Max Koppers - Concepedia

Author

Max Koppers

University Medical Center Utrecht ORCID

Also Known As

Jian Yang, Koppers, Max, M J Koppers, M. Koppers, Max Koppers, Myrthe J A Koppers

Publications

4.3K

Citations

H-Index

Concepts

All Affiliations

University Medical Center Utrecht University of Cambridge Amsterdam UMC Location University of Amsterdam Radboud University Nijmegen Utrecht University

About

Max Koppers is an author at University Medical Center Utrecht specializing in medicine, neurodegenerative diseases, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	1.1K
2	Cell Biology	4	4	350
3	Natural Sciences	2	2	56
4	Social Sciences	1	1	150
5	Cellular Physiology	1	1	34

Max Koppers

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis Chi-Hong Wu, Claudia Fallini, Nicola Ticozzi, Nature Neurodegenerative DiseasesAmyotrophic Lateral SclerosisDevelopmental BiologyProfilin 1Genetic Disorder	2012	594
Late Endosomes Act as mRNA Translation Platforms and Sustain Mitochondria in Axons Jean-Michel Cioni, Julie Qiaojin Lin, Anne Holtermann, Cell	2019	434
<scp>C</scp>9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits Max Koppers, Anna M. Blokhuis, Henk‐Jan Westeneng, Annals of Neurology	2015	244
On-Site Ribosome Remodeling by Locally Synthesized Ribosomal Proteins in Axons Toshiaki Shigeoka, Max Koppers, Hovy Ho‐Wai Wong, Cell Reports	2019	175
ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN Ewout J. N. Groen, Katsumi Fumoto, Anna M. Blokhuis, Human Molecular Genetics Neurological DisorderGeneticsMolecular BiologySocial SciencesNeuropathology	2013	150
UNC13A is a modifier of survival in amyotrophic lateral sclerosis Frank P. Diekstra, Paul W.J. van Vught, Wouter van Rheenen, Neurobiology of Aging Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurochemical BiomarkersNeuroscienceNeurology	2011	144
Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathways Anna M. Blokhuis, Max Koppers, Ewout J. N. Groen, Acta Neuropathologica	2016	142
VCP mutations in familial and sporadic amyotrophic lateral sclerosis Max Koppers, Marka van Blitterswijk, Lotte Vlam, Neurobiology of Aging Neurodegenerative DiseasesAmyotrophic Lateral SclerosisGenetic DisorderGeneticsNeurology	2011	139
VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient Marka van Blitterswijk, Michael A. van Es, Max Koppers, Neurobiology of Aging	2012	76
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis Hylke M. Blauw, Wouter van Rheenen, Max Koppers, Human Molecular Genetics	2012	62

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