A. E. Harding

15.4k citations
88 papers · 11.1k · 4 hit papers · h-index 45

Impact in

Papers in

Co-authors
J A Morgan-Hughes (16 shared papers)Ian Holt (11 shared papers)Kenneth H. Fischbeck (1 shared paper)Albert R. La Spada (1 shared paper)Dennis B. Lubahn (1 shared paper)Elizabeth Wilson (1 shared paper)Richard Petty (3 shared papers)C. D. Marsden (11 shared papers)
Journals
Brain (10 papers)Movement Disorders (10 papers)Annals of Neurology (10 papers)Journal of Neurology Neurosurgery & Psychiatry (9 papers)The Lancet (5 papers)
Partner nations
United KingdomUnited StatesIndia

In The Last Decade

A. E. Harding

88 papers receiving 10.7k citations

A. E. Harding's Hit Papers

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy 1991 · 2.1k citations
2.1k0+14+28Years since publication50010001.5k2.0k
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

  • it has ≥500 total citations;
  • it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
  • it reaches the top citation threshold in at least one of its specific research topics.
  1. 1991 Nature
  2. 1990 PubMed
  3. 1988 Nature
  4. 1983 The Lancet

Peers

A. E. Harding
Comparison fields: 5 of 130
  • Clinical Biochemistry 3.1k
  • Cellular and Molecular Neuroscience 4.7k
  • Neurology 2.6k
  • Neurology 1.3k
  • Molecular Biology 7.6k
Replace Laurence A. Bindoff with:
Laurence A. Bindoff Norway
Massimo Pandolfo Belgium
Caterina Mariotti Italy
Laurie J. Ozelius United States
Albert R. La Spada United States
Maurizio Moggio Italy
Thomas D. Bird United States
Yu‐ichi Goto Japan
Tetsuo Ashizawa United States
Robert H. Baloh United States
A. E. Harding relative to Laurence A. Bindoff Norway Laurence A. Bindoff's profile →
Citations per field
00.5×2×3.3×
Laurence A. Bindoff · 1×
Citations per year

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-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.

Border = papers with A. E. Harding Line = papers co-authored together A. E. Harding links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 88 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
Nature ·Albert R. La Spada, Elizabeth Wilson, Dennis B. Lubahn, A. E. Harding, Kenneth H. Fischbeck
Hit paper breakdown →		19912124
2
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
Nature ·Ian Holt, A. E. Harding, J A Morgan-Hughes
Hit paper breakdown →		19881352
3
A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.
PubMed ·Ian Holt, A. E. Harding, Richard Petty, J A Morgan-Hughes
Hit paper breakdown →		1990776
4
CLASSIFICATION OF THE HEREDITARY ATAXIAS AND PARAPLEGIAS
The Lancet ·A. E. Harding
Hit paper breakdown →		1983697
5
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
Brain ·Paul Riordan‐Eva, M D Sanders, G.G. Govan, Mary G. Sweeney, J Da Costa, A. E. Harding
1995374
6
Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease
The Lancet ·Colin Smith, C. Roland Wolf, A C Gough, Nigel K. Spurr, P. Nigel Leigh, Beatrice A. Summers, A. E. Harding, D.M Maranganore, S. Sturman, Adrian C. Williams, Anthony H.V. Schapira
1992346
7
Clinical features and classification of inherited ataxias.
PubMed ·A. E. Harding
1993339
8
THE CLINICAL FEATURES OF MITOCHONDRIAL MYOPATHY
Brain ·Richard Petty, A. E. Harding, J A Morgan-Hughes
1986315
9
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA
The Lancet ·William Reardon, Marcus Pembrey, Richard C. Trembath, Richard Ross, Mary G. Sweeney, A. E. Harding, Linda Luxon
1992295
10
Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA
Annals of Neurology ·Ian Holt, A. E. Harding, Jonathan M. Cooper, Anthony H.V. Schapira, António Toscano, J. B. Clark, J A Morgan-Hughes
1989264
11
Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA.
PubMed ·M A McShane, Simon Hammans, M G Sweeney, Ian Holt, T. James Beattie, E M Brett, A. E. Harding
1991191
12
Neuroacanthocytosis. A clinical, haematological and pathological study of 19 cases.
PubMed ·R Hardie, H. PULLON, A. E. Harding, J.S. Owen, Manuel Melo Pires, Geoff Daniels, Y Imai, Virendra Misra, R. H. M. King, Judith M. Jacobs
1991180
13
A genetic study of idiopathic focal dystonias
Annals of Neurology ·Heather Waddy, Nicholas Fletcher, A. E. Harding, C. D. Marsden
1991175
14
Striatal D1 and D2 dopamine receptor loss in asymptomatic mutation carriers of Huntington's disease
Annals of Neurology ·R. A. Weeks, Paola Piccini, A. E. Harding, David J. Brooks
1996160
15
Parkinson's disease in twins studied with 18 F‐dopa and positron emission tomography
Neurology ·David J. Burn, M. H. Mark, E. Diane Playford, Demetrius M. Maraganore, Thomas Zimmerman, Roger C. Duvoisin, A. E. Harding, C. D. Marsden, David J. Brooks
1992153
16
INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION: 2. CLINICAL AND PATHOLOGICAL FEATURES
Brain ·John Collinge, Jeremy M. Brown, John Hardy, Michael Mullan, Martin N. Rossor, H. F. Baker, T.J. Crow, R. Lofthouse, Mark Poulter, R.M. Ridley, F. Owen, Craig L. Bennett, Gary R. Dunn, A. E. Harding, Niall Quinn, Bhavya S. Doshi, G.W. Roberts, Mrinalini Honavar, I. Janota, P. L. Lantos
1992139
17
Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples
The Lancet ·Simon Hammans, M G Sweeney, Martin Brockington, J A Morgan-Hughes, A. E. Harding
1991137
18
The mitochondrial DNA transfer RNA Leu(UUR) A→G(3243) mutation: A clinical and genetic study
Brain ·Simon Hammans, Mary G. Sweeney, Michael G. Hanna, Martin Brockington, J A Morgan-Hughes, A. E. Harding
1995123
19
A clinical and genetic study of familial Parkinson's disease
Movement Disorders ·Demetrius M. Maraganore, A. E. Harding, C. D. Marsden
1991113
20
Striatal D1 and D2 receptor binding in patients with Huntington's disease and other choreas A PET study
Brain ·N. Turjanski, R. A. Weeks, Raymond J. Dolan, A. E. Harding, David J. Brooks
1995108

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 88 papers that have together received 11.1k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (39 papers), Genetic Neurodegenerative Diseases (31 papers), Metabolism and Genetic Disorders (30 papers), Hereditary Neurological Disorders (15 papers), Neurological disorders and treatments (13 papers), Neurological diseases and metabolism (13 papers), ATP Synthase and ATPases Research (11 papers) and Botulinum Toxin and Related Neurological Disorders (7 papers). The work is most often cited by research in Clinical Biochemistry (3.1k citations), Cellular and Molecular Neuroscience (4.7k citations), Neurology (2.6k citations), Neurology (1.3k citations) and Molecular Biology (7.6k citations). A. E. Harding has collaborated with scholars based in United Kingdom, United States and India. Frequent 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. Their work appears in journals such as Brain, Movement Disorders, Annals of Neurology, Journal of Neurology Neurosurgery & Psychiatry and The Lancet.

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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