Muotri, Alysson R.
University of California San Diego
28 papers on CoChatORCID 0000-0003-0867-2875
Most cited papers
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A Model for Neural Development and Treatment of Rett Syndrome Using Human Induced Pluripotent Stem Cells
Marchetto, M. C. N., Carromeu, C., Acab, A., Yu, D., Yeo, G. W., Mu, Y., Chen, G., Gage, F. H., & Muotri, A. R. (2010) · Cell
Genetics and Neurodevelopmental DisordersPluripotent Stem Cells Research
Cited by 1,329
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The Brazilian Zika virus strain causes birth defects in experimental models
Cugola, F. R., Fernandes, I. R., Russo, F. B., Freitas, B. C., Dias, J. L. M., Guimarães, K. P., Benazzato, C., Almeida, N., Pignatari, G. C., Romero, S., et al. (2016) · Nature
Mosquito-borne diseases and controlVirology and Viral Diseases
Cited by 1,326
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Complex Oscillatory Waves Emerging from Cortical Organoids Model Early Human Brain Network Development
Trujillo, C. A., Gao, R., Negraes, P. D., Gu, J., Buchanan, J., Preissl, S., Wang, A., Wu, W., Haddad, G. G., Chaim, I. A., et al. (2019) · Cell Stem Cell
Neural dynamics and brain functionNeurogenesis and neuroplasticity mechanisms
Cited by 974
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Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition
Muotri, A. R., Chu, V. T., Marchetto, M. C. N., Deng, W., Moran, J. V., & Gage, F. H. (2005) · Nature
Chromosomal and Genetic VariationsNeurogenesis and neuroplasticity mechanisms
Cited by 942
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Wnt-mediated activation of NeuroD1 and retro-elements during adult neurogenesis
Kuwabara, T., Hsieh, J., Muotri, A., Yeo, G., Warashina, M., Lie, D. C., Moore, L., Nakashima, K., Asashima, M., & Gage, F. H. (2009) · Nature Neuroscience
Neurogenesis and neuroplasticity mechanismsWnt/β-catenin signaling in development and cancer
Cited by 648
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L1 retrotransposition in neurons is modulated by MeCP2
Muotri, A. R., Marchetto, M. C. N., Coufal, N. G., Oefner, R., Yeo, G., Nakashima, K., & Gage, F. H. (2010) · Nature
Genetics and Neurodevelopmental DisordersChromosomal and Genetic Variations
Cited by 626
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Non-Cell-Autonomous Effect of Human SOD1G37R Astrocytes on Motor Neurons Derived from Human Embryonic Stem Cells
Marchetto, M. C. N., Muotri, A. R., Mu, Y., Smith, A. M., Cezar, G. G., & Gage, F. H. (2008) · Cell Stem Cell
Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments
Cited by 475
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Altered proliferation and networks in neural cells derived from idiopathic autistic individuals
Marchetto, M. C., Belinson, H., Tian, Y., Freitas, B. C., Fu, C., Vadodaria, K. C., Beltrao-Braga, P. C., Trujillo, C. A., Mendes, A. P. D., Padmanabhan, K., et al. (2017) · Molecular Psychiatry
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 466
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Modeling of TREX1-dependent autoimmune disease using human stem cells highlights L1 accumulation as a source of neuroinflammation
Thomas, C. A., Tejwani, L., Trujillo, C. A., Negraes, P. D., Herai, R. H., Mesci, P., Macia, A., Crow, Y. J., & Muotri, A. R. (2017) · Cell Stem Cell
interferon and immune responsesSystemic Lupus Erythematosus Research
Cited by 330
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Efficient generation of human iPSCs by a synthetic self-replicative RNA
Yoshioka, N., Gros, E., Li, H.-R., Kumar, S., Deacon, D. C., Maron, C., Muotri, A. R., Chi, N. C., Fu, X.-D., Yu, B. D., et al. (2013) · Cell stem cell
Pluripotent Stem Cells ResearchRNA Interference and Gene Delivery
Cited by 312
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Getting to the cores of autism
Iakoucheva, L. M., Muotri, A. R., & Sebat, J. (2019) · Cell
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 260
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Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons
Griesi-Oliveira, K., Acab, A., Gupta, A. R., Sunaga, D. Y., Chailangkarn, T., Nicol, X., Nunez, Y., Walker, M. F., Murdoch, J. D., Sanders, S. J., et al. (2015) · Molecular Psychiatry
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 236
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Ataxia telangiectasia mutated (ATM) modulates long interspersed element-1 (L1) retrotransposition in human neural stem cells
Coufal, N. G., Garcia-Perez, J. L., Peng, G. E., Marchetto, M. C. N., Muotri, A. R., Mu, Y., Carson, C. T., Macia, A., Moran, J. V., & Gage, F. H. (2011) · Proceedings of the National Academy of Sciences
Chromosomal and Genetic VariationsGenomic variations and chromosomal abnormalities
Cited by 229
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Paternally inherited cis-regulatory structural variants are associated with autism
Brandler, W. M., Antaki, D., Gujral, M., Kleiber, M. L., Whitney, J., Maile, M. S., Hong, O., Chapman, T. R., Tan, S., Tandon, P., et al. (2018) · Science
Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities
Cited by 209
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A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex
Antaki, D., Guevara, J., Maihofer, A. X., Klein, M., Gujral, M., Grove, J., Carey, C. E., Hong, O., Arranz, M. J., Hervas, A., et al. (2022) · Nature Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 206
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A Quantitative Framework to Evaluate Modeling of Cortical Development by Neural Stem Cells
Stein, J. L., de la Torre-Ubieta, L., Tian, Y., Parikshak, N. N., Hernández, I. A., Marchetto, M. C., Baker, D. K., Lu, D., Hinman, C. R., Lowe, J. K., et al. (2014) · Neuron
Neurogenesis and neuroplasticity mechanismsPluripotent Stem Cells Research
Cited by 201
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L1-associated genomic regions are deleted in somatic cells of the healthy human brain
Erwin, J. A., Paquola, A. C. M., Singer, T., Gallina, I., Novotny, M., Quayle, C., Bedrosian, T. A., Alves, F. I. A., Butcher, C. R., Herdy, J. R., et al. (2016) · Nature Neuroscience
Genomic variations and chromosomal abnormalitiesChromosomal and Genetic Variations
Cited by 195
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A human neurodevelopmental model for Williams syndrome
Chailangkarn, T., Trujillo, C. A., Freitas, B. C., Hrvoj-Mihic, B., Herai, R. H., Yu, D. X., Brown, T. T., Marchetto, M. C., Bardy, C., McHenry, L., et al. (2016) · Nature
Williams Syndrome ResearchGenetics and Neurodevelopmental Disorders
Cited by 195
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Transposable Elements, Inflammation, and Neurological Disease
Saleh, A., Macia, A., & Muotri, A. R. (2019) · Frontiers in Neurology
Chromosomal and Genetic VariationsNeuroinflammation and Neurodegeneration Mechanisms
Cited by 149
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Species-specific maturation profiles of human, chimpanzee and bonobo neural cells
Marchetto, M. C., Hrvoj-Mihic, B., Kerman, B. E., Yu, D. X., Vadodaria, K. C., Linker, S. B., Narvaiza, I., Santos, R., Denli, A. M., Mendes, A. P., et al. (2019) · eLife
Neurogenesis and neuroplasticity mechanismsPluripotent Stem Cells Research
Cited by 132
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Altered neuronal network and rescue in a human MECP2 duplication model
Nageshappa, S., Carromeu, C., Trujillo, C. A., Mesci, P., Espuny-Camacho, I., Pasciuto, E., Vanderhaeghen, P., Verfaillie, C. M., Raitano, S., Kumar, A., et al. (2016) · Molecular Psychiatry
Genetics and Neurodevelopmental DisordersEpigenetics and DNA Methylation
Cited by 117
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Frequency and complexity of de novo structural mutation in autism
Brandler, W. M., Antaki, D., Gujral, M., Noor, A., Rosanio, G., Chapman, T. R., Barrera, D. J., Lin, G. N., Malhotra, D., Watts, A. C., et al. (2016) · The American Journal of Human Genetics
Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research
Cited by 104
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Pharmacological reversal of synaptic and network pathology in human MECP2‐KO neurons and cortical organoids
Trujillo, C. A., Adams, J. W., Negraes, P. D., Carromeu, C., Tejwani, L., Acab, A., Tsuda, B., Thomas, C. A., Sodhi, N., Fichter, K. M., et al. (2021) · EMBO Molecular Medicine
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 101
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Therapeutically viable generation of neurons with antisense oligonucleotide suppression of PTB
Maimon, R., Chillon-Marinas, C., Snethlage, C. E., Singhal, S. M., McAlonis-Downes, M., Ling, K., Rigo, F., Bennett, C. F., Da Cruz, S., Hnasko, T. S., et al. (2021) · Nature Neuroscience
Neurogenesis and neuroplasticity mechanismsNeuroscience and Neuropharmacology Research
Cited by 62
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