Nathaniel J. Tear-Hafford
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
Genetic and Demographic Determinants of Fuchs Endothelial Corneal Dystrophy Risk and Severity.
Journal: JAMA ophthalmology
Published: March 13, 2025
Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencing.
Journal: NAR genomics and bioinformatics
Published: August 02, 2022
Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophy.
Journal: Acta ophthalmologica
Published: November 17, 2021
TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated disease.
Journal: Progress in retinal and eye research
Published: April 15, 2020
CUGC for posterior polymorphous corneal dystrophy (PPCD).
Journal: European journal of human genetics : EJHG
Published: February 12, 2019
CRISPR/Cas9-targeted enrichment and long-read sequencing of the Fuchs endothelial corneal dystrophy-associated TCF4 triplet repeat.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 30, 2018
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis.
Journal: Experimental eye research
Published: October 31, 2018
Antisense Therapy for a Common Corneal Dystrophy Ameliorates TCF4 Repeat Expansion-Mediated Toxicity.
Journal: American journal of human genetics
Published: January 03, 2018
Showing 1-9 of 9
Last Updated: 09/26/2026