Wolfram Kreß
Impact in
-
- Genetic Neurodegenerative Diseases
- Genetics top 2%
- Neurogenetic and Muscular Disorders Research
Papers in
-
- Muscle Physiology and Disorders 37
- RNA modifications and cancer 13
- RNA Research and Splicing 10
- Mitochondrial Function and Pathology 9
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- Genetic Neurodegenerative Diseases 32
- Co-authors
- K. Ricker (3 shared papers)Christina L. Liquori (1 shared paper)Melinda L. Moseley (1 shared paper)Laura P.W. Ranum (1 shared paper)Susan L. Naylor (1 shared paper)Benedikt Schoser (11 shared papers)Clemens R. Müller (9 shared papers)Jocelyn Laporte (7 shared papers)
- Journals
- Neuromuscular Disorders (11 papers)Muscle & Nerve (9 papers)European Journal of Human Genetics (8 papers)Human Mutation (7 papers)Journal of Organometallic Chemistry (6 papers)
- Partner nations
- GermanyFranceUnited States
In The Last Decade
Wolfram Kreß
111 papers receiving 3.9k citations
Wolfram Kreß's Hit Papers
Peers
Comparison fields: 5 of 113
- Cellular and Molecular Neuroscience 1.4k
- Genetics 389
- Molecular Biology 2.7k
- Neurology 500
- Cardiology and Cardiovascular Medicine 567
Countries citing papers authored by Wolfram Kreß
This map shows the geographic impact of Wolfram Kreß'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 Wolfram Kreß with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wolfram Kreß more than expected).
Fields of papers citing papers by Wolfram Kreß
This network shows the impact of papers produced by Wolfram Kreß. 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 Wolfram Kreß. The network helps show where Wolfram Kreß may publish in the future.
Co-authors
The 25 scholars most cited alongside Wolfram Kreß, 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 113 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9 Hit paper breakdown → | 2001 | 925 |
| 2 | 2004 | 177 | |
| 3 | 2000 | 168 | |
| 4 | 2008 | 113 | |
| 5 | 2006 | 104 | |
| 6 | 2012 | 103 | |
| 7 | 2005 | 93 | |
| 8 | 2003 | 91 | |
| 9 | 2011 | 81 | |
| 10 | 2013 | 81 | |
| 11 | 1995 | 75 | |
| 12 | 2014 | 75 | |
| 13 | 2010 | 67 | |
| 14 | 2004 | 61 | |
| 15 | 1997 | 60 | |
| 16 | 1999 | 58 | |
| 17 | 2001 | 56 | |
| 18 | 2004 | 55 | |
| 19 | 2005 | 53 | |
| 20 | 2013 | 52 |
About Wolfram Kreß
Wolfram Kreß is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Cardiology and Cardiovascular Medicine, Genetics and Cell Biology, having authored 113 papers that have together received 4.0k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (37 papers), Genetic Neurodegenerative Diseases (32 papers), Cardiomyopathy and Myosin Studies (20 papers), RNA modifications and cancer (13 papers), Cellular transport and secretion (10 papers), RNA Research and Splicing (10 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Mitochondrial Function and Pathology (9 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.4k citations), Genetics (389 citations), Molecular Biology (2.7k citations), Neurology (500 citations) and Cardiology and Cardiovascular Medicine (567 citations). Wolfram Kreß has collaborated with scholars based in Germany, France and United States. Frequent co-authors include K. Ricker, Christina L. Liquori, Melinda L. Moseley, Laura P.W. Ranum, Susan L. Naylor, Benedikt Schoser, Clemens R. Müller, Jocelyn Laporte, Jean‐Louis Mandel and T. Grimm. Their work appears in journals such as Neuromuscular Disorders, Muscle & Nerve, European Journal of Human Genetics, Human Mutation and Journal of Organometallic 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.