Andrew E. Fry
Impact in
- Developmental Neuroscience top 10%
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Hemoglobinopathies and Related Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 18
- Genetics and Neurodevelopmental Disorders 6
- Genetic Associations and Epidemiology 3
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- Daniela T. Pilz (9 shared papers)Thomas D. Cushion (4 shared papers)Dominic Kwiatkowski (11 shared papers)Taane G. Clark (8 shared papers)Kirk A. Rockett (9 shared papers)Anna Richardson (7 shared papers)Sarah Auburn (7 shared papers)Mark I. Rees (2 shared papers)
- Journals
- Clinical Genetics (3 papers)European Journal of Human Genetics (3 papers)European Journal of Medical Genetics (2 papers)PLoS ONE (2 papers)Human Molecular Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesGambia
In The Last Decade
Andrew E. Fry
36 papers receiving 952 citations
Peers
Comparison fields: 5 of 111
- Developmental Neuroscience 47
- Genetics 275
- Genetics 84
- Cell Biology 137
- Pediatrics, Perinatology and Child Health 133
Countries citing papers authored by Andrew E. Fry
This map shows the geographic impact of Andrew E. Fry'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 Andrew E. Fry with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew E. Fry more than expected).
Fields of papers citing papers by Andrew E. Fry
This network shows the impact of papers produced by Andrew E. Fry. 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 Andrew E. Fry. The network helps show where Andrew E. Fry may publish in the future.
Co-authors
The 25 scholars most cited alongside Andrew E. Fry, 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 | 2007 | 119 | |
| 2 | 2013 | 103 | |
| 3 | 2018 | 93 | |
| 4 | 2009 | 91 | |
| 5 | 2014 | 67 | |
| 6 | 2017 | 44 | |
| 7 | 2009 | 43 | |
| 8 | 2018 | 36 | |
| 9 | 2016 | 33 | |
| 10 | 2012 | 30 | |
| 11 | 2008 | 29 | |
| 12 | 2008 | 26 | |
| 13 | 2009 | 23 | |
| 14 | 2013 | 23 | |
| 15 | 2008 | 21 | |
| 16 | 2016 | 20 | |
| 17 | 2008 | 18 | |
| 18 | 2019 | 17 | |
| 19 | 2010 | 16 | |
| 20 | 2018 | 13 |
About Andrew E. Fry
Andrew E. Fry is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Immunology, having authored 37 papers that have together received 968 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Malaria Research and Control (5 papers), Fetal and Pediatric Neurological Disorders (4 papers), Neurogenesis and neuroplasticity mechanisms (3 papers), Microtubule and mitosis dynamics (3 papers), Complement system in diseases (3 papers), Genetic Associations and Epidemiology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Developmental Neuroscience (47 citations), Genetics (275 citations), Genetics (84 citations), Cell Biology (137 citations) and Pediatrics, Perinatology and Child Health (133 citations). Andrew E. Fry has collaborated with scholars based in United Kingdom, United States and Gambia. Frequent co-authors include Daniela T. Pilz, Thomas D. Cushion, Dominic Kwiatkowski, Taane G. Clark, Kirk A. Rockett, Anna Richardson, Sarah Auburn, Mark I. Rees, Mahamadou Diakité and Kerrin S. Small. Their work appears in journals such as Clinical Genetics, European Journal of Human Genetics, European Journal of Medical Genetics, PLoS ONE and Human Molecular 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.