Meng-Han Tsai (M-H Tsai)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 34

Top Topics

Temporal Lobe Epilepsy

Mitochondrial Dna

Top Venues

Brain and behavior

Acta neuropathologica

This page only lists publications with an associated author ORCID identifier.

Publications

Meng-Han Tsai, Hao-Chen Ke, Wan-Cian Lin, Fang-Shin Nian, Chia-Wei Huang, Haw-Yuan Cheng, Chi-Sin Hsu, Tiziana Granata, Chien-Hui Chang, Barbara Castellotti, Shin-Yi Lin, Fabio M Doniselli, Cheng-Ju Lu, Silvana Franceschetti, Francesca Ragona, Pei-Shan Hou, Laura Canafoglia, Chien-Yi Tung, Mei-Hsuan Lee, Won-Jing Wang, Jin-Wu Tsai
Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations. Acta neuropathologica 147 (1) (2024)
Meng-Han Tsai, Hao-Chen Ke, Wan-Cian Lin, Fang-Shin Nian, Chia-Wei Huang, Haw-Yuan Cheng, Chi-Sin Hsu, Tiziana Granata, Chien-Hui Chang, Barbara Castellotti, Shin-Yi Lin, Fabio M Doniselli, Cheng-Ju Lu, Silvana Franceschetti, Francesca Ragona, Pei-Shan Hou, Laura Canafoglia, Chien-Yi Tung, Mei-Hsuan Lee, Won-Jing Wang, Jin-Wu Tsai
Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations. Acta neuropathologica 147 (1) (2024)
Meng-Han Tsai, Hao-Chen Ke, Wan-Cian Lin, Fang-Shin Nian, Chia-Wei Huang, Haw-Yuan Cheng, Chi-Sin Hsu, Tiziana Granata, Chien-Hui Chang, Barbara Castellotti, Shin-Yi Lin, Fabio M Doniselli, Cheng-Ju Lu, Silvana Franceschetti, Francesca Ragona, Pei-Shan Hou, Laura Canafoglia, Chien-Yi Tung, Mei-Hsuan Lee, Won-Jing Wang, Jin-Wu Tsai
Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations. Acta neuropathologica 147 (1) (2024)
Meng-Han Tsai, Hao-Chen Ke, Wan-Cian Lin, Fang-Shin Nian, Chia-Wei Huang, Haw-Yuan Cheng, Chi-Sin Hsu, Tiziana Granata, Chien-Hui Chang, Barbara Castellotti, Shin-Yi Lin, Fabio M Doniselli, Cheng-Ju Lu, Silvana Franceschetti, Francesca Ragona, Pei-Shan Hou, Laura Canafoglia, Chien-Yi Tung, Mei-Hsuan Lee, Won-Jing Wang, Jin-Wu Tsai
Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations. Acta neuropathologica 147 (1) (2024)
Meng-Han Tsai, Hao-Chen Ke, Wan-Cian Lin, Fang-Shin Nian, Chia-Wei Huang, Haw-Yuan Cheng, Chi-Sin Hsu, Tiziana Granata, Chien-Hui Chang, Barbara Castellotti, Shin-Yi Lin, Fabio M Doniselli, Cheng-Ju Lu, Silvana Franceschetti, Francesca Ragona, Pei-Shan Hou, Laura Canafoglia, Chien-Yi Tung, Mei-Hsuan Lee, Won-Jing Wang, Jin-Wu Tsai
Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations. Acta neuropathologica 147 (1) (2024)
Shih-Ying Chen, Chen-Rui Ho, Yan-Ting Lu, Chih-Hsiang Lin, Min-Yu Lan, Meng-Han Tsai
The Genetics of Primary Familial Brain Calcification: A Literature Review. International journal of molecular sciences 24 (13) (2023)
Cheng-Yen Kuo, Meng-Han Tsai, Hsi-Hsien Lin, Yu-Chi Wang, Abhishek Kumar Singh, Chin-Chen Chang, Jainn-Jim Lin, Po-Cheng Hung, Kuang-Lin Lin
Identification and clinical characteristics of a novel missense ADGRG1 variant in bilateral Frontoparietal Polymicrogyria: The electroclinical change from infancy to adulthood after Callosotomy in three siblings. Epilepsia open 8 (1) (2023)
Chih-Hsiang Lin, Sung-Chou Li, Ming-Hong Lin, Chen-Jui Ho, Yan-Ting Lu, Yuyu Lin, Pei-Hsien Lin, Kuo-Wang Tsai, Meng-Han Tsai
S100A6 participates in initiation of autoimmune encephalitis and is under epigenetic control. Brain and behavior (2023)
Chih-Hsiang Lin, Sung-Chou Li, Ming-Hong Lin, Chen-Jui Ho, Yan-Ting Lu, Yuyu Lin, Pei-Hsien Lin, Kuo-Wang Tsai, Meng-Han Tsai
S100A6 participates in initiation of autoimmune encephalitis and is under epigenetic control. Brain and behavior 13 (3) (2023)
Cheng-Yen Kuo, Meng-Han Tsai, Hsi-Hsien Lin, Yu-Chi Wang, Abhishek Kumar Singh, Chin-Chen Chang, Jainn-Jim Lin, Po-Cheng Hung, Kuang-Lin Lin
Identification and clinical characteristics of a novel missense ADGRG1 variant in bilateral Frontoparietal Polymicrogyria: The electroclinical change from infancy to adulthood after Callosotomy in three siblings. Epilepsia open 8 (1) (2023)
Cheng-Yen Kuo, Meng-Han Tsai, Hsi-Hsien Lin, Yu-Chi Wang, Abhishek Kumar Singh, Chin-Chen Chang, Jainn-Jim Lin, Po-Cheng Hung, Kuang-Lin Lin
Identification and clinical characteristics of a novel missense ADGRG1 variant in bilateral Frontoparietal Polymicrogyria: The electroclinical change from infancy to adulthood after Callosotomy in three siblings. Epilepsia open 8 (1) (2023)
Chih-Hsiang Lin, Sung-Chou Li, Ming-Hong Lin, Chen-Jui Ho, Yan-Ting Lu, Yuyu Lin, Pei-Hsien Lin, Kuo-Wang Tsai, Meng-Han Tsai
S100A6 participates in initiation of autoimmune encephalitis and is under epigenetic control. Brain and behavior 13 (3) (2023)
Yan-Ting Lu, Chih-Hsiang Lin, Chen-Jui Ho, Shih-Ying Chen, Meng-Han Tsai
Validating Prediction Tools for Autoimmune Encephalitis in Adult Taiwanese Patients: A Retrospective Study. Biomedicines 11 (7) (2023)
Chih-Hsiang Lin, Sung-Chou Li, Ming-Hong Lin, Chen-Jui Ho, Yan-Ting Lu, Yuyu Lin, Pei-Hsien Lin, Kuo-Wang Tsai, Meng-Han Tsai
S100A6 participates in initiation of autoimmune encephalitis and is under epigenetic control. Brain and behavior 13 (3) (2023)
I-Jun Chou, Ju-Yin Hou, Wen-Lang Fan, Meng-Han Tsai, Kuang-Lin Lin
Long-Term Outcome of Neonatal Seizure with PACS2 Mutation: Case Series and Literature Review. Children (Basel, Switzerland) 10 (4) (2023)
Tatiana Maroilley, Meng-Han Tsai, Rumika Mascarenhas, Catherine Diao, Maryam Khanbabaei, Sabine Kaya, Christel Depienne, Maja Tarailo-Graovac, Karl Martin Klein
A novel FAME1 repeat configuration in a European family identified using a combined genomics approach. Epilepsia open (2023)
Chih-Hsiang Lin, Sung-Chou Li, Ming-Hong Lin, Chen-Jui Ho, Yan-Ting Lu, Yuyu Lin, Pei-Hsien Lin, Kuo-Wang Tsai, Meng-Han Tsai
S100A6 participates in initiation of autoimmune encephalitis and is under epigenetic control. Brain and behavior (2023)
Cheng-Yen Kuo, Meng-Han Tsai, Hsi-Hsien Lin, Yu-Chi Wang, Abhishek Kumar Singh, Chin-Chen Chang, Jainn-Jim Lin, Po-Cheng Hung, Kuang-Lin Lin
Identification and clinical characteristics of a novel missense ADGRG1 variant in bilateral Frontoparietal Polymicrogyria: The electroclinical change from infancy to adulthood after Callosotomy in three siblings. Epilepsia open 8 (1) (2023)
I-Jun Chou, Ju-Yin Hou, Wen-Lang Fan, Meng-Han Tsai, Kuang-Lin Lin
Long-Term Outcome of Neonatal Seizure with PACS2 Mutation: Case Series and Literature Review. Children (Basel, Switzerland) 10 (4) (2023)
Tatiana Maroilley, Meng-Han Tsai, Rumika Mascarenhas, Catherine Diao, Maryam Khanbabaei, Sabine Kaya, Christel Depienne, Maja Tarailo-Graovac, Karl Martin Klein
A novel FAME1 repeat configuration in a European family identified using a combined genomics approach. Epilepsia open (2023)
Chih-Hsiang Lin, Sung-Chou Li, Ming-Hong Lin, Chen-Jui Ho, Yan-Ting Lu, Yuyu Lin, Pei-Hsien Lin, Kuo-Wang Tsai, Meng-Han Tsai
S100A6 participates in initiation of autoimmune encephalitis and is under epigenetic control. Brain and behavior 13 (3) (2023)
Jun-Ru Lin, Ju-Fang Cheng, Yo-Tsen Liu, Ting-Rong Hsu, Kao-Min Lin, Chien Chen, Chia-Ling Lin, Meng-Han Tsai, Jin-Wu Tsai
Novel lissencephaly-associated DCX variants in the C-terminal DCX domain affect microtubule binding and dynamics. Epilepsia 63 (5) (2022)
Cheng-Yen Kuo, Meng-Han Tsai, Hsi-Hsien Lin, Yu-Chi Wang, Abhishek Kumar Singh, Chin-Chen Chang, Jainn-Jim Lin, Po-Cheng Hung, Kuang-Lin Lin
Identification and clinical characteristics of a novel missense ADGRG1 variant in bilateral Frontoparietal Polymicrogyria: The electroclinical change from infancy to adulthood after Callosotomy in three siblings. Epilepsia open (2022)
Cheng-Yen Kuo, Meng-Han Tsai, Hsi-Hsien Lin, Yu-Chi Wang, Abhishek Kumar Singh, Chang-Chih Chen, Jainn-Jim Lin, Po-Cheng Hung, Kuang-Lin Lin
Identification and Clinical Characteristics of a Novel Missense ADGRG1 Variant in Bilateral Frontoparietal Polymicrogyria: the Electroclinical Change from Infancy to Adulthood after Callosotomy in Three Siblings. Epilepsia open (2022)
Cheng-Yen Kuo, Meng-Han Tsai, Hsi-Hsien Lin, Yu-Chi Wang, Abhishek Kumar Singh, Chang-Chih Chen, Jainn-Jim Lin, Po-Cheng Hung, Kuang-Lin Lin
Identification and clinical characteristics of a novel missense ADGRG1 variant in bilateral Frontoparietal Polymicrogyria: The electroclinical change from infancy to adulthood after Callosotomy in three siblings. Epilepsia open (2022)
Shih-Ying Chen, Chen-Jui Ho, Yan-Ting Lu, Chih-Hsiang Lin, Meng-Han Tsai
ADCY5-related dyskinesia: a case report. Neurological research and practice 4 (1) (2022)
Ting-Ying Fu, Chen-Rui Ho, Chih-Hsiang Lin, Yan-Ting Lu, Wei-Che Lin, Meng-Han Tsai
Hippocampal Malrotation: A Genetic Developmental Anomaly Related to Epilepsy? Brain sciences 11 (4) (2021)
Chia-Wei Liou, Shih-Hsuan Chen, Tsu-Kung Lin, Meng-Han Tsai, Chiung-Chih Chang
Oxidative Stress Biomarkers and Mitochondrial DNA Copy Number Associated with APOE4 Allele and Cholinesterase Inhibitor Therapy in Patients with Alzheimer's Disease. Antioxidants (Basel, Switzerland) 10 (12) (2021)
Meng-Han Tsai, Chung-Wen Kuo, Tsu-Kung Lin, Chen-Rui Ho, Pei-Wen Wang, Jiin-Haur Chuang, Chia-Wei Liou
Ischemic Stroke Risk Associated with Mitochondrial Haplogroup F in the Asian Population. Cells 9 (8) (2020)
Shang-Der Chen, Hsiu-Yung Pan, Jyun-Bin Huang, Xuan-Ping Liu, Jie-Hau Li, Chen-Jui Ho, Meng-Han Tsai, Jenq-Lin Yang, Shu-Fang Chen, Nai-Ching Chen, Yao-Chung Chuang
Circulating MicroRNAs from Serum Exosomes May Serve as a Putative Biomarker in the Diagnosis and Treatment of Patients with Focal Cortical Dysplasia. Cells 9 (8) (2020)
Shih-Hsuan Chen, Chung-Wen Kuo, Tsu-Kung Lin, Meng-Han Tsai, Chia-Wei Liou
Dopamine Therapy and the Regulation of Oxidative Stress and Mitochondrial DNA Copy Number in Patients with Parkinson's Disease. Antioxidants (Basel, Switzerland) 9 (11) (2020)
Meng-Han Tsai, Fang-Shin Nian, Mei-Hsin Hsu, Wei-Szu Liu, Yo-Tsen Liu, Chen Liu, Po-Hsi Lin, Daw-Yang Hwang, Yao-Chung Chuang, Jin-Wu Tsai
PRRT2 missense mutations cluster near C-terminus and frequently lead to protein mislocalization. Epilepsia 60 (5) (2019)
Chih-Hsiang Lin, Chen-Jui Ho, Yan-Ting Lu, Fu-Yuan Shih, Yao-Chung Chuang, Meng-Han Tsai
Predicting the Functional Outcome of Adult Patients with Status Epilepticus. Journal of clinical medicine 8 (7) (2019)
Meng-Han Tsai, C-K Chan, Y-C Chang, Y-T Yu, S-T Chuang, W-L Fan, S-C Li, T-Y Fu, W-N Chang, C-W Liou, Y-C Chuang, C-C Ng, D-Y Hwang, K-S Lim
DEPDC5 mutations in familial and sporadic focal epilepsy. Clinical genetics 92 (4) (2017)