David Bourn
Impact in
Papers in
- Genetics 14
- Genomics and Rare Diseases 9
- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 2
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- Neurofibromatosis and Schwannoma Cases 6
- Co-authors
- D. Gareth Evans (4 shared papers)Tom Strachan (3 shared papers)T Strachan (3 shared papers)Simon A. Carter (1 shared paper)Lisa Strain (2 shared papers)Judith Goodship (2 shared papers)Paul Warwicker (1 shared paper)Judith A. Goodship (1 shared paper)
- Journals
- Human Genetics (3 papers)The American Journal of Human Genetics (3 papers)Journal of Medical Genetics (2 papers)Nature Communications (2 papers)Human Molecular Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
David Bourn
41 papers receiving 1.5k citations
David Bourn's Hit Papers
Peers
Comparison fields: 5 of 78
- Genetics 606
- Neurology 197
- Psychiatry and Mental health 174
- Immunology 187
- Cell Biology 76
Countries citing papers authored by David Bourn
This map shows the geographic impact of David Bourn'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 David Bourn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Bourn more than expected).
Fields of papers citing papers by David Bourn
This network shows the impact of papers produced by David Bourn. 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 David Bourn. The network helps show where David Bourn may publish in the future.
Co-authors
The 25 scholars most cited alongside David Bourn, 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 | 2006 | 176 | |
| 3 | 2017 | 113 | |
| 4 | 2018 | 95 | |
| 5 | 1994 | 82 | |
| 6 | 2006 | 81 | |
| 7 | 2019 | 63 | |
| 8 | A mutation in the neurofibromatosis type 2 tumor-suppressor gene, giving rise to widely different clinical phenotypes in two unrelated individuals. | 1994 | 59 |
| 9 | 2019 | 49 | |
| 10 | 2021 | 44 | |
| 11 | 2014 | 34 | |
| 12 | 2012 | 29 | |
| 13 | 1995 | 25 | |
| 14 | 1995 | 23 | |
| 15 | 2017 | 23 | |
| 16 | 2009 | 20 | |
| 17 | 1995 | 19 | |
| 18 | 2018 | 17 | |
| 19 | 2015 | 15 | |
| 20 | 2013 | 13 |
About David Bourn
David Bourn is a scholar working on Genetics, Neurology, Hematology, Dermatology and Pulmonary and Respiratory Medicine, having authored 41 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Neurofibromatosis and Schwannoma Cases (6 papers), RNA and protein synthesis mechanisms (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Molecular Biology Techniques and Applications (3 papers), Electrolyte and hormonal disorders (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and Skin and Cellular Biology Research (2 papers). The work is most often cited by research in Genetics (606 citations), Neurology (197 citations), Psychiatry and Mental health (174 citations), Immunology (187 citations) and Cell Biology (76 citations). David Bourn has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include D. Gareth Evans, Tom Strachan, T Strachan, Simon A. Carter, Lisa Strain, Judith Goodship, Paul Warwicker, Judith A. Goodship, Paul Mead and Yves Pirson. Their work appears in journals such as Human Genetics, The American Journal of Human Genetics, Journal of Medical Genetics, Nature Communications and Human Molecular 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.