Stephen Abbs
- Genetics top 1%
- Neurogenetic and Muscular Disorders Research 14
- Molecular Biology top 2%
- Muscle Physiology and Disorders 42
- RNA Research and Splicing 12
- RNA regulation and disease 6
- Ion channel regulation and function 6
- Immunology and Allergy top 2%
- Genetics top 2%
- Neurogenetic and Muscular Disorders Research 14
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- Cardiomyopathy and Myosin Studies 19
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- Genetic Neurodegenerative Diseases 9
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- Cellular transport and secretion 5
- Co-authors
- Martin BobrowCaroline A. SewryChristopher G. MathewShu C. YauFrancesco MuntoniLucy FengHeinz JungbluthSebahattin Çirak
- Journals
- Neuromuscular Disorders (22 papers)European Journal of Human Genetics (8 papers)Journal of Medical Genetics (7 papers)
- Partner nations
- United KingdomItalyUnited States
In The Last Decade
Stephen Abbs
81 papers receiving 3.9k citations
Hit Papers
Peers
Comparison fields: 5 of 108
- Genetics 853
- Molecular Biology 3.0k
- Immunology and Allergy 230
- Genetics 1.0k
- Cardiology and Cardiovascular Medicine 805
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 39 | |
| 2 | 2018 | 23 | |
| 3 | 2017 | 6 | |
| 4 | 2013 | 40 | |
| 5 | 2011 | 18 | |
| 6 | 2011 | 3 | |
| 7 | Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation studybreakdown → | 2011 | 656 |
| 8 | 2011 | 3 | |
| 9 | 2011 | 6 | |
| 10 | 2011 | 72 | |
| 11 | 2011 | 30 | |
| 12 | 2010 | 11 | |
| 13 | 2010 | 9 | |
| 14 | 2009 | 28 | |
| 15 | 2006 | 108 | |
| 16 | 2006 | 105 | |
| 17 | Analysis of dystrophin mRNA show nonsense, splice and cryptic splice site mutations cause Becker muscular dystrophy. | 2003 | 2 |
| 18 | 2001 | 160 | |
| 19 | 1997 | 23 | |
| 20 | 1989 | 53 |
About Stephen Abbs
Stephen Abbs is a scholar working on Genetics, Molecular Biology, Cardiology and Cardiovascular Medicine, Immunology and Allergy and Cell Biology, having authored 83 papers that have together received 4.0k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (42 papers), Cardiomyopathy and Myosin Studies (19 papers), Neurogenetic and Muscular Disorders Research (14 papers), RNA Research and Splicing (12 papers), Genetic Neurodegenerative Diseases (9 papers), RNA regulation and disease (6 papers), Ion channel regulation and function (6 papers) and Cellular transport and secretion (5 papers). The work is most often cited by research in Genetics (853 citations), Molecular Biology (3.0k citations), Immunology and Allergy (230 citations), Genetics (1.0k citations) and Cardiology and Cardiovascular Medicine (805 citations). Stephen Abbs has collaborated with scholars based in United Kingdom, Italy and United States. Frequent co-authors include Martin Bobrow, Caroline A. Sewry, Christopher G. Mathew, Shu C. Yau, Francesco Muntoni, Lucy Feng, Heinz Jungbluth, Sebahattin Çirak, Silvia Torelli and Volker Straub. Their work appears in journals such as Neuromuscular Disorders, European Journal of Human Genetics, Journal of Medical 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.