Stuart W. Tompson

2.2k total citations
16 papers, 716 citations indexed

About

Stuart W. Tompson is a scholar working on Molecular Biology, Genetics and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Stuart W. Tompson has authored 16 papers receiving a total of 716 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Stuart W. Tompson's work include Hedgehog Signaling Pathway Studies (4 papers), Connective tissue disorders research (4 papers) and Corneal surgery and disorders (4 papers). Stuart W. Tompson is often cited by papers focused on Hedgehog Signaling Pathway Studies (4 papers), Connective tissue disorders research (4 papers) and Corneal surgery and disorders (4 papers). Stuart W. Tompson collaborates with scholars based in United States, United Kingdom and Spain. Stuart W. Tompson's co-authors include Víctor L. Ruiz‐Pérez, Judith A. Goodship, Daniel H. Cohn, Deborah Krakow, Michael Wright, Terri L. Young, Stanley F. Nelson, David L. Rimoin, Ralph S. Lachman and Helen J. Blair and has published in prestigious journals such as Nature Communications, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Stuart W. Tompson

16 papers receiving 701 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stuart W. Tompson United States	12	482	429	65	55	53	16	716
Sandra D. Dreyer United States	10	499 1.0×	285 0.7×	35 0.5×	62 1.1×	32 0.6×	11	818
Jameela Shinwari Saudi Arabia	9	217 0.5×	200 0.5×	47 0.7×	33 0.6×	43 0.8×	15	488
Olaf Rittinger Austria	17	433 0.9×	384 0.9×	18 0.3×	47 0.9×	15 0.3×	40	785
Annie McNinch United Kingdom	13	145 0.3×	379 0.9×	124 1.9×	78 1.4×	94 1.8×	23	573
Hiroto Obata Japan	15	326 0.7×	113 0.3×	161 2.5×	45 0.8×	75 1.4×	24	890
Annalaura Torella Italy	18	697 1.4×	286 0.7×	35 0.5×	47 0.9×	8 0.2×	77	983
C. Herbert Pratt United States	12	295 0.6×	113 0.3×	20 0.3×	43 0.8×	15 0.3×	20	898
Ghislaine Plessis France	18	431 0.9×	341 0.8×	33 0.5×	26 0.5×	11 0.2×	31	810
Katherine Holman Australia	15	529 1.1×	522 1.2×	62 1.0×	34 0.6×	6 0.1×	31	911
Maree Flaherty Australia	14	286 0.6×	257 0.6×	153 2.4×	18 0.3×	10 0.2×	30	566

Countries citing papers authored by Stuart W. Tompson

Since Specialization

Citations

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

Fields of papers citing papers by Stuart W. Tompson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stuart W. Tompson. 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 Stuart W. Tompson. The network helps show where Stuart W. Tompson may publish in the future.

Co-authorship network of co-authors of Stuart W. Tompson

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

All Works

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16 of 16 papers shown

Young, Terri L., et al.. (2022). Sonic Hedgehog Intron Variant Associated With an Unusual Pediatric Cortical Cataract. Investigative Ophthalmology & Visual Science. 63(6). 25–25. 2 indexed citations

Thomson, Benjamin R., Pan Liu, Tuncer Onay, et al.. (2021). Cellular crosstalk regulates the aqueous humor outflow pathway and provides new targets for glaucoma therapies. Nature Communications. 12(1). 6072–6072. 52 indexed citations

Seow, Wei Jie, Cheryl Ngo, Hong Pan, et al.. (2019). In-utero epigenetic factors are associated with early-onset myopia in young children. PLoS ONE. 14(5). e0214791–e0214791. 18 indexed citations

Bradfield, Yasmin S., et al.. (2019). Comparative Intraoperative Anterior Segment OCT Findings in Pediatric Patients with and without Glaucoma. Ophthalmology Glaucoma. 2(4). 232–239. 11 indexed citations

Tompson, Stuart W., Kristina N. Whisenhunt, Samuel J. Huang, et al.. (2017). Exome Sequence Analysis of 14 Families With High Myopia. Investigative Ophthalmology & Visual Science. 58(4). 1982–1982. 13 indexed citations

Tompson, Stuart W. & Terri L. Young. (2017). Assaying the Effects of Splice Site Variants by Exon Trapping in a Mammalian Cell Line. BIO-PROTOCOL. 7(10). 24 indexed citations

Tompson, Stuart W., Charles A. Johnson, Diana Abbott, et al.. (2017). Reduced penetrance in a large Caucasian pedigree with Stickler syndrome. Ophthalmic Genetics. 38(1). 43–50. 4 indexed citations

Tompson, Stuart W., et al.. (2016). Whole Exome Sequencing Identifies a Rare Variant Co-segregating with High Myopia. Investigative Ophthalmology & Visual Science. 57(12). 3606–3606. 1 indexed citations

Weinstein, Michael M., Stuart W. Tompson, Yuqing Chen, Brendan Lee, & Daniel H. Cohn. (2014). Mice Expressing Mutant Trpv4 Recapitulate the Human TRPV4 Disorders. Journal of Bone and Mineral Research. 29(8). 1815–1822. 20 indexed citations

10.

Lee, Hane, John M. Graham, David L. Rimoin, et al.. (2012). Exome Sequencing Identifies PDE4D Mutations in Acrodysostosis. The American Journal of Human Genetics. 90(4). 746–751. 95 indexed citations

11.

Tompson, Stuart W., Eissa Faqeih, Leena Ala‐Kokko, et al.. (2012). Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2. American Journal of Medical Genetics Part A. 158A(2). 309–314. 13 indexed citations

12.

Blair, Helen J., Stuart W. Tompson, Yuning Liu, et al.. (2011). Evc2 is a positive modulator of Hedgehog signalling that interacts with Evc at the cilia membrane and is also found in the nucleus. BMC Biology. 9(1). 14–14. 72 indexed citations

13.

Tompson, Stuart W., Carlos A. Bacino, Nicole P. Safina, et al.. (2010). Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene. The American Journal of Human Genetics. 87(5). 708–712. 54 indexed citations

14.

Tompson, Stuart W., Barry Merriman, Vincent Funari, et al.. (2008). A Recessive Skeletal Dysplasia, SEMD Aggrecan Type, Results from a Missense Mutation Affecting the C-Type Lectin Domain of Aggrecan. The American Journal of Human Genetics. 84(1). 72–79. 101 indexed citations

15.

Tompson, Stuart W., Víctor L. Ruiz‐Pérez, Helen J. Blair, et al.. (2006). Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis–van Creveld syndrome patients. Human Genetics. 120(5). 663–670. 83 indexed citations

16.

Ruiz‐Pérez, Víctor L., Stuart W. Tompson, Pablo Lapunzina, et al.. (2003). Mutations in Two Nonhomologous Genes in a Head-to-Head Configuration Cause Ellis-van Creveld Syndrome. The American Journal of Human Genetics. 72(3). 728–732. 153 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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