A E Harding
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
-
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Papers in
-
- Mitochondrial Function and Pathology 31
- ATP Synthase and ATPases Research 13
-
- Genetic Neurodegenerative Diseases 11
- Hereditary Neurological Disorders 6
- Co-authors
- P. K. Thomas (2 shared papers)David H. Miller (5 shared papers)Mary G. Sweeney (7 shared papers)J A Morgan-Hughes (7 shared papers)P K Thomas (1 shared paper)D. A. S. Compston (4 shared papers)R. M. Chalmers (7 shared papers)H. Kellar-Wood (4 shared papers)
- Journals
- Journal of Neurology Neurosurgery & Psychiatry (12 papers)Journal of the Neurological Sciences (8 papers)Annals of Neurology (5 papers)Journal of Medical Genetics (5 papers)Brain (4 papers)
- Partner nations
- United KingdomIndiaMexico
In The Last Decade
A E Harding
61 papers receiving 3.2k citations
A E Harding's Hit Papers
Peers
Comparison fields: 5 of 87
- Clinical Biochemistry 692
- Cellular and Molecular Neuroscience 1.4k
- Neurology 444
- Neurology 746
- Molecular Biology 1.7k
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-authors
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
Showing the 20 most-cited of 63 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | THE CLINICAL FEATURES OF HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPES I AND II Hit paper breakdown → | 1980 | 654 |
| 2 | 1992 | 311 | |
| 3 | 1982 | 193 | |
| 4 | 1980 | 156 | |
| 5 | 1989 | 133 | |
| 6 | 1994 | 120 | |
| 7 | 1993 | 120 | |
| 8 | 1996 | 103 | |
| 9 | 1983 | 90 | |
| 10 | 1997 | 70 | |
| 11 | Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation. | 1995 | 70 |
| 12 | Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy. | 1992 | 67 |
| 13 | 1994 | 66 | |
| 14 | 1997 | 61 | |
| 15 | 1996 | 58 | |
| 16 | 1991 | 51 | |
| 17 | 1996 | 51 | |
| 18 | Vitamin E and the nervous system. | 1987 | 51 |
| 19 | 1990 | 50 | |
| 20 | 1983 | 50 |
About A E Harding
A E Harding is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Clinical Biochemistry, Neurology and Neurology, having authored 63 papers that have together received 3.4k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (31 papers), Metabolism and Genetic Disorders (16 papers), ATP Synthase and ATPases Research (13 papers), Genetic Neurodegenerative Diseases (11 papers), Neurological diseases and metabolism (9 papers), Hereditary Neurological Disorders (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Neurological disorders and treatments (4 papers). The work is most often cited by research in Clinical Biochemistry (692 citations), Cellular and Molecular Neuroscience (1.4k citations), Neurology (444 citations), Neurology (746 citations) and Molecular Biology (1.7k citations). A E Harding has collaborated with scholars based in United Kingdom, India and Mexico. Frequent co-authors include P. K. Thomas, David H. Miller, Mary G. Sweeney, J A Morgan-Hughes, P K Thomas, D. A. S. Compston, R. M. Chalmers, H. Kellar-Wood, Ian Holt and G.G. Govan. Their work appears in journals such as Journal of Neurology Neurosurgery & Psychiatry, Journal of the Neurological Sciences, Annals of Neurology, Journal of Medical Genetics and Brain.
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.