Ms Caitlin Bennett
Research Assistant - Epilepsy Research
Department of Medicine
18 Scholarly works
0 Projects
HIGHLIGHTS
2025
Journal article
Improving genetic diagnostic yield in familial and sporadic cerebral cavernous malformations: detection of copy number and deep Intronic variants
DOI: 10.1093/hmg/ddaf0772025
Journal article
Genome-wide association meta-analyses of drug-resistant epilepsy
DOI: 10.1016/j.ebiom.2025.1056752024
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
Applying the ILAE diagnostic criteria for Lennox-Gastaut syndrome in the real-world setting: A multicenter retrospective cohort study
DOI: 10.1002/epi4.128942023
Journal article
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
DOI: 10.1038/s41467-023-39539-62023
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-w2023
Journal article
Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practice
DOI: 10.1111/dmcn.15308
RECENT SCHOLARLY WORKS
2022
Journal article
Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions
DOI: 10.1093/hmg/ddab3662022
Journal article
Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy
DOI: 10.1093/brain/awac0822021
Journal article
Erratum: Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals (The American Journal of Human Genetics (2021) 108(6) (965–982), (S0002929721001403), (10.1016/j.ajhg.2021.04.009))
DOI: 10.1016/j.ajhg.2021.08.008