S. J. Bowne

632 total citations · 1 hit paper
4 papers, 466 citations indexed

About

S. J. Bowne is a scholar working on Molecular Biology, Ophthalmology and Epidemiology. According to data from OpenAlex, S. J. Bowne has authored 4 papers receiving a total of 466 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 1 paper in Ophthalmology and 1 paper in Epidemiology. Recurrent topics in S. J. Bowne's work include Retinal Development and Disorders (2 papers), Biochemical and Molecular Research (1 paper) and Retinal Diseases and Treatments (1 paper). S. J. Bowne is often cited by papers focused on Retinal Development and Disorders (2 papers), Biochemical and Molecular Research (1 paper) and Retinal Diseases and Treatments (1 paper). S. J. Bowne collaborates with scholars based in United States. S. J. Bowne's co-authors include L.S. Sullivan, Stephen P. Daiger, Sarah Mortimer, Eric A. Pierce, Jay‐Jiguang Zhu, Jing Zhu, Dianna H. Wheaton, David G. Birch, Anisa Gire and Lizbeth Hedstrom and has published in prestigious journals such as Human Molecular Genetics, Investigative Ophthalmology & Visual Science and Clinical Genetics.

In The Last Decade

S. J. Bowne

4 papers receiving 462 citations

Hit Papers

Genes and mutations causing retinitis pigmentosa 2013 2026 2017 2021 2013 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
S. J. Bowne United States 3 436 209 121 57 54 4 466
L.S. Sullivan United States 3 431 1.0× 210 1.0× 120 1.0× 59 1.0× 56 1.0× 6 463
Sally Justus United States 13 536 1.2× 207 1.0× 138 1.1× 87 1.5× 55 1.0× 18 596
Ruben Jauregui United States 14 432 1.0× 291 1.4× 98 0.8× 65 1.1× 88 1.6× 37 509
Regine Mühlfriedel Germany 12 393 0.9× 215 1.0× 150 1.2× 52 0.9× 73 1.4× 24 468
Xufeng Dai China 12 558 1.3× 251 1.2× 193 1.6× 126 2.2× 81 1.5× 20 609
Wen-Hsuan Wu United States 9 550 1.3× 177 0.8× 152 1.3× 82 1.4× 75 1.4× 18 617
Waldo Herrera United States 6 405 0.9× 235 1.1× 112 0.9× 39 0.7× 41 0.8× 7 446
R. Barhoum Spain 6 299 0.7× 97 0.5× 108 0.9× 56 1.0× 28 0.5× 6 396
Avril Kennan Ireland 11 542 1.2× 189 0.9× 137 1.1× 66 1.2× 36 0.7× 16 612
T. P. Dryja United States 7 320 0.7× 147 0.7× 78 0.6× 57 1.0× 30 0.6× 10 371

Countries citing papers authored by S. J. Bowne

Since Specialization
Citations

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

Fields of papers citing papers by S. J. Bowne

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. J. Bowne. 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 S. J. Bowne. The network helps show where S. J. Bowne may publish in the future.

Co-authorship network of co-authors of S. J. Bowne

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

All Works

4 of 4 papers shown
1.
Daiger, Stephen P., L.S. Sullivan, & S. J. Bowne. (2013). Genes and mutations causing retinitis pigmentosa. Clinical Genetics. 84(2). 132–141. 456 indexed citations breakdown →
2.
Cukras, Catherine A., et al.. (2005). A Potential Interaction Between the RP1 and IMPDH1 Proteins. Investigative Ophthalmology & Visual Science. 46(13). 1710–1710. 2 indexed citations
3.
Sullivan, L.S., Sarah Mortimer, Lizbeth Hedstrom, et al.. (2005). Mutations in IMPDH1 Are Associated With Leber Congenital Amaurosis. 46(13). 1815–1815. 1 indexed citations
4.
Bowne, S. J.. (2002). Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa. Human Molecular Genetics. 11(5). 559–568. 7 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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