Edward Nylen
Impact in
-
- Genetic Neurodegenerative Diseases
- Molecular Biology top 10%
- Muscle Physiology and Disorders
- RNA Research and Splicing
- Nuclear Structure and Function
- Ubiquitin and proteasome pathways
Papers in
-
- Muscle Physiology and Disorders 10
- RNA Research and Splicing 3
- Sexual Differentiation and Disorders 2
-
- Genetic Neurodegenerative Diseases 7
- Co-authors
- Klaus Wrogemann (16 shared papers)Cheryl R. Greenberg (10 shared papers)Tracey Weiler (5 shared papers)Kenneth Morgan (6 shared papers)Takuya Fujiwara (5 shared papers)Eduardo Rosenmann (3 shared papers)Patrick Frosk (2 shared papers)Thangirala Sudha (1 shared paper)
- Journals
- The American Journal of Human Genetics (2 papers)Experimental Neurology (1 paper)Transfusion (1 paper)Advances in experimental medicine and biology (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- CanadaUnited KingdomNetherlands
In The Last Decade
Edward Nylen
17 papers receiving 859 citations
Peers
Comparison fields: 5 of 68
- Cellular and Molecular Neuroscience 229
- Molecular Biology 800
- Genetics 108
- Cardiology and Cardiovascular Medicine 192
- Cell Biology 135
Countries citing papers authored by Edward Nylen
This map shows the geographic impact of Edward Nylen'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 Edward Nylen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Edward Nylen more than expected).
Fields of papers citing papers by Edward Nylen
This network shows the impact of papers produced by Edward Nylen. 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 Edward Nylen. The network helps show where Edward Nylen may publish in the future.
Co-authors
The 25 scholars most cited alongside Edward Nylen, 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 | 2002 | 188 | |
| 2 | 1999 | 142 | |
| 3 | 2000 | 102 | |
| 4 | 1998 | 84 | |
| 5 | 1988 | 77 | |
| 6 | Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype. | 1996 | 74 |
| 7 | 2004 | 53 | |
| 8 | 1991 | 47 | |
| 9 | 1988 | 28 | |
| 10 | 1991 | 23 | |
| 11 | 1983 | 17 | |
| 12 | 1985 | 14 | |
| 13 | 1997 | 11 | |
| 14 | 2004 | 10 | |
| 15 | 2006 | 8 | |
| 16 | 1977 | 6 | |
| 17 | 1993 | 4 |
About Edward Nylen
Edward Nylen is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Cardiology and Cardiovascular Medicine, Cell Biology and Physiology, having authored 17 papers that have together received 888 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (10 papers), Genetic Neurodegenerative Diseases (7 papers), Muscle metabolism and nutrition (4 papers), Hormonal and reproductive studies (3 papers), RNA Research and Splicing (3 papers), Cardiomyopathy and Myosin Studies (3 papers), Sexual Differentiation and Disorders (2 papers) and Adipose Tissue and Metabolism (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (229 citations), Molecular Biology (800 citations), Genetics (108 citations), Cardiology and Cardiovascular Medicine (192 citations) and Cell Biology (135 citations). Edward Nylen has collaborated with scholars based in Canada, United Kingdom and Netherlands. Frequent co-authors include Klaus Wrogemann, Cheryl R. Greenberg, Tracey Weiler, Kenneth Morgan, Takuya Fujiwara, Eduardo Rosenmann, Patrick Frosk, Thangirala Sudha, Marshall J. Glesby and Kate Bushby. Their work appears in journals such as The American Journal of Human Genetics, Experimental Neurology, Transfusion, Advances in experimental medicine and biology 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.