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Transient Photoreceptor Deconstruction by CNTF Enhances rAAV-Mediated Cone Functional Rescue in Late Stage CNGB3-Achromatopsia

Molecular therapy, 2013-06, Vol.21 (6), p.1131-1141

2013

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A novel form of progressive retinal atrophy in Swedish vallhund dogs

PloS one, 2014-09, Vol.9 (9), p.e106610-e106610

2014

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Insight from OPN1LW Gene Haplotypes into the Cause and Prevention of Myopia

Genes, 2022-05, Vol.13 (6), p.942

2022

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Gene therapy rescues cone function in congenital achromatopsia

Human molecular genetics, 2010-07, Vol.19 (13), p.2581-2593

2010

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New quantitative trait loci for carotid atherosclerosis identified in an intercross derived from apolipoprotein E-deficient mouse strains

Physiological genomics, 2013-04, Vol.45 (8), p.332-342

2013

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Role of a Dual Splicing and Amino Acid Code in Myopia, Cone Dysfunction and Cone Dystrophy Associated with L / M Opsin Interchange Mutations

Translational vision science & technology, 2017-05, Vol.6 (3), p.2

2017

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Atherosclerosis Susceptibility Loci Identified in an Extremely Atherosclerosis‐Resistant Mouse Strain

Journal of the American Heart Association, 2013-08, Vol.2 (4), p.e000260-n/a

2013

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Genetic analysis of atherosclerosis and glucose homeostasis in an intercross between C57BL/6 and BALB/cJ apolipoprotein E-deficient mice

Circulation. Cardiovascular genetics, 2012-04, Vol.5 (2), p.190-201

2012

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Quantitative Trait Locus Analysis of Neointimal Formation in an Intercross Between C57BL/6 and C3H/HeJ Apolipoprotein E-Deficient Mice

Circulation. Cardiovascular genetics, 2009-06, Vol.2 (3), p.220-228

2009

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Equine Multiple Congenital Ocular Anomalies (MCOA) syndrome in PMEL17 (Silver) mutant ponies: five cases

Veterinary ophthalmology, 2011-09, Vol.14 (5), p.313-320

2011

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Gene therapy rescues cone function in congenital achromatopsia

Human molecular genetics, 2011-12, Vol.20 (24), p.5024-5024

2011

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Quantitative trait locus analysis of circulating adhesion molecules in hyperlipidemic apolipoprotein E-deficient mice

Molecular genetics and genomics : MGG, 2008-11, Vol.280 (5), p.375-383

2008

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Insight from IOPN1LW/I Gene Haplotypes into the Cause and Prevention of Myopia

Genes, 2022-05, Vol.13 (6)

2022

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Mutations in the Canine CNGB3 Channel Subunit in Two Achromatopsia Models Leads to Mis-Localization of CNGA3 Expression in Retinal Outer Segments

Biophysical journal, 2011-02, Vol.100 (3), p.104a-104a

2011

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Characterization of Gene Therapy Associated Uveitis Following Intravitreal Adeno-Associated Virus Injection in Mice

Investigative ophthalmology & visual science, 2021-02, Vol.62 (2), p.41-41

2021

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Poster Session II: Intravitreal gene therapy in primate reaches extrafoveal cones

Journal of vision (Charlottesville, Va.), 2023-12, Vol.23 (15), p.66

2023

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CFH Haploinsufficiency and Complement Alterations in Early-Onset Macular Degeneration

Investigative ophthalmology & visual science, 2024-04, Vol.65 (4), p.43-43

2024

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Tritan color vision deficiency may be associated with an OPN1SW splicing defect and haploinsufficiency

Journal of the Optical Society of America. A, Optics, image science, and vision, 2020-04, Vol.37 (4), p.A26

2020

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Transient Photoreceptor Deconstruction by CNTF Enhances rAAV-Mediated Cone Functional Rescue in Late Stage CNGB3-Achromatopsia

A novel form of progressive retinal atrophy in Swedish vallhund dogs

Insight from OPN1LW Gene Haplotypes into the Cause and Prevention of Myopia

Gene therapy rescues cone function in congenital achromatopsia

New quantitative trait loci for carotid atherosclerosis identified in an intercross derived from apolipoprotein E-deficient mouse strains

Role of a Dual Splicing and Amino Acid Code in Myopia, Cone Dysfunction and Cone Dystrophy Associated with L / M Opsin Interchange Mutations

Atherosclerosis Susceptibility Loci Identified in an Extremely Atherosclerosis‐Resistant Mouse Strain

Genetic analysis of atherosclerosis and glucose homeostasis in an intercross between C57BL/6 and BALB/cJ apolipoprotein E-deficient mice

Quantitative Trait Locus Analysis of Neointimal Formation in an Intercross Between C57BL/6 and C3H/HeJ Apolipoprotein E-Deficient Mice

Equine Multiple Congenital Ocular Anomalies (MCOA) syndrome in PMEL17 (Silver) mutant ponies: five cases

Gene therapy rescues cone function in congenital achromatopsia

Quantitative trait locus analysis of circulating adhesion molecules in hyperlipidemic apolipoprotein E-deficient mice

Insight from IOPN1LW/I Gene Haplotypes into the Cause and Prevention of Myopia

Mutations in the Canine CNGB3 Channel Subunit in Two Achromatopsia Models Leads to Mis-Localization of CNGA3 Expression in Retinal Outer Segments

Characterization of Gene Therapy Associated Uveitis Following Intravitreal Adeno-Associated Virus Injection in Mice

Poster Session II: Intravitreal gene therapy in primate reaches extrafoveal cones

CFH Haploinsufficiency and Complement Alterations in Early-Onset Macular Degeneration

Tritan color vision deficiency may be associated with an OPN1SW splicing defect and haploinsufficiency

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