C. Anthony Scott

696 total citations
18 papers, 456 citations indexed

About

C. Anthony Scott is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, C. Anthony Scott has authored 18 papers receiving a total of 456 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Immunology. Recurrent topics in C. Anthony Scott's work include Epigenetics and DNA Methylation (4 papers), Genetic Syndromes and Imprinting (3 papers) and RNA regulation and disease (3 papers). C. Anthony Scott is often cited by papers focused on Epigenetics and DNA Methylation (4 papers), Genetic Syndromes and Imprinting (3 papers) and RNA regulation and disease (3 papers). C. Anthony Scott collaborates with scholars based in United States, Gambia and Canada. C. Anthony Scott's co-authors include Diane C. Slusarski, Eleonora Laritsky, Harry A. Mackay, Maria S. Baker, Cristian Coarfa, Val C. Sheffield, Robert A. Waterland, Jack Duryea, Erika Tavares and Nina Nuangchamnong and has published in prestigious journals such as Nature Communications, The Journal of Immunology and Biophysical Journal.

In The Last Decade

C. Anthony Scott

18 papers receiving 453 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C. Anthony Scott United States 13 322 146 57 48 34 18 456
David McGaughey United States 14 433 1.3× 145 1.0× 28 0.5× 57 1.2× 20 0.6× 20 587
Aurore Caqueret Canada 9 219 0.7× 95 0.7× 30 0.5× 53 1.1× 19 0.6× 10 344
Thomas B. Nicholson United States 10 768 2.4× 136 0.9× 35 0.6× 31 0.6× 53 1.6× 14 867
Kelly E. Jackson United States 8 204 0.6× 211 1.4× 24 0.4× 26 0.5× 50 1.5× 15 375
Majida Charif Morocco 17 417 1.3× 114 0.8× 24 0.4× 37 0.8× 24 0.7× 51 617
Lijia Huang Canada 14 370 1.1× 180 1.2× 19 0.3× 44 0.9× 31 0.9× 32 541
Michael J. Szego Canada 9 294 0.9× 141 1.0× 28 0.5× 42 0.9× 44 1.3× 16 454
Ender Karaca Türkiye 13 265 0.8× 247 1.7× 37 0.6× 40 0.8× 40 1.2× 25 544
Maaike Vreeburg Netherlands 15 355 1.1× 261 1.8× 28 0.5× 58 1.2× 15 0.4× 29 530
Fuchou Tang China 5 460 1.4× 136 0.9× 22 0.4× 16 0.3× 50 1.5× 6 523

Countries citing papers authored by C. Anthony Scott

Since Specialization
Citations

This map shows the geographic impact of C. Anthony Scott'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 C. Anthony Scott with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. Anthony Scott more than expected).

Fields of papers citing papers by C. Anthony Scott

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. Anthony Scott. 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 C. Anthony Scott. The network helps show where C. Anthony Scott may publish in the future.

Co-authorship network of co-authors of C. Anthony Scott

This figure shows the co-authorship network connecting the top 25 collaborators of C. Anthony Scott. A scholar is included among the top collaborators of C. Anthony Scott 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 C. Anthony Scott. C. Anthony Scott is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Gunasekara, Chathura, Harry A. Mackay, C. Anthony Scott, et al.. (2023). Systemic interindividual epigenetic variation in humans is associated with transposable elements and under strong genetic control. Genome biology. 24(1). 2–2. 19 indexed citations
2.
Tucker, Budd A., Erin R. Burnight, Cathryn M. Cranston, et al.. (2021). Development and biological characterization of a clinical gene transfer vector for the treatment of MAK-associated retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 29(5). 259–288. 1 indexed citations
3.
Scott, C. Anthony, et al.. (2021). Functional Role of the RNA-Binding Protein Rbm24a and Its Target sox2 in Microphthalmia. Biomedicines. 9(2). 100–100. 5 indexed citations
4.
Scott, C. Anthony, Jack Duryea, Harry A. Mackay, et al.. (2020). Identification of cell type-specific methylation signals in bulk whole genome bisulfite sequencing data. Genome biology. 21(1). 156–156. 20 indexed citations
5.
Dash, Soma, et al.. (2019). RNA binding proteins in eye development: rbm24a regulates sox2 and leads to microphthalmia and visual processing defects in zebrafish. Investigative Ophthalmology & Visual Science. 60(9). 4952–4952. 1 indexed citations
6.
Gunasekara, Chathura, C. Anthony Scott, Eleonora Laritsky, et al.. (2019). A genomic atlas of systemic interindividual epigenetic variation in humans. Genome biology. 20(1). 105–105. 68 indexed citations
7.
Mackay, Harry A., C. Anthony Scott, Jack Duryea, et al.. (2019). DNA methylation in AgRP neurons regulates voluntary exercise behavior in mice. Nature Communications. 10(1). 5364–5364. 32 indexed citations
8.
Scott, C. Anthony, et al.. (2019). DHHC5 Mediates β-Adrenergic Signaling in Cardiomyocytes by Targeting Gα Proteins. Biophysical Journal. 118(4). 826–835. 28 indexed citations
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Scott, C. Anthony, et al.. (2019). A High-Throughput Assay for Congenital and Age-Related Eye Diseases in Zebrafish. Biomedicines. 7(2). 28–28. 13 indexed citations
11.
Schneider, Igor, C. Anthony Scott, Trudi A. Westfall, et al.. (2017). The Nkd EF-hand domain modulates divergent wnt signaling outputs in zebrafish. Developmental Biology. 434(1). 63–73. 2 indexed citations
12.
Scott, C. Anthony, Michael R. Rebagliati, Qihong Zhang, et al.. (2017). Nuclear/cytoplasmic transport defects in BBS6 underlie congenital heart disease through perturbation of a chromatin remodeling protein. PLoS Genetics. 13(7). e1006936–e1006936. 23 indexed citations
13.
Héon, Elise, Gun‐Hee Kim, Erika Tavares, et al.. (2016). Mutations inC8ORF37cause Bardet Biedl syndrome (BBS21). Human Molecular Genetics. 25(11). 2283–2294. 77 indexed citations
14.
Scott, C. Anthony, et al.. (2016). Automated, high‐throughput, in vivo analysis of visual function using the zebrafish. Developmental Dynamics. 245(5). 605–613. 25 indexed citations
15.
DeLuca, Adam P., S. Scott Whitmore, Tasneem P. Sharma, et al.. (2015). Hypomorphic mutations inTRNT1cause retinitis pigmentosa with erythrocytic microcytosis. Human Molecular Genetics. 25(1). 44–56. 56 indexed citations
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Gruss, H J, C. Anthony Scott, Barrett J. Rollins, Marion A. Brach, & F Herrmann. (1996). Human fibroblasts express functional IL-2 receptors formed by the IL-2R α- and β-chain subunits: association of IL-2 binding with secretion of the monocyte chemoattractant protein-1. The Journal of Immunology. 157(2). 851–857. 29 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.

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