| Mitochondrial dysfunction in Parkinson’s disease: new mechanistic insights and therapeutic perspectives JS Park, RL Davis, CM Sue Current neurology and neuroscience reports 18, 1-11, 2018 | 527 | 2018 |
| Parkinson's disease-linked human PARK9/ATP13A2 maintains zinc homeostasis and promotes α-Synuclein externalization via exosomes SMY Kong, BKK Chan, JS Park, KJ Hill, JB Aitken, L Cottle, H Farghaian, ... Human molecular genetics 23 (11), 2816-2833, 2014 | 261 | 2014 |
| A crucial role for matrix metalloproteinase 2 in osteocytic canalicular formation and bone metabolism K Inoue, Y Mikuni-Takagaki, K Oikawa, T Itoh, M Inada, T Noguchi, ... Journal of biological chemistry 281 (44), 33814-33824, 2006 | 215 | 2006 |
| The role of ATP13A2 in Parkinson's disease: Clinical phenotypes and molecular mechanisms JS Park, NF Blair, CM Sue Movement Disorders 30 (6), 770-779, 2015 | 188 | 2015 |
| Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene K Lohmann, RA Wilcox, S Winkler, A Ramirez, A Rakovic, JS Park, B Arns, ... Annals of neurology 73 (4), 537-545, 2013 | 175 | 2013 |
| Nix restores mitophagy and mitochondrial function to protect against PINK1/Parkin-related Parkinson’s disease B Koentjoro, JS Park, CM Sue Scientific Reports 7, 44373, 2017 | 171 | 2017 |
| Parkinson's disease-associated human ATP13A2 (PARK9) deficiency causes zinc dyshomeostasis and mitochondrial dysfunction JS Park, B Koentjoro, D Veivers, A Mackay-Sim, CM Sue Human molecular genetics 23 (11), 2802-2815, 2014 | 167 | 2014 |
| Pathogenic effects of novel mutations in the P‐type ATPase ATP13A2 (PARK9) causing Kufor‐Rakeb syndrome, a form of early‐onset parkinsonism JS Park, P Mehta, AA Cooper, D Veivers, A Heimbach, B Stiller, ... Human mutation 32 (8), 956-964, 2011 | 145 | 2011 |
| Thioredoxin interacting protein (TXNIP) regulates tubular autophagy and mitophagy in diabetic nephropathy through the mTOR signaling pathway C Huang, Y Zhang, DJ Kelly, CYR Tan, A Gill, D Cheng, F Braet, JS Park, ... Scientific reports 6 (1), 29196, 2016 | 120 | 2016 |
| Activin A is essential for neurogenesis following neurodegeneration A Abdipranoto‐Cowley, JS Park, D Croucher, J Daniel, S Henshall, ... Stem Cells 27 (6), 1330-1346, 2009 | 96 | 2009 |
| In vitro and in vivo safety studies of cinnamon extract (Cinnamomum cassia) on general and genetic toxicology JW Yun, JR You, YS Kim, SH Kim, EY Cho, JH Yoon, E Kwon, JJ Jang, ... Regulatory Toxicology and Pharmacology 95, 115-123, 2018 | 54 | 2018 |
| Molecular mechanisms of the 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin-induced inverted U-shaped dose responsiveness in anchorage independent growth and cell proliferation of human … NS Ahn, H Hu, JS Park, JS Park, JS Kim, S An, G Kong, OI Aruoma, ... Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 579 (1 …, 2005 | 44 | 2005 |
| Requirement of metabolic activation for estrogenic activity of Pueraria mirifica YS Lee, JS Park, SD Cho, JK Son, W Cherdshewasart, KS Kang Journal of veterinary science 3 (4), 273-277, 2002 | 39 | 2002 |
| Molecular evidence for two-stage learning and partial laterality in eyeblink conditioning of mice JS Park, T Onodera, S Nishimura, RF Thompson, S Itohara Proceedings of the National Academy of Sciences 103 (14), 5549-5554, 2006 | 32 | 2006 |
| Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis RL Davis, KR Kumar, C Puttick, C Liang, KE Ahmad, F Edema-Hildebrand, ... Neurology 99 (7), e730-e742, 2022 | 31 | 2022 |
| High degree of genetic heterogeneity for hereditary cerebellar ataxias in Australia C Kang, C Liang, KE Ahmad, Y Gu, SF Siow, JG Colebatch, S Whyte, ... The Cerebellum 18, 137-146, 2019 | 26 | 2019 |
| Hormonal effects of several chemicals in recombinant yeast, MCF-7 cells and uterotrophic assays in mice JS Park, BJ Lee, KS Kang, JH Tai, JJ Cho, MH Cho, T Inoue, YS Lee Journal of microbiology and biotechnology 10 (3), 293-299, 2000 | 25 | 2000 |
| Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variants F Vulinovic, V Krajka, TJ Hausrat, P Seibler, D Alvarez‐Fischer, H Madoev, ... Human mutation 39 (12), 1901-1915, 2018 | 24 | 2018 |
| Loss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell models JS Park, B Koentjoro, RL Davis, CM Sue Parkinsonism & related disorders 27, 67-73, 2016 | 23 | 2016 |
| Phenotypic variability of parkin mutations in single kindred B Koentjoro, JS Park, AD Ha, CM Sue Movement Disorders 27 (10), 1299-1303, 2012 | 23 | 2012 |
