Brian Harding

161 papers receiving 6.6k citations

Brian Harding's Hit Papers

A common molecular basis for three inherited kidney stone diseases 1996 · 559 citations
5590+10+20Years since publication100200300400500

Peers

Brian Harding
Comparison fields: 5 of 121
  • Nephrology 566
  • Clinical Biochemistry 435
  • Psychiatry and Mental health 847
  • Genetics 585
  • Neurology 693
Replace Hans Scheffer with:
Hans Scheffer Netherlands
Thierry Frébourg France
Didier Lacombe France
Raphael Schiffmann United States
Lionel Van Maldergem Belgium
Marcella Devoto Italy
David M. Kurnit United States
Robert Kleta United Kingdom
Tania Attié‐Bitach France
G.A.P. Bruns United States
Brian Harding relative to Hans Scheffer Netherlands Hans Scheffer's profile →
Citations per field
00.5×6.7×
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-authors

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

Showing the 20 most-cited of 162 papers — load more, or switch the sort, to bring in the rest.

#Work
1
A common molecular basis for three inherited kidney stone diseases
Hit paper breakdown →
1996559
2 2000403
3 2002365
4 1988355
5 1998296
6 2004122
7 1994119
8 2007110
9
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.
1970110
10 1990104
11 197199
12 200498
13 201489
14 200584
15 200683
16 200079
17 200779
18 200977
19 200376
20 199476

About Brian Harding

Brian Harding is a scholar working on Molecular Biology, Epidemiology, Genetics, Genetics and Oncology, having authored 162 papers that have together received 6.9k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (20 papers), Epilepsy research and treatment (16 papers), Mitochondrial Function and Pathology (15 papers), Neuroendocrine Tumor Research Advances (14 papers), Metabolism and Genetic Disorders (12 papers), Parathyroid Disorders and Treatments (12 papers), Neuroblastoma Research and Treatments (10 papers) and RNA regulation and disease (9 papers). The work is most often cited by research in Nephrology (566 citations), Clinical Biochemistry (435 citations), Psychiatry and Mental health (847 citations), Genetics (585 citations) and Neurology (693 citations). Brian Harding has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include Rajesh V. Thakker, Maria Thom, I. C. M. MacLennan, Sanjay M. Sisodiya, J. Helen Cross, M. V. Squier, Sarah E. Lloyd, M. Andrew Nesbit, P. Perrino and John P. Blass. Their work appears in journals such as Neuropathology and Applied Neurobiology, The Journal of Clinical Endocrinology & Metabolism, Journal of Neuropathology & Experimental Neurology, Clinical Endocrinology 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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