A E Harding
- Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases 27
- Hereditary Neurological Disorders 7
- Neurology top 0.5%
- Neurological diseases and metabolism 10
- Neurological disorders and treatments 8
- Parkinson's Disease Mechanisms and Treatments 6
- Neurology top 0.5%
- Neurological diseases and metabolism 10
- Neurological disorders and treatments 8
- Parkinson's Disease Mechanisms and Treatments 6
- Molecular Biology top 2%
- Mitochondrial Function and Pathology 24
- Amyloidosis: Diagnosis, Treatment, Outcomes 8
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders 10
A E Harding
71 papers receiving 4.7k citations
Hit Papers
Peers
Comparison fields: 5 of 110
- Cellular and Molecular Neuroscience 2.5k
- Neurology 1.7k
- Neurology 893
- Molecular Biology 2.6k
- Clinical Biochemistry 258
Countries citing papers authored by A E Harding
This map shows the geographic impact of A E Harding'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 A E Harding with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A E Harding more than expected).
Fields of papers citing papers by A E Harding
This network shows the impact of papers produced by A E Harding. 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 A E Harding. The network helps show where A E Harding may publish in the future.
Co-authorship network
The 25 scholars most cited alongside A E Harding, 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 | 1997 | 32 | |
| 2 | The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus. | 1996 | 52 |
| 3 | 1995 | 20 | |
| 4 | 1995 | 69 | |
| 5 | 1994 | 92 | |
| 6 | 1994 | 48 | |
| 7 | 1994 | 29 | |
| 8 | 1994 | 284 | |
| 9 | 1994 | 43 | |
| 10 | 1993 | 135 | |
| 11 | 1992 | 31 | |
| 12 | 1991 | 31 | |
| 13 | 1990 | 107 | |
| 14 | 1989 | 114 | |
| 15 | 1988 | 20 | |
| 16 | 1987 | 367 | |
| 17 | The hereditary ataxias and related disorders | 1984 | 218 |
| 18 | 1984 | 8 | |
| 19 | 1982 | 309 | |
| 20 | FRIEDREICH'S ATAXIA: A CLINICAL AND GENETIC STUDY OF 90 FAMILIES WITH AN ANALYSIS OF EARLY DIAGNOSTIC CRITERIA AND INTRAFAMILIAL CLUSTERING OF CLINICAL FEATURESbreakdown → | 1981 | 698 |
About A E Harding
A E Harding is a scholar working on Cellular and Molecular Neuroscience, Clinical Biochemistry, Neurology, Neurology and Rheumatology, having authored 72 papers that have together received 4.9k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (27 papers), Mitochondrial Function and Pathology (24 papers), Neurological diseases and metabolism (10 papers), Metabolism and Genetic Disorders (10 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (8 papers), Neurological disorders and treatments (8 papers), Hereditary Neurological Disorders (7 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (2.5k citations), Neurology (1.7k citations), Neurology (893 citations), Molecular Biology (2.6k citations) and Clinical Biochemistry (258 citations). A E Harding has collaborated with scholars based in United Kingdom, India and France. Frequent co-authors include W. I. McDonald, Paul S. Tofts, David H. Miller, D. P. R. Muller, P. K. Thomas, C. D. Marsden, Philip D. Thompson, M G Sweeney, L J Findley and Peter G. Bain. Their work appears in journals such as Journal of Neurology Neurosurgery & Psychiatry, Brain, Movement Disorders, Journal of Medical Genetics and Acta Neuropathologica.
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.