Christopher Bennett
Impact in
- Genetics top 1%
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Connective tissue disorders research
- Developmental Biology top 5%
Papers in
- Genetics 27
- Genomics and Rare Diseases 12
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 4
- Genetic and rare skin diseases. 4
- Genetic and Kidney Cyst Diseases 4
- Connective tissue disorders research 4
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- Glycogen Storage Diseases and Myoclonus 4
- Co-authors
- Mushtaq Ahmed (4 shared papers)David Bruce Grant (1 shared paper)MaryJ. Seller (3 shared papers)Pramila Ramani (1 shared paper)J. Ross Hawkins (1 shared paper)Stephanie A. Robb (1 shared paper)Zoe Docherty (1 shared paper)Sandeep Uppal (2 shared papers)
- Journals
- Journal of Medical Genetics (7 papers)The American Journal of Human Genetics (3 papers)Nature Genetics (3 papers)Nature Communications (2 papers)Human Mutation (2 papers)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Christopher Bennett
39 papers receiving 2.8k citations
Christopher Bennett's Hit Papers
Peers
Comparison fields: 5 of 95
- Genetics 1.5k
- Developmental Biology 38
- Rheumatology 240
- Psychiatry and Mental health 217
- Clinical Biochemistry 48
Countries citing papers authored by Christopher Bennett
This map shows the geographic impact of Christopher Bennett'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 Christopher Bennett with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher Bennett more than expected).
Fields of papers citing papers by Christopher Bennett
This network shows the impact of papers produced by Christopher Bennett. 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 Christopher Bennett. The network helps show where Christopher Bennett may publish in the future.
Co-authors
The 25 scholars most cited alongside Christopher Bennett, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Evidence for 28 genetic disorders discovered by combining healthcare and research data Hit paper breakdown → | 2020 | 417 |
| 2 | 2008 | 246 | |
| 3 | 2006 | 240 | |
| 4 | 2012 | 184 | |
| 5 | 1993 | 148 | |
| 6 | 2011 | 142 | |
| 7 | 2018 | 137 | |
| 8 | 2014 | 134 | |
| 9 | 2014 | 113 | |
| 10 | 2017 | 113 | |
| 11 | 2018 | 95 | |
| 12 | Novel mutations and deletions of the KIT (steel factor receptor) gene in human piebaldism. | 1995 | 86 |
| 13 | 2007 | 81 | |
| 14 | 2012 | 75 | |
| 15 | 2012 | 68 | |
| 16 | 2019 | 63 | |
| 17 | 1991 | 61 | |
| 18 | 2017 | 56 | |
| 19 | 2019 | 49 | |
| 20 | 2012 | 48 |
About Christopher Bennett
Christopher Bennett is a scholar working on Genetics, Rheumatology, Developmental Biology, Pediatrics, Perinatology and Child Health and Psychiatry and Mental health, having authored 41 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetic and rare skin diseases. (4 papers), Glycogen Storage Diseases and Myoclonus (4 papers), Genetic and Kidney Cyst Diseases (4 papers), Connective tissue disorders research (4 papers) and Congenital limb and hand anomalies (3 papers). The work is most often cited by research in Genetics (1.5k citations), Developmental Biology (38 citations), Rheumatology (240 citations), Psychiatry and Mental health (217 citations) and Clinical Biochemistry (48 citations). Christopher Bennett has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Mushtaq Ahmed, David Bruce Grant, MaryJ. Seller, Pramila Ramani, J. Ross Hawkins, Stephanie A. Robb, Zoe Docherty, Sandeep Uppal, Ian Carr and David T. Bonthron. Their work appears in journals such as Journal of Medical Genetics, The American Journal of Human Genetics, Nature Genetics, Nature Communications and Human Mutation.
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.