Meredith Wilson
Impact in
- Archeology top 5%
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
-
- Mitochondrial Function and Pathology 7
- RNA modifications and cancer 6
- Congenital heart defects research 6
- Genetics 27
- Genomic variations and chromosomal abnormalities 10
- Genetics and Neurodevelopmental Disorders 8
- Genetic Syndromes and Imprinting 6
- Co-authors
- David Mowat (8 shared papers)Lesley C. Adès (3 shared papers)Bronwyn Kerr (4 shared papers)Ági K. Gedeon (3 shared papers)John Christodoulou (7 shared papers)David R. Moore (1 shared paper)John C. Mulley (3 shared papers)Jennifer E. Mossop (1 shared paper)
- Journals
- The American Journal of Human Genetics (5 papers)Human Mutation (4 papers)European Journal of Human Genetics (3 papers)American Journal of Neuroradiology (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Meredith Wilson
89 papers receiving 3.2k citations
Peers
Comparison fields: 5 of 141
- Archeology 45
- Genetics 1.1k
- Sensory Systems 149
- Genetics 266
- Molecular Biology 1.6k
Countries citing papers authored by Meredith Wilson
This map shows the geographic impact of Meredith Wilson'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 Meredith Wilson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Meredith Wilson more than expected).
Fields of papers citing papers by Meredith Wilson
This network shows the impact of papers produced by Meredith Wilson. 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 Meredith Wilson. The network helps show where Meredith Wilson may publish in the future.
Co-authors
The 25 scholars most cited alongside Meredith Wilson, 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 92 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 385 | |
| 2 | 2012 | 209 | |
| 3 | 1998 | 173 | |
| 4 | 1997 | 171 | |
| 5 | 2013 | 157 | |
| 6 | 2014 | 120 | |
| 7 | 2000 | 113 | |
| 8 | 1993 | 104 | |
| 9 | 2007 | 101 | |
| 10 | 2014 | 89 | |
| 11 | 2004 | 81 | |
| 12 | 2012 | 77 | |
| 13 | 2003 | 69 | |
| 14 | 2007 | 68 | |
| 15 | 1998 | 63 | |
| 16 | 2005 | 60 | |
| 17 | 2014 | 58 | |
| 18 | 2014 | 56 | |
| 19 | 1999 | 55 | |
| 20 | 2015 | 52 |
About Meredith Wilson
Meredith Wilson is a scholar working on Molecular Biology, Genetics, Geography, Planning and Development, Surgery and Pediatrics, Perinatology and Child Health, having authored 92 papers that have together received 3.3k indexed citations. Recurring topics across this work include Pacific and Southeast Asian Studies (13 papers), Genomic variations and chromosomal abnormalities (10 papers), Congenital gastrointestinal and neural anomalies (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Mitochondrial Function and Pathology (7 papers), Genetic Syndromes and Imprinting (6 papers), RNA modifications and cancer (6 papers) and Congenital heart defects research (6 papers). The work is most often cited by research in Archeology (45 citations), Genetics (1.1k citations), Sensory Systems (149 citations), Genetics (266 citations) and Molecular Biology (1.6k citations). Meredith Wilson has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include David Mowat, Lesley C. Adès, Bronwyn Kerr, Ági K. Gedeon, John Christodoulou, David R. Moore, John C. Mulley, Jennifer E. Mossop, Donald M. Caspary and Michel Goossens. Their work appears in journals such as The American Journal of Human Genetics, Human Mutation, European Journal of Human Genetics, American Journal of Neuroradiology and Journal of Medical 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.