David Ravine
Impact in
- Genetics top 0.2%
- Genetic and Kidney Cyst Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Nephrology top 2%
Papers in
- Genetics 48
- Genetic and Kidney Cyst Diseases 19
- Genetics and Neurodevelopmental Disorders 19
- Genetic Syndromes and Imprinting 6
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 4
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- Renal and related cancers 13
- RNA modifications and cancer 6
- Co-authors
- Robert N. Gibson (4 shared papers)Helen Leonard (14 shared papers)Eliécer Coto (4 shared papers)D. M. Danks (2 shared papers)P Kincaid-Smith (2 shared papers)Martijn H. Breuning (3 shared papers)John Christodoulou (9 shared papers)Roser Torrá (3 shared papers)
- Journals
- Journal of Medical Genetics (9 papers)The Lancet (6 papers)Kidney International (5 papers)Human Mutation (4 papers)The Medical Journal of Australia (3 papers)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
David Ravine
73 papers receiving 4.7k citations
David Ravine's Hit Papers
Peers
Comparison fields: 5 of 115
- Genetics 3.4k
- Nephrology 264
- Cognitive Neuroscience 706
- Molecular Biology 2.0k
- Pediatrics, Perinatology and Child Health 382
Countries citing papers authored by David Ravine
This map shows the geographic impact of David Ravine'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 Ravine with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Ravine more than expected).
Fields of papers citing papers by David Ravine
This network shows the impact of papers produced by David Ravine. 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 Ravine. The network helps show where David Ravine may publish in the future.
Co-authors
The 25 scholars most cited alongside David Ravine, 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 74 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Unified Criteria for Ultrasonographic Diagnosis of ADPKD Hit paper breakdown → | 2008 | 506 |
| 2 | 1999 | 437 | |
| 3 | 1994 | 430 | |
| 4 | 2006 | 274 | |
| 5 | 1994 | 251 | |
| 6 | 1997 | 237 | |
| 7 | 2008 | 203 | |
| 8 | 1993 | 191 | |
| 9 | 2001 | 171 | |
| 10 | 1992 | 134 | |
| 11 | 1993 | 114 | |
| 12 | 2017 | 85 | |
| 13 | 2006 | 81 | |
| 14 | 1997 | 81 | |
| 15 | 1997 | 77 | |
| 16 | 2010 | 74 | |
| 17 | 2006 | 74 | |
| 18 | 2007 | 73 | |
| 19 | 2004 | 71 | |
| 20 | 2006 | 71 |
About David Ravine
David Ravine is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Genetics and Pediatrics, Perinatology and Child Health, having authored 74 papers that have together received 4.8k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (19 papers), Genetics and Neurodevelopmental Disorders (19 papers), Renal and related cancers (13 papers), Autism Spectrum Disorder Research (12 papers), Genetic Syndromes and Imprinting (6 papers), RNA modifications and cancer (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Genetics (3.4k citations), Nephrology (264 citations), Cognitive Neuroscience (706 citations), Molecular Biology (2.0k citations) and Pediatrics, Perinatology and Child Health (382 citations). David Ravine has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Robert N. Gibson, Helen Leonard, Eliécer Coto, D. M. Danks, P Kincaid-Smith, Martijn H. Breuning, John Christodoulou, Roser Torrá, Nicholas de Klerk and Nick Hateboer. Their work appears in journals such as Journal of Medical Genetics, The Lancet, Kidney International, Human Mutation and The Medical Journal of Australia.
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.