Andreas Roos
Impact in
- Neurology top 2%
- Amyotrophic Lateral Sclerosis Research
- Myasthenia Gravis and Thymoma
-
- Hereditary Neurological Disorders
Papers in
-
- Hereditary Neurological Disorders 25
- Genetic Neurodegenerative Diseases 10
- Neurology 28
- Myasthenia Gravis and Thymoma 17
- Co-authors
- Hanns Lochmüller (46 shared papers)Joachim Weis (31 shared papers)René Peiman Zahedi (15 shared papers)Ulrike Schara (48 shared papers)Rita Horváth (25 shared papers)Jan Senderek (14 shared papers)Stephan Buchkremer (10 shared papers)Anand Goswami (4 shared papers)
- Journals
- Brain (10 papers)Acta Neuropathologica (10 papers)Neuromuscular Disorders (8 papers)Cells (8 papers)Human Molecular Genetics (7 papers)
- Partner nations
- GermanyCanadaUnited Kingdom
In The Last Decade
Andreas Roos
168 papers receiving 3.5k citations
Peers
Comparison fields: 5 of 105
- Neurology 539
- Cellular and Molecular Neuroscience 589
- Cell Biology 308
- Molecular Biology 1.3k
- Genetics 467
Countries citing papers authored by Andreas Roos
This map shows the geographic impact of Andreas Roos'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 Andreas Roos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Roos more than expected).
Fields of papers citing papers by Andreas Roos
This network shows the impact of papers produced by Andreas Roos. 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 Andreas Roos. The network helps show where Andreas Roos may publish in the future.
Co-authors
The 25 scholars most cited alongside Andreas Roos, 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 179 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 191 | |
| 2 | 2013 | 138 | |
| 3 | 2009 | 137 | |
| 4 | 2006 | 120 | |
| 5 | 2021 | 118 | |
| 6 | 2007 | 115 | |
| 7 | 2019 | 100 | |
| 8 | 2009 | 92 | |
| 9 | 2017 | 89 | |
| 10 | 2015 | 84 | |
| 11 | 2010 | 83 | |
| 12 | 2013 | 68 | |
| 13 | 2018 | 60 | |
| 14 | 2017 | 56 | |
| 15 | 2013 | 55 | |
| 16 | 2020 | 52 | |
| 17 | 2019 | 51 | |
| 18 | 2018 | 47 | |
| 19 | 2016 | 45 | |
| 20 | 2018 | 44 |
About Andreas Roos
Andreas Roos is a scholar working on Cellular and Molecular Neuroscience, Neurology, Genetics, Molecular Biology and Genetics, having authored 179 papers that have together received 3.6k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (51 papers), Genomics and Rare Diseases (30 papers), Hereditary Neurological Disorders (25 papers), Myasthenia Gravis and Thymoma (17 papers), Neurogenetic and Muscular Disorders Research (16 papers), Genetics and Neurodevelopmental Disorders (11 papers), Genetic Neurodegenerative Diseases (10 papers) and Inflammatory Myopathies and Dermatomyositis (10 papers). The work is most often cited by research in Neurology (539 citations), Cellular and Molecular Neuroscience (589 citations), Cell Biology (308 citations), Molecular Biology (1.3k citations) and Genetics (467 citations). Andreas Roos has collaborated with scholars based in Germany, Canada and United Kingdom. Frequent co-authors include Hanns Lochmüller, Joachim Weis, René Peiman Zahedi, Ulrike Schara, Rita Horváth, Jan Senderek, Stephan Buchkremer, Anand Goswami, Thomas Eggermann and Albert Sickmann. Their work appears in journals such as Brain, Acta Neuropathologica, Neuromuscular Disorders, Cells and Human Molecular Genetics.
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.