Simon Holden
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
-
- Genetic Neurodegenerative Diseases
Papers in
-
- Congenital heart defects research 5
- Mitochondrial Function and Pathology 3
- Genetics 15
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 4
- Genetic and rare skin diseases. 4
- Genomics and Rare Diseases 3
- Co-authors
- Sarah Mason (1 shared paper)Thomas B. Stoker (2 shared papers)Julia C. Greenland (1 shared paper)Roger A. Barker (2 shared papers)Christine Patch (2 shared papers)Evangelos Vassos (2 shared papers)Cathryn M. Lewis (2 shared papers)F. Lucy Raymond (1 shared paper)
- Journals
- Clinical and Experimental Dermatology (6 papers)Journal of Medical Genetics (3 papers)British Journal of Dermatology (3 papers)Gene (2 papers)Clinical Genetics (2 papers)
- Partner nations
- United KingdomFranceUnited States
In The Last Decade
Simon Holden
32 papers receiving 559 citations
Peers
Comparison fields: 5 of 78
- Genetics 219
- Cellular and Molecular Neuroscience 87
- Molecular Biology 296
- Neurology 61
- Developmental Biology 7
Countries citing papers authored by Simon Holden
This map shows the geographic impact of Simon Holden'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 Simon Holden with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simon Holden more than expected).
Fields of papers citing papers by Simon Holden
This network shows the impact of papers produced by Simon Holden. 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 Simon Holden. The network helps show where Simon Holden may publish in the future.
Co-authors
The 25 scholars most cited alongside Simon Holden, 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 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 119 | |
| 2 | 2021 | 112 | |
| 3 | 2004 | 54 | |
| 4 | 2006 | 48 | |
| 5 | 2013 | 33 | |
| 6 | 2011 | 30 | |
| 7 | 2010 | 29 | |
| 8 | 2009 | 23 | |
| 9 | 2007 | 19 | |
| 10 | 2017 | 15 | |
| 11 | 2010 | 13 | |
| 12 | 2003 | 11 | |
| 13 | 2013 | 10 | |
| 14 | 2019 | 8 | |
| 15 | 2015 | 7 | |
| 16 | 2012 | 6 | |
| 17 | 2016 | 6 | |
| 18 | 2014 | 5 | |
| 19 | 2019 | 4 | |
| 20 | 2023 | 4 |
About Simon Holden
Simon Holden is a scholar working on Molecular Biology, Genetics, Surgery, Pathology and Forensic Medicine and Cell Biology, having authored 35 papers that have together received 585 indexed citations. Recurring topics across this work include Congenital heart defects research (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genetic and rare skin diseases. (4 papers), Mitochondrial Function and Pathology (3 papers), Skin and Cellular Biology Research (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (219 citations), Cellular and Molecular Neuroscience (87 citations), Molecular Biology (296 citations), Neurology (61 citations) and Developmental Biology (7 citations). Simon Holden has collaborated with scholars based in United Kingdom, France and United States. Frequent co-authors include Sarah Mason, Thomas B. Stoker, Julia C. Greenland, Roger A. Barker, Christine Patch, Evangelos Vassos, Cathryn M. Lewis, F. Lucy Raymond, David Collier and Dan Rujescu. Their work appears in journals such as Clinical and Experimental Dermatology, Journal of Medical Genetics, British Journal of Dermatology, Gene and Clinical 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.