| Year |
Citation |
Score |
| 2024 |
Koppers M, Özkan N, Nguyen HH, Jurriens D, McCaughey J, Nguyen DTM, Li CH, Stucchi R, Altelaar M, MacGillavry HD, Kapitein LC, Hoogenraad CC, Farías GG. Axonal endoplasmic reticulum tubules control local translation via P180/RRBP1-mediated ribosome interactions. Developmental Cell. PMID 38815583 DOI: 10.1016/j.devcel.2024.05.005 |
0.623 |
|
| 2022 |
Koppers M, Holt CE. Receptor-Ribosome Coupling: A Link Between Extrinsic Signals and mRNA Translation in Neuronal Compartments. Annual Review of Neuroscience. PMID 34985917 DOI: 10.1146/annurev-neuro-083021-110015 |
0.65 |
|
| 2021 |
Özkan N, Koppers M, van Soest I, van Harten A, Jurriens D, Liv N, Klumperman J, Kapitein LC, Hoogenraad CC, Farías GG. ER - lysosome contacts at a pre-axonal region regulate axonal lysosome availability. Nature Communications. 12: 4493. PMID 34301956 DOI: 10.1038/s41467-021-24713-5 |
0.525 |
|
| 2021 |
Koppers M, Farías GG. Organelle distribution in neurons: Logistics behind polarized transport. Current Opinion in Cell Biology. 71: 46-54. PMID 33706233 DOI: 10.1016/j.ceb.2021.02.004 |
0.363 |
|
| 2019 |
Shigeoka T, Koppers M, Wong HH, Lin JQ, Cagnetta R, Dwivedy A, de Freitas Nascimento J, van Tartwijk FW, Ströhl F, Cioni JM, Schaeffer J, Carrington M, Kaminski CF, Jung H, Harris WA, et al. On-Site Ribosome Remodeling by Locally Synthesized Ribosomal Proteins in Axons. Cell Reports. 29: 3605-3619.e10. PMID 31825839 DOI: 10.1016/J.Celrep.2019.11.025 |
0.672 |
|
| 2019 |
Koppers M, Cagnetta R, Shigeoka T, Wunderlich LC, Vallejo-Ramirez P, Qiaojin Lin J, Zhao S, Jakobs MA, Dwivedy A, Minett MS, Bellon A, Kaminski CF, Harris WA, Flanagan J, Holt CE. Receptor-specific interactome as a hub for rapid cue-induced selective translation in axons. Elife. 8. PMID 31746735 DOI: 10.7554/Elife.48718 |
0.73 |
|
| 2019 |
Koppers M, Cagnetta R, Shigeoka T, Wunderlich LC, Vallejo-Ramirez P, Lin JQ, Zhao S, Jakobs MA, Dwivedy A, Minett MS, Bellon A, Kaminski CF, Harris WA, Flanagan JG, Holt CE. Author response: Receptor-specific interactome as a hub for rapid cue-induced selective translation in axons Elife. DOI: 10.7554/Elife.48718.Sa2 |
0.811 |
|
| 2018 |
Cioni JM, Lin JQ, Holtermann AV, Koppers M, Jakobs MAH, Azizi A, Turner-Bridger B, Shigeoka T, Franze K, Harris WA, Holt CE. Late Endosomes Act as mRNA Translation Platforms and Sustain Mitochondria in Axons. Cell. PMID 30612743 DOI: 10.1016/J.Cell.2018.11.030 |
0.682 |
|
| 2018 |
Cioni JM, Koppers M, Holt CE. Molecular control of local translation in axon development and maintenance. Current Opinion in Neurobiology. 51: 86-94. PMID 29549711 DOI: 10.1016/J.Conb.2018.02.025 |
0.844 |
|
| 2016 |
van Rheenen W, Shatunov A, Dekker AM, McLaughlin RL, Diekstra FP, Pulit SL, van der Spek RA, Võsa U, de Jong S, Robinson MR, Yang J, Fogh I, van Doormaal PT, Tazelaar GH, Koppers M, et al. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nature Genetics. 48: 1043-8. PMID 27455348 DOI: 10.1038/Ng.3622 |
0.675 |
|
| 2016 |
Blokhuis AM, Koppers M, Groen EJ, van den Heuvel DM, Dini Modigliani S, Anink JJ, Fumoto K, van Diggelen F, Snelting A, Sodaar P, Verheijen BM, Demmers JA, Veldink JH, Aronica E, Bozzoni I, et al. Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathways. Acta Neuropathologica. 132: 175-96. PMID 27164932 DOI: 10.1007/s00401-016-1575-8 |
0.768 |
|
| 2013 |
Groen EJ, Fumoto K, Blokhuis AM, Engelen-Lee J, Zhou Y, van den Heuvel DM, Koppers M, van Diggelen F, van Heest J, Demmers JA, Kirby J, Shaw PJ, Aronica E, Spliet WG, Veldink JH, et al. ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN. Human Molecular Genetics. 22: 3690-704. PMID 23681068 DOI: 10.1093/hmg/ddt222 |
0.814 |
|
| 2013 |
Blokhuis AM, Groen EJ, Koppers M, van den Berg LH, Pasterkamp RJ. Protein aggregation in amyotrophic lateral sclerosis. Acta Neuropathologica. 125: 777-94. PMID 23673820 DOI: 10.1007/s00401-013-1125-6 |
0.667 |
|
| 2013 |
Koppers M, Groen EJ, van Vught PW, van Rheenen W, Witteveen E, van Es MA, Pasterkamp RJ, van den Berg LH, Veldink JH. Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3. Neurobiology of Aging. 34: 1518.e5-7. PMID 23141412 DOI: 10.1016/j.neurobiolaging.2012.09.018 |
0.63 |
|
| 2012 |
Groen EJ, van Rheenen W, Koppers M, van Doormaal PT, Vlam L, Diekstra FP, Dooijes D, Pasterkamp RJ, van den Berg LH, Veldink JH. CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis. Neurobiology of Aging. 33: 1852.e1-3. PMID 22507827 DOI: 10.1016/j.neurobiolaging.2012.03.007 |
0.634 |
|
| 2012 |
Koppers M, van Blitterswijk MM, Vlam L, Rowicka PA, van Vught PW, Groen EJ, Spliet WG, Engelen-Lee J, Schelhaas HJ, de Visser M, van der Kooi AJ, van der Pol WL, Pasterkamp RJ, Veldink JH, van den Berg LH. VCP mutations in familial and sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. 33: 837.e7-13. PMID 22078486 DOI: 10.1016/j.neurobiolaging.2011.10.006 |
0.625 |
|
| 2011 |
van Es MA, Schelhaas HJ, van Vught PW, Ticozzi N, Andersen PM, Groen EJ, Schulte C, Blauw HM, Koppers M, Diekstra FP, Fumoto K, LeClerc AL, Keagle P, Bloem BR, Scheffer H, et al. Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis. Annals of Neurology. 70: 964-73. PMID 22190368 DOI: 10.1002/Ana.22611 |
0.72 |
|
| 2010 |
Blauw HM, Al-Chalabi A, Andersen PM, van Vught PWJ, Diekstra FP, van Es MA, Saris CGJ, Groen EJN, van Rheenen W, Koppers M, Slot Rvt, Strengman E, Estrada K, Rivadeneira F, Hofman A, et al. A large genome scan for rare CNVs in amyotrophic lateral sclerosis Human Molecular Genetics. 19: 4091-4099. PMID 20685689 DOI: 10.1093/Hmg/Ddq323 |
0.627 |
|
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