John Christodoulou
Impact in
- Clinical Biochemistry top 0.05%
- Metabolism and Genetic Disorders
- Genetics top 0.1%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
-
- Mitochondrial Function and Pathology 83
- RNA modifications and cancer 34
- Biochemical and Molecular Research 20
- ATP Synthase and ATPases Research 18
- Genetics 136
- Genetics and Neurodevelopmental Disorders 86
- Genomics and Rare Diseases 36
- Co-authors
- Helen Leonard (41 shared papers)David R. Thorburn (52 shared papers)Carolyn Ellaway (37 shared papers)Sarah Williamson (17 shared papers)Gladys Ho (24 shared papers)Angus Clarke (6 shared papers)Bruce Bennetts (16 shared papers)Patrick Tam (10 shared papers)
- Journals
- Journal of Inherited Metabolic Disease (22 papers)European Journal of Human Genetics (17 papers)Human Mutation (16 papers)The American Journal of Human Genetics (15 papers)The Journal of Pediatrics (13 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
John Christodoulou
309 papers receiving 11.6k citations
John Christodoulou's Hit Papers
Peers
Comparison fields: 5 of 155
- Clinical Biochemistry 2.6k
- Genetics 5.2k
- Cognitive Neuroscience 1.9k
- Molecular Biology 6.2k
- Biochemistry 336
Countries citing papers authored by John Christodoulou
This map shows the geographic impact of John Christodoulou'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 John Christodoulou with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John Christodoulou more than expected).
Fields of papers citing papers by John Christodoulou
This network shows the impact of papers produced by John Christodoulou. 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 John Christodoulou. The network helps show where John Christodoulou may publish in the future.
Co-authors
The 25 scholars most cited alongside John Christodoulou, 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 319 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Rett syndrome: Revised diagnostic criteria and nomenclature Hit paper breakdown → | 2010 | 1005 |
| 2 | Leigh syndrome: Clinical features and biochemical and DNA abnormalities Hit paper breakdown → | 1996 | 578 |
| 3 | 2004 | 377 | |
| 4 | Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high. | 1992 | 374 |
| 5 | 2012 | 346 | |
| 6 | 2006 | 274 | |
| 7 | 2012 | 210 | |
| 8 | 2010 | 173 | |
| 9 | 2006 | 160 | |
| 10 | 2008 | 154 | |
| 11 | 2017 | 153 | |
| 12 | 2008 | 151 | |
| 13 | 2015 | 137 | |
| 14 | 2005 | 135 | |
| 15 | 2003 | 133 | |
| 16 | 2009 | 130 | |
| 17 | 2011 | 126 | |
| 18 | 2019 | 111 | |
| 19 | 2017 | 105 | |
| 20 | 2015 | 104 |
About John Christodoulou
John Christodoulou is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Cognitive Neuroscience and Pediatrics, Perinatology and Child Health, having authored 319 papers that have together received 11.8k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (88 papers), Genetics and Neurodevelopmental Disorders (86 papers), Mitochondrial Function and Pathology (83 papers), Genomics and Rare Diseases (36 papers), RNA modifications and cancer (34 papers), Autism Spectrum Disorder Research (32 papers), Biochemical and Molecular Research (20 papers) and ATP Synthase and ATPases Research (18 papers). The work is most often cited by research in Clinical Biochemistry (2.6k citations), Genetics (5.2k citations), Cognitive Neuroscience (1.9k citations), Molecular Biology (6.2k citations) and Biochemistry (336 citations). John Christodoulou has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Helen Leonard, David R. Thorburn, Carolyn Ellaway, Sarah Williamson, Gladys Ho, Angus Clarke, Bruce Bennetts, Patrick Tam, Gregory J. Pelka and Denise M. Kirby. Their work appears in journals such as Journal of Inherited Metabolic Disease, European Journal of Human Genetics, Human Mutation, The American Journal of Human Genetics and The Journal of Pediatrics.
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.