Publications by authors named "Simone C Yendle"

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Mutations in KCNT1 cause a spectrum of focal epilepsies.
Rikke S Møller, Sarah E Heron, Line H G Larsen, Chiao Xin Lim, Michael G Ricos, Simone C Yendle

Epilepsia· September 2015

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GRIN2A mutations cause epilepsy-aphasia spectrum disorders.
Gemma L Carvill, Brigid M Regan, Simone C Yendle, Brian J O'Roak, Natalia Lozovaya

Nat Genet· September 2013

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Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, Jacinta M McMahon, Brian J O'Roak

Nat Genet· July 2013

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Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies.
Sarah E Heron, Yeh Sze Ong, Simone C Yendle, Jacinta M McMahon, Samuel F Berkovic

Epilepsia· May 2013

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Rare copy number variants are an important cause of epileptic encephalopathies.
Heather C Mefford, Simone C Yendle, Cynthia Hsu, Joseph Cook, Eileen Geraghty

Ann Neurol· December 2011

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Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.
Claudia B Catarino, Joan Y W Liu, Ioannis Liagkouras, Vaneesha S Gibbons, Robyn W Labrum, Simone C Yendle

Brain· October 2011

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Cyclin-dependent kinase-like 5 (CDKL5) mutation screening in Rett syndrome and related disorders.
Rose White, Gladys Ho, Swetlana Schmidt, Ingrid E Scheffer, Alexandra Fischer, Simone C Yendle

Twin Res Hum Genet· April 2010

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