Robyn M. Rautenbach
Cape Town, WC, South Africa
Last Updated: 09/26/2026
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Found 8 publications
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome.
Journal: Human molecular genetics
Published: December 13, 2018
Extraocular Muscle Findings in Myasthenia Gravis Associated Treatment-Resistant Ophthalmoplegia.
Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society
Published: July 26, 2017
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
The African-387 C>T TGFB1 variant is functional and associates with the ophthalmoplegic complication in juvenile myasthenia gravis.
Journal: Journal of human genetics
Published: July 15, 2015
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
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.
Journal: Nature genetics
Published: August 08, 2014
The role of lysyl oxidase-like 1 DNA copy number variants in exfoliation glaucoma.
Journal: Molecular vision
Published: August 29, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026