Peter G. Procopis
Impact in
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
- Neurology top 10%
- Peripheral Neuropathies and Disorders
Papers in
-
- RNA regulation and disease 3
- Mitochondrial Function and Pathology 3
- ATP Synthase and ATPases Research 2
-
- Neonatal Health and Biochemistry 2
- Pharmacological Effects and Toxicity Studies 2
- Co-authors
- Robert Ouvrier (5 shared papers)Monique M. Ryan (4 shared papers)Jayne Antony (4 shared papers)Padraic J. Grattan‐Smith (2 shared papers)Graeme Morgan (1 shared paper)B Turner (2 shared papers)Brian Turner (1 shared paper)John Christodoulou (3 shared papers)
- Journals
- The Medical Journal of Australia (5 papers)Pediatric Neurology (2 papers)Acta Paediatrica (1 paper)Mitochondrion (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- AustraliaUnited StatesSingapore
In The Last Decade
Peter G. Procopis
28 papers receiving 430 citations
Peers
Comparison fields: 5 of 59
- Clinical Biochemistry 72
- Neurology 100
- Cellular and Molecular Neuroscience 83
- Psychiatry and Mental health 39
- Genetics 78
Countries citing papers authored by Peter G. Procopis
This map shows the geographic impact of Peter G. Procopis'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 Peter G. Procopis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter G. Procopis more than expected).
Fields of papers citing papers by Peter G. Procopis
This network shows the impact of papers produced by Peter G. Procopis. 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 Peter G. Procopis. The network helps show where Peter G. Procopis may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter G. Procopis, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 76 | |
| 2 | 2014 | 58 | |
| 3 | 2018 | 57 | |
| 4 | 1979 | 43 | |
| 5 | 1972 | 37 | |
| 6 | 1999 | 30 | |
| 7 | 2000 | 27 | |
| 8 | 1971 | 15 | |
| 9 | 1967 | 13 | |
| 10 | 2010 | 12 | |
| 11 | 2000 | 11 | |
| 12 | 1971 | 11 | |
| 13 | 1992 | 10 | |
| 14 | 1987 | 10 | |
| 15 | 1982 | 9 | |
| 16 | 1991 | 8 | |
| 17 | 1975 | 8 | |
| 18 | 2019 | 7 | |
| 19 | 2002 | 7 | |
| 20 | 1986 | 5 |
About Peter G. Procopis
Peter G. Procopis is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Infectious Diseases, Surgery and Neurology, having authored 28 papers that have together received 466 indexed citations. Recurring topics across this work include RNA regulation and disease (3 papers), Metabolism and Genetic Disorders (3 papers), Mitochondrial Function and Pathology (3 papers), Neonatal Health and Biochemistry (2 papers), ATP Synthase and ATPases Research (2 papers), Infectious Encephalopathies and Encephalitis (2 papers), Neurological and metabolic disorders (2 papers) and Pharmacological Effects and Toxicity Studies (2 papers). The work is most often cited by research in Clinical Biochemistry (72 citations), Neurology (100 citations), Cellular and Molecular Neuroscience (83 citations), Psychiatry and Mental health (39 citations) and Genetics (78 citations). Peter G. Procopis has collaborated with scholars based in Australia, United States and Singapore. Frequent co-authors include Robert Ouvrier, Monique M. Ryan, Jayne Antony, Padraic J. Grattan‐Smith, Graeme Morgan, B Turner, Brian Turner, John Christodoulou, Claire Cooke‐Yarborough and Christopher Troedson. Their work appears in journals such as The Medical Journal of Australia, Pediatric Neurology, Acta Paediatrica, Mitochondrion and The American Journal of Human 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.