Trevor Carmichael - Concepedia

Author

Trevor Carmichael

Also Known As

André Reis, Ari Ziskind, Donald L Budenz, T Carmichael, T R Carmichael, Trevor Carmichael, Trevor R Carmichael, Trevor R. Carmichael, Trevor Robin Carmichael

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

University of the Witwatersrand Duke University Singapore National Eye Center University of Limpopo Stellenbosch University

About

Trevor Carmichael is an author at University of the Witwatersrand specializing in medicine, natural sciences, and chromatin structure.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	95
2	Natural Sciences	1	1	79
3	Public Health	1	1	16
4	Cell Biology	1	1	79
5	Epidemiology	1	1	16

Trevor Carmichael

Publications

676

Citations

H-Index

Page 1

	Year	Citations
Implantation of a Miniature Glaucoma Device Under a Scleral Flap Elie Dahan, Trevor Carmichael Journal of Glaucoma	2005	188
Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population. Susan Williams, Benjamin T. Whigham, Yutao Liu, PubMed	2010	99
Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the<i>LOXL1</i>locus Michael A. Hauser, Inas F. Aboobakar, Yutao Liu, Human Molecular Genetics Exfoliation SyndromeGeneticsGenetic EpidemiologyPathologyMolecular Genetics	2015	79
Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry Michael A. Hauser, R. Rand Allingham, Tin Aung, JAMA	2019	70
Topical steroids in the treatment of central and paracentral corneal ulcers. Trevor Carmichael, Yevgeniy Gelfand, N H Welsh British Journal of Ophthalmology	1990	65
The Genetics of POAG in Black South Africans: A Candidate Gene Association Study Susan Williams, Trevor Carmichael, R. Rand Allingham, Scientific Reports	2015	42
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome Daniel Berner, Ursula Hoja, Matthias Zenkel, Human Molecular Genetics	2019	30
Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in <i>PAX6</i> in a South African family. Saadiah Goolam, Nadia Carstens, Mark T. Ross, PubMed	2018	21
Chronic inflammatory cells and damaged limbal cells in pterygium Peter Anguria, Trevor Carmichael, Sam Ntuli, African Health Sciences	2013	20
Young patient’s age determines pterygium recurrence after surgery Peter Anguria, Sam Ntuli, Trevor Carmichael African Health Sciences	2014	18

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