James McGill
Impact in
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
- Genetics top 5%
- Connective tissue disorders research
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 14
- Connective tissue disorders research 8
- Genomic variations and chromosomal abnormalities 3
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- Mitochondrial Function and Pathology 3
- Glycosylation and Glycoproteins Research 2
- Co-authors
- Vazken M. Der Kaloustian (2 shared papers)Sharron Townshend (5 shared papers)Robert S. Ware (5 shared papers)David Sillence (5 shared papers)Ravi Savarirayan (5 shared papers)Andreas Zankl (5 shared papers)J. Ault (5 shared papers)Verity Pacey (5 shared papers)
- Journals
- The Medical Journal of Australia (4 papers)Journal of Inherited Metabolic Disease (4 papers)Journal of Medical Genetics (3 papers)Developmental Medicine & Child Neurology (2 papers)Clinical Genetics (2 papers)
- Partner nations
- AustraliaUnited StatesCanada
In The Last Decade
James McGill
36 papers receiving 738 citations
Peers
Comparison fields: 5 of 97
- Clinical Biochemistry 165
- Genetics 377
- Pediatrics, Perinatology and Child Health 110
- Molecular Biology 335
- Rheumatology 56
Countries citing papers authored by James McGill
This map shows the geographic impact of James McGill'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 James McGill with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James McGill more than expected).
Fields of papers citing papers by James McGill
This network shows the impact of papers produced by James McGill. 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 James McGill. The network helps show where James McGill may publish in the future.
Co-authors
The 25 scholars most cited alongside James McGill, 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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1996 | 83 | |
| 2 | 1999 | 78 | |
| 3 | 1994 | 56 | |
| 4 | 2011 | 53 | |
| 5 | 1990 | 51 | |
| 6 | 2012 | 50 | |
| 7 | 2010 | 34 | |
| 8 | 2006 | 31 | |
| 9 | 2007 | 28 | |
| 10 | 1990 | 26 | |
| 11 | 1991 | 26 | |
| 12 | 2018 | 23 | |
| 13 | 2009 | 22 | |
| 14 | 2011 | 19 | |
| 15 | 1992 | 19 | |
| 16 | 2019 | 18 | |
| 17 | 1995 | 18 | |
| 18 | 1991 | 16 | |
| 19 | 2005 | 15 | |
| 20 | 1999 | 14 |
About James McGill
James McGill is a scholar working on Genetics, Molecular Biology, Clinical Biochemistry, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 37 papers that have together received 777 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (12 papers), Connective tissue disorders research (8 papers), Neonatal Health and Biochemistry (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Mitochondrial Function and Pathology (3 papers), Glycosylation and Glycoproteins Research (2 papers), Galectins and Cancer Biology (2 papers) and Carbohydrate Chemistry and Synthesis (2 papers). The work is most often cited by research in Clinical Biochemistry (165 citations), Genetics (377 citations), Pediatrics, Perinatology and Child Health (110 citations), Molecular Biology (335 citations) and Rheumatology (56 citations). James McGill has collaborated with scholars based in Australia, United States and Canada. Frequent co-authors include Vazken M. Der Kaloustian, Sharron Townshend, Robert S. Ware, David Sillence, Ravi Savarirayan, Andreas Zankl, J. Ault, Verity Pacey, Leanne M. Johnston and David Coman. Their work appears in journals such as The Medical Journal of Australia, Journal of Inherited Metabolic Disease, Journal of Medical Genetics, Developmental Medicine & Child Neurology and Clinical 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.