A. E. Harding

15.4k total citations · 4 hit papers
88 papers, 11.1k citations indexed

About

A. E. Harding is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, A. E. Harding has authored 88 papers receiving a total of 11.1k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 40 papers in Cellular and Molecular Neuroscience and 30 papers in Clinical Biochemistry. Recurrent topics in A. E. Harding's work include Mitochondrial Function and Pathology (39 papers), Genetic Neurodegenerative Diseases (31 papers) and Metabolism and Genetic Disorders (30 papers). A. E. Harding is often cited by papers focused on Mitochondrial Function and Pathology (39 papers), Genetic Neurodegenerative Diseases (31 papers) and Metabolism and Genetic Disorders (30 papers). A. E. Harding collaborates with scholars based in United Kingdom, United States and India. A. E. Harding's co-authors include J A Morgan-Hughes, Ian Holt, Kenneth H. Fischbeck, Albert R. La Spada, Dennis B. Lubahn, Elizabeth Wilson, Richard Petty, C. D. Marsden, Mary G. Sweeney and Nicholas Fletcher and has published in prestigious journals such as Nature, The Lancet and Nucleic Acids Research.

In The Last Decade

A. E. Harding

88 papers receiving 10.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1991 2.1k citations A. E. Harding et al. profile →
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1988 1.4k citations Ian Holt, A. E. Harding et al. profile →
A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.

1990 776 citations Ian Holt, A. E. Harding et al. PubMed profile →
CLASSIFICATION OF THE HEREDITARY ATAXIAS AND PARAPLEGIAS

1983 697 citations A. E. Harding profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
A. E. Harding United Kingdom	45	7.6k	4.7k	3.1k	2.6k	1.3k	88	11.1k
Laurence A. Bindoff Norway	48	6.3k 0.8×	1.4k 0.3×	3.4k 1.1×	878 0.3×	643 0.5×	187	8.0k
Caterina Mariotti Italy	45	4.4k 0.6×	3.7k 0.8×	766 0.2×	1.8k 0.7×	642 0.5×	158	6.3k
Massimo Pandolfo Belgium	55	7.3k 1.0×	6.2k 1.3×	497 0.2×	2.3k 0.9×	750 0.6×	207	10.0k
Albert R. La Spada United States	52	7.8k 1.0×	5.5k 1.2×	327 0.1×	2.8k 1.1×	810 0.6×	146	11.3k
Thomas D. Bird United States	52	4.2k 0.6×	5.9k 1.3×	252 0.1×	2.7k 1.0×	1.8k 1.4×	170	8.6k
Maurizio Moggio Italy	44	4.4k 0.6×	1.0k 0.2×	1.1k 0.4×	1.0k 0.4×	394 0.3×	195	6.2k
Laurie J. Ozelius United States	58	2.8k 0.4×	5.7k 1.2×	397 0.1×	7.6k 2.9×	1.1k 0.8×	231	11.6k
Tetsuo Ashizawa United States	56	9.4k 1.2×	9.4k 2.0×	263 0.1×	4.1k 1.5×	626 0.5×	249	12.2k
Giuseppe De Michele Italy	43	3.0k 0.4×	3.9k 0.8×	266 0.1×	3.2k 1.2×	1.2k 0.9×	208	6.8k
Yu‐ichi Goto Japan	47	7.7k 1.0×	1.0k 0.2×	3.3k 1.0×	391 0.1×	255 0.2×	288	10.2k

Countries citing papers authored by A. E. Harding

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of A. E. Harding

This figure shows the co-authorship network connecting the top 25 collaborators of A. E. Harding. A scholar is included among the top collaborators of A. E. Harding based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with A. E. Harding. A. E. Harding is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Riordan‐Eva, Paul & A. E. Harding. (1995). Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations.. Journal of Medical Genetics. 32(2). 81–87. 89 indexed citations

Sweeney, Mary G., Simon Hammans, L. W. Duchen, et al.. (1994). Mitochondrial DNA mutation underlying Leigh's syndrome: Clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsy. Journal of the Neurological Sciences. 121(1). 57–65. 43 indexed citations

Morrison, Karen & A. E. Harding. (1994). Disorders of the motor neurone.. PubMed. 3(2). 431–45. 7 indexed citations

Alcolado, John, Aneela Majid, Martin Brockington, et al.. (1994). Mitochondrial gene defects in patients with NIDDM. Diabetologia. 37(4). 372–376. 60 indexed citations

Rinne, J. O., S. E. Daniel, F Scaravilli, et al.. (1994). The neuropathological features of neuroacanthocytosis. Movement Disorders. 9(3). 297–304. 58 indexed citations

Gregory, Robert A., P. K. Thomas, R. H. M. King, et al.. (1993). Coexistence of hereditary motor and sensory neuropathy type IA and IGM paraproteinemic neuropathy. Annals of Neurology. 33(6). 649–652. 24 indexed citations

Harding, A. E., Ian Holt, M G Sweeney, Martin Brockington, & Mary B. Davis. (1992). Prenatal diagnosis of mitochondrial DNA8993 T----G disease.. PubMed. 50(3). 629–33. 76 indexed citations

Harding, A. E. & Simon Hammans. (1992). Deletions of the mitochondrial genome. Journal of Inherited Metabolic Disease. 15(4). 480–486. 23 indexed citations

Maraganore, Demetrius M., A. E. Harding, & C. D. Marsden. (1991). A clinical and genetic study of familial Parkinson's disease. Movement Disorders. 6(3). 205–211. 113 indexed citations

10.

Hardie, R, A. E. Harding, J.S. Owen, et al.. (1991). Neuroacanthocytosis. A clinical, haematological and pathological study of 19 cases.. PubMed. 114 ( Pt 1A). 13–49. 180 indexed citations

11.

Morgan-Hughes, J A, Jonathan M. Cooper, Anthony H.V. Schapira, et al.. (1991). The molecular pathology of human respiratory chain defects.. PubMed. 147(6-7). 450–4. 5 indexed citations

12.

Schapira, Anthony H.V., Ian Holt, Mary G. Sweeney, et al.. (1990). Mitochondrial DNA analysis in Parkinson's disease. Movement Disorders. 5(4). 294–297. 87 indexed citations

13.

Fletcher, Nicholas, A. E. Harding, & C. D. Marsden. (1990). A GENETIC STUDY OF IDIOPATHIC TORSION DYSTONIA IN THE UNITED KINGDOM. Brain. 113(2). 379–395. 72 indexed citations

14.

Waddy, Heather, et al.. (1990). Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: A magnetic stimulation study. Annals of Neurology. 28(1). 43–49. 43 indexed citations

15.

Truong, Daniel, A. E. Harding, F Scaravilli, et al.. (1990). Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies. Movement Disorders. 5(2). 109–117. 45 indexed citations

16.

Holt, Ian, A. E. Harding, & J A Morgan-Hughes. (1988). Mitochondrial DNA polymorphism in mitochondrial myopathy. Human Genetics. 79(1). 53–57. 27 indexed citations

17.

Harding, A. E.. (1988). The inherited ataxias.. PubMed. 48. 37–46. 20 indexed citations

18.

Harding, A. E., Richard Petty, & J A Morgan-Hughes. (1988). Mitochondrial myopathy: a genetic study of 71 cases.. Journal of Medical Genetics. 25(8). 528–535. 24 indexed citations

19.

Lim, Lyn‐li, M. A. Ron, Joel David, et al.. (1988). Psychiatric and Neurological Manifestations in Systemic Lupus Erythematosus. QJM. 66(249). 27–38. 50 indexed citations

20.

Evans, Nathaniel R., L J Farrow, A. E. Harding, & James S. Stewart. (1970). New techniques for speeding small intestinal biopsy.. Gut. 11(1). 88–89. 16 indexed citations

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.

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