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Max Koppers

Utrecht University · NL
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Area of research
Neurology · Genetics
Research interest
Research interests include Biology, Cell biology, Amyotrophic lateral sclerosis, Organelle, Genome-wide association study, and C9orf72.
h-index
citations
1,757
works
11
NIH funding
primary concept
email

Recent publications

Axonal endoplasmic reticulum tubules control local translation via P180/RRBP1-mediated ribosome interactions
Developmental Cell 2024cited by 39position: firstdoi
Spatiotemporal proteomics reveals the biosynthetic lysosomal membrane protein interactome in neurons
Nature Communications 2024cited by 16position: middledoi
Receptor-Ribosome Coupling: A Link Between Extrinsic Signals and mRNA Translation in Neuronal Compartments
Annual Review of Neuroscience 2022cited by 16position: firstdoi
ER – lysosome contacts at a pre-axonal region regulate axonal lysosome availability
Nature Communications 2021cited by 61position: middledoi
Organelle distribution in neurons: Logistics behind polarized transport
Current Opinion in Cell Biology 2021cited by 34position: firstdoi
Complex Interactions Between Membrane-Bound Organelles, Biomolecular Condensates and the Cytoskeleton
Frontiers in Cell and Developmental Biology 2020cited by 59position: firstdoi
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Nature Genetics 2016cited by 624position: middledoi
Full ablation of C9orf72 in mice causes immune system-related pathology and neoplastic events but no motor neuron defects
Acta Neuropathologica 2016cited by 127position: middledoi
<scp><i>C9orf72</i></scp> and <scp><i>UNC13A</i></scp> are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: A genome‐wide meta‐analysis
Annals of Neurology 2014cited by 123position: middledoi
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
Nature 2012cited by 595position: middledoi
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis
Human Molecular Genetics 2012cited by 63position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Ginny G. Farı́as · Utrecht University5 papers (2020–2024)Nazmiye Özkan · Utrecht University4 papers (2020–2024)Daphne Jurriens · Utrecht University2 papers (2021–2024)Maarten Altelaar · Utrecht University2 papers (2024–2024)Lukas C. Kapitein · Utrecht University2 papers (2021–2024)D. Nguyen · Ho Chi Minh City University of Transport2 papers (2024–2024)Casper C. Hoogenraad · Utrecht University2 papers (2021–2024)R. Jeroen Pasterkamp · Utrecht University2 papers (2012–2016)Leonard H. van den Berg · Utrecht University2 papers (2012–2016)Chun Hei Li · Utrecht University2 papers (2024–2024)Jan H. Veldink · University Medical Center Utrecht2 papers (2012–2016)Albert C. Ludolph · German Center for Neurodegenerative Diseases1 papers (2012–2012)Alexandra van Harten · Utrecht University1 papers (2021–2021)Inge van Soest · Utrecht University1 papers (2021–2021)Alain de Bruin · Utrecht University1 papers (2016–2016)Henk‐Jan Westeneng · Utrecht University1 papers (2016–2016)Riccardo Stucchi · Utrecht University1 papers (2024–2024)Philip Van Damme · Universitair Ziekenhuis Leuven1 papers (2012–2012)Sameh A. Youssef · Utrecht University1 papers (2016–2016)Robin Lemmens · KU Leuven1 papers (2012–2012)
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