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Zebrafish--on the move towards ophthalmological research

Eye (London), 2014-04, Vol.28 (4), p.367-380

2014

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Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiatives

Progress in retinal and eye research, 2020-07, Vol.77, p.100827-100827, Article 100827

2020

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Full-field stimulus testing: Role in the clinic and as an outcome measure in clinical trials of severe childhood retinal disease

Progress in retinal and eye research, 2022-03, Vol.87, p.101000-101000, Article 101000

2022

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Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement

Proceedings of the National Academy of Sciences - PNAS, 2013-02, Vol.110 (6), p.1984-1984

2013

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Toenail onychomycosis: an important global disease burden

Journal of clinical pharmacy and therapeutics, 2010-10, Vol.35 (5), p.497-519

2010

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Predeployment Sleep Duration and Insomnia Symptoms as Risk Factors for New-Onset Mental Health Disorders Following Military Deployment

Sleep (New York, N.Y.), 2013-07, Vol.36 (7), p.1009-1018

2013

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Canine retina has a primate fovea-like bouquet of cone photoreceptors which is affected by inherited macular degenerations

PloS one, 2014-03, Vol.9 (3), p.e90390-e90390

2014

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Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing

PloS one, 2016-01, Vol.11 (1), p.e0145951-e0145951

2016

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Probing Mechanisms of Photoreceptor Degeneration in a New Mouse Model of the Common Form of Autosomal Dominant Retinitis Pigmentosa due to P23H Opsin Mutations

The Journal of biological chemistry, 2011-03, Vol.286 (12), p.10551-10567

2011

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The caloric irrigation test

Handbook of Clinical Neurology, 2016, Vol.137, p.119-131

2016

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Visual Function and Central Retinal Structure in Choroideremia

Investigative ophthalmology & visual science, 2016-07, Vol.57 (9), p.OCT377-OCT387

2016

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In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations

Cell reports (Cambridge), 2017-07, Vol.20 (2), p.384-396

2017

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Magnitude of problematic anger and its predictors in the Millennium Cohort

BMC public health, 2020-07, Vol.20 (1), p.1-1168, Article 1168

2020

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Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease

Human molecular genetics, 2013-12, Vol.22 (25), p.5136-5145

2013

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Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosa

Proceedings of the National Academy of Sciences - PNAS, 2011-08, Vol.108 (34), p.E569-E576

2011

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Soil carbon sequestration in agroforestry systems: a meta-analysis

Agroforestry systems, 2018-04, Vol.92 (2), p.285-299

2018

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Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial

Human gene therapy, 2008-10, Vol.19 (10), p.979-990

2008

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A G86R mutation in the calcium-sensor protein GCAP1 alters regulation of retinal guanylyl cyclase and causes dominant cone-rod degeneration

The Journal of biological chemistry, 2019-03, Vol.294 (10), p.3476-3488

2019

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Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics

Proceedings of the National Academy of Sciences - PNAS, 2008-09, Vol.105 (39), p.15112-15117

2008

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NTFP income contribution to household economy and related socio-economic factors: Lessons from Bangladesh

Forest policy and economics, 2012-01, Vol.14 (1), p.136-142

2012

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Gene therapy restores vision in a canine model of childhood blindness

Nature genetics, 2001-05, Vol.28 (1), p.92-95

2001

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Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa

Proceedings of the National Academy of Sciences - PNAS, 2012-02, Vol.109 (6), p.2132-2137

2012

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Gene therapy reforms photoreceptor structure and restores vision in NPHP5-associated Leber congenital amaurosis

Molecular therapy, 2021-08, Vol.29 (8), p.2456-2468

2021

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Storable, neglected, and underutilized species of Southern Africa for greater agricultural resilience

Plant-environment interactions (Hoboken, N.J. : 2018), 2024-08, Vol.5 (4), p.e70004-n/a

2024

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Zebrafish--on the move towards ophthalmological research

Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiatives

Full-field stimulus testing: Role in the clinic and as an outcome measure in clinical trials of severe childhood retinal disease

Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect

Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement

Toenail onychomycosis: an important global disease burden

Predeployment Sleep Duration and Insomnia Symptoms as Risk Factors for New-Onset Mental Health Disorders Following Military Deployment

Canine retina has a primate fovea-like bouquet of cone photoreceptors which is affected by inherited macular degenerations

Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing

Probing Mechanisms of Photoreceptor Degeneration in a New Mouse Model of the Common Form of Autosomal Dominant Retinitis Pigmentosa due to P23H Opsin Mutations

The caloric irrigation test

Visual Function and Central Retinal Structure in Choroideremia

In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations

Magnitude of problematic anger and its predictors in the Millennium Cohort

Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease

Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosa

Soil carbon sequestration in agroforestry systems: a meta-analysis

Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial

A G86R mutation in the calcium-sensor protein GCAP1 alters regulation of retinal guanylyl cyclase and causes dominant cone-rod degeneration

Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics

NTFP income contribution to household economy and related socio-economic factors: Lessons from Bangladesh

Gene therapy restores vision in a canine model of childhood blindness

Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa

Gene therapy reforms photoreceptor structure and restores vision in NPHP5-associated Leber congenital amaurosis

Storable, neglected, and underutilized species of Southern Africa for greater agricultural resilience

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