| Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis CH Wu, C Fallini, N Ticozzi, PJ Keagle, PC Sapp, K Piotrowska, P Lowe, ... Nature 488 (7412), 499-503, 2012 | 765 | 2012 |
| Protein aggregation in amyotrophic lateral sclerosis AM Blokhuis, EJN Groen, M Koppers, LH van den Berg, RJ Pasterkamp Acta neuropathologica 125, 777-794, 2013 | 712 | 2013 |
| Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ... Nature genetics 48 (9), 1043-1048, 2016 | 633 | 2016 |
| Late endosomes act as mRNA translation platforms and sustain mitochondria in axons JM Cioni, JQ Lin, AV Holtermann, M Koppers, MAH Jakobs, A Azizi, ... Cell 176 (1), 56-72. e15, 2019 | 401 | 2019 |
| C 9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits M Koppers, AM Blokhuis, HJ Westeneng, ML Terpstra, CAC Zundel, ... Annals of neurology 78 (3), 426-438, 2015 | 338 | 2015 |
| Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis MA Van Es, HJ Schelhaas, PWJ Van Vught, N Ticozzi, PM Andersen, ... Annals of neurology 70 (6), 964-973, 2011 | 221 | 2011 |
| Full ablation of C9orf72 in mice causes immune system-related pathology and neoplastic events but no motor neuron defects E Sudria-Lopez, M Koppers, M de Wit, C van der Meer, HJ Westeneng, ... Acta neuropathologica 132, 145-147, 2016 | 162 | 2016 |
| ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN EJN Groen, K Fumoto, AM Blokhuis, JY Engelen-Lee, Y Zhou, ... Human molecular genetics 22 (18), 3690-3704, 2013 | 160 | 2013 |
| Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathways AM Blokhuis, M Koppers, EJN Groen, DMA van den Heuvel, ... Acta neuropathologica 132, 175-196, 2016 | 159 | 2016 |
| On-site ribosome remodeling by locally synthesized ribosomal proteins in axons T Shigeoka, M Koppers, HHW Wong, JQ Lin, R Cagnetta, A Dwivedy, ... Cell reports 29 (11), 3605-3619. e10, 2019 | 155 | 2019 |
| VCP mutations in familial and sporadic amyotrophic lateral sclerosis M Koppers, MM van Blitterswijk, L Vlam, PA Rowicka, PWJ van Vught, ... Neurobiology of aging 33 (4), 837. e7-837. e13, 2012 | 155 | 2012 |
| UNC13A is a modifier of survival in amyotrophic lateral sclerosis FP Diekstra, PWJ van Vught, W van Rheenen, M Koppers, RJ Pasterkamp, ... Neurobiology of aging 33 (3), 630. e3-630. e8, 2012 | 155 | 2012 |
| C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: A genome‐wide meta‐analysis FP Diekstra, VM Van Deerlin, JC Van Swieten, A Al‐Chalabi, AC Ludolph, ... Annals of neurology 76 (1), 120-133, 2014 | 128 | 2014 |
| Molecular control of local translation in axon development and maintenance JM Cioni, M Koppers, CE Holt Current opinion in neurobiology 51, 86-94, 2018 | 125 | 2018 |
| VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient M van Blitterswijk, MA van Es, M Koppers, W van Rheenen, J Medic, ... Neurobiology of aging 33 (12), 2950. e1-2950. e4, 2012 | 89 | 2012 |
| A large genome scan for rare CNVs in amyotrophic lateral sclerosis HM Blauw, A Al-Chalabi, PM Andersen, PWJ van Vught, FP Diekstra, ... Human molecular genetics 19 (20), 4091-4099, 2010 | 78 | 2010 |
| Receptor-specific interactome as a hub for rapid cue-induced selective translation in axons M Koppers, R Cagnetta, T Shigeoka, LCS Wunderlich, P Vallejo-Ramirez, ... Elife 8, e48718, 2019 | 72 | 2019 |
| NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis HM Blauw, W van Rheenen, M Koppers, P Van Damme, S Waibel, ... Human molecular genetics 21 (11), 2497-2502, 2012 | 60 | 2012 |
| ER–lysosome contacts at a pre-axonal region regulate axonal lysosome availability N Özkan, M Koppers, I van Soest, A van Harten, D Jurriens, N Liv, ... Nature communications 12 (1), 4493, 2021 | 53 | 2021 |
| Complex interactions between membrane-bound organelles, biomolecular condensates and the cytoskeleton M Koppers, N Özkan, GG Farías Frontiers in Cell and Developmental Biology 8, 618733, 2020 | 43 | 2020 |
Jeroen PasterkampDepartment of Translational Neuroscience, UMC Utrechtumcutrecht.nl의 이메일 확인됨