Ylva Mende
Impact in
- Genetics top 5%
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
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- RNA modifications and cancer
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
- Cancer-related gene regulation
- RNA regulation and disease
Papers in
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- RNA modifications and cancer 5
- RNA Research and Splicing 3
- Cancer-related gene regulation 2
- Epigenetics and DNA Methylation 1
- Muscle Physiology and Disorders 1
- Prion Diseases and Protein Misfolding 1
- Genetics 2
- Neurogenetic and Muscular Disorders Research 2
- Co-authors
- Brunhilde Wirth (5 shared papers)Markus Rießland (2 shared papers)Ingmar Blümcke (1 shared paper)Jan Hauke (1 shared paper)Lutz Garbes (1 shared paper)Eric Hahnen (1 shared paper)Anja Förster (1 shared paper)Branko Zevnik (1 shared paper)
- Journals
- Human Molecular Genetics (2 papers)Virus Research (1 paper)PLoS Genetics (1 paper)PLoS ONE (1 paper)Journal of Biological Chemistry (1 paper)
- Partner nations
- GermanyUnited StatesSlovenia
In The Last Decade
Ylva Mende
7 papers receiving 322 citations
Peers
Comparison fields: 5 of 44
- Genetics 174
- Molecular Biology 290
- Cancer Research 20
- Surgery 57
- Genetics 32
Countries citing papers authored by Ylva Mende
This map shows the geographic impact of Ylva Mende'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 Ylva Mende with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ylva Mende more than expected).
Fields of papers citing papers by Ylva Mende
This network shows the impact of papers produced by Ylva Mende. 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 Ylva Mende. The network helps show where Ylva Mende may publish in the future.
Co-authors
The 25 scholars most cited alongside Ylva Mende, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 177 | |
| 2 | 2011 | 61 | |
| 3 | 2010 | 47 | |
| 4 | 2016 | 18 | |
| 5 | 2012 | 16 | |
| 6 | 2004 | 6 | |
| 7 | 2011 | 1 |
About Ylva Mende
Ylva Mende is a scholar working on Molecular Biology, Genetics, Cardiology and Cardiovascular Medicine, Physiology and Genetics, having authored 7 papers that have together received 326 indexed citations. Recurring topics across this work include RNA modifications and cancer (5 papers), RNA Research and Splicing (3 papers), Cancer-related gene regulation (2 papers), Neurogenetic and Muscular Disorders Research (2 papers), Epigenetics and DNA Methylation (1 paper), Muscle Physiology and Disorders (1 paper), Cardiomyopathy and Myosin Studies (1 paper) and Prion Diseases and Protein Misfolding (1 paper). The work is most often cited by research in Genetics (174 citations), Molecular Biology (290 citations), Cancer Research (20 citations), Surgery (57 citations) and Genetics (32 citations). Ylva Mende has collaborated with scholars based in Germany, United States and Slovenia. Frequent co-authors include Brunhilde Wirth, Markus Rießland, Ingmar Blümcke, Jan Hauke, Lutz Garbes, Eric Hahnen, Anja Förster, Branko Zevnik, Frank J. Schoenen and Thorsten Buch. Their work appears in journals such as Human Molecular Genetics, Virus Research, PLoS Genetics, PLoS ONE and Journal of Biological Chemistry.
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.