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
- Genetic and Kidney Cyst Diseases 2
- Diabetes and associated disorders 2
- Genetic Syndromes and Imprinting 2
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- Chromatin Remodeling and Cancer 2
- Ubiquitin and proteasome pathways 2
- Co-authors
- Elizabeth Baker (2 shared papers)David F. Callen (2 shared papers)Sian Ellard (2 shared papers)Erica Woollatt (1 shared paper)Eric Haan (1 shared paper)Peter Thompson (1 shared paper)Elizabeth Thompson (1 shared paper)Meryl Altree (1 shared paper)
- Journals
- The American Journal of Human Genetics (2 papers)Orphanet Journal of Rare Diseases (1 paper)Pediatric Nephrology (1 paper)British Journal of Educational Studies (1 paper)The Journal of Physiology (1 paper)
- Partner nations
- United KingdomAustraliaNetherlands
In The Last Decade
Angus Dobbie
19 papers receiving 661 citations
Peers
Comparison fields: 5 of 71
- Genetics 284
- Clinical Biochemistry 67
- Molecular Biology 402
- Genetics 36
- Nephrology 24
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 | 91 | |
| 4 | 2011 | 61 | |
| 5 | 2016 | 59 | |
| 6 | 2016 | 50 | |
| 7 | 2011 | 33 | |
| 8 | 2008 | 33 | |
| 9 | 2002 | 29 | |
| 10 | 2013 | 27 | |
| 11 | 2018 | 25 | |
| 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, Cellular and Molecular Neuroscience and Neurology, having authored 20 papers that have together received 675 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Pancreatic function and diabetes (2 papers), Genetic and Kidney Cyst Diseases (2 papers), Diabetes and associated disorders (2 papers), Genetic Syndromes and Imprinting (2 papers), Chromatin Remodeling and Cancer (2 papers) and Ubiquitin and proteasome pathways (2 papers). The work is most often cited by research in Genetics (284 citations), Clinical Biochemistry (67 citations), Molecular Biology (402 citations), Genetics (36 citations) and Nephrology (24 citations). Angus Dobbie has collaborated with scholars based in United Kingdom, Australia and Netherlands. Frequent co-authors include Elizabeth Baker, David F. Callen, Sian Ellard, Erica Woollatt, Eric Haan, Peter Thompson, Elizabeth Thompson, Meryl Altree, Helen J. Eyre and Grant R. Sutherland. Their work appears in journals such as The American Journal of Human Genetics, Orphanet Journal of Rare Diseases, Pediatric Nephrology, British Journal of Educational Studies and The Journal of Physiology.
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.