Armin Pscherer
Impact in
- Cancer Research top 5%
- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
- Genetics top 5%
- Chronic Lymphocytic Leukemia Research
Papers in
-
- RNA modifications and cancer 5
- RNA Research and Splicing 4
- Genomics and Chromatin Dynamics 3
- Oncology 5
- Cancer-related Molecular Pathways 3
- Co-authors
- Peter Lichter (12 shared papers)Reinhard Buettner (7 shared papers)Markus Moser (5 shared papers)Roland Schüle (4 shared papers)Hartmut Döhner (6 shared papers)Stephan Stilgenbauer (6 shared papers)Axel Imhof (4 shared papers)Reinhard Bauer (4 shared papers)
- Journals
- International Journal of Cancer (2 papers)Nucleic Acids Research (2 papers)Blood (2 papers)Cancer Research (1 paper)Genes Chromosomes and Cancer (1 paper)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Armin Pscherer
22 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 83
- Cancer Research 377
- Genetics 178
- Molecular Biology 1.0k
- Pathology and Forensic Medicine 160
- Genetics 234
Countries citing papers authored by Armin Pscherer
This map shows the geographic impact of Armin Pscherer'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 Armin Pscherer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Armin Pscherer more than expected).
Fields of papers citing papers by Armin Pscherer
This network shows the impact of papers produced by Armin Pscherer. 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 Armin Pscherer. The network helps show where Armin Pscherer may publish in the future.
Co-authors
The 25 scholars most cited alongside Armin Pscherer, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 226 | |
| 2 | 1995 | 220 | |
| 3 | 2012 | 161 | |
| 4 | 2002 | 116 | |
| 5 | 2004 | 96 | |
| 6 | 2008 | 79 | |
| 7 | 2008 | 70 | |
| 8 | 2013 | 58 | |
| 9 | 1994 | 55 | |
| 10 | The helix-loop-helix transcription factor SEF-2 regulates the activity of a novel initiator element in the promoter of the human somatostatin receptor II gene. | 1996 | 55 |
| 11 | 1996 | 54 | |
| 12 | 2011 | 41 | |
| 13 | 1999 | 38 | |
| 14 | 2005 | 37 | |
| 15 | 2009 | 36 | |
| 16 | 2013 | 29 | |
| 17 | 2011 | 26 | |
| 18 | 2006 | 20 | |
| 19 | 2010 | 14 | |
| 20 | 1993 | 14 |
About Armin Pscherer
Armin Pscherer is a scholar working on Molecular Biology, Oncology, Cancer Research, Genetics and Pathology and Forensic Medicine, having authored 22 papers that have together received 1.5k indexed citations. Recurring topics across this work include MicroRNA in disease regulation (5 papers), RNA modifications and cancer (5 papers), Chronic Lymphocytic Leukemia Research (4 papers), RNA Research and Splicing (4 papers), Genomics and Chromatin Dynamics (3 papers), Cancer-related molecular mechanisms research (3 papers), Lymphoma Diagnosis and Treatment (3 papers) and Cancer-related Molecular Pathways (3 papers). The work is most often cited by research in Cancer Research (377 citations), Genetics (178 citations), Molecular Biology (1.0k citations), Pathology and Forensic Medicine (160 citations) and Genetics (234 citations). Armin Pscherer has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Peter Lichter, Reinhard Buettner, Markus Moser, Roland Schüle, Hartmut Döhner, Stephan Stilgenbauer, Axel Imhof, Reinhard Bauer, Fred Sinowatz and Daniel Mertens. Their work appears in journals such as International Journal of Cancer, Nucleic Acids Research, Blood, Cancer Research and Genes Chromosomes and Cancer.
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.