Cuddapah, Vishnu Anand

Methyl-CpG-binding protein 2 ( MECP2 ) mutation type is associated with disease severity in Rett syndrome

Cuddapah, V. A., Pillai, R. B., Shekar, K. V., Lane, J. B., Motil, K. J., Skinner, S. A., Tarquinio, D. C., Glaze, D. G., McGwin, G., Kaufmann, W. E., et al. (2014) · Journal of Medical Genetics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 311

GABAergic disinhibition and impaired KCC2 cotransporter activity underlie tumor-associated epilepsy: Reduced KCC2 Underlie Tumor-Related Epilepsy

Campbell, S. L., Robel, S., Cuddapah, V. A., Robert, S., Buckingham, S. C., Kahle, K. T., & Sontheimer, H. (2015) · Glia

Epilepsy research and treatmentNeuroscience and Neuropharmacology Research

Cited by 185