Andrew E. Fry

5.7k total citations
37 papers, 956 citations indexed

About

Andrew E. Fry is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Andrew E. Fry has authored 37 papers receiving a total of 956 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 18 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Andrew E. Fry's work include Genetics and Neurodevelopmental Disorders (6 papers), Malaria Research and Control (5 papers) and Complement system in diseases (4 papers). Andrew E. Fry is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Malaria Research and Control (5 papers) and Complement system in diseases (4 papers). Andrew E. Fry collaborates with scholars based in United Kingdom, United States and Gambia. Andrew E. Fry's co-authors include Daniela T. Pilz, Thomas D. Cushion, Dominic Kwiatkowski, Taane G. Clark, Kirk A. Rockett, Sarah Auburn, Anna Richardson, Kerrin S. Small, Fatou Sisay-Joof and Mahamadou Diakité and has published in prestigious journals such as PLoS ONE, Brain and Genome Research.

In The Last Decade

Andrew E. Fry

36 papers receiving 937 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Andrew E. Fry United Kingdom 18 361 315 158 154 145 37 956
Anthi Drousiotou Cyprus 14 465 1.3× 368 1.2× 96 0.6× 150 1.0× 91 0.6× 47 1.1k
Petra Zwijnenburg Netherlands 17 451 1.2× 179 0.6× 79 0.5× 109 0.7× 104 0.7× 27 1.1k
Abdelhamid Barakat Morocco 23 774 2.1× 491 1.6× 137 0.9× 88 0.6× 84 0.6× 132 1.6k
Neil Dear United Kingdom 9 664 1.8× 250 0.8× 75 0.5× 62 0.4× 281 1.9× 11 1.2k
Fabrizio Dutly Switzerland 23 559 1.5× 385 1.2× 48 0.3× 189 1.2× 72 0.5× 48 1.7k
Michał Witt Poland 25 690 1.9× 671 2.1× 175 1.1× 158 1.0× 46 0.3× 87 1.7k
Sebastian Eck Germany 12 366 1.0× 448 1.4× 50 0.3× 40 0.3× 72 0.5× 23 1.0k
Beryl B. Cummings United States 12 862 2.4× 694 2.2× 95 0.6× 49 0.3× 75 0.5× 18 1.6k
Ahmad Abou Tayoun United Arab Emirates 23 892 2.5× 838 2.7× 57 0.4× 117 0.8× 65 0.4× 81 2.0k
Guénet Jl France 15 557 1.5× 229 0.7× 56 0.4× 67 0.4× 88 0.6× 32 884

Countries citing papers authored by Andrew E. Fry

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Andrew E. Fry

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew E. Fry. A scholar is included among the top collaborators of Andrew E. Fry based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Andrew E. Fry. Andrew E. Fry is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Brasch‐Andersen, Charlotte, Helen Cox, Michael Parker, et al.. (2020). A new 1p36.13‐1p36.12 microdeletion syndrome characterized by learning disability, behavioral abnormalities, and ptosis. Clinical Genetics. 97(6). 927–932. 2 indexed citations
2.
Whatley, Sharon D., Shivaram Hegde, Johann te Water Naudé, et al.. (2020). Focal segmental glomerulosclerosis and mild intellectual disability in a patient with a novel de novo truncating TRIM8 mutation. European Journal of Medical Genetics. 63(9). 103972–103972. 6 indexed citations
3.
Angius, Andrea, Paolo Uva, Manuela Oppo, et al.. (2019). Exome sequencing in Crisponi/cold‐induced sweating syndrome–like individuals reveals unpredicted alternative diagnoses. Clinical Genetics. 95(5). 607–614. 9 indexed citations
4.
Myers, Kenneth A., Susan M. White, Shehla Mohammed, et al.. (2018). Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome. Epilepsy Research. 140. 166–170. 13 indexed citations
5.
O’Neill, Adam C., Christina Kyrousi, Richard J. Leventer, et al.. (2018). A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal Migration. Cell Reports. 25(10). 2729–2741.e6. 34 indexed citations
6.
Fry, Andrew E., Thomas D. Cushion, & Daniela T. Pilz. (2014). The genetics of lissencephaly. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(2). 198–210. 67 indexed citations
7.
Fry, Andrew E., et al.. (2014). Congenital glaucoma in Wagner syndrome. Journal of American Association for Pediatric Ophthalmology and Strabismus. 18(3). 291–293. 5 indexed citations
8.
Cushion, Thomas D., William B. Dobyns, Jonathan G.L. Mullins, et al.. (2013). Overlapping cortical malformations and mutations in TUBB2B and TUBA1A. Brain. 136(2). 536–548. 101 indexed citations
9.
Kloeckener‐Gruissem, Barbara, John Neidhardt, I Magyar, et al.. (2012). Novel VCAN mutations and evidence for unbalanced alternative splicing in the pathogenesis of Wagner syndrome. European Journal of Human Genetics. 21(3). 352–356. 30 indexed citations
10.
Auburn, Sarah, Andrew E. Fry, Taane G. Clark, et al.. (2010). Further Evidence Supporting a Role for Gs Signal Transduction in Severe Malaria Pathogenesis. PLoS ONE. 5(4). e10017–e10017. 16 indexed citations
11.
Teo, Yik Ying, Andrew E. Fry, Kanishka Bhattacharya, et al.. (2009). Genome-wide comparisons of variation in linkage disequilibrium. Genome Research. 19(10). 1849–1860. 44 indexed citations
12.
Fry, Andrew E., Claus Klingenberg, Jean Matthes, et al.. (2009). Connective tissue involvement in two patients with features of cranioectodermal dysplasia. American Journal of Medical Genetics Part A. 149A(10). 2212–2215. 11 indexed citations
13.
Campino, Susana, Julian Forton, Sarah Auburn, et al.. (2009). TLR9 polymorphisms in African populations: no association with severe malaria, but evidence of cis-variants acting on gene expression. Malaria Journal. 8(1). 44–44. 23 indexed citations
14.
Hennig, Branwen J., Andrew E. Fry, K Hirai, et al.. (2008). PTPRC (CD45) variation and disease association studied using single nucleotide polymorphism tagging. Tissue Antigens. 71(5). 458–463. 5 indexed citations
15.
Teo, Yik Ying, Kerrin S. Small, Andrew E. Fry, et al.. (2008). Power consequences of linkage disequilibrium variation between populations. Genetic Epidemiology. 33(2). 128–135. 26 indexed citations
16.
Campino, Susana, Julian Forton, Srilakshmi M. Raj, et al.. (2008). Validating Discovered Cis-Acting Regulatory Genetic Variants: Application of an Allele Specific Expression Approach to HapMap Populations. PLoS ONE. 3(12). e4105–e4105. 21 indexed citations
17.
Teo, Yik Ying, Andrew E. Fry, Miguel SanJoaquin, et al.. (2008). Assessing Genuine Parents-Offspring Trios for Genetic Association Studies. Human Heredity. 67(1). 26–37. 8 indexed citations
18.
19.
Fry, Andrew E., Michael J. Griffiths, Sarah Auburn, et al.. (2007). Common variation in the ABO glycosyltransferase is associated with susceptibility to severe Plasmodium falciparum malaria. Human Molecular Genetics. 17(4). 567–576. 117 indexed citations
20.
Fry, Andrew E., et al.. (2006). Haplotype Homozygosity and Derived Alleles in the Human Genome. The American Journal of Human Genetics. 78(6). 1053–1059. 9 indexed citations

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Anthi Drousiotou Breakdown of academic impact, for papers by Petra Zwijnenburg Breakdown of academic impact, for papers by Abdelhamid Barakat Breakdown of academic impact, for papers by Neil Dear Breakdown of academic impact, for papers by Fabrizio Dutly Breakdown of academic impact, for papers by Michał Witt Breakdown of academic impact, for papers by Sebastian Eck Breakdown of academic impact, for papers by Beryl B. Cummings Breakdown of academic impact, for papers by Ahmad Abou Tayoun Breakdown of academic impact, for papers by Guénet Jl
Rankless by CCL
2026