David J. Bunyan
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Ocular Disorders and Treatments
- Genomics and Rare Diseases
- Congenital Ear and Nasal Anomalies
- Nephrology top 5%
- Renal Diseases and Glomerulopathies
Papers in
- Genetics 34
- Genomic variations and chromosomal abnormalities 12
- Congenital Ear and Nasal Anomalies 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genetics and Neurodevelopmental Disorders 5
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- RNA regulation and disease 6
- RNA Research and Splicing 5
- Co-authors
- N. Simon Thomas (15 shared papers)David Robinson (11 shared papers)I. Karen Temple (6 shared papers)Diana Eccles (7 shared papers)Katherine Lachlan (2 shared papers)Sarah Ennis (8 shared papers)Anneke Lucassen (1 shared paper)Eleanor G. Seaby (4 shared papers)
- Journals
- Human Genetics (4 papers)European Journal of Human Genetics (3 papers)British Journal of Cancer (3 papers)Journal of Medical Genetics (3 papers)Genetics in Medicine (2 papers)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
David J. Bunyan
58 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 92
- Genetics 979
- Nephrology 188
- Developmental Biology 45
- Genetics 216
- Pathology and Forensic Medicine 304
Countries citing papers authored by David J. Bunyan
This map shows the geographic impact of David J. Bunyan'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 J. Bunyan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David J. Bunyan more than expected).
Fields of papers citing papers by David J. Bunyan
This network shows the impact of papers produced by David J. Bunyan. 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 J. Bunyan. The network helps show where David J. Bunyan may publish in the future.
Co-authors
The 25 scholars most cited alongside David J. Bunyan, 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 60 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 170 | |
| 2 | 2015 | 165 | |
| 3 | Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene. | 1996 | 138 |
| 4 | 2007 | 129 | |
| 5 | 2006 | 108 | |
| 6 | 2020 | 103 | |
| 7 | 2008 | 82 | |
| 8 | 2007 | 79 | |
| 9 | 2007 | 67 | |
| 10 | 2009 | 67 | |
| 11 | 2008 | 61 | |
| 12 | 2009 | 60 | |
| 13 | 2005 | 48 | |
| 14 | 2006 | 47 | |
| 15 | 2017 | 46 | |
| 16 | 2009 | 46 | |
| 17 | 2009 | 43 | |
| 18 | 2006 | 41 | |
| 19 | 2018 | 38 | |
| 20 | 1995 | 29 |
About David J. Bunyan
David J. Bunyan is a scholar working on Genetics, Molecular Biology, Genetics, Pathology and Forensic Medicine and Surgery, having authored 60 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Congenital Ear and Nasal Anomalies (8 papers), Genetic factors in colorectal cancer (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), RNA regulation and disease (6 papers), RNA Research and Splicing (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Cell Adhesion Molecules Research (4 papers). The work is most often cited by research in Genetics (979 citations), Nephrology (188 citations), Developmental Biology (45 citations), Genetics (216 citations) and Pathology and Forensic Medicine (304 citations). David J. Bunyan has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include N. Simon Thomas, David Robinson, I. Karen Temple, Diana Eccles, Katherine Lachlan, Sarah Ennis, Anneke Lucassen, Eleanor G. Seaby, John F. Harvey and Matthew Lyon. Their work appears in journals such as Human Genetics, European Journal of Human Genetics, British Journal of Cancer, Journal of Medical Genetics and Genetics in Medicine.
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.