J. Cameron

Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes.

I. Scheffer, A. Palotie, P. Striano, 2021, American journal of human genetics.

Encephalopathies with KCNC1 variants: genotype‐phenotype‐functional correlations

Ye Htet Aung, S. Berkovic, S. Petrou, 2019, Annals of clinical and translational neurology.

Individual fixel-based white matter abnormalities in the epilepsies

I. Scheffer, R. Smith, S. Berkovic, 2023, medRxiv.

Recognition and epileptology of protracted CLN3 disease

I. Scheffer, S. Berkovic, P. Carney, 2023, Epilepsia.

IRF2BPL: A new genotype for progressive myoclonus epilepsies

S. Berkovic, S. Franceschetti, C. Calvello, 2023, Epilepsia.

Exploring individual fixel-based white matter abnormalities in epilepsy

S. Berkovic, H. Pardoe, R. Mito, 2023, Brain communications.