Brian Harding

11.2k total citations · 1 hit paper
162 papers, 6.9k citations indexed

About

Brian Harding is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, Brian Harding has authored 162 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Molecular Biology, 30 papers in Epidemiology and 26 papers in Genetics. Recurrent topics in Brian Harding's work include Glioma Diagnosis and Treatment (23 papers), Epilepsy research and treatment (19 papers) and Neuroendocrine Tumor Research Advances (16 papers). Brian Harding is often cited by papers focused on Glioma Diagnosis and Treatment (23 papers), Epilepsy research and treatment (19 papers) and Neuroendocrine Tumor Research Advances (16 papers). Brian Harding collaborates with scholars based in United Kingdom, United States and Canada. Brian Harding's co-authors include Rajesh V. Thakker, I. C. M. MacLennan, Maria Thom, Sanjay M. Sisodiya, J. Helen Cross, M. V. Squier, Sarah E. Lloyd, M. Andrew Nesbit, John P. Blass and Gary E. Gibson and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Brian Harding

162 papers receiving 6.6k 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.

A common molecular basis for three inherited kidney stone diseases

1996 556 citations Sarah E. Lloyd, Brian Harding et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Brian Harding United Kingdom	46	2.8k	1.1k	1.1k	1.0k	969	162	6.9k
Marcella Devoto Italy	45	2.7k 0.9×	354 0.3×	1.8k 1.7×	490 0.5×	160 0.2×	161	6.6k
Anthony T. Yachnis United States	46	2.4k 0.9×	750 0.7×	934 0.9×	588 0.6×	187 0.2×	143	6.4k
Wuh‐Liang Hwu Taiwan	47	3.2k 1.1×	733 0.7×	1.3k 1.2×	236 0.2×	548 0.6×	394	8.9k
Thierry Frébourg France	60	6.5k 2.3×	384 0.3×	2.7k 2.5×	4.5k 4.3×	518 0.5×	276	14.1k
Didier Lacombe France	48	4.0k 1.4×	819 0.7×	2.7k 2.5×	561 0.5×	160 0.2×	322	7.8k
Hans Scheffer Netherlands	47	3.7k 1.3×	465 0.4×	2.7k 2.5×	341 0.3×	340 0.4×	191	7.9k
David M. Kurnit United States	37	4.7k 1.6×	281 0.3×	1.5k 1.4×	690 0.7×	140 0.1×	116	8.0k
Dirk Troost Netherlands	59	4.4k 1.5×	982 0.9×	629 0.6×	1.1k 1.0×	1.4k 1.5×	197	11.3k
Kiyoshi Hayasaka Japan	38	2.5k 0.9×	745 0.7×	1.0k 0.9×	157 0.1×	400 0.4×	235	6.0k
G.A.P. Bruns United States	50	6.0k 2.1×	492 0.4×	1.9k 1.7×	805 0.8×	142 0.1×	108	9.7k

Countries citing papers authored by Brian Harding

Since Specialization

Citations

This map shows the geographic impact of Brian 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 Brian Harding with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brian Harding more than expected).

Fields of papers citing papers by Brian Harding

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brian 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 Brian Harding. The network helps show where Brian Harding may publish in the future.

Co-authorship network of co-authors of Brian Harding

This figure shows the co-authorship network connecting the top 25 collaborators of Brian Harding. A scholar is included among the top collaborators of Brian 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 Brian Harding. Brian 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

McCormick, Elizabeth M., Julie P. Taylor, Alison J. Coffey, et al.. (2023). Expert Panel Curation of 113 Primary Mitochondrial Disease Genes for the Leigh Syndrome Spectrum. Annals of Neurology. 94(4). 696–712. 23 indexed citations

Boda, Enrica, Roberta Parolisi, Brian Harding, et al.. (2022). Molecular and functional heterogeneity in dorsal and ventral oligodendrocyte progenitor cells of the mouse forebrain in response to DNA damage. Nature Communications. 13(1). 2331–2331. 14 indexed citations

Helman, Guy, Ayelet Zerem, Sarah Woidill, et al.. (2021). Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating Leukodystrophy. Pediatric Neurology. 121. 11–19. 4 indexed citations

Harding, Brian, Séverine Drunat, Omar Soukarieh, et al.. (2016). Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons. The American Journal of Human Genetics. 99(2). 511–520. 47 indexed citations

Gorvin, Caroline M., Martijn J. Wilmer, Siân E. Piret, et al.. (2013). Receptor-mediated endocytosis and endosomal acidification is impaired in proximal tubule epithelial cells of Dent disease patients. Proceedings of the National Academy of Sciences. 110(17). 7014–7019. 67 indexed citations

Walls, Gerard, Michael R. Bowl, Jeshmi Jeyabalan, et al.. (2009). Mice deleted for the hyperparathyroidism-jaw tumour (HPT-JT) syndrome allele have abnormal parathyroids with increased proliferation rates. 19. 1 indexed citations

Christie, Paul T., et al.. (2007). Characterisation of 25 calcium-sensing receptor mutations in disorders of calcium homeostasis. 13(6). 1767–1780. 1 indexed citations

Lemos, Manuel C., Brian Harding, Michael R. Bowl, et al.. (2007). Mice deleted for a Multiple Endocrine Neoplasia Type 1 (MEN1) allele develop pancreatic, pituitary and parathyroid tumours in association with hypercalcaemia. 2 indexed citations

Lemos, Manuel C., Brian Harding, & Rajesh V. Thakker. (2007). Genetic background influences expression of Multiple Endocrine Neoplasia type 1 (MEN1) mutation, implicating a role for genetic modifiers. 2 indexed citations

10.

McLellan, Ailsa, Sharon Davies, Isobel Heyman, et al.. (2007). Psychopathology in children with epilepsy before and after temporal lobe resection. Developmental Medicine & Child Neurology. 47(10). 666–672. 23 indexed citations

11.

Kennedy, Ann, Paul T. Christie, Brian Harding, et al.. (2003). Matrix metalloproteinase 13 (MMP13) mutation causes spondyloepimetaphyseal dysplasia (SEMD), Missouri variant. 5(18). 25–6. 2 indexed citations

12.

Christie, Paul T., Brian Harding, Michael R. Bowl, et al.. (2002). An activating calcium sensing receptor mutation associated with normocalcemic (idiopathic) hypercalciuric nephrolithiasis.. Journal of Bone and Mineral Research. 17. 3 indexed citations

13.

Gordon, I., et al.. (2002). Correlation of SPECT with pathology and seizure outcome in children undergoing epilepsy surgery. Developmental Medicine & Child Neurology. 44(10). 676–680. 11 indexed citations

14.

Sisodiya, Sanjay M., et al.. (2002). Drug resistance in epilepsy: expression of drug resistance proteins in common causes of refractory epilepsy. Brain. 125(1). 22–31. 364 indexed citations

15.

Harding, Brian, et al.. (2001). Bilateral hippocampal granule cell dispersion: autopsy study of 3 infants. Neuropathology and Applied Neurobiology. 27(3). 245–251. 19 indexed citations

16.

Christie, Paul T., Brian Harding, M. Andrew Nesbit, Michael P. Whyte, & Rajesh V. Thakker. (2001). X-Linked Hypophosphatemia Attributable to Pseudoexons of the PHEX Gene. The Journal of Clinical Endocrinology & Metabolism. 86(8). 3840–3844. 48 indexed citations

17.

Bassett, J. H. Duncan, Penny Rashbass, Brian Harding, et al.. (1999). Studies of the Murine Homolog of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene, men1. Journal of Bone and Mineral Research. 14(1). 3–10. 39 indexed citations

18.

Pang, J T, Sarah E. Lloyd, C Wooding, et al.. (1996). Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11g13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene. Human Genetics. 97(6). 732–741. 29 indexed citations

19.

Harding, Brian, David B. Dunger, David Grant, & Magda Erdohazi. (1988). Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities.. Journal of Neurology Neurosurgery & Psychiatry. 51(3). 385–390. 49 indexed citations

20.

MacLennan, I. C. M., G. Loewi, & Brian Harding. (1970). The role of immunoglobulins in lymphocyte-mediated cell damage, in vitro. I. Comparison of the effects of target cell specific antibody and normal serum factors on cellular damage by immune and non-immune lymphocytes.. PubMed. 18(3). 397–404. 110 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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