Andrew E. Fry
Impact in
- Developmental Neuroscience top 10%
- Genetics top 10%
- Hemoglobinopathies and Related Disorders
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 19
- Genetics and Neurodevelopmental Disorders 6
- Genetic Associations and Epidemiology 4
- Genomic variations and chromosomal abnormalities 4
- 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)Sarah Auburn (7 shared papers)Anna Richardson (7 shared papers)Mahamadou Diakité (6 shared papers)
- Journals
- European Journal of Human Genetics (3 papers)Clinical Genetics (3 papers)Human Molecular Genetics (2 papers)European Journal of Medical Genetics (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesGambia
In The Last Decade
Andrew E. Fry
36 papers receiving 937 citations
Peers
Comparison fields: 5 of 118
- Developmental Neuroscience 48
- Genetics 122
- Genetics 315
- Cell Biology 145
- Pediatrics, Perinatology and Child Health 154
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 | 117 | |
| 2 | 2013 | 101 | |
| 3 | 2009 | 91 | |
| 4 | 2018 | 90 | |
| 5 | 2014 | 67 | |
| 6 | 2009 | 44 | |
| 7 | 2017 | 44 | |
| 8 | 2018 | 34 | |
| 9 | 2016 | 33 | |
| 10 | 2012 | 30 | |
| 11 | 2008 | 29 | |
| 12 | 2008 | 26 | |
| 13 | 2009 | 23 | |
| 14 | 2013 | 22 | |
| 15 | 2008 | 21 | |
| 16 | 2016 | 19 | |
| 17 | 2008 | 18 | |
| 18 | 2019 | 18 | |
| 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 956 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Malaria Research and Control (5 papers), Genetic Associations and Epidemiology (4 papers), Fetal and Pediatric Neurological Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Complement system in diseases (4 papers), Microtubule and mitosis dynamics (3 papers) and Pain Management and Placebo Effect (3 papers). The work is most often cited by research in Developmental Neuroscience (48 citations), Genetics (122 citations), Genetics (315 citations), Cell Biology (145 citations) and Pediatrics, Perinatology and Child Health (154 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, Sarah Auburn, Anna Richardson, Mahamadou Diakité, Kerrin S. Small and Mark I. Rees. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, Human Molecular Genetics, European Journal of Medical Genetics 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.