Projects per year
Personal profile
Education
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
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Collaborations and top research areas from the last five years
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Exploring the Genetics and Molecular Mechanism of Familial Adult Myoclonic Epilepsy
Tsai, M.-H. (PI), Chiou, H.-Y. C. (CoPI), Fan, W. L. (CoPI) & Lin, C. H. (CoPI)
01/08/24 → 31/07/25
Project: National Science and Technology Council › National Science and Technology Council Academic Grants
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Unraveling the Roles of Centrosome and Actin Related New Lissencephaly Genes in Neuronal Migration
Tsai, M.-H. (PI), Fan, W. L. (CoPI), Li, S. C. (CoPI), Lin, C. H. (CoPI) & Tsai, J. W. (CoPI)
01/08/23 → 31/07/24
Project: National Science and Technology Council › National Science and Technology Council Academic Grants
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Unraveling the Roles of Centrosome and Actin Related New Lissencephaly Genes in Neuronal Migration
Tsai, M.-H. (PI), Fan, W. L. (CoPI), Li, S. C. (CoPI), Lin, C. H. (CoPI) & Tsai, J. W. (CoPI)
01/08/22 → 31/07/23
Project: National Science and Technology Council › National Science and Technology Council Academic Grants
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Unraveling the Roles of Centrosome and Actin Related New Lissencephaly Genes in Neuronal Migration
Tsai, M.-H. (PI), Fan, W. L. (CoPI), Li, S. C. (CoPI), Lin, C. H. (CoPI) & Tsai, J. W. (CoPI)
01/08/21 → 31/07/22
Project: National Science and Technology Council › National Science and Technology Council Academic Grants
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Dravet-like syndrome with PCDH19 mutations in Taiwan ― A multicenter study
Liu, Y. H., Liang, J. S., Chang, M. Y., Hung, P. L., Tsai, M. H., Chou, I. J., Hou, J. Y., Lee, W. T. & Lin, K. L., 05 2025, In: Pediatrics and Neonatology. 66, 3, p. 230-234 5 p.Research output: Contribution to journal › Journal Article › peer-review
Open Access -
ILAE genetic literacy series: Focal cortical dysplasia
the ILAE Genetics Commission* and the ILAE Genetics Literacy Taskforce**, 02 2025, In: Epileptic disorders : international epilepsy journal with videotape. 27, 1, p. 1-8 8 p.Research output: Contribution to journal › Journal Article › peer-review
Open Access -
A lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development
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., 15 01 2024, In: Development (Cambridge). 151, 2, dev201912.Research output: Contribution to journal › Journal Article › peer-review
Open Access2 Scopus citations -
Clinical and molecular characterization of patients with YWHAG-related epilepsy
Cetica, V., Pisano, T., Lesca, G., Marafi, D., Licchetta, L., Riccardi, F., Mei, D., Chung, H. Y. B., Bayat, A., Balasubramanian, M., Lowenstein, D. H., Endzinienė, M., Alotaibi, M., Villeneuve, N., Jacobs, J., Isidor, B., Solazzi, R., den Hollander, N. S., Marjanovic, D. & Rougeot-Jung, C. & 14 others, , 05 2024, In: Epilepsia. 65, 5, p. 1439-1450 12 p.Research output: Contribution to journal › Journal Article › peer-review
Open Access3 Scopus citations -
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Epi25 Collaborative, 10 2024, In: Nature Neuroscience. 27, 10, p. 1864-1879 16 p.Research output: Contribution to journal › Journal Article › peer-review
Open Access6 Scopus citations