John Broxholme

4.4k total citations
25 papers, 898 citations indexed

About

John Broxholme is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, John Broxholme has authored 25 papers receiving a total of 898 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Immunology. Recurrent topics in John Broxholme's work include Genetic Associations and Epidemiology (4 papers), Single-cell and spatial transcriptomics (2 papers) and Genetic Mapping and Diversity in Plants and Animals (2 papers). John Broxholme is often cited by papers focused on Genetic Associations and Epidemiology (4 papers), Single-cell and spatial transcriptomics (2 papers) and Genetic Mapping and Diversity in Plants and Animals (2 papers). John Broxholme collaborates with scholars based in United Kingdom, United States and Germany. John Broxholme's co-authors include Helen Lockstone, Edward Blair, Sandra Marisa Oliveira, Houman Ashrafian, Bronwyn Kerr, Ingegerd Östman‐Smith, Hugh Watkins, Charles Redwood, Anthony P. Salmon and Eshita Sharma and has published in prestigious journals such as Nature Communications, Bioinformatics and PLoS ONE.

In The Last Decade

John Broxholme

25 papers receiving 888 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
John Broxholme United Kingdom 16 465 258 143 104 98 25 898
Damián Heine‐Suñer Spain 18 447 1.0× 311 1.2× 153 1.1× 140 1.3× 66 0.7× 50 879
André Schaller Switzerland 19 697 1.5× 145 0.6× 125 0.9× 80 0.8× 64 0.7× 74 1.2k
Dorota Monies Saudi Arabia 22 579 1.2× 507 2.0× 188 1.3× 99 1.0× 25 0.3× 48 1.3k
Haike Reznik‐Wolf Israel 15 554 1.2× 171 0.7× 128 0.9× 83 0.8× 23 0.2× 39 888
Pieter Faber United States 15 1.0k 2.2× 190 0.7× 200 1.4× 78 0.8× 26 0.3× 22 1.6k
Weihong Zhao China 15 402 0.9× 260 1.0× 91 0.6× 67 0.6× 36 0.4× 24 742
Yves Sznajer Belgium 19 623 1.3× 373 1.4× 117 0.8× 106 1.0× 27 0.3× 50 1.1k
Lifeng Tian United States 15 474 1.0× 366 1.4× 81 0.6× 82 0.8× 23 0.2× 47 900
Pagon Ra United States 6 450 1.0× 260 1.0× 86 0.6× 49 0.5× 57 0.6× 291 791
Koichiro Higasa Japan 20 794 1.7× 229 0.9× 149 1.0× 88 0.8× 23 0.2× 72 1.4k

Countries citing papers authored by John Broxholme

Since Specialization
Citations

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

Fields of papers citing papers by John Broxholme

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John Broxholme

This figure shows the co-authorship network connecting the top 25 collaborators of John Broxholme. A scholar is included among the top collaborators of John Broxholme 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 John Broxholme. John Broxholme is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Thackray, Benjamin D., Vicky Ball, Brett W. C. Kennedy, et al.. (2024). AICAR confers prophylactic cardioprotection in doxorubicin-induced heart failure in rats. Journal of Molecular and Cellular Cardiology. 191. 12–22. 3 indexed citations
2.
Mifsud, Karen R., et al.. (2023). Genomic regulation of Krüppel-like-factor family members by corticosteroid receptors in the rat brain. Neurobiology of Stress. 23. 100532–100532. 7 indexed citations
3.
Mifsud, Karen R., Silvia Salatino, Eshita Sharma, et al.. (2021). Distinct regulation of hippocampal neuroplasticity and ciliary genes by corticosteroid receptors. Nature Communications. 12(1). 4737–4737. 37 indexed citations
4.
Hargreaves, Chantal E., Silvia Salatino, Sarah C. Sasson, et al.. (2021). Decreased ATM Function Causes Delayed DNA Repair and Apoptosis in Common Variable Immunodeficiency Disorders. Journal of Clinical Immunology. 41(6). 1315–1330. 8 indexed citations
5.
Timm, Kerstin N., Vicky Ball, John A. Henry, et al.. (2020). Early detection of doxorubicin-induced cardiotoxicity in rats by its cardiac metabolic signature assessed with hyperpolarized MRI. Communications Biology. 3(1). 692–692. 32 indexed citations
6.
Goulart, Michelle R., Yu‐Mei Chang, Gerry Polton, et al.. (2019). Phenotypic and transcriptomic characterization of canine myeloid-derived suppressor cells. Scientific Reports. 9(1). 3574–3574. 28 indexed citations
7.
Attar, Moustafa, Eshita Sharma, Shuqiang Li, et al.. (2018). A practical solution for preserving single cells for RNA sequencing. Scientific Reports. 8(1). 2151–2151. 47 indexed citations
8.
Wills, Quin F., Esther Mellado-Gomez, Rory Nolan, et al.. (2017). The nature and nurture of cell heterogeneity: accounting for macrophage gene-environment interactions with single-cell RNA-Seq. BMC Genomics. 18(1). 53–53. 14 indexed citations
9.
Shanks, Morag, Susan M. Downes, Richard R. Copley, et al.. (2012). Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease. European Journal of Human Genetics. 21(3). 274–280. 104 indexed citations
10.
Min, Josine L., Jennifer M. Taylor, J. Brent Richards, et al.. (2011). The Use of Genome-Wide eQTL Associations in Lymphoblastoid Cell Lines to Identify Novel Genetic Pathways Involved in Complex Traits. PLoS ONE. 6(7). e22070–e22070. 28 indexed citations
11.
Vandiedonck, Claire, Martin S. Taylor, Helen Lockstone, et al.. (2011). Pervasive haplotypic variation in the spliceo-transcriptome of the human major histocompatibility complex. Genome Research. 21(7). 1042–1054. 58 indexed citations
12.
Lawrence, Robert, Aaron Day-Williams, Richard Mott, et al.. (2009). GLIDERS - A web-based search engine for genome-wide linkage disequilibrium between HapMap SNPs. BMC Bioinformatics. 10(1). 367–367. 23 indexed citations
13.
Hennig, Branwen J., Katherine Fielding, John Broxholme, et al.. (2008). Host Genetic Factors and Vaccine-Induced Immunity to Hepatitis B Virus Infection. PLoS ONE. 3(3). e1898–e1898. 81 indexed citations
14.
Morar, Nilesh, Stephan Weidinger, Wei‐Li Di, et al.. (2007). Positional cloning of susceptibility genes for atopic dermatitis in the epidermal differentiation complex. mediaTUM (Technical University of Munich). 1 indexed citations
15.
Hoffmann, Sigrid, Pamela J. Kaisaki, Patrick Danoy, et al.. (2005). Missense Mutation in Sterile α Motif of Novel Protein SamCystin is Associated with Polycystic Kidney Disease in (cy/+) Rat. Journal of the American Society of Nephrology. 16(12). 3517–3526. 73 indexed citations
16.
Ke, Xiayi, Marcos Miretti, John Broxholme, et al.. (2005). A comparison of tagging methods and their tagging space. Human Molecular Genetics. 14(18). 2757–2767. 30 indexed citations
17.
Traherne, James A., Michael Hill, Pirro G. Hysi, et al.. (2003). LD mapping of maternally and non-maternally derived alleles and atopy in FcεRI-β. Human Molecular Genetics. 12(20). 2577–2585. 29 indexed citations
18.
Williams, Charlene J., Yun Zhang, Andrew E. Timms, et al.. (2002). Autosomal Dominant Familial Calcium Pyrophosphate Dihydrate Deposition Disease Is Caused by Mutation in the Transmembrane Protein ANKH. The American Journal of Human Genetics. 71(4). 985–991. 85 indexed citations
19.
Anderson, Gavin, N. I. Leaves, Sumit Bhattacharyya, et al.. (2002). Positive association to IgE levels and a physical map of the 13q14 atopy locus. European Journal of Human Genetics. 10(4). 266–270. 17 indexed citations
20.
Blair, Edward, Charles Redwood, Houman Ashrafian, et al.. (2001). Mutations in the gamma2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis.. Journal of Medical Genetics. 38. 115 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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