Brian Harding

11.2k citations
162 papers · 6.9k indexed · 1 hit paper · h-index 46

Brian Harding

162 papers receiving 6.6k citations

Hit Papers

A common molecular basis for three inherited kidney stone...5561996202620062016100200300400500

Peers

Brian Harding
Comparison fields: 5 of 124
  • Nephrology 597
  • Clinical Biochemistry 477
  • Genetics 701
  • Psychiatry and Mental health 969
  • Pediatrics, Perinatology and Child Health 1.1k
Replace Hans Scheffer with:
Hans Scheffer Netherlands
Kiyoshi Hayasaka Japan
Raphael Schiffmann United States
Thierry Frébourg France
Didier Lacombe France
Lionel Van Maldergem Belgium
Marcella Devoto Italy
Robert Kleta United Kingdom
David M. Kurnit United States
G.A.P. Bruns United States
Brian Harding relative to Hans Scheffer Netherlands Hans Scheffer's profile →
Citations per field
00.5×6.1×
Hans Scheffer · 1×
Citations per year

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

The 25 scholars most cited alongside Brian 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 Brian Harding Line = papers co-authored together Brian Harding links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 202323
2 202214
3 20214
4 201647
5 201367
6
Mice deleted for the hyperparathyroidism-jaw tumour (HPT-JT) syndrome allele have abnormal parathyroids with increased proliferation rates
20091
7 200831
8
Genetic background influences expression of Multiple Endocrine Neoplasia type 1 (MEN1) mutation, implicating a role for genetic modifiers
20072
9
Mice deleted for a Multiple Endocrine Neoplasia Type 1 (MEN1) allele develop pancreatic, pituitary and parathyroid tumours in association with hypercalcaemia
20072
10 200723
11 200348
12
An activating calcium sensing receptor mutation associated with normocalcemic (idiopathic) hypercalciuric nephrolithiasis.
20023
13 200211
14 200148
15 200119
16 200130
17 200021
18 199629
19 199521
20 198849

About Brian Harding

Brian Harding is a scholar working on Genetics, Nephrology and Developmental Neuroscience, having authored 162 papers that have together received 6.9k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (23 papers), Epilepsy research and treatment (19 papers), Neuroendocrine Tumor Research Advances (16 papers), Mitochondrial Function and Pathology (15 papers), Metabolism and Genetic Disorders (13 papers), Parathyroid Disorders and Treatments (12 papers), Neuroblastoma Research and Treatments (11 papers) and Neuroscience and Neuropharmacology Research (11 papers). The work is most often cited by research in Nephrology (597 citations), Clinical Biochemistry (477 citations) and Genetics (701 citations). Brian Harding has collaborated with scholars based in United Kingdom, United States and Canada. Frequent 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, Andrew C. Baker and Magda Erdohazi. Their work appears in journals such as Neuropathology and Applied Neurobiology, The Journal of Clinical Endocrinology & Metabolism, Journal of Neuropathology & Experimental Neurology, Brain and Journal of Medical Genetics.

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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