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Tsai, Meng Han and Muir, Alison M. and Wang, Won nJing and Kang, Yi Ning and Yang, Kun Chuan and Chao, Nian Hsin and Wu, Mei Feng and Chang, Ying Chao and Porter, Brenda E. and Jansen, Laura A. and Sebire, Guillaume and Deconinck, Nicolas and Fan, Wen Lang and Su, Shih Chi and Chung, Wen Hung and Almanza Fuerte, Edith P. and Mehaffey, Michele G. and Ng, Ching Ching and Chan, Chung Kin and Lim, Kheng Seang and Leventer, Richard J. and Lockhart, Paul J. and Riney, Kate and Damiano, John A. and Hildebrand, Michael S. and Mirzaa, Ghayda M. and Dobyns, William B. and Berkovic, Samuel F. and Scheffer, Ingrid E. and Tsai, Jin Wu and Mefford, Heather C. (2020) Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly. Neuron, 106 (2). 237-245.e8. ISSN 0896-6273, DOI https://doi.org/10.1016/j.neuron.2020.01.027.
Tsai, Meng Han and Chan, Chung Kin and Chang, Ying Chao and Lin, Chih Hsiang and Liou, Chia Wei and Chang, Wen Neng and Ng, Ching Ching and Lim, Kheng Seang and Hwang, Daw Yang (2018) Molecular Genetic Characterization of Patients With Focal Epilepsy Using a Customized Targeted Resequencing Gene Panel. Frontiers in Neurology, 9. p. 515. ISSN 1664-2295, DOI https://doi.org/10.3389/fneur.2018.00515.
Tsai, Meng Han and Chan, Chung Kin and Chang, Ying Chao and Yu, Y.T. and Chuang, S.T. and Fan, W.L. and Ling, S.C. and Fu, Ting Ying and Chang, Wen Neng and Liou, Chia Wei and Chuang, Yao Chung and Ng, Ching Ching and Hwang, Daw Yang and Lim, Kheng Seang (2017) DEPDC5 mutations in familial and sporadic focal epilepsy. Clinical Genetics, 92 (4). pp. 397-404. ISSN 0009-9163, DOI https://doi.org/10.1111/cge.12992.
