日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Epilepsy-associated FOXJ3 variants link a transcriptional program of the PTEN-mTOR pathway to neuronal specification and cortical lamination.

与癫痫相关的 FOXJ3 变异将 PTEN-mTOR 通路的转录程序与神经元分化和皮质分层联系起来。

Cheng Haw-Yuan, Liu Chen, Nien Chiao-Wen, Huang Hui-Chin, Zhao Hong-Jun, Nian Fang-Shin, Chen Chien, Custodio Helena Martins, Sisodiya Sanjay M, Lu Chien, Chen Hsin-Hung, Hsu Chih-Sin, Pi Wen-Chieh, Chu Chia-Chi, Hsu Jacob Shu-Jui, Chen Pei-Lung, Chang Fu-Pang, Tung Chien-Yi, Chou Shen-Ju, Alavi Shahryar, Houlden Henry, Chen Wei-Yi, Liu Yo-Tsen, Hou Pei-Shan, Tsai Jin-Wu

Knowledge graph representation of the mappings between seizure semiology and epileptogenic zones

癫痫发作症状学与致痫灶之间映射关系的知识图谱表示

Yang, Shihao; Wen, Zirui; Zhan, Wenxin; Fotedar, Neel; Shih, Yen-Cheng; Ding, Jun-En; Bernardo, Danilo; Kallioniemi, Elisa; Weil, Alexander G; Huang, Xiying; Rosenow, Felix; Sun, Hai; Liu, Yo-Tsen; Wu, Shasha; Liu, Feng

Multidisciplinary Approaches for Diagnosing Underrecognized Transthyretin Amyloidosis in Real-World Practice

真实世界中诊断未被充分认识的转甲状腺素蛋白淀粉样变性的多学科方法

Chang, Hao-Chih; Kuo, Ling; Yu, Tsyr-Yan; Liu, Yo-Tsen; Lin, Kon-Ping; Yu, Wen-Chung

Relationship between executive function and dual-task walking in people with Parkinson's disease

帕金森病患者执行功能与双任务行走之间的关系

Zhou, Jun-Hong; Wang, Ray-Yau; Liu, Yo-Tsen; Cheng, Shih-Jung; Liu, Hsin-Hsuan; Yang, Yea-Ru

Clinical impact of pharmacogenetic risk variants in a large chinese cohort

药物遗传风险变异在中国大型人群队列中的临床影响

Wei, Chun-Yu; Wen, Ming-Shien; Cheng, Chih-Kuang; Sheen, Yi-Jing; Yao, Tsung-Chieh; Lee, Sing-Lian; Wu, Jer-Yuarn; Tsai, Ming-Fang; Li, Ling-Hui; Chen, Chun-Houh; Fann, Cathy S-J; Yang, Hsin-Chou; Huang, Yen-Tsung; Chen, Hung-Hsin; Liu, Yi-Min; Yeh, Erh-Chan; Peng, Yu-Ching; Wang, Shuu-Jiun; Chen, Shih-Pin; Tsai, Ming-Tsun; Huo, Teh-Ia; Su, Chien-Wei; Tarng, Der-Cherng; Huang, Chin-Chou; Fuh, Jong-Ling; Lan, Keng-Hsin; Liu, Yo-Tsen; Lu, Ching-Liang; Lee, Yi-Chung; Huang, Yi-Hsiang; Li, Chung-Pin; Wang, Yen-Feng; Hsieh, Yu-Cheng; Chen, Yi-Ming; Hsiao, Tzu-Hung; Lin, Ching-Heng; Chen, Yen-Ju; Chen, I-Chieh; Mao, Chien-Lin; Chang, Shu-Jung; Chang, Yen-Lin; Liao, Yi-Ju; Lai, Chih-Hung; Lee, Wei-Ju; Tung, Hsin; Yen, Ting-Ting; Yen, Hsin-Chien; Chang, Jer-Hwa; Huang, Chun-Yao; Chan, Lung; Lin, Yung-Wei; Hsiao, Bu-Yuan; Hu, Chaur-Jong; Lin, Yung-Kuo; Lin, Yung-Feng; Chang, Tung-Cheng; Wu, Deng-Chyang; Kan, Jung-Yu; Hsu, Chung-Yao; Chen, Szu-Chia; Li, Ching-Chia; Huang, Chung-Feng; Sheu, Chau-Chyun; Yang, Lii-Jia; Chen, Chung-Hwan; Chen, Kuan-Mao; Chang, Shu-Min; Liou, Min-Shiuan; Wang, Shi-Ping; Lin, Kuan-Ting; Chuang, Hui-Ping; Chen, Ying-Ju; Sin, Joey; Chen, Ying-Ting; Chang, Chiung-Chih; Kuo, Chang-Fu; Lin, Jing-Chi; Kuo, Ho-Chang; Chan, Tien-Min; Lee, Chao-Wei; Lai, Jenn-Haung; Luo, Shue-Fen; Cheng, Hao-Tsai; Lin, Lian-Yu; Chang, Li-Chun; Tsai, Chia-Ti; Kao, Hsien-Li; Yu, Jian-Jyun; Jeng, Jiann-Shing; Chiu, Min-Chin; Hong, Tzu-Chan; Yang, Shun-Fa; Lu, Hsueh-Ju; Su, Sheng-Chiang; Chu, Pauling; Li, Peng-Fei; Tsai, Chia-Lin; Tsai, Chia-Kuang; Tang, Shih-En; Lin, Chien-Ming; Wu, Yung-Fu; Huang, Chih-Yang; Ling, Shinn-Zong; Chang, Chun-Chun; Lin, Tzu-Kai; Hsiao, Sheng-Mou; Chang, Chih-Hung; Chen, Chih-Dao; Ma, Gwo-Chin; Chang, Ting-Yu; Hwang, Juey-Jen; Lu, Chien-Lin; Kao, Kuo-Jang; Hung, Chen-Fang; Chen, Shiou-Sheng; Chen, Po-Yueh; Tsui, Kochung; Chen, Yuan-Tsong; Chen, Chien-Hsiun; Chien, Chih-Cheng; Chiang, Han-Sun; Chiu, Yen-Ling; Chen, Hsiang-Cheng; Kwok, Pui-Yan

Monogenic Causes in Familial Stroke Across Intracerebral Hemorrhage and Ischemic Stroke Subtypes Identified by Whole-Exome Sequencing

全外显子组测序鉴定出脑出血和缺血性卒中亚型中家族性卒中的单基因病因

Chang, Li-Hsin; Chi, Nai-Fang; Chen, Chun-Yu; Lin, Yung-Shuan; Hsu, Shao-Lun; Tsai, Jui-Yao; Huang, Hui-Chi; Lin, Chun-Jen; Chung, Chih-Ping; Tung, Chien-Yi; Jeng, Chung-Jiuan; Lee, Yi-Chung; Liu, Yo-Tsen; Lee, I-Hui

The clinical and imaging features of FLNA positive and negative periventricular nodular heterotopia

FLNA阳性和阴性脑室周围结节性异位症的临床和影像学特征

Lu, Yan-Ting; Hsu, Chung-Yao; Liu, Yo-Tsen; Chan, Chung-Kin; Chuang, Yao-Chung; Lin, Chih-Hsiang; Chang, Kai-Ping; Ho, Chen-Jui; Ng, Ching-Ching; Lim, Kheng-Seang; Tsai, Meng-Han

Cellular secretion and cytotoxicity of transthyretin mutant proteins underlie late-onset amyloidosis and neurodegeneration

转甲状腺素蛋白突变蛋白的细胞分泌和细胞毒性是晚发性淀粉样变性和神经退行性的基础

Ridwan Babatunde Ibrahim, Ssu-Yu Yeh, Kon-Ping Lin, Frans Ricardo, Tsyr-Yan Yu, Chih-Chiang Chan, Jin-Wu Tsai, Yo-Tsen Liu3

PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementation

PDXK 突变导致多发性神经病,对 5'-磷酸吡哆醛补充剂有反应

Viorica Chelban, Matthew P Wilson, Jodi Warman Chardon, Jana Vandrovcova, M Natalia Zanetti, Eleni Zamba-Papanicolaou, Stephanie Efthymiou, Simon Pope, Maria R Conte, Giancarlo Abis, Yo-Tsen Liu, Eloise Tribollet, Nourelhoda A Haridy, Juan A Botía, Mina Ryten, Paschalis Nicolaou, Anna Minaidou, Kypr

Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan

台湾遗传性转甲状腺素蛋白淀粉样变性的临床和遗传特征

Chao, Hua-Chuan; Liao, Yi-Chu; Liu, Yo-Tsen; Guo, Yuh-Cherng; Chang, Fu-Pang; Lee, Yi-Chung; Lin, Kon-Ping