John Broxholme
Impact in
- Genetics top 10%
- Genetic and Kidney Cyst Diseases
- Genetic Associations and Epidemiology
- Nephrology top 10%
Papers in
-
- Single-cell and spatial transcriptomics 2
- RNA Research and Splicing 2
- Epigenetics and DNA Methylation 2
- Genetics 7
- Genetic Associations and Epidemiology 4
- Co-authors
- Helen Lockstone (5 shared papers)Sandra Marisa Oliveira (1 shared paper)Ingegerd Östman‐Smith (1 shared paper)Charles Redwood (1 shared paper)Hugh Watkins (1 shared paper)Anthony P. Salmon (1 shared paper)Edward Blair (1 shared paper)Bronwyn Kerr (1 shared paper)
- Journals
- PLoS ONE (3 papers)Human Molecular Genetics (2 papers)European Journal of Human Genetics (2 papers)Scientific Reports (2 papers)Nature Communications (1 paper)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
John Broxholme
25 papers receiving 898 citations
Peers
Comparison fields: 5 of 95
- Genetics 237
- Nephrology 53
- Immunology 129
- Molecular Biology 418
- Behavioral Neuroscience 19
Countries citing papers authored by John Broxholme
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
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-authors
The 25 scholars most cited alongside John Broxholme, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 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. | 2001 | 115 |
| 2 | 2012 | 105 | |
| 3 | 2002 | 85 | |
| 4 | 2008 | 81 | |
| 5 | 2005 | 74 | |
| 6 | 2011 | 59 | |
| 7 | 2007 | 56 | |
| 8 | 2018 | 47 | |
| 9 | 2021 | 39 | |
| 10 | 2020 | 34 | |
| 11 | 2005 | 31 | |
| 12 | 2003 | 29 | |
| 13 | 2019 | 28 | |
| 14 | 2011 | 28 | |
| 15 | 2009 | 23 | |
| 16 | 2002 | 17 | |
| 17 | 2017 | 14 | |
| 18 | 2012 | 10 | |
| 19 | 2021 | 8 | |
| 20 | 2022 | 7 |
About John Broxholme
John Broxholme is a scholar working on Molecular Biology, Genetics, Immunology, Epidemiology and Dermatology, having authored 25 papers that have together received 909 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (4 papers), Hepatitis B Virus Studies (2 papers), T-cell and B-cell Immunology (2 papers), Dermatology and Skin Diseases (2 papers), Electron Spin Resonance Studies (2 papers), Single-cell and spatial transcriptomics (2 papers), RNA Research and Splicing (2 papers) and Epigenetics and DNA Methylation (2 papers). The work is most often cited by research in Genetics (237 citations), Nephrology (53 citations), Immunology (129 citations), Molecular Biology (418 citations) and Behavioral Neuroscience (19 citations). John Broxholme has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Helen Lockstone, Sandra Marisa Oliveira, Ingegerd Östman‐Smith, Charles Redwood, Hugh Watkins, Anthony P. Salmon, Edward Blair, Bronwyn Kerr, Houman Ashrafian and Eshita Sharma. Their work appears in journals such as PLoS ONE, Human Molecular Genetics, European Journal of Human Genetics, Scientific Reports and Nature Communications.
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.