| Parkinson’s disease–associated VPS35 mutant reduces mitochondrial membrane potential and impairs PINK1/Parkin-mediated mitophagy KY Ma, MR Fokkens, F Reggiori, M Mari, DS Verbeek Translational neurodegeneration 10, 1-17, 2021 | 37 | 2021 |
| Fast Fluorescence Lifetime Imaging Reveals the Aggregation Processes of α-Synuclein and Polyglutamine in Aging Caenorhabditis elegans RF Laine, T Sinnige, KY Ma, AJ Haack, C Poudel, P Gaida, N Curry, ... ACS chemical biology 14 (7), 1628-1636, 2019 | 27 | 2019 |
| A gain‐of‐function variant in dopamine D2 receptor and progressive chorea and dystonia phenotype MCM van der Weijden, D Rodriguez‐Contreras, CCS Delnooz, ... Movement Disorders 36 (3), 729-739, 2021 | 25 | 2021 |
| Comparative Studies in the A30P and A53T α-Synuclein C. elegans Strains to Investigate the Molecular Origins of Parkinson's Disease M Perni, A Van der Goot, R Limbocker, TJ Van Ham, FA Aprile, CK Xu, ... Frontiers in Cell and Developmental Biology 9, 552549, 2021 | 16 | 2021 |
| Cerebellar developmental deficits underlie neurodegenerative disorder spinocerebellar ataxia type 23 CJLM Smeets, KY Ma, SE Fisher, DS Verbeek Brain Pathology 31 (2), 239-252, 2021 | 8 | 2021 |
| Systematic analysis of PINK1 variants of unknown significance shows intact mitophagy function for most variants KY Ma, MR Fokkens, T van Laar, DS Verbeek npj Parkinson's Disease 7 (1), 113, 2021 | 7 | 2021 |
| Crystal structure of truncated human coatomer protein complex subunit ζ1 (Copζ1) S Lunev, MFW Semmelink, JL Xian, KY Ma, AJA Leenders, ASS Dömling, ... Acta Crystallographica Section F: Structural Biology Communications 73 (1), 1-8, 2017 | 3 | 2017 |
| Reply: PLD3 and spinocerebellar ataxia KY Ma, DS Verbeek Brain 141 (11), e79-e79, 2018 | 2 | 2018 |
| Gene: PINK1 KY Ma, MR Fokkens, DS Teus van Laar Molecular genetics of monogenic movement disorders: making meaning of rare …, 2022 | | 2022 |
| Chromosome 20: 1,978,757-1,994,285 reverse strand CJLM Smeets, KY Ma, SE Fisher, DS Verbeek Molecular genetics of monogenic movement disorders: making meaning of rare …, 2022 | | 2022 |
| Molecular genetics of monogenic movement disorders: making meaning of rare variants KY Ma | | 2022 |
| Comparative Studies in the A30P and A53T α-Synuclein C. elegans Strains to Investigate the Molecular Origins of Parkinson’s Disease K Nishioka, E Vayndorf, PJ Kahle, EAA Nollen, M Vendruscolo Intracellular Mechanisms of α-Synuclein Processing, 2021 | | 2021 |
| De novo mutations in the Kv4. 3 channel reduce the availability of native A-type current by affecting channel localization and function in mammalian cells C Tiecher, A Catte, KY Ma, MR Fokkens, K van Gassen, N Verbeek, ... A comprehensive study of the voltage-gated potassium channel Kv4. 3, 101, 0 | | |
