Alexander Rotenberg

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 31

Top Topics

Autism Spectrum Disorder

Transcranial Magnetic Stimulation

Top Venues

Journal of inherited metabolic disease

Journal of neurodevelopmental disorders

Annals of clinical and translational neurology

Journal of sleep research

This page only lists publications with an associated author ORCID identifier.

Publications

Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Christopher Mark LaCoursiere, Jeremy F P Ullmann, Hyun Yong Koh, Laura Turner, Cristina M Baker, Barbara Robens, Wanqing Shao, Alexander Rotenberg, Christopher Michael McGraw, Annapurna H Poduri
Zebrafish models of candidate human epilepsy-associated genes provide evidence of hyperexcitability. bioRxiv : the preprint server for biology (2024)
Christopher Mark LaCoursiere, Jeremy F P Ullmann, Hyun Yong Koh, Laura Turner, Cristina M Baker, Barbara Robens, Wanqing Shao, Alexander Rotenberg, Christopher Michael McGraw, Annapurna H Poduri
Zebrafish models of candidate human epilepsy-associated genes provide evidence of hyperexcitability. bioRxiv : the preprint server for biology (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Christopher Mark LaCoursiere, Jeremy F P Ullmann, Hyun Yong Koh, Laura Turner, Cristina M Baker, Barbara Robens, Wanqing Shao, Alexander Rotenberg, Christopher Michael McGraw, Annapurna H Poduri
Zebrafish models of candidate human epilepsy-associated genes provide evidence of hyperexcitability. bioRxiv : the preprint server for biology (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease (2024)
Itay Tokatly Latzer, Edward Yang, Onur Afacan, Erland Arning, Alexander Rotenberg, Henry Hing Cheong Lee, Jean-Baptiste Roullet, Phillip L Pearl
Glymphatic dysfunction coincides with lower GABA levels and sleep disturbances in succinic semialdehyde dehydrogenase deficiency. Journal of sleep research 33 (4) (2023)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Samuele Cesaro, Melissa L DiBacco, Erland Arning, Alexander Rotenberg, Henry Hing Cheong Lee, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mariarita Bertoldi, Phillip L Pearl
Phenotypic correlates of structural and functional protein impairments resultant from ALDH5A1 variants. Human genetics (2023)
Itay Tokatly Latzer, Edward Yang, Onur Afacan, Erland Arning, Alexander Rotenberg, Henry Hing Cheong Lee, Jean-Baptiste Roullet, Phillip L Pearl
Glymphatic dysfunction coincides with lower GABA levels and sleep disturbances in succinic semialdehyde dehydrogenase deficiency. Journal of sleep research 33 (4) (2023)
Itay Tokatly Latzer, Ellen Hanson, Mariarita Bertoldi, Ángeles García-Cazorla, Melissa Tsuboyama, Paul MacMullin, Alexander Rotenberg, Jean-Baptiste Roullet, Phillip L Pearl, null null
Autism spectrum disorder and GABA levels in children with succinic semialdehyde dehydrogenase deficiency. Developmental medicine and child neurology (2023)
Sameer C Dhamne, Meera E Modi, Audrey Gray, Simone Bonazzi, Lucas Craig, Elizabeth Bainbridge, Lahin Lalani, Chloe E Super, Samantha Schaeffer, Ketthsy Capre, Danuta Lubicka, Guiqing Liang, Doug Burdette, Stephanie M McTighe, Sarika Gurnani, Sheryl Anne D Vermudez, Daniel Curtis, Christopher J Wilson, Mustafa Q Hameed, Angelica D'Amore, Alexander Rotenberg, Mustafa Sahin
Seizure reduction in TSC2-mutant mouse model by an mTOR catalytic inhibitor. Annals of clinical and translational neurology (2023)
Itay Tokatly Latzer, Edward Yang, Onur Afacan, Erland Arning, Alexander Rotenberg, Henry Hing Cheong Lee, Jean-Baptiste Roullet, Phillip L Pearl
Glymphatic dysfunction coincides with lower GABA levels and sleep disturbances in succinic semialdehyde dehydrogenase deficiency. Journal of sleep research (2023)
Itay Tokatly Latzer, Edward Yang, Onur Afacan, Erland Arning, Alexander Rotenberg, Henry Hing Cheong Lee, Jean-Baptiste Roullet, Phillip L Pearl
Glymphatic dysfunction coincides with lower GABA levels and sleep disturbances in succinic semialdehyde dehydrogenase deficiency. Journal of sleep research (2023)
Mustafa Q Hameed, Benjamin Hui, Rui Lin, Paul C MacMullin, Andres Pascual-Leone, Sheryl Anne D Vermudez, Alexander Rotenberg
Depressed glutamate transporter 1 expression in a mouse model of Dravet syndrome. Annals of clinical and translational neurology (2023)
Itay Tokatly Latzer, Edward Yang, Onur Afacan, Erland Arning, Alexander Rotenberg, Henry Hing Cheong Lee, Jean-Baptiste Roullet, Phillip L Pearl
Glymphatic dysfunction coincides with lower GABA levels and sleep disturbances in succinic semialdehyde dehydrogenase deficiency. Journal of sleep research (2023)
Alisa Pasichnik, Melissa Tsuboyama, Ali Jannati, Clemente Vega, Harper L Kaye, Ugur Damar, Jeffrey Bolton, Scellig S D Stone, Joseph R Madsen, Ralph O Suarez, Alexander Rotenberg
Discrepant expressive language lateralization in children and adolescents with epilepsy. Annals of clinical and translational neurology 9 (9) (2022)
Mustafa Q Hameed, Nathaniel W Hodgson, Henry Hing Cheong Lee, Andres Pascual-Leone, Paul C MacMullin, Ali Jannati, Sameer C Dhamne, Takao K Hensch, Alexander Rotenberg
N-acetylcysteine treatment mitigates loss of cortical parvalbumin-positive interneuron and perineuronal net integrity resulting from persistent oxidative stress in a rat TBI model. Cerebral cortex (New York, N.Y. : 1991) (2022)
Tsung-Hsun Hsieh, Xiao-Kuo He, Hui-Hua Liu, Jia-Jin Jason Chen, Chih-Wei Peng, Hao-Li Liu, Alexander Rotenberg, Ko-Ting Chen, Ming-Yuan Chang, Yung-Hsiao Chiang, Pi-Kai Chang, Chi-Wei Kuo
Early Repetitive Transcranial Magnetic Stimulation Exerts Neuroprotective Effects and Improves Motor Functions in Hemiparkinsonian Rats. Neural plasticity 2021 (2021)
Christopher J Yuskaitis, Leigh-Ana Rossitto, Karenna J Groff, Sameer C Dhamne, Bo Zhang, Lahin K Lalani, Achint K Singh, Alexander Rotenberg, Mustafa Sahin
Factors influencing the acute pentylenetetrazole-induced seizure paradigm and a literature review. Annals of clinical and translational neurology 8 (7) (2021)
Yan Sun, Sameer C Dhamne, Alejandro Carretero-Guillén, Ricardo Salvador, Marti C Goldenberg, Brianna R Godlewski, Alvaro Pascual-Leone, Joseph R Madsen, Scellig S D Stone, Giulio Ruffini, Javier Márquez-Ruiz, Alexander Rotenberg
Drug-Responsive Inhomogeneous Cortical Modulation by Direct Current Stimulation. Annals of neurology 88 (3) (2020)
Roman Gersner, Carmen Paredes, Mustafa Q Hameed, Sameer C Dhamne, Álvaro Pascual-Leone, Alexander Rotenberg
Transcranial magnetic stimulation tracks subminute changes in cortical excitability during propofol anesthesia. Annals of clinical and translational neurology 7 (3) (2020)
Fae B Kayarian, Ali Jannati, Alexander Rotenberg, Emiliano Santarnecchi
Targeting Gamma-Related Pathophysiology in Autism Spectrum Disorder Using Transcranial Electrical Stimulation: Opportunities and Challenges. Autism research : official journal of the International Society for Autism Research 13 (7) (2020)