David E. Barton
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Statistics and Probability top 1%
Papers in
- Genetics 34
- Genomics and Rare Diseases 12
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- Advanced Statistical Methods and Models 8
- Co-authors
- David John Finney (1 shared paper)Uta Francke (25 shared papers)F. Noble David (19 shared papers)Norman T. J. Bailey (1 shared paper)John Riordan (1 shared paper)Byoung Se Kwon (2 shared papers)David Chaim Rubinsztein (8 shared papers)Rik Derynck (2 shared papers)
- Journals
- Biometrika (20 papers)Journal of Medical Genetics (12 papers)European Journal of Human Genetics (10 papers)Genomics (9 papers)Annals of Human Genetics (7 papers)
- Partner nations
- United KingdomUnited StatesIreland
In The Last Decade
David E. Barton
188 papers receiving 7.2k citations
David E. Barton's Hit Papers
Peers
Comparison fields: 5 of 200
- Genetics 1.4k
- Statistics and Probability 370
- Molecular Biology 2.9k
- Cellular and Molecular Neuroscience 758
- Urology 211
Countries citing papers authored by David E. Barton
This map shows the geographic impact of David E. Barton'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 E. Barton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David E. Barton more than expected).
Fields of papers citing papers by David E. Barton
This network shows the impact of papers produced by David E. Barton. 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 E. Barton. The network helps show where David E. Barton may publish in the future.
Co-authors
The 25 scholars most cited alongside David E. Barton, 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 194 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Statistical Method in Biological Assay. Hit paper breakdown → | 1966 | 787 |
| 2 | 1988 | 386 | |
| 3 | The Elements of Stochastic Processes with Applications to the Natural Sciences. Hit paper breakdown → | 1965 | 364 |
| 4 | 1988 | 327 | |
| 5 | 1959 | 227 | |
| 6 | 2018 | 167 | |
| 7 | 2001 | 158 | |
| 8 | 1988 | 150 | |
| 9 | 1991 | 139 | |
| 10 | 1987 | 137 | |
| 11 | 1994 | 125 | |
| 12 | 2017 | 124 | |
| 13 | 1993 | 119 | |
| 14 | 1952 | 118 | |
| 15 | Selective blockade of the endothelin subtype A receptor decreases early atherosclerosis in hamsters fed cholesterol. | 1995 | 112 |
| 16 | 2002 | 107 | |
| 17 | 2001 | 102 | |
| 18 | 2000 | 100 | |
| 19 | 2013 | 93 | |
| 20 | 1994 | 90 |
About David E. Barton
David E. Barton is a scholar working on Genetics, Statistics and Probability, Pediatrics, Perinatology and Child Health, Molecular Biology and Cellular and Molecular Neuroscience, having authored 194 papers that have together received 7.9k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (15 papers), Genomics and Rare Diseases (12 papers), Pediatric Urology and Nephrology Studies (12 papers), Cystic Fibrosis Research Advances (12 papers), Urological Disorders and Treatments (9 papers), Advanced Statistical Methods and Models (8 papers), Neonatal Respiratory Health Research (8 papers) and Mitochondrial Function and Pathology (8 papers). The work is most often cited by research in Genetics (1.4k citations), Statistics and Probability (370 citations), Molecular Biology (2.9k citations), Cellular and Molecular Neuroscience (758 citations) and Urology (211 citations). David E. Barton has collaborated with scholars based in United Kingdom, United States and Ireland. Frequent co-authors include David John Finney, Uta Francke, F. Noble David, Norman T. J. Bailey, John Riordan, Byoung Se Kwon, David Chaim Rubinsztein, Rik Derynck, Andrew Green and Maxine Merrington. Their work appears in journals such as Biometrika, Journal of Medical Genetics, European Journal of Human Genetics, Genomics and Annals of Human 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.