Caitlin A. Bennett

245 Burgundy St
Heidelberg, VIC 3084, Australia

Last Updated: 09/26/2026

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Found 13 publications

Genome sequencing boosts diagnostic yield for the developmental and epileptic encephalopathies.

Genome sequencing boosts diagnostic yield for the developmental and epileptic encephalopathies.

Journal: medRxiv : the preprint server for health sciences

Published: May 07, 2026

Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia.

Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia.

Journal: medRxiv : the preprint server for health sciences

Published: December 03, 2025

Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia.

Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia.

Journal: Progress in neuro-psychopharmacology & biological psychiatry

Published: November 23, 2025

Improving genetic diagnostic yield in familial and sporadic cerebral cavernous malformations: detection of copy number and deep Intronic variants.

Improving genetic diagnostic yield in familial and sporadic cerebral cavernous malformations: detection of copy number and deep Intronic variants.

Journal: Human molecular genetics

Published: October 10, 2024

Genome-wide association meta-analyses of drug-resistant epilepsy.

Genome-wide association meta-analyses of drug-resistant epilepsy.

Journal: EBioMedicine

Published: August 12, 2024

Applying the ILAE diagnostic criteria for Lennox-Gastaut syndrome in the real-world setting: A multicenter retrospective cohort study.

Applying the ILAE diagnostic criteria for Lennox-Gastaut syndrome in the real-world setting: A multicenter retrospective cohort study.

Journal: Epilepsia open

Published: July 11, 2023

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Journal: medRxiv : the preprint server for health sciences

Published: March 03, 2023

Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practice.

Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practice.

Journal: Developmental medicine and child neurology

Published: December 21, 2021

Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions.

Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions.

Journal: Human molecular genetics

Published: November 04, 2021

Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy.

Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy.

Journal: Brain : a journal of neurology

Published: August 18, 2021

Avelumab Combined with Stereotactic Ablative Body Radiotherapy in Metastatic Castration-resistant Prostate Cancer: The Phase 2 ICE-PAC Clinical Trial.

Avelumab Combined with Stereotactic Ablative Body Radiotherapy in Metastatic Castration-resistant Prostate Cancer: The Phase 2 ICE-PAC Clinical Trial.

Journal: European urology

Published: May 20, 2021

Nursing Implications of Recent Changes in Management Practices for Metastatic Prostate Cancer.

Nursing Implications of Recent Changes in Management Practices for Metastatic Prostate Cancer.

Journal: Seminars in oncology nursing

Published: July 26, 2020

Showing 1-12 of 13

Last Updated: 09/26/2026