Epilepsy Genetics Program
Recent publications
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Poduri A, Chopra SS, Neilan EG, Christina Elhosary P, Kurian MA, Meyer E, Barry BJ, Khwaja OS, Salih MA, Stodberg T, Scheffer IE, Maher ER, Sahin M, Wu BL, Berry GT, Walsh CA, Picker J, Kothare SV. (2012) Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy. Epilepsia.
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Poduri A, Evrony GD, Cai X, Elhosary PC, Beroukhim R, Lehtinen MK, Hills LB, Heinzen EL, Hill A, Hill RS, Barry BJ, Bourgeois BF, Riviello JJ, Barkovich AJ, Black PM, Ligon KL, Walsh CA. (2012) Somatic activation of AKT3 causes hemispheric developmental brain malformations. Neuron 74:41-48.
