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Max Koppers, Ph.D. - Publications

Affiliations: 
2010-2016 Translational Neuroscience Utrecht University, Utrecht, Netherlands 
 2016- Physiology, Development and Neuroscience University of Cambridge, Cambridge, England, United Kingdom 
Area:
Neurodegeneration, Axon guidance, Developmental Neuroscience, Local translation
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17 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.634
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  0.515
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  0.364
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  0.701
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  0.766
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  0.8
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  0.655
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  0.832
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  0.686
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  0.771
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  0.679
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  0.645
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  0.648
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  0.64
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  0.723
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  0.641
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