David John Coman
Impact in
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
- Physiology top 10%
- Lysosomal Storage Disorders Research
- Diet and metabolism studies
Papers in
-
- Metabolism and Genetic Disorders 22
- Genetics 24
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 6
- Co-authors
- Joy Yaplito‐Lee (2 shared papers)Avihu Boneh (2 shared papers)Peter J. Lewindon (3 shared papers)Pekka Kannus (3 shared papers)Jaak Jaeken (6 shared papers)R. J McKinlay Gardner (4 shared papers)James J. McGill (7 shared papers)Sophie Calvert (3 shared papers)
- Journals
- Molecular Genetics and Metabolism (4 papers)European Journal of Human Genetics (4 papers)Pediatric Nephrology (3 papers)Journal of Inherited Metabolic Disease (3 papers)Fetal Diagnosis and Therapy (2 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
David John Coman
83 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 94
- Clinical Biochemistry 308
- Physiology 302
- Biochemistry 76
- Genetics 284
- Molecular Biology 600
Countries citing papers authored by David John Coman
This map shows the geographic impact of David John Coman'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 John Coman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David John Coman more than expected).
Fields of papers citing papers by David John Coman
This network shows the impact of papers produced by David John Coman. 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 John Coman. The network helps show where David John Coman may publish in the future.
Co-authors
The 25 scholars most cited alongside David John Coman, 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 90 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 140 | |
| 2 | 2008 | 74 | |
| 3 | 2017 | 56 | |
| 4 | 2010 | 56 | |
| 5 | 2011 | 54 | |
| 6 | 2013 | 52 | |
| 7 | 2007 | 49 | |
| 8 | 2020 | 49 | |
| 9 | 2006 | 43 | |
| 10 | 2008 | 43 | |
| 11 | 2010 | 39 | |
| 12 | 2006 | 37 | |
| 13 | 2007 | 35 | |
| 14 | 2010 | 35 | |
| 15 | 2009 | 33 | |
| 16 | 2009 | 31 | |
| 17 | 2013 | 30 | |
| 18 | 2007 | 29 | |
| 19 | 2018 | 28 | |
| 20 | 2015 | 25 |
About David John Coman
David John Coman is a scholar working on Clinical Biochemistry, Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health and Physiology, having authored 90 papers that have together received 1.5k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (22 papers), Mitochondrial Function and Pathology (14 papers), Glycosylation and Glycoproteins Research (10 papers), Genomic variations and chromosomal abnormalities (7 papers), Neonatal Health and Biochemistry (6 papers), Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Galectins and Cancer Biology (5 papers). The work is most often cited by research in Clinical Biochemistry (308 citations), Physiology (302 citations), Biochemistry (76 citations), Genetics (284 citations) and Molecular Biology (600 citations). David John Coman has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Joy Yaplito‐Lee, Avihu Boneh, Peter J. Lewindon, Pekka Kannus, Jaak Jaeken, R. J McKinlay Gardner, James J. McGill, Sophie Calvert, Pauline Mary Rudd and Eileen P. Treacy. Their work appears in journals such as Molecular Genetics and Metabolism, European Journal of Human Genetics, Pediatric Nephrology, Journal of Inherited Metabolic Disease and Fetal Diagnosis and Therapy.
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.