S.A. Rundle
Impact in
-
- Genetic Neurodegenerative Diseases
- Neurology top 5%
- Parkinson's Disease Mechanisms and Treatments
Papers in
-
- Mitochondrial Function and Pathology 5
- Ubiquitin and proteasome pathways 2
- Fungal and yeast genetics research 2
- RNA modifications and cancer 2
- DNA Repair Mechanisms 1
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- Genetic Neurodegenerative Diseases 12
- Co-authors
- J. David Brook (14 shared papers)William Reardon (4 shared papers)David E. Housman (3 shared papers)Alan Buckler (2 shared papers)D J Shaw (2 shared papers)Peter S. Harper (1 shared paper)H G Harley (16 shared papers)Steve Crow (6 shared papers)
- Journals
- Nucleic Acids Research (3 papers)Journal of Medical Genetics (3 papers)Genomics (2 papers)Human Genetics (2 papers)Nature (1 paper)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
S.A. Rundle
19 papers receiving 1.2k citations
S.A. Rundle's Hit Papers
Peers
Comparison fields: 5 of 74
- Cellular and Molecular Neuroscience 885
- Neurology 300
- Molecular Biology 820
- Genetics 249
- Virology 32
Countries citing papers authored by S.A. Rundle
This map shows the geographic impact of S.A. Rundle'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 S.A. Rundle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S.A. Rundle more than expected).
Fields of papers citing papers by S.A. Rundle
This network shows the impact of papers produced by S.A. Rundle. 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 S.A. Rundle. The network helps show where S.A. Rundle may publish in the future.
Co-authors
The 25 scholars most cited alongside S.A. Rundle, 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 | Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy Hit paper breakdown → | 1992 | 589 |
| 2 | 1992 | 143 | |
| 3 | 1991 | 127 | |
| 4 | Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker. | 1991 | 80 |
| 5 | 1993 | 56 | |
| 6 | A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus. | 1990 | 45 |
| 7 | 1993 | 32 | |
| 8 | 1991 | 26 | |
| 9 | 1992 | 26 | |
| 10 | 1991 | 17 | |
| 11 | 1992 | 16 | |
| 12 | 1993 | 13 | |
| 13 | 1991 | 12 | |
| 14 | 1992 | 8 | |
| 15 | 2022 | 7 | |
| 16 | 1990 | 5 | |
| 17 | 1990 | 3 | |
| 18 | 2008 | 2 | |
| 19 | 1990 | 2 |
About S.A. Rundle
S.A. Rundle is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Neurology and Epidemiology, having authored 19 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (12 papers), Mitochondrial Function and Pathology (5 papers), Ubiquitin and proteasome pathways (2 papers), Fungal and yeast genetics research (2 papers), Parkinson's Disease Mechanisms and Treatments (2 papers), Genomic variations and chromosomal abnormalities (2 papers), RNA modifications and cancer (2 papers) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (885 citations), Neurology (300 citations), Molecular Biology (820 citations), Genetics (249 citations) and Virology (32 citations). S.A. Rundle has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include J. David Brook, William Reardon, David E. Housman, Alan Buckler, D J Shaw, Peter S. Harper, H G Harley, Steve Crow, Peter S. Harper and Duncan J. Shaw. Their work appears in journals such as Nucleic Acids Research, Journal of Medical Genetics, Genomics, Human Genetics and Nature.
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.