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Sofia B. Lizarraga

Affiliations: 
University of South Carolina, Columbia, SC 
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"Sofia Lizarraga"
Mean distance: 14.83 (cluster 46)
 
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Parents

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Yixian Zheng grad student 2003 Johns Hopkins
 (Regulation of spindle assembly by the Ran pathway.)
Chris A. Walsh post-doc Harvard Medical School
Eric Morrow post-doc 2010-2014 Brown
 (Tenure-track Assistant Professor at University of South Carolina Columbia as of 2015)
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Publications

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Vacharasin JM, Ward JA, McCord MM, et al. (2024) Neuroimmune mechanisms in autism etiology - untangling a complex problem using human cellular models. Oxford Open Neuroscience. 3: kvae003
Ghate PS, Vacharasin JM, Ward JA, et al. (2023) The Warburg micro syndrome protein RAB3GAP1 modulates neuronal morphogenesis and interacts with axon elongation end ER-Golgi trafficking factors. Neurobiology of Disease. 106215
Ritchie FD, Lizarraga SB. (2023) The role of histone methyltransferases in neurocognitive disorders associated with brain size abnormalities. Frontiers in Neuroscience. 17: 989109
Leung CS, Rosenzweig S, Yoon B, et al. (2023) Dysregulation of the chromatin environment leads to differential alternative splicing as a mechanism of disease in a human model of autism spectrum disorder. Human Molecular Genetics
Cheon S, Culver AM, Bagnell AM, et al. (2022) Counteracting epigenetic mechanisms regulate the structural development of neuronal circuitry in human neurons. Molecular Psychiatry
Lizarraga SB, Ma L, Maguire AM, et al. (2021) Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Science Translational Medicine. 13
Chukwurah E, Osmundsen A, Davis SW, et al. (2019) All Together Now: Modeling the Interaction of Neural With Non-neural Systems Using Organoid Models. Frontiers in Neuroscience. 13: 582
Xu M, Ouyang Q, Gong J, et al. (2017) Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6-Null Mouse Model of Christianson Syndrome. Eneuro. 4
Hollingsworth EW, Vaughn JE, Orack JC, et al. (2017) iPhemap: an atlas of phenotype to genotype relationships of human iPSC models of neurological diseases. Embo Molecular Medicine
Ouyang Q, Nakayama T, Baytas O, et al. (2016) Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features. Proceedings of the National Academy of Sciences of the United States of America
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