Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
2023 | Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study | Rizig, Mie; Bandres-Ciga, Sara; Makarious, Mary B; Ojo, Oluwadamilola Omolara; Crea, Peter Wild; Abiodun, Oladunni Victoria; Levine, Kristin S; Abubakar, Sani Atta; Achoru, Charles Obiora; Vitale, Dan; Adeniji, Olaleye Akinmola; Agabi, Osigwe Paul; Koretsky, Mathew J; Agulanna, Uchechi; Hall, Deborah A; Akinyemi, Rufus Olusola; Xie, Tao; Ali, Mohammed Wulgo; Shamim, Ejaz A; Ani-Osheku, Ifeyinwa; Padmanaban, Mahesh; Arigbodi, Ohwotemu Michael; Standaert, David G; Bello, Abiodun Hamzat; Dean, Marissa N; Erameh, Cyril Oshomah; Elsayed, Inas; Farombi, Temitope Hannah; Okunoye, Olaitan; Fawale, Michael Bimbola; Billingsley, Kimberley J; Imarhiagbe, Frank Aiwansoba; Jerez, Pilar Alvarez; Iwuozo, Emmanuel Uzodinma; Baker, Breeana; Komolafe, Morenikeji Adeyoyin; Malik, Laksh; Nwani, Paul Osemeke; Daida, Kensuke; Nwazor, Ernest Okwundu; Miano-Burkhardt, Abigail; Nyandaiti, Yakub Wilberforce; Fang, Zih-Hua; Obiabo, Yahaya Olugbo; Kluss, Jillian H; Odeniyi, Olanike Adedoyin; Hernandez, Dena G; Odiase, Francis Ehidiamen; Tayebi, Nahid; Ojini, Francis Ibe; Sidranksy, Ellen; Onwuegbuzie, Gerald Awele; D'Souza, Andrea M; Osaigbovo, Godwin Osawaru; Berhe, Bahafta; Osemwegie, Nosakhare; Reed, Xylena; Oshinaike, Olajumoke Olufemi; Leonard, Hampton L; Otubogun, Folajimi Morenikeji; Alvarado, Chelsea X; Oyakhire, Shyngle Imiewan; Ozomma, Simon Izuchukwu; Samuel, Sarah Chabiri; Taiwo, Funmilola Tolulope; Wahab, Kolawole Wasiu; Zubair, Yusuf Agboola; Iwaki, Hirotaka; Kim, Jonggeol Jeffrey; Morris, Huw R; Hardy, John; Nalls, Mike A; Heilbron, Karl; Norcliffe-Kaufmann, Lucy; Blauwendraat, Cornelis; Houlden, Henry; Singleton, Andrew; Okubadejo, Njideka Ulunma; CHIN-HSIEN LIN | The Lancet. Neurology | 10 | | |
2017 | Identification of VPS35 p.D620N mutation-related Parkinson's disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: A case report and literature review | Chen Y.-F.; Chang Y.-Y.; Lan M.-Y.; PEI-LUNG CHEN ; CHIN-HSIEN LIN | BMC Neurology | 22 | 14 | |
2015 | The impact of nonmotor symptoms on quality of life in patients with parkinson's disease in Taiwan | Liu W.-M.; Lin R.-J.; Yu R.-L.; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; RUEY-MEEI WU | Neuropsychiatric Disease and Treatment | 31 | 26 | |
2021 | In vitro genome editing rescues parkinsonism phenotypes in induced pluripotent stem cells-derived dopaminergic neurons carrying LRRK2 p.G2019S mutation | Chang, Kuo-Hsuan; Huang, Cheng-Yen; Ou-Yang, Chih-Hsin; Ho, Chang-Han; Lin, Han-Yi; Hsu, Chia-Lang; YOU-TZUNG CHEN ; Chou, Yu-Chi; Chen, Yi-Jing; Chen, Ying; Lin, Jia-Li; Wang, Ji-Kuan; Lin, Pei-Wen; Lin, Ying-Ru; MIAO-HSIA LIN ; CHI-KANG TSENG ; CHIN-HSIEN LIN | Stem Cell Research and Therapy | 19 | 13 | |
2021 | Integrated 18F-T807 Tau PET, Structural MRI, and Plasma Tau in Tauopathy Neurodegenerative Disorders | Li, Cheng-Hsuan; TA-FU CHEN ; MING-JANG CHIU ; RUOH-FANG YEN ; Shih, Ming-Chieh; CHIN-HSIEN LIN | Frontiers in Aging Neuroscience | 13 | 13 | |
2022 | An integrated biometric voice and facial features for early detection of Parkinson’s disease | Lim, Wee Shin; Chiu, Shu-I; Wu, Meng-Ciao; Tsai, Shu-Fen; Wang, Pu-He; Kun-Pei Lin ; YUNG-MING CHEN ; Peng, Pei-Ling; YUNG-YAW CHEN ; JYH-SHING JANG ; CHIN-HSIEN LIN | NPJ Parkinson's disease | 8 | 5 | |
2020 | Integrated Plasma and Neuroimaging Biomarkers Associated with Motor and Cognition Severity in Parkinson's Disease | CHIH-HAO CHEN ; BO-CHING LEE ; CHIN-HSIEN LIN | Journal of Parkinson's Disease | 25 | 20 | |
2017 | Intrafamilial phenotypic heterogeneity in a Taiwanese family with a MAPT p.R5H mutation: A case report and literature review | Lin H.-C.; CHIN-HSIEN LIN ; PEI-LUNG CHEN ; Cheng S.-J.; Chen P.-H. | BMC Neurology | 12 | 10 | |
2022 | Investigating DYT1 in a Taiwanese dystonia cohort | MENG-CHEN WU ; Chang, Yung-Yee; Chen, Ying-Fa; Lan, Min-Yu; PEI-LUNG CHEN ; CHUN-HWEI TAI ; CHIN-HSIEN LIN | Journal of the Formosan Medical Association | 2 | 2 | |
2023 | Irritable bowel syndrome based on Rome IV diagnostic criteria associates with non-motor symptoms of Parkinson's disease | Tai, Yi-Cheng; Liao, Peng-Hsiang; Leta, Valentina; CHIN-HSIEN LIN ; Chaudhuri, K Ray | Parkinsonism & related disorders | 1 | 0 | |
2024 | Isotropic multi-scale neuronal reconstruction from high-ratio expansion microscopy with contrastive unsupervised deep generative models | Chang, Gary Han; Wu, Meng Yun; Yen, Ling Hui; Huang, Da Yu; Lin, Ya Hui; Luo, Yi Ru; Liu, Ya Ding; Xu, Bin; Leong, Kam W.; WEN-SUNG LAI ; Chiang, Ann Shyn; Wang, Kuo Chuan; CHIN-HSIEN LIN ; Wang, Shih Luen; Chu, Li An | Computer Methods and Programs in Biomedicine | | | |
2014 | Lack of C9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders | CHIN-HSIEN LIN ; TA-FU CHEN ; MING-JANG CHIU ; Lin H.-I.; RUEY-MEEI WU | Frontiers in Neurology | 11 | 15 | |
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 | |
2009 | Lack of evidence for association of a parkin promoter polymorphism with early-onset Parkinson's disease in a Chinese population | Taylor J.M.; RUEY-MEEI WU ; CHIN-HSIEN LIN ; Delatycki M.B.; Lockhart P.J. | Parkinsonism and Related Disorders | 2 | 2 | |
2004 | Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism | Lockhart P.J.; Bounds R.; Hulihan M.; Kachergus J.; Lincoln S.; CHIN-HSIEN LIN ; RUEY-MEEI WU ; Farrer M.J. | Movement Disorders | 29 | 15 | |
2007 | Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (Ethnic Chinese) cohort of familial and early-onset parkinsonism | CHIN-HSIEN LIN ; WUH-LIANG HWU ; Chiang S.-C.; CHUN-HWEI TAI ; RUEY-MEEI WU | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 8 | 7 | |
2021 | Lack of PTRHD1 mutation in patients with young-onset and familial Parkinson's disease in a Taiwanese population | Chen S.-J.; Ho C.-H.; Lin H.-Y.; CHIN-HSIEN LIN ; RUEY-MEEI WU | Neurobiology of Aging | 4 | 4 | |
2017 | Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort | Lin H.-H.; RUEY-MEEI WU ; Lin H.-I.; Chen M.-L.; CHUN-HWEI TAI ; CHIN-HSIEN LIN | Neurobiology of Aging | 9 | 8 | |
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 | |
2017 | A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: A case study and literature review | Hsueh S.-J.; NI-CHUNG LEE ; SHU-HUA YANG ; Lin H.-I.; CHIN-HSIEN LIN | BMC Neurology | 5 | 5 | |