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
- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 4
- Genetic and rare skin diseases. 4
- Genomics and Rare Diseases 3
- Co-authors
- F. Lucy Raymond (2 shared papers)Thomas B. Stoker (2 shared papers)Roger A. Barker (2 shared papers)Sarah Mason (1 shared paper)Julia C. Greenland (1 shared paper)Riza Yosia Sunindijo (1 shared paper)Christine Patch (2 shared papers)Cathryn M. Lewis (2 shared papers)
- Journals
- Clinical and Experimental Dermatology (6 papers)Journal of Medical Genetics (3 papers)British Journal of Dermatology (3 papers)European Journal of Human Genetics (2 papers)Gene (2 papers)
- Partner nations
- United KingdomFranceUnited States
In The Last Decade
Simon Holden
34 papers receiving 653 citations
Peers
Comparison fields: 5 of 98
- Genetics 231
- Cellular and Molecular Neuroscience 102
- Neurology 60
- Molecular Biology 279
- Radiological and Ultrasound Technology 16
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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2021 | 128 | |
| 2 | 2010 | 124 | |
| 3 | 2004 | 56 | |
| 4 | 2006 | 55 | |
| 5 | 2013 | 42 | |
| 6 | 2018 | 40 | |
| 7 | 2011 | 34 | |
| 8 | 2010 | 30 | |
| 9 | 2010 | 29 | |
| 10 | 2009 | 28 | |
| 11 | 2007 | 22 | |
| 12 | 2017 | 16 | |
| 13 | 2013 | 13 | |
| 14 | 2003 | 11 | |
| 15 | 2015 | 9 | |
| 16 | 2019 | 8 | |
| 17 | 2012 | 6 | |
| 18 | 2016 | 6 | |
| 19 | 2014 | 5 | |
| 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 37 papers that have together received 701 indexed citations. Recurring topics across this work include Congenital heart defects research (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetic and rare skin diseases. (4 papers), Genetic Neurodegenerative Diseases (3 papers), Skin and Cellular Biology Research (3 papers), Genomics and Rare Diseases (3 papers) and Mitochondrial Function and Pathology (3 papers). The work is most often cited by research in Genetics (231 citations), Cellular and Molecular Neuroscience (102 citations), Neurology (60 citations), Molecular Biology (279 citations) and Radiological and Ultrasound Technology (16 citations). Simon Holden has collaborated with scholars based in United Kingdom, France and United States. Frequent co-authors include F. Lucy Raymond, Thomas B. Stoker, Roger A. Barker, Sarah Mason, Julia C. Greenland, Riza Yosia Sunindijo, Christine Patch, Cathryn M. Lewis, Evangelos Vassos and Dan Rujescu. Their work appears in journals such as Clinical and Experimental Dermatology, Journal of Medical Genetics, British Journal of Dermatology, European Journal of Human Genetics and Gene.
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.