Kellen Diamond Winden
Affiliations: | 2010 | University of California, Los Angeles, Los Angeles, CA |
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"Kellen Winden"Mean distance: 16.66 (cluster 6) | S | N | B | C | P |
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Sign in to add mentorDaniel Geschwind | grad student | 2010 | UCLA | |
(Systems level analysis of neuronal transcriptome organization and transcriptional dysregulation in epilepsy.) |
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Publications
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Afshar-Saber W, Teaney NA, Winden KD, et al. (2023) ALDH5A1-deficient iPSC-derived excitatory and inhibitory neurons display cell type specific alterations. Neurobiology of Disease. 106386 |
Winden KD, Pham TT, Teaney NA, et al. (2023) Increased degradation of FMRP contributes to neuronal hyperexcitability in tuberous sclerosis complex. Cell Reports. 42: 112838 |
Buttermore ED, Anderson NC, Chen PF, et al. (2022) 16p13.11 deletion variants associated with neuropsychiatric disorders cause morphological and synaptic changes in induced pluripotent stem cell-derived neurons. Frontiers in Psychiatry. 13: 924956 |
Sundberg M, Pinson H, Smith RS, et al. (2021) 16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro. Nature Communications. 12: 2897 |
Di Nardo A, Lenoël I, Winden KD, et al. (2020) Phenotypic Screen with TSC-Deficient Neurons Reveals Heat-Shock Machinery as a Druggable Pathway for mTORC1 and Reduced Cilia. Cell Reports. 31: 107780 |
Winden KD, Sundberg M, Yang C, et al. (2019) Biallelic mutations in lead to abnormalities associated with cortical tubers in human iPSC-derived neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
Winden KD, Ebrahimi-Fakhari D, Sahin M. (2018) Abnormal mTOR Activation in Autism. Annual Review of Neuroscience |
Sundberg M, Tochitsky I, Buchholz DE, et al. (2018) Purkinje cells derived from TSC patients display hypoexcitability and synaptic deficits associated with reduced FMRP levels and reversed by rapamycin. Molecular Psychiatry |
Ercan E, Han JM, Di Nardo A, et al. (2017) Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex. The Journal of Experimental Medicine |
Wertz MH, Winden K, Neveu P, et al. (2016) Cell type-specific miR-431 dysregulation in a motor neuron model of Spinal Muscular Atrophy. Human Molecular Genetics |