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Meeting Abstract (8)
Journal Articles (3)

Journal

Investigative Ophthalmology & Visual Science (11)

Article Type

ARVO Annual Meeting Abstract (8)
Cornea (3)

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Cornea (3)
Eye Anatomy and Disorders (3)
Genetics (3)

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endothelium (2)
family (2)
hereditary corneal dystrophy (2)
mutation (2)
single nucleotide polymorphism (2)
alleles (1)
amyloid (1)
chromosomes (1)
cornea (1)
dna, mitochondrial (1)

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Cornea July 2014

Mitochondrial Polymorphism A10398G and Haplogroup I Are Associated With Fuchs' Endothelial Corneal Dystrophy

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Yi-Ju Li; Mollie A. Minear; Xuejun Qin; Jacqueline Rimmler; Michael A. Hauser; R. Rand Allingham; Robert P. Igo; Jonathan H. Lass; Sudha K. Iyengar; Gordon K. Klintworth; Natalie A. Afshari; Simon G. Gregory
TAGS: dna, mitochondrial, endothelium, hereditary corneal dystrophy, mitochondria, polymorphism, alleles, genetics, smoking, single nucleotide polymorphism, genome-wide association study
Invest. Ophthalmol. Vis. Sci.. 2014; 55(7):4577-4584. doi: https://doi.org/10.1167/iovs.13-13517

ARVO Annual Meeting Abstract April 2014

Common variants in TCF4 and three novel genes increase susceptibility to Fuchs Dystrophy

Sudha K Iyengar; Yi-Ju Li; Robert P Igo; Kathryn P Burdon; John H Fingert; John Gottsch; Gordon K Klintworth; Jonathan H Lass; Natalie A Afshari; FECD Genetics Consortium

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):4070. doi:

ARVO Annual Meeting Abstract June 2013

An Investigation of Mitochondrial Haplogroups in Fuchs Endothelial Corneal Dystrophy

Yi-Ju Li; Mollie Minear; Jacqueline Rimmler; Elmer Balajonda; Michael Hauser; R Rand Allingham; Gordon Klintworth; Simon Gregory; Natalie Afshari

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):4725. doi:

ARVO Annual Meeting Abstract June 2013

Proteolytic processing in lattice corneal dystrophy

Ebbe Toftgaard Poulsen; Kasper Runager; Michael Risør; Ida B. Thøgersen; Thomas Dyrlund; Line Thomsen; Gordon Klintworth; Jan Enghild

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):4735. doi:

ARVO Annual Meeting Abstract June 2013

Insights into the molecular mechanisms of TGFBIp aggregation in corneal dystrophies

Kasper Runager; Jarl Underhaug; Charlotte Sørensen; Henrik Karring; Gordon Klintworth; Niels Nielsen; Jan Enghild

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):4738. doi:

ARVO Annual Meeting Abstract June 2013

A Family-based Investigation of the Role of TCF4 Trinucleotide Repeat Expansion in Fuchs Endothelial Corneal Dystrophy (FECD)

Keith Baratz; Ross Aleff; Yi-Ju Li; Malinda Butz; Simon Gregory; Gordon Klintworth; W. Edward Highsmith; Natalie Afshari; Eric Wieben

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):4560. doi:

ARVO Annual Meeting Abstract March 2012

Genetic screen of African-Americans with Fuchs endothelial corneal dystrophy

Natalie A. Afshari; Mollie A. Minear; Jacqueline Rimmler; Elmer Balajonda; Shera Watson; Michael A. Hauser; R R. Allingham; Gordon K. Klintworth; Yi-Ju Li; Simon G. Gregory

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):5987. doi:

ARVO Annual Meeting Abstract April 2011

Replication Of Association And Linkage To The FCD2/TCF4 Locus On Chromosome 18 In Fuchs Endothelial Corneal Dystrophy

Mollie A. Minear; Yi-Ju Li; Jacqueline Rimmler; R. R. Allingham; S. A. Riazuddin; Nicholas Katsanis; John D. Gottsch; Simon G. Gregory; Gordon K. Klintworth; Natalie A. Afshari

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):1087. doi:

ARVO Annual Meeting Abstract April 2011

Effects of Conditional Dicer Knockdown on the Outflow Pathway in Living Mice

Pedro Gonzalez; Pratap Challa; Lucinda J. Camras; Fan Yuan; Iris D. Navarro; Guorong Li; Coralia Luna; Jing Wu; Gordon K. Klintworth; David L. Epstein

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):6610. doi:

Cornea March 2009

Genome-wide Linkage Scan in Fuchs Endothelial Corneal Dystrophy

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Natalie A. Afshari; Yi-Ju Li; Margaret A. Pericak-Vance; Simon Gregory; Gordon K. Klintworth
TAGS: endothelium, family, genome, hereditary corneal dystrophy, chromosomes, single nucleotide polymorphism, genetic linkage analysis, mutation
Invest. Ophthalmol. Vis. Sci.. 2009; 50(3):1093-1097. doi: https://doi.org/10.1167/iovs.08-1839

Cornea May 2004

Two Mutations in the TGFBI ( BIGH3 ) Gene Associated with Lattice Corneal Dystrophy in an Extensively Studied Family

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Gordon K. Klintworth; Wenjun Bao; Natalie A. Afshari
TAGS: family, genes, meretoja syndrome, mutation, cornea, amyloid, nucleotides
Invest. Ophthalmol. Vis. Sci.. 2004; 45(5):1382-1388. doi: https://doi.org/10.1167/iovs.03-1228

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Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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