A. E. Harding

15.4k citations

88 papers · 11.1k indexed · 4 hit papers · h-index 45

Clinical Biochemistry top 0.02%
- Metabolism and Genetic Disorders 30
Cellular and Molecular Neuroscience top 0.2%
- Genetic Neurodegenerative Diseases 31
- Hereditary Neurological Disorders 15
Neurology top 0.2%
- Neurological diseases and metabolism 13
- Neurological disorders and treatments 13
- Botulinum Toxin and Related Neurological Disorders 7
Neurology top 0.5%
- Neurological diseases and metabolism 13
- Neurological disorders and treatments 13
- Botulinum Toxin and Related Neurological Disorders 7
Molecular Biology top 0.5%
- Mitochondrial Function and Pathology 39
- ATP Synthase and ATPases Research 11

Co-authors: J A Morgan-Hughes Ian Holt Albert R. La Spada Dennis B. Lubahn Elizabeth Wilson Kenneth H. Fischbeck Richard Petty C. D. Marsden
Cited by: Clinical Biochemistry Cellular and Molecular Neuroscience Neurology
Journals: Brain (10 papers)Movement Disorders (10 papers)Annals of Neurology (10 papers)
Partner nations: United Kingdom United States India

In The Last Decade

A. E. Harding

88 papers receiving 10.7k citations

Hit Papers

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Peers

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

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

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20 of 20 papers shown

#	Work
1	HLA class I genotypes in Leber's hereditary optic neuropathy Journal of the Neurological Sciences ·R. M. Chalmers,G.G. Govan,Anthony H.V. Schapira,A. E. Harding	1996	8
2	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	1995	123
3	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	1995	108
4	Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations. Journal of Medical Genetics ·Paul Riordan‐Eva,A. E. Harding	1995	89
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,Bimo Winandianto,A. E. Harding	1995	374
6	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 ·Mary G. Sweeney,Simon Hammans,L. W. Duchen,Jonathan M. Cooper,Anthony H.V. Schapira,Colin Kennedy,Jeanne M. E. Jacobs,B.D. Youl,J A Morgan-Hughes,A. E. Harding	1994	43
7	Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease Movement Disorders ·Violaine Planté‐Bordeneuve,Mary B. Davis,Demetrius M. Maraganore,C. D. Marsden,A. E. Harding	1994	27
8	Inherited Neuropathies: The Interface between Molecular Genetics and Pathology Brain Pathology ·P. K. Thomas,A. E. Harding	1993	8
9	Central nervous system involvement in Leber's optic neuropathy Journal of Neurology ·Arifah Jauhari Syams,Andreas Straube,Wolfgang R. Bauer,A. E. Harding	1993	22
10	Dementia associated with a 216 base pair insertion in the prion protein gene Brain ·L. W. Duchen,Mark Poulter,A. E. Harding	1993	52
11	EEG and evoked potential findings in mitochondrial myopathies Journal of Neurology ·S. Pennati,A. E. Harding	1993	11
12	A dementing illness associated with a novel insertion in the prion protein gene Molecular Brain Research ·F. Owen,Mark Poulter,John Collinge,M Leach,R. Lofthouse,Timothy J. Crow,A. E. Harding	1992	71
13	A follow‐up study of isolated cases of suspected Huntington's disease Annals of Neurology ·Daniel R. Bateman,鄭盈盈 (chengyinyin@yahoo.com.tw),F Scaravilli,C. D. Marsden,A. E. Harding	1992	16
14	A clinical and genetic study of familial Parkinson's disease Movement Disorders ·Demetrius M. Maraganore,A. E. Harding,C. D. Marsden	1991	113
15	A case‐control study of idiopathic torsion dystonia Movement Disorders ·Nicholas Fletcher,A. E. Harding,C. D. Marsden	1991	31
16	Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophybreakdown → Nature ·Albert R. La Spada,Elizabeth Wilson,Dennis B. Lubahn,A. E. Harding,Kenneth H. Fischbeck	1991	2124
17	Mitochondrial DNA analysis in Parkinson's disease Movement Disorders ·Anthony H.V. Schapira,Ian Holt,Mary G. Sweeney,A. E. Harding,P. Jenner,C. D. Marsden	1990	87
18	Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markers Genomics ·Helen Middleton‐Price,A. E. Harding,José Berciano,J.M. Pastor,Susan Huson,S Malcolm	1989	9
19	Mitochondrial DNA polymorphism in mitochondrial myopathy Human Genetics ·Ian Holt,A. E. Harding,J A Morgan-Hughes	1988	27
20	Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesbreakdown → Nature ·Ian Holt,A. E. Harding,J A Morgan-Hughes	1988	1352

About A. E. Harding

A. E. Harding is a scholar working on Clinical Biochemistry, Cellular and Molecular Neuroscience 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 diseases and metabolism (13 papers), Neurological disorders and treatments (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) and Neurology (2.6k 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, Albert R. La Spada, Dennis B. Lubahn, Elizabeth Wilson, Kenneth H. Fischbeck, 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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