Max Koppers
Impact in
Papers in
- Co-authors
- R. Jeroen Pasterkamp (10 shared papers)Anna M. Blokhuis (4 shared papers)Leonard H. van den Berg (7 shared papers)Ewout J. N. Groen (6 shared papers)Christine E. Holt (5 shared papers)Jean-Michel Cioni (3 shared papers)Jan Herman Veldink (10 shared papers)William A. Harris (3 shared papers)
- Journals
- Neurobiology of Aging (5 papers)Acta Neuropathologica (3 papers)Annals of Neurology (3 papers)Human Molecular Genetics (3 papers)Current Opinion in Cell Biology (2 papers)
- Partner nations
- NetherlandsUnited KingdomUnited States
In The Last Decade
Max Koppers
29 papers receiving 3.4k citations
Max Koppers's Hit Papers
Peers
Comparison fields: 5 of 89
- Neurology 2.0k
- Genetics 1.2k
- Neurology 533
- Cellular and Molecular Neuroscience 507
- Cell Biology 395
Countries citing papers authored by Max Koppers
This map shows the geographic impact of Max Koppers's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Max Koppers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Max Koppers more than expected).
Fields of papers citing papers by Max Koppers
This network shows the impact of papers produced by Max Koppers. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Max Koppers. The network helps show where Max Koppers may publish in the future.
Co-authors
The 25 scholars most cited alongside Max Koppers, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis Hit paper breakdown → | 2012 | 498 |
| 2 | Protein aggregation in amyotrophic lateral sclerosis Hit paper breakdown → | 2013 | 471 |
| 3 | Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis Hit paper breakdown → | 2016 | 453 |
| 4 | Late Endosomes Act as mRNA Translation Platforms and Sustain Mitochondria in Axons Hit paper breakdown → | 2019 | 320 |
| 5 | 2015 | 220 | |
| 6 | 2011 | 172 | |
| 7 | 2013 | 125 | |
| 8 | 2019 | 122 | |
| 9 | 2011 | 117 | |
| 10 | 2016 | 112 | |
| 11 | 2011 | 110 | |
| 12 | 2016 | 107 | |
| 13 | 2018 | 96 | |
| 14 | 2014 | 88 | |
| 15 | 2012 | 67 | |
| 16 | 2010 | 49 | |
| 17 | 2019 | 48 | |
| 18 | 2021 | 44 | |
| 19 | 2012 | 42 | |
| 20 | 2020 | 38 |
About Max Koppers
Max Koppers is a scholar working on Neurology, Genetics, Cell Biology, Neurology and Molecular Biology, having authored 30 papers that have together received 3.4k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (17 papers), Neurogenetic and Muscular Disorders Research (11 papers), RNA Research and Splicing (6 papers), Cellular transport and secretion (6 papers), Neurological diseases and metabolism (5 papers), RNA regulation and disease (4 papers), Endoplasmic Reticulum Stress and Disease (4 papers) and Microtubule and mitosis dynamics (3 papers). The work is most often cited by research in Neurology (2.0k citations), Genetics (1.2k citations), Neurology (533 citations), Cellular and Molecular Neuroscience (507 citations) and Cell Biology (395 citations). Max Koppers has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include R. Jeroen Pasterkamp, Anna M. Blokhuis, Leonard H. van den Berg, Ewout J. N. Groen, Christine E. Holt, Jean-Michel Cioni, Jan Herman Veldink, William A. Harris, Toshiaki Shigeoka and Julie Qiaojin Lin. Their work appears in journals such as Neurobiology of Aging, Acta Neuropathologica, Annals of Neurology, Human Molecular Genetics and Current Opinion in Cell Biology.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.