Simone C. Yendle

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

Gemma L. Carvill, Sinéad B. Heavin, Simone C. Yendle et al. · Nature Genetics · 2013 · 683 citations · Full text

Genetics, Novo Mutations, Neurotransmission +5

<i>KCNQ2</i> encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy

Sarah Weckhuysen, Simone Mandelstam, Arvid Suls et al. · Annals of Neurology · 2011 · 494 citations

GRIN2A mutations cause epilepsy-aphasia spectrum disorders

Gemma L. Carvill, Brigid M. Regan, Simone C. Yendle et al. · Nature Genetics · 2013 · 372 citations · Full text

Genetic Disorder, Grin2a Mutations, Neurology +4

Rare copy number variants are an important cause of epileptic encephalopathies

Heather C. Mefford, Simone C. Yendle, Cynthia L. Hsu et al. · Annals of Neurology · 2011 · 243 citations

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology

Claudia B. Catarino, Joan Liu, Ioannis Liagkouras et al. · Brain · 2011 · 218 citations · Full text