Simone C. Yendle

mTOR and neuroinflammation in epilepsy: implications for disease progression and treatment

CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions

Rare copy number variants are an important cause of epileptic encephalopathies

Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations