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EMBO Molecular Medicine|November 8, 2021
Neonatal neuronal WWOX gene therapy rescues Wwox null phenotypesSrinivasarao Repudi, Irina Kustanovich, Sara Abu-Swai, et al.
Stem Cell Research|February 14, 2025
Generation of human induced pluripotent stem cell lines HUJIi004 and HUJIi005 from two individuals carrying autosomal-dominant mutations in the CTNBB1 gene resulting in CTNNB1 neurodevelopmental disorderDaniel J Steinberg, Kian Maroun, Srinivasarao Repudi, et al.
Neurobiology of Disease|October 11, 2021
Altered neocortical oscillations and cellular excitability in an in vitro Wwox knockout mouse model of epileptic encephalopathyVanessa L Breton, Mark S Aquilino, Srinivasarao Repudi, et al.
Molecular Therapy. Advances|July 9, 2026
Neuron-specific WWOX gene therapy produces dose-dependent, durable rescue in a model of WWOX-related epileptic encephalopathyMustafa Obeid, Rania Akkawi, Srinivasarao Repudi, et al.
EMBO Molecular Medicine|July 16, 2021
Modeling genetic epileptic encephalopathies using brain organoidsDaniel J Steinberg, Srinivasarao Repudi, Afifa Saleem, et al.
Brain : a Journal of Neurology|April 29, 2021
Neuronal deletion of Wwox, associated with WOREE syndrome, causes epilepsy and myelin defectsSrinivasarao Repudi, Daniel J Steinberg, Nimrod Elazar, et al.
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