Stephen Abbs
Impact in
- Genetics top 1%
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 2%
- Muscle Physiology and Disorders
- RNA Research and Splicing
- Ion channel regulation and function
Papers in
-
- Muscle Physiology and Disorders 40
- RNA Research and Splicing 10
- RNA regulation and disease 5
- Ion channel regulation and function 5
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- Cardiomyopathy and Myosin Studies 17
- Co-authors
- Martin Bobrow (14 shared papers)Caroline A. Sewry (19 shared papers)Christopher G. Mathew (6 shared papers)Shu C. Yau (10 shared papers)Francesco Muntoni (10 shared papers)Heinz Jungbluth (17 shared papers)Lucy Feng (7 shared papers)Volker Straub (6 shared papers)
- Journals
- Neuromuscular Disorders (22 papers)Journal of Medical Genetics (7 papers)European Journal of Human Genetics (7 papers)Genomics (4 papers)BMC Nephrology (2 papers)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
Stephen Abbs
79 papers receiving 4.2k citations
Stephen Abbs's Hit Papers
Peers
Comparison fields: 5 of 105
- Genetics 823
- Molecular Biology 3.0k
- Cardiology and Cardiovascular Medicine 854
- Immunology and Allergy 224
- Genetics 876
Countries citing papers authored by Stephen Abbs
This map shows the geographic impact of Stephen Abbs'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 Stephen Abbs with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephen Abbs more than expected).
Fields of papers citing papers by Stephen Abbs
This network shows the impact of papers produced by Stephen Abbs. 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 Stephen Abbs. The network helps show where Stephen Abbs may publish in the future.
Co-authors
The 25 scholars most cited alongside Stephen Abbs, 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 81 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study Hit paper breakdown → | 2011 | 691 |
| 2 | 2010 | 206 | |
| 3 | 2001 | 167 | |
| 4 | 2019 | 156 | |
| 5 | 1996 | 148 | |
| 6 | 2010 | 145 | |
| 7 | 2006 | 125 | |
| 8 | 2006 | 120 | |
| 9 | 2013 | 112 | |
| 10 | 2005 | 105 | |
| 11 | 2013 | 103 | |
| 12 | 1988 | 101 | |
| 13 | 2008 | 96 | |
| 14 | 1991 | 96 | |
| 15 | 1998 | 95 | |
| 16 | 2011 | 89 | |
| 17 | 2011 | 87 | |
| 18 | 2010 | 84 | |
| 19 | 1990 | 84 | |
| 20 | 1992 | 81 |
About Stephen Abbs
Stephen Abbs is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine, Genetics, Cell Biology and Genetics, having authored 81 papers that have together received 4.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (40 papers), Cardiomyopathy and Myosin Studies (17 papers), Neurogenetic and Muscular Disorders Research (13 papers), RNA Research and Splicing (10 papers), Genetic Neurodegenerative Diseases (7 papers), RNA regulation and disease (5 papers), Ion channel regulation and function (5 papers) and Cellular transport and secretion (4 papers). The work is most often cited by research in Genetics (823 citations), Molecular Biology (3.0k citations), Cardiology and Cardiovascular Medicine (854 citations), Immunology and Allergy (224 citations) and Genetics (876 citations). Stephen Abbs has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Martin Bobrow, Caroline A. Sewry, Christopher G. Mathew, Shu C. Yau, Francesco Muntoni, Heinz Jungbluth, Lucy Feng, Volker Straub, Sebahattin Çirak and Silvia Torelli. Their work appears in journals such as Neuromuscular Disorders, Journal of Medical Genetics, European Journal of Human Genetics, Genomics and BMC Nephrology.
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.