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Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons.
Deneault E, White SH, Rodrigues DC, Ross PJ, Faheem M, Zaslavsky K, Wang Z, Alexandrova R, Pellecchia G, Wei W, Piekna A, Kaur G, Howe JL, Kwan V, Thiruvahindrapuram B, Walker S, Lionel AC, Pasceri P, Merico D, Yuen RKC, Singh KK, Ellis J, Scherer SW. Deneault E, et al. Among authors: wei w. Stem Cell Reports. 2018 Nov 13;11(5):1211-1225. doi: 10.1016/j.stemcr.2018.10.003. Epub 2018 Nov 1. Stem Cell Reports. 2018. PMID: 30392976 Free PMC article.
Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation.
Hildebrandt MR, Reuter MS, Wei W, Tayebi N, Liu J, Sharmin S, Mulder J, Lesperance LS, Brauer PM, Mok RSF, Kinnear C, Piekna A, Romm A, Howe J, Pasceri P, Meng G, Rozycki M, Rodrigues DC, Martinez EC, Szego MJ, Zúñiga-Pflücker JC, Anderson MK, Prescott SA, Rosenblum ND, Kamath BM, Mital S, Scherer SW, Ellis J. Hildebrandt MR, et al. Among authors: wei w. Stem Cell Reports. 2019 Dec 10;13(6):1126-1141. doi: 10.1016/j.stemcr.2019.11.003. Stem Cell Reports. 2019. PMID: 31813827 Free PMC article.
Shifts in Ribosome Engagement Impact Key Gene Sets in Neurodevelopment and Ubiquitination in Rett Syndrome.
Rodrigues DC, Mufteev M, Weatheritt RJ, Djuric U, Ha KCH, Ross PJ, Wei W, Piekna A, Sartori MA, Byres L, Mok RSF, Zaslavsky K, Pasceri P, Diamandis P, Morris Q, Blencowe BJ, Ellis J. Rodrigues DC, et al. Among authors: wei w. Cell Rep. 2020 Mar 24;30(12):4179-4196.e11. doi: 10.1016/j.celrep.2020.02.107. Cell Rep. 2020. PMID: 32209477 Free article.
Identification of TIA1 mRNA targets during human neuronal development.
Byres LP, Mufteev M, Yuki KE, Wei W, Piekna A, Wilson MD, Rodrigues DC, Ellis J. Byres LP, et al. Among authors: wei w. Mol Biol Rep. 2021 Sep;48(9):6349-6361. doi: 10.1007/s11033-021-06634-0. Epub 2021 Aug 19. Mol Biol Rep. 2021. PMID: 34410578 Free PMC article.
Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutations.
Mok RSF, Zhang W, Sheikh TI, Pradeepan K, Fernandes IR, DeJong LC, Benigno G, Hildebrandt MR, Mufteev M, Rodrigues DC, Wei W, Piekna A, Liu J, Muotri AR, Vincent JB, Muller L, Martinez-Trujillo J, Salter MW, Ellis J. Mok RSF, et al. Among authors: wei w. Transl Psychiatry. 2022 Oct 18;12(1):450. doi: 10.1038/s41398-022-02216-1. Transl Psychiatry. 2022. PMID: 36253345 Free PMC article.
Disruption of DDX53 coding sequence has limited impact on iPSC-derived human NGN2 neurons.
Faheem M, Deneault E, Alexandrova R, Rodrigues DC, Pellecchia G, Shum C, Zarrei M, Piekna A, Wei W, Howe JL, Thiruvahindrapuram B, Lamoureux S, Ross PJ, Bradley CA, Ellis J, Scherer SW. Faheem M, et al. Among authors: wei w. BMC Med Genomics. 2023 Jan 12;16(1):5. doi: 10.1186/s12920-022-01425-3. BMC Med Genomics. 2023. PMID: 36635662 Free PMC article.
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