  | Nian, F.-S.* , Liao, B.-K.* , Su, Y.-L., Wu, P.-R., Tsai, J.-W., & Hou, P.-S.*. (April 2025). Oscillatory DeltaC Expression in Neural Progenitors Primes the Prototype of Forebrain Development. Molecular Neurobiology, 62 (4), 4076 - 4092. doi:10.1007/s12035-024-04530-9  Peer Reviewed verified by ORBi* These authors have contributed equally to this work. |
 | Tsai, M.-H., Ke, H.-C., Lin, W.-C., Nian, F.-S., Huang, C.-W., Cheng, H.-Y., Hsu, C.-S., Granata, T., Chang, C.-H., Castellotti, B., Lin, S.-Y., Doniselli, F. M., Lu, C.-J., Franceschetti, S., Ragona, F., Hou, P.-S., Canafoglia, L., Tung, C.-Y., Lee, M.-H., ... Tsai, J.-W. (2024). Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations. Acta Neuropathologica, 147 (1). doi:10.1007/s00401-023-02665-y Peer Reviewed verified by ORBi |
 | Tsai, M.-H., Lin, W.-C., Chen, S.-Y., Hsieh, M.-Y., Nian, F.-S., Cheng, H.-Y., Zhao, H.-J., Hung, S.-S., Hsu, C.-H., Hou, P.-S., Tung, C.-Y., Lee, M.-H., & Tsai, J.-W. (2024). A lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development. Development, 151 (2). doi:10.1242/dev.201912 Peer Reviewed verified by ORBi |
 | Huang, C.-W., Lee, K.-Y., Lin, P.-T., Nian, F.-S., Cheng, H.-Y., Chang, C.-H., Liao, C.-Y., Su, Y.-L., Seah, C., Li, C., Chen, Y.-F., Lee, M.-H., & Tsai, J.-W. (2023). Muscleblind-like 2 knockout shifts adducin 1 isoform expression and alters dendritic spine dynamics of cortical neurons during brain development. Neuropathology and Applied Neurobiology, 49 (2). doi:10.1111/nan.12890 Peer Reviewed verified by ORBi |
Cheng, H.-Y., Nian, F.-S., Ou, Y.-W., & Tsai, J.-W. (2023). Assessment of Dynein-Mediated Nuclear Migration in the Developing Cortex by Live-Tissue Microscopy. In Methods in Molecular Biology. Humana Press Inc. doi:10.1007/978-1-0716-2958-1_4 Editorial reviewed |
 | Nian, F.-S., & Hou, P.-S. (2022). Evolving Roles of Notch Signaling in Cortical Development. Frontiers in Neuroscience, 16, 844410. doi:10.3389/fnins.2022.844410 Peer Reviewed verified by ORBi |
 | Yang, C.-P., Yang, W.-S., Wong, Y.-H., Wang, K.-H., Teng, Y.-C., Chang, M.-H., Liao, K.-H., Nian, F.-S., Chao, C.-C., Tsai, J.-W., Hwang, W.-L., Lin, M.-W., Tzeng, T.-Y., Wang, P.-N., Campbell, M., Chen, L.-K., Tsai, T.-F., Chang, P.-C., & Kung, H.-J. (May 2020). Muscle atrophy-related myotube-derived exosomal microRNA in neuronal dysfunction: Targeting both coding and long noncoding RNAs. Aging Cell, 19 (5), 13107. doi:10.1111/acel.13107 Peer Reviewed verified by ORBi |
 | Tsai, M.-H.* , Cheng, H.-Y.* , Nian, F.-S.* , Liu, C., Chao, N.-H., Chiang, K.-L., Chen, S.-F., & Tsai, J.-W. (2020). Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation. Acta Neuropathologica Communications, 8 (1). doi:10.1186/s40478-020-00971-0 Peer Reviewed verified by ORBi* These authors have contributed equally to this work. |
  | Nian, F.-S., Li, L.-L., Cheng, C.-Y., Wu, P.-C., Lin, Y.-T., Tang, C.-Y., Ren, B.-S., Tai, C.-Y., Fann, M.-J., Kao, L.-S., Hong, C.-J., & Tsai, J.-W. (September 2019). Rab18 Collaborates with Rab7 to Modulate Lysosomal and Autophagy Activities in the Nervous System: an Overlapping Mechanism for Warburg Micro Syndrome and Charcot-Marie-Tooth Neuropathy Type 2B. Molecular Neurobiology, 56 (9), 6095 - 6105. doi:10.1007/s12035-019-1471-z Peer Reviewed verified by ORBi |
 | Tsai, M.-H.* , Nian, F.-S.* , Hsu, M.-H., Liu, W.-S., Liu, Y.-T., Liu, C., Lin, P.-H., Hwang, D.-Y., Chuang, Y.-C., & Tsai, J.-W. (May 2019). PRRT2 missense mutations cluster near C-terminus and frequently lead to protein mislocalization. Epilepsia, 60 (5), 807 - 817. doi:10.1111/epi.14725 Peer Reviewed verified by ORBi* These authors have contributed equally to this work. |
 | Liu, Y.-T., Nian, F.-S., Chou, W.-J., Tai, C.-Y., Kwan, S.-Y., Chen, C., Kuo, P.-W., Lin, P.-H., Chen, C.-Y., Huang, C.-W., Lee, Y.-C., Soong, B.-W., & Tsai, J.-W. (28 June 2016). PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defects. Oncotarget, 7 (26), 39184 - 39196. doi:10.18632/oncotarget.9258 Peer Reviewed verified by ORBi |
 | Chakraborty, S., Nian, F.-S., Tsai, J.-W., Karmenyan, A., & Chiou, A. (13 January 2016). Quantification of the Metabolic State in Cell-Model of Parkinson's Disease by Fluorescence Lifetime Imaging Microscopy. Scientific Reports, 6 (1), 19145. doi:10.1038/srep19145 Peer Reviewed verified by ORBi |
 | Cheng, C.-Y., Wu, J.-C., Tsai, J.-W., Nian, F.-S., Wu, P.-C., Kao, L.-S., Fann, M.-J., Tsai, S.-J., Liou, Y.-J., Tai, C.-Y., & Hong, C.-J. (May 2015). ENU mutagenesis identifies mice modeling Warburg Micro Syndrome with sensory axon degeneration caused by a deletion in Rab18. Experimental Neurology, 267, 143 - 151. doi:10.1016/j.expneurol.2015.03.003 Peer Reviewed verified by ORBi |
 | Liou, Y.-J., Chen, C.-H., Cheng, C.-Y., Chen, S.-Y., Chen, T.-J., Yu, Y. W.-Y., Nian, F.-S., Tsai, S.-J., & Hong, C.-J. (2012). Convergent evidence from mouse and human studies suggests the involvement of zinc finger protein 326 gene in antidepressant treatment response. PLoS ONE, 7 (5), 32984. doi:10.1371/journal.pone.0032984 Peer Reviewed verified by ORBi |
