Stuart W. Tompson - Concepedia

Author

Stuart W. Tompson

Also Known As

S W J Tompson, Stuart Tompson, Stuart W Tompson, Stuart W. J. Tompson, Stuart W. Tompson, Stuart W. Tompson, Tompson, Stuart W., W.J. Stuart Tompson

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

University of Wisconsin–Madison National University of Singapore University of California, Los Angeles Cedars-Sinai Medical Center Flinders University

About

Stuart W. Tompson is an author at University of Wisconsin–Madison specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	925
2	Molecular Genetics	3	3	510
3	Cell Biology	1	1	81
4	Cellular Physiology	1	1	196
5	Molecular Biology	1	1	136

Stuart W. Tompson

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity Tomokazu Souma, Stuart W. Tompson, Benjamin R. Thomson, Journal of Clinical Investigation	2016	286
Mutations in Two Nonhomologous Genes in a Head-to-Head Configuration Cause Ellis-van Creveld Syndrome Víctor L. Ruiz‐Pérez, Stuart W. Tompson, J. Helen Blair, The American Journal of Human Genetics Developmental BiologyGenetic DisorderMedicineGeneticsCraniofacial Development	2003	229
Angiopoietin-1 is required for Schlemm’s canal development in mice and humans Benjamin R. Thomson, Tomokazu Souma, Stuart W. Tompson, Journal of Clinical Investigation Ocular DiseaseSchlemm ’Cellular PhysiologyInflammationAngiogenesis	2017	196
A Recessive Skeletal Dysplasia, SEMD Aggrecan Type, Results from a Missense Mutation Affecting the C-Type Lectin Domain of Aggrecan Stuart W. Tompson, Barry Merriman, Vincent Funari, The American Journal of Human Genetics Genetic DisorderGeneticsPathologyMolecular GeneticsDisease Gene Identification	2008	145
Exome Sequencing Identifies PDE4D Mutations in Acrodysostosis Hane Lee, John M. Graham, David L. Rimoin, The American Journal of Human Genetics Genetic DisorderMedicineGeneticsMolecular BiologyMolecular Genetics	2012	136
Cellular crosstalk regulates the aqueous humor outflow pathway and provides new targets for glaucoma therapies Benjamin R. Thomson, Pan Liu, Tuncer Onay, Nature Communications	2021	132
Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis–van Creveld syndrome patients Stuart W. Tompson, Víctor L. Ruiz‐Pérez, Helen J. Blair, Human Genetics Genetic DisorderGeneticsEllis–van CreveldPathologyEvc2 Identifies Mutations	2006	119
Evc2 is a positive modulator of Hedgehog signalling that interacts with Evc at the cilia membrane and is also found in the nucleus Helen J. Blair, Stuart W. Tompson, Yuning Liu, BMC Biology	2011	91
Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium Yee-Ling Wong, Pirro G. Hysi, Chui Ming Gemmy Cheung, PLoS ONE	2019	85
Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene Stuart W. Tompson, Carlos A. Bacino, Nicole P. Safina, The American Journal of Human Genetics Fibrochondrogenesis ResultsFibrosisPathologyMatrix BiologyMedicine	2010	81

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