Publications by authors named "Eileen Geraghty"

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Intragenic deletions of ALDH7A1 in pyridoxine-dependent epilepsy caused by Alu-Alu recombination.
Heather C Mefford, Matthew Zemel, Eileen Geraghty, Joseph Cook, Peter T Clayton

Neurology· September 2015

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GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.
Gemma L Carvill, Sarah Weckhuysen, Jacinta M McMahon, Corinna Hartmann, Rikke S Møller, Eileen Geraghty

Neurology· April 2014

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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, Eileen Geraghty

Nat Genet· September 2013

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Deletions of 16p11.2 and 19p13.2 in a family with intellectual disability and generalized epilepsy.
Alexander G Bassuk, Eileen Geraghty, Shu Wu, Saul A Mullen, Samuel F Berkovic

Am J Med Genet A· July 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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