| Year |
Citation |
Score |
| 2023 |
Yang R, Feng X, Arias-Cavieres A, Mitchell RM, Polo A, Hu K, Zhong R, Qi C, Zhang RS, Westneat N, Portillo CA, Nobrega MA, Hansel C, Garcia Iii AJ, Zhang X. Upregulation of SYNGAP1 expression in mice and human neurons by redirecting alternative splicing. Neuron. PMID 36917980 DOI: 10.1016/j.neuron.2023.02.021 |
0.72 |
|
| 2023 |
Li Y, Ritchie EM, Steinke CL, Qi C, Chen L, Zheng B, Jin Y. Correction: Activation of MAP3K DLK and LZK in Purkinje cells causes rapid and slow degeneration depending on signaling strength. Elife. 12. PMID 36779959 DOI: 10.7554/eLife.86472 |
0.5 |
|
| 2022 |
Qi C, Luo LD, Feng I, Ma S. Molecular mechanisms of synaptogenesis. Frontiers in Synaptic Neuroscience. 14: 939793. PMID 36176941 DOI: 10.3389/fnsyn.2022.939793 |
0.594 |
|
| 2022 |
Ma S, Skarica M, Li Q, Xu C, Risgaard RD, Tebbenkamp ATN, Mato-Blanco X, Kovner R, Krsnik Ž, de Martin X, Luria V, Martí-Pérez X, Liang D, Karger A, Schmidt DK, ... ... Qi C, et al. Molecular and cellular evolution of the primate dorsolateral prefrontal cortex. Science (New York, N.Y.). eabo7257. PMID 36007006 DOI: 10.1126/science.abo7257 |
0.705 |
|
| 2021 |
Qi C, Feng I, Costa AR, Pinto-Costa R, Neil JE, Caluseriu O, Li D, Ganetzky RD, Brasch-Andersen C, Fagerberg C, Hansen LK, Bupp C, Muraresku CC, Ruan X, Kang B, et al. Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humans. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 34906466 DOI: 10.1016/j.gim.2021.09.014 |
0.594 |
|
| 2021 |
Ruan X, Kang B, Qi C, Lin W, Wang J, Zhang X. Progenitor cell diversity in the developing mouse neocortex. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 33649223 DOI: 10.1073/pnas.2018866118 |
0.679 |
|
| 2021 |
Li Y, Ritchie EM, Steinke CL, Qi C, Chen L, Zheng B, Jin Y. Activation of MAP3K DLK and LZK in Purkinje cells causes rapid and slow degeneration depending on signaling strength. Elife. 10. PMID 33475086 DOI: 10.7554/eLife.63509 |
0.574 |
|
| 2017 |
Qin R, Cao S, Lyu T, Qi C, Zhang W, Wang Y. CDYL Deficiency Disrupts Neuronal Migration and Increases Susceptibility to Epilepsy. Cell Reports. 18: 380-390. PMID 28076783 DOI: 10.1016/j.celrep.2016.12.043 |
0.422 |
|
| 2014 |
Qi C, Liu S, Qin R, Zhang Y, Wang G, Shang Y, Wang Y, Liang J. Coordinated regulation of dendrite arborization by epigenetic factors CDYL and EZH2. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 4494-508. PMID 24671995 DOI: 10.1523/Jneurosci.3647-13.2014 |
0.455 |
|
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