A E Harding

6.6k total citations · 1 hit paper
72 papers, 4.9k citations indexed

About

A E Harding is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, A E Harding has authored 72 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 31 papers in Cellular and Molecular Neuroscience and 19 papers in Neurology. Recurrent topics in A E Harding's work include Genetic Neurodegenerative Diseases (27 papers), Mitochondrial Function and Pathology (24 papers) and Neurological diseases and metabolism (10 papers). A E Harding is often cited by papers focused on Genetic Neurodegenerative Diseases (27 papers), Mitochondrial Function and Pathology (24 papers) and Neurological diseases and metabolism (10 papers). A E Harding collaborates with scholars based in United Kingdom, India and France. A E Harding's 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 and has published in prestigious journals such as New England Journal of Medicine, The Lancet and Brain.

In The Last Decade

A E Harding

71 papers receiving 4.7k 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.

FRIEDREICH'S ATAXIA: A CLINICAL AND GENETIC STUDY OF 90 FAMILIES WITH AN ANALYSIS OF EARLY DIAGNOSTIC CRITERIA AND INTRAFAMILIAL CLUSTERING OF CLINICAL FEATURES

1981 698 citations A E Harding Brain 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	33	2.6k	2.5k	1.7k	893	612	72	4.9k
Hidenao Sasaki Japan	41	2.2k 0.8×	2.0k 0.8×	2.1k 1.2×	532 0.6×	912 1.5×	240	5.3k
James Garbern United States	39	2.2k 0.8×	1.4k 0.5×	612 0.4×	755 0.8×	478 0.8×	78	4.2k
Davide Pareyson Italy	46	2.4k 0.9×	4.5k 1.8×	3.6k 2.1×	1.3k 1.5×	341 0.6×	252	7.9k
Anne Baron‐Van Evercooren France	42	2.8k 1.1×	2.9k 1.2×	345 0.2×	1.3k 1.4×	881 1.4×	99	7.0k
A E Harding United Kingdom	31	1.7k 0.6×	1.3k 0.5×	791 0.5×	468 0.5×	223 0.4×	61	3.1k
Maria Teresa Dotti Italy	37	1.8k 0.7×	791 0.3×	1.5k 0.9×	672 0.8×	117 0.2×	173	4.5k
Jacqueline Trotter Germany	48	3.8k 1.5×	2.4k 0.9×	374 0.2×	1.4k 1.6×	476 0.8×	85	7.1k
Xinghua Yin United States	23	1.3k 0.5×	1.2k 0.5×	485 0.3×	1.2k 1.3×	749 1.2×	31	3.5k
Patrice D. Smith Canada	20	1.8k 0.7×	2.1k 0.8×	960 0.6×	577 0.6×	240 0.4×	33	3.9k
Stefan M. Pulst United States	44	4.1k 1.6×	3.3k 1.3×	2.3k 1.3×	457 0.5×	169 0.3×	157	6.2k

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

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20 of 20 papers shown

Wenning, Gregor K., Eduard Kraft, Clare J. Fowler, et al.. (1997). Cerebellar presentation of multiple system atrophy. Movement Disorders. 12(1). 115–117. 32 indexed citations

David, Gilles, Paola Giunti, N. Abbas, et al.. (1996). 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.. PubMed. 59(6). 1328–36. 52 indexed citations

Reilly, Mary M., David Adams, Mary B. Davis, G. Saïd, & A E Harding. (1995). Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77). Journal of Neurology. 242(10). 664–668. 20 indexed citations

Morgan-Hughes, J A, M G Sweeney, Jonathan M. Cooper, et al.. (1995). Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1271(1). 135–140. 69 indexed citations

Enevoldson, T P, M. D. Sanders, & A E Harding. (1994). Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy. A clinical and genetic study of eight familes. Brain. 117(3). 445–460. 92 indexed citations

Giunti, Paola, M G Sweeney, M. Spadaro, et al.. (1994). The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias. Brain. 117(4). 645–649. 48 indexed citations

Dexter, David T., David J. Brooks, A E Harding, et al.. (1994). Nigrostriatal function in vitamin E deficiency: Clinical, experimental, and positron emission tomographic studies. Annals of Neurology. 35(3). 298–303. 29 indexed citations

Bain, Peter G., L J Findley, Philip D. Thompson, et al.. (1994). A study of hereditary essential tremor. Brain. 117(4). 805–824. 284 indexed citations

Thompson, Philip D., Kailash P. Bhatia, Peter Brown, et al.. (1994). Cortical myoclonus in huntington's disease. Movement Disorders. 9(6). 633–641. 43 indexed citations

10.

Harding, A E. (1993). Hereditary Spastic Paraplegias. Seminars in Neurology. 13(4). 333–336. 135 indexed citations

11.

Kartsounis, L. D., et al.. (1992). The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies. Archives of Neurology. 49(2). 158–160. 31 indexed citations

12.

Misra, V.P., R. H. M. King, A E Harding, J. R. Muddle, & P. K. Thomas. (1991). Peripheral neuropathy in the Chediak-Higashi syndrome. Acta Neuropathologica. 81(3). 354–358. 31 indexed citations

13.

Plant, Gordon T., Tamás Révész, Rita Barnard, A E Harding, & P. C. Gautier-Smith. (1990). FAMILIAL CEREBRAL AMYLOID ANGIOPATHY WITH NONNEURITIC AMYLOID PLAQUE FORMATION. Brain. 113(3). 721–747. 107 indexed citations

14.

Collinge, John, F. Owen, R. Lofthouse, et al.. (1989). DIAGNOSIS OF GERSTMANN-STRÄUSSLER SYNDROME IN FAMILIAL DEMENTIA WITH PRION PROTEIN GENE ANALYSIS. The Lancet. 334(8653). 15–17. 114 indexed citations

15.

Coleman, R., S. Robb, Brian Lake, E M Brett, & A E Harding. (1988). The diverse neurological features of Niemann‐Pick disease type C: A report of two cases. Movement Disorders. 3(4). 295–299. 20 indexed citations

16.

Ormerod, I E, David H. Miller, W. I. McDonald, et al.. (1987). THE ROLE OF NMR IMAGING IN THE ASSESSMENT OF MULTIPLE SCLEROSIS AND ISOLATED NEUROLOGICAL LESIONS. Brain. 110(6). 1579–1616. 367 indexed citations

17.

Harding, A E. (1984). The hereditary ataxias and related disorders. Churchill Livingstone eBooks. 218 indexed citations

18.

Harding, A E. (1984). Subdural haematoma in two patients with chronic neurological disorders.. BMJ. 288(6435). 1986–1987. 8 indexed citations

19.

Harding, A E. (1982). THE CLINICAL FEATURES AND CLASSIFICATION OF THE LATE ONSET AUTOSOMAL DOMINANT CEREBELLAR ATAXIAS. Brain. 105(1). 1–28. 309 indexed citations

20.

Harding, A E. (1981). FRIEDREICH'S ATAXIA: A CLINICAL AND GENETIC STUDY OF 90 FAMILIES WITH AN ANALYSIS OF EARLY DIAGNOSTIC CRITERIA AND INTRAFAMILIAL CLUSTERING OF CLINICAL FEATURES. Brain. 104(3). 589–620. 698 indexed citations breakdown →

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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