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Nathaniel J Hafford-Tear

Showing results (1-10 of 9) with videos related to

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Acta Ophthalmologica|February 17, 2022
Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophyPetra Liskova, Nathaniel J Hafford-Tear, Pavlina Skalicka, et al.
European Journal of Human Genetics : EJHG|June 16, 2019
CUGC for posterior polymorphous corneal dystrophy (PPCD)Alice E Davidson, Nathaniel J Hafford-Tear, Lubica Dudakova, et al.
Progress in Retinal and Eye Research|August 1, 2020
TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated diseaseMichael P Fautsch, Eric D Wieben, Keith H Baratz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 9, 2019
CRISPR/Cas9-targeted enrichment and long-read sequencing of the Fuchs endothelial corneal dystrophy-associated TCF4 triplet repeatNathaniel J Hafford-Tear, Yu-Chih Tsai, Amanda N Sadan, et al.
Experimental Eye Research|March 10, 2019
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosisLubica Dudakova, Cerys J Evans, Nikolas Pontikos, et al.
American Journal of Human Genetics|March 13, 2018
Antisense Therapy for a Common Corneal Dystrophy Ameliorates TCF4 Repeat Expansion-Mediated ToxicityChristina Zarouchlioti, Beatriz Sanchez-Pintado, Nathaniel J Hafford Tear, et al.
Plos Genetics|May 7, 2024
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated diseaseNihar Bhattacharyya, Niuzheng Chai, Nathaniel J Hafford-Tear, et al.
JAMA Ophthalmology|March 13, 2025
Genetic and Demographic Determinants of Fuchs Endothelial Corneal Dystrophy Risk and SeveritySiyin Liu, Amanda N Sadan, Nihar Bhattacharyya, et al.
NAR Genomics and Bioinformatics|December 8, 2022
Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencingAlysha S Taylor, Dinis Barros, Nastassia Gobet, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Acta Ophthalmologica|February 17, 2022
Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophyPetra Liskova, Nathaniel J Hafford-Tear, Pavlina Skalicka, et al.
European Journal of Human Genetics : EJHG|June 16, 2019
CUGC for posterior polymorphous corneal dystrophy (PPCD)Alice E Davidson, Nathaniel J Hafford-Tear, Lubica Dudakova, et al.
Progress in Retinal and Eye Research|August 1, 2020
TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated diseaseMichael P Fautsch, Eric D Wieben, Keith H Baratz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 9, 2019
CRISPR/Cas9-targeted enrichment and long-read sequencing of the Fuchs endothelial corneal dystrophy-associated TCF4 triplet repeatNathaniel J Hafford-Tear, Yu-Chih Tsai, Amanda N Sadan, et al.
Experimental Eye Research|March 10, 2019
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosisLubica Dudakova, Cerys J Evans, Nikolas Pontikos, et al.
American Journal of Human Genetics|March 13, 2018
Antisense Therapy for a Common Corneal Dystrophy Ameliorates TCF4 Repeat Expansion-Mediated ToxicityChristina Zarouchlioti, Beatriz Sanchez-Pintado, Nathaniel J Hafford Tear, et al.
Plos Genetics|May 7, 2024
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated diseaseNihar Bhattacharyya, Niuzheng Chai, Nathaniel J Hafford-Tear, et al.
JAMA Ophthalmology|March 13, 2025
Genetic and Demographic Determinants of Fuchs Endothelial Corneal Dystrophy Risk and SeveritySiyin Liu, Amanda N Sadan, Nihar Bhattacharyya, et al.
NAR Genomics and Bioinformatics|December 8, 2022
Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencingAlysha S Taylor, Dinis Barros, Nastassia Gobet, et al.
Pageof 1