation of epilepsy clinic letters for the development of information extraction tools
Longitudinal analysis of the relationship between motor and psychiatric symptoms in idiopathic dystonia
Development and validation of an automated basal cell carcinoma histopathology information extraction system using natural language processing