Steve Crow
Impact in
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- Genetic Neurodegenerative Diseases
- Neurology top 5%
- Parkinson's Disease Mechanisms and Treatments
Papers in ⓘ
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- Genetic Neurodegenerative Diseases 7
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- Mitochondrial Function and Pathology 4
- Ubiquitin and proteasome pathways 2
- DNA Repair Mechanisms 1
- Fungal and yeast genetics research 1
- Co-authors
- J. David Brook (7 shared papers)William Reardon (3 shared papers)Duncan J. Shaw (6 shared papers)J Myring (2 shared papers)S.A. Rundle (6 shared papers)H G Harley (6 shared papers)Iain Fenton (1 shared paper)P S Harper (1 shared paper)
- Journals
- Journal of Medical Genetics (2 papers)Human Molecular Genetics (1 paper)Genomics (1 paper)The Lancet (1 paper)Change The Magazine of Higher Learning (1 paper)
- Partner nations
- United KingdomUnited States
In The Last Decade
Steve Crow
8 papers receiving 596 citations
Peers
Comparison fields: 5 of 48
- Cellular and Molecular Neuroscience 517
- Neurology 234
- Molecular Biology 491
- Genetics 117
- Genetics 23
Countries citing papers authored by Steve Crow
This map shows the geographic impact of Steve Crow'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 Steve Crow with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Steve Crow more than expected).
Fields of papers citing papers by Steve Crow
This network shows the impact of papers produced by Steve Crow. 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 Steve Crow. The network helps show where Steve Crow may publish in the future.
Co-authors
The 21 scholars most cited alongside Steve Crow, 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 | Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy. | 1993 | 303 |
| 2 | 1992 | 143 | |
| 3 | Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker. | 1991 | 80 |
| 4 | 1993 | 32 | |
| 5 | 1992 | 26 | |
| 6 | 1992 | 16 | |
| 7 | 1992 | 8 | |
| 8 | 2005 | 4 |
About Steve Crow
Steve Crow is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Genetics and Infectious Diseases, having authored 8 papers that have together received 612 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (4 papers), Ubiquitin and proteasome pathways (2 papers), Parkinson's Disease Mechanisms and Treatments (1 paper), DNA Repair Mechanisms (1 paper), Fungal and yeast genetics research (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (517 citations), Neurology (234 citations), Molecular Biology (491 citations), Genetics (117 citations) and Genetics (23 citations). Steve Crow has collaborated with scholars based in United Kingdom and United States. Frequent co-authors include J. David Brook, William Reardon, Duncan J. Shaw, J Myring, S.A. Rundle, H G Harley, Iain Fenton, P S Harper, J. MacMillan and Peter S. Harper. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, Genomics, The Lancet and Change The Magazine of Higher Learning.
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.