公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
2016 | Clinical heterogeneity of LRRK2 p.I2012T mutation | Fan T.-S.; RUEY-MEEI WU ; PEI-LUNG CHEN ; TA-FU CHEN ; Li H.-Y.; Lin Y.-H.; Chen C.-Y.; Chen M.-L.; CHUN-HWEI TAI ; Lin H.-I.; CHIEN-YU CHEN | Parkinsonism and Related Disorders | 14 | 14 | |
2015 | Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population | Fan T.-S.; Lin H.-I.; CHIN-HSIEN LIN ; RUEY-MEEI WU | Neurobiology of Aging | 17 | 17 | |
2017 | Lack of TMEM230 mutations in patients with familial and sporadic Parkinson's disease in a Taiwanese population | Fan T.-S.; CHIN-HSIEN LIN ; Lin H.-I.; Chen M.-L.; RUEY-MEEI WU | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 9 | 8 | |
2018 | PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population | Fan T.-S.; RUEY-MEEI WU ; Lin H.-I.; Cheng C.; CHIN-HSIEN LIN | Neurobiology of Aging | 1 | 1 |