Helmut Fuchs
Impact in
- Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
- Molecular Biology top 2%
- RNA modifications and cancer
- Connexins and lens biology
- RNA and protein synthesis mechanisms
- RNA regulation and disease
Papers in
-
- Connexins and lens biology 13
- Mitochondrial Function and Pathology 9
- Retinal Development and Disorders 6
- Genetics 26
- Genetics and Neurodevelopmental Disorders 8
- Co-authors
- Martin Hrabě de Angelis (175 shared papers)Valérie Gailus‐Durner (102 shared papers)Eckhard Wolf (43 shared papers)Birgit Rathkolb (39 shared papers)Rudi Balling (9 shared papers)Gregory S. Barsh (5 shared papers)Wolfgang Wurst (29 shared papers)Karen B. Avraham (7 shared papers)
- Journals
- Mammalian Genome (15 papers)PLoS ONE (12 papers)PLoS Genetics (6 papers)Human Molecular Genetics (5 papers)Investigative Ophthalmology & Visual Science (5 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Helmut Fuchs
181 papers receiving 5.4k citations
Peers
Comparison fields: 5 of 159
- Sensory Systems 641
- Molecular Biology 2.6k
- Cell Biology 591
- Behavioral Neuroscience 116
- Endocrine and Autonomic Systems 190
Countries citing papers authored by Helmut Fuchs
This map shows the geographic impact of Helmut Fuchs'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 Helmut Fuchs with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Helmut Fuchs more than expected).
Fields of papers citing papers by Helmut Fuchs
This network shows the impact of papers produced by Helmut Fuchs. 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 Helmut Fuchs. The network helps show where Helmut Fuchs may publish in the future.
Co-authors
The 25 scholars most cited alongside Helmut Fuchs, 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 185 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 276 | |
| 2 | 2009 | 243 | |
| 3 | 2002 | 215 | |
| 4 | 2001 | 179 | |
| 5 | 2009 | 165 | |
| 6 | 2008 | 162 | |
| 7 | 2004 | 139 | |
| 8 | 2008 | 124 | |
| 9 | 2003 | 110 | |
| 10 | Clinical Chemistry Reference Intervals for C57BL/6J, C57BL/6N, and C3HeB/FeJ Mice (Mus musculus). | 2016 | 92 |
| 11 | 2004 | 87 | |
| 12 | 2007 | 85 | |
| 13 | 2018 | 85 | |
| 14 | 2008 | 75 | |
| 15 | 2010 | 73 | |
| 16 | 2015 | 73 | |
| 17 | 2002 | 73 | |
| 18 | 2010 | 69 | |
| 19 | 2014 | 69 | |
| 20 | 2020 | 64 |
About Helmut Fuchs
Helmut Fuchs is a scholar working on Molecular Biology, Genetics, Cell Biology, Physiology and Sensory Systems, having authored 185 papers that have together received 5.4k indexed citations. Recurring topics across this work include Connexins and lens biology (13 papers), Hearing, Cochlea, Tinnitus, Genetics (12 papers), Adipose Tissue and Metabolism (9 papers), Mitochondrial Function and Pathology (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Metabolism and Genetic Disorders (8 papers), Retinal Development and Disorders (6 papers) and Cardiomyopathy and Myosin Studies (6 papers). The work is most often cited by research in Sensory Systems (641 citations), Molecular Biology (2.6k citations), Cell Biology (591 citations), Behavioral Neuroscience (116 citations) and Endocrine and Autonomic Systems (190 citations). Helmut Fuchs has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Martin Hrabě de Angelis, Valérie Gailus‐Durner, Eckhard Wolf, Birgit Rathkolb, Rudi Balling, Gregory S. Barsh, Wolfgang Wurst, Karen B. Avraham, Karen P. Steel and Sabine M. Hölter. Their work appears in journals such as Mammalian Genome, PLoS ONE, PLoS Genetics, Human Molecular Genetics and Investigative Ophthalmology & Visual Science.
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.