Trevor R. Carmichael

Johannesburg, GT, South Africa

Last Updated: 09/26/2026

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Found 22 publications

Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye.

Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye.

Journal: JAMA

Published: February 23, 2021

Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry.

Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry.

Journal: JAMA

Published: November 06, 2019

The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome.

The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome.

Journal: Human molecular genetics

Published: December 13, 2018

Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in PAX6 in a South African family.

Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in PAX6 in a South African family.

Journal: Molecular vision

Published: July 07, 2017

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

Journal: Nature genetics

Published: September 30, 2016

Novel mutation in the CHST6 gene causes macular corneal dystrophy in a black South African family.

Novel mutation in the CHST6 gene causes macular corneal dystrophy in a black South African family.

Journal: BMC medical genetics

Published: August 06, 2015

Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.

Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.

Journal: Nature genetics

Published: May 29, 2015

Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus.

Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus.

Journal: Human molecular genetics

Published: April 29, 2015

The genetics of POAG in black South Africans: a candidate gene association study.

The genetics of POAG in black South Africans: a candidate gene association study.

Journal: Scientific reports

Published: October 22, 2014

MYOC mutations in black south african patients with primary open-angle glaucoma: genetic testing and cascade screening.

MYOC mutations in black south african patients with primary open-angle glaucoma: genetic testing and cascade screening.

Journal: Ophthalmic genetics

Published: October 21, 2014

A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.

A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.

Journal: Nature genetics

Published: August 08, 2014

In vitro pharmaceutical characterization and statistical optimization of a novel topically applied instantly-soluble solid eye drop matrix.

In vitro pharmaceutical characterization and statistical optimization of a novel topically applied instantly-soluble solid eye drop matrix.

Journal: Pharmaceutical development and technology

Published: June 21, 2014

Showing 1-12 of 22

Last Updated: 09/26/2026