Angus Dobbie
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
Papers in
- Genetics 11
- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 3
- Diabetes and associated disorders 2
- Genetic and Kidney Cyst Diseases 2
-
- Ubiquitin and proteasome pathways 1
- Co-authors
- David F. Callen (2 shared papers)Elizabeth Baker (2 shared papers)Sian Ellard (2 shared papers)Helen J. Eyre (1 shared paper)Peter Thompson (1 shared paper)Elizabeth Thompson (1 shared paper)Meryl Altree (1 shared paper)Eric Haan (1 shared paper)
- Journals
- The American Journal of Human Genetics (2 papers)Pediatric Nephrology (1 paper)PLoS ONE (1 paper)Orphanet Journal of Rare Diseases (1 paper)British Journal of Educational Studies (1 paper)
- Partner nations
- United KingdomAustraliaNetherlands
In The Last Decade
Angus Dobbie
19 papers receiving 672 citations
Peers
Comparison fields: 5 of 68
- Genetics 250
- Clinical Biochemistry 57
- Molecular Biology 363
- Nephrology 21
- Neurology 43
Countries citing papers authored by Angus Dobbie
This map shows the geographic impact of Angus Dobbie'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 Angus Dobbie with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Angus Dobbie more than expected).
Fields of papers citing papers by Angus Dobbie
This network shows the impact of papers produced by Angus Dobbie. 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 Angus Dobbie. The network helps show where Angus Dobbie may publish in the future.
Co-authors
The 25 scholars most cited alongside Angus Dobbie, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 122 | |
| 2 | 2001 | 102 | |
| 3 | 2013 | 93 | |
| 4 | 2011 | 63 | |
| 5 | 2016 | 61 | |
| 6 | 2016 | 50 | |
| 7 | 2011 | 35 | |
| 8 | 2008 | 34 | |
| 9 | 2002 | 29 | |
| 10 | 2013 | 27 | |
| 11 | 2018 | 26 | |
| 12 | 2013 | 24 | |
| 13 | 2014 | 8 | |
| 14 | Panorthosia or Universal Reform | 1993 | 3 |
| 15 | 2003 | 2 | |
| 16 | 2005 | 2 | |
| 17 | EAST SYNDROME (EPILEPSY, ATAXIA, SENSORINEURAL DEAFNESS AND TUBULOPATHY) IS CAUSED BY MUTATIONS IN KCNJ10 | 2009 | 1 |
| 18 | Panglottia, or, Universal Language Being Part Five of His Universal Deliberation on the Reform of Human Affairs | 1989 | 1 |
| 19 | 2012 | 1 | |
| 20 | 1988 | 1 |
About Angus Dobbie
Angus Dobbie is a scholar working on Genetics, Molecular Biology, Surgery, Neurology and Oncology, having authored 20 papers that have together received 685 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Diabetes and associated disorders (2 papers), Genetic and Kidney Cyst Diseases (2 papers), Pancreatic function and diabetes (2 papers), Diabetes Management and Research (1 paper), Ubiquitin and proteasome pathways (1 paper) and Hyperglycemia and glycemic control in critically ill and hospitalized patients (1 paper). The work is most often cited by research in Genetics (250 citations), Clinical Biochemistry (57 citations), Molecular Biology (363 citations), Nephrology (21 citations) and Neurology (43 citations). Angus Dobbie has collaborated with scholars based in United Kingdom, Australia and Netherlands. Frequent co-authors include David F. Callen, Elizabeth Baker, Sian Ellard, Helen J. Eyre, Peter Thompson, Elizabeth Thompson, Meryl Altree, Eric Haan, Grant R. Sutherland and Erica Woollatt. Their work appears in journals such as The American Journal of Human Genetics, Pediatric Nephrology, PLoS ONE, Orphanet Journal of Rare Diseases and British Journal of Educational Studies.
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.