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ARVO Annual Meeting Abstract June 2024

Rapid molecular diagnosis in pediatric cataract using gene panel testing

Sarah Hull; Nusha Mirza; Andrea L Vincent

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):4646.

ARVO Annual Meeting Abstract June 2023

Clinical and molecular characterization of foveal hypoplasia

Sarah Hull; Jay Kumar; Andrea L Vincent

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):453.

ARVO Annual Meeting Abstract June 2023

Genotype and Phenotypic investigation of a New Zealand Cohort of Inherited Optic neuropathies

Andrea L Vincent; Glynis Hanrahan; Sarah Hull

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):2777.

ARVO Annual Meeting Abstract June 2022

Characterising the natural history of retinal degeneration progression associated with a founder mutation in the PDE6B gene.

Andrea L Vincent; Elena Edgar - Nemec; Sarah Hull

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):620 – A0335.

ARVO Annual Meeting Abstract June 2022

Lamination of the outer plexiform layer in dominant Wolfram disease

Sarah Hull; Andrea L Vincent

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):513 – A0090.

ARVO Annual Meeting Abstract June 2022

Collagen hydrogels covalently crosslinked by bioorthogonal click chemistry resist cell-induced contraction while preserving encapsulated corneal stromal cell phenotype

Lucia G. Brunel; Sarah M. Hull; Patrik K. Johansson; David Myung; Sarah C. Heilshorn

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):94 – A0192.

ARVO Annual Meeting Abstract June 2021

Phenotypic variability of WFS1 related eye disease

Sarah Hull; Leo Sheck; Alec Hou; Andrea L Vincent

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):1563.

ARVO Annual Meeting Abstract June 2021

Bio-orthogonally Crosslinked Matrix Therapies for Corneal Defect Repair

David Myung; Fang Chen; Gabriella Fernandes-Cunha; Peter Le; Sarah Hull; Sarah Heilshorn

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):947.

ARVO Annual Meeting Abstract June 2021

Harboyan Syndrome with biallelic SLC4A11 pathogenic variants misdiagnosed as congenital CMV infection

Andrea L Vincent; Gulunay Kiray; Sarah Hull

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):1498.

ARVO Annual Meeting Abstract June 2020

Molecular and phenotypic investigation of a New Zealand cohort of childhood-onset retinal dystrophy

Sarah Hull; Gulunay Kiray; John Chiang; Andrea L Vincent

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2383.

ARVO Annual Meeting Abstract June 2020

Detailed characterization of an inherited optic atrophy cohort demonstrates highly variable phenotypes and uncommon molecular associations

Andrea L Vincent; Alec Lin Hou; Sarah Hull; Leo Sheck

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2404.

ARVO Annual Meeting Abstract June 2020

Bioengineered, In Situ-Crosslinked Collagen Gels for Suture-Free Stromal Defect Reconstruction of the Cornea

David Myung; Ali R Djalilian; Sarah Heilshorn; Fang Chen; Peter Le; Sarah Hull; Gabriella Fernandes-Cunha; Kyung-Sun Na

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3555.

ARVO Annual Meeting Abstract July 2019

Biophysical characterization of a simultaneous interpenetrating polymer network composed of crosslinked collagen and hyaluronic acid

Krystal Ya-Fong Lai; Hyun Jong Lee; Sarah Hull; Gabriella Fernandes-Cunha; David Myung

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4097.

ARVO Annual Meeting Abstract July 2019

Characterization of bioorthogonally crosslinked collagen gels with encapsulated corneal stromal stem cells

Sarah Hull; Gabriella Fernandes-Cunha; Ilham Putra; Medi Eslani; Ali R Djalilian; Sarah Heilshorn; David Myung

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4110.

ARVO Annual Meeting Abstract July 2019

Effects of mesenchymal stem cells encapsulated within crosslinked collagen carrier gels on alkali burns in a corneal organ culture model

Ignacio Jesus Blanco; Gabriella Fernandes-Cunha; Sarah Hull; Hyun Jong Lee; Kyung-Sun Na; Ali R Djalilian; David Myung

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4685.

ARVO Annual Meeting Abstract July 2019

Leber Congenital Amaurosis associated with GUCY2D variants: A Retrospective Natural History Study in preparation for future Therapies.

ZAINA Ibrahim BOUZIA; Michalis Georgiou; Sarah Hull; Anthony G Robson; Andrew Webster; Alison J Hardcastle; Alessia Fiorentino; Michel Michaelides

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5421.

ARVO Annual Meeting Abstract July 2018

Effects of engineered cellular microenvironments on the secretome of human mesenchymal stem cells

Sarah Hull; Gabriella Fernandes-Cunha; Hyun Jong Lee; Sarah Heilshorn; David Myung

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2293.

Genetics November 2016

Mutations in AGBL5 , Encoding α-Tubulin Deglutamylase, Are Associated With Autosomal Recessive Retinitis Pigmentosa

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Galuh D. N. Astuti; Gavin Arno; Sarah Hull; Laurence Pierrache; Hanka Venselaar; Keren Carss; F. Lucy Raymond; Rob W. J. Collin; Sultana M. H. Faradz; L. Ingeborgh van den Born; Andrew R. Webster; Frans P. M. Cremers
TAGS: autosomal recessive inheritance, mutation, retinitis pigmentosa, tubulin, family, genes, proteins
Invest. Ophthalmol. Vis. Sci.. 2016; 57(14):6180-6187. https://doi.org/10.1167/iovs.16-20148

ARVO Annual Meeting Abstract September 2016

Survey of ophthalmic and systemic features in patients with PNPLA6 -related disorders

Robert B Hufnagel; Sarah Hull; Jose Luiz Pedroso; Shuan Dai; Andrea Nemeth; Helene Dollfus; Brian Patrick Brooks; Robert Sisk; Michel Michaelides; Anthony T Moore; Zubair Ahmed

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):6564.

ARVO Annual Meeting Abstract September 2016

Molecular study of the MFRP gene in patients with posterior microphthalmia (MCOP) supports its role in autosomal recessive MCOP pathogenesis

Basamat Almoallem; Gavin Arno; Julie De Zaeytijd; Sarah Hull; Martina Suzani; Thomy J. L. de Ravel; Andrew Webster; Bart Peter Leroy; Tony Moore; Elfride De Baere

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):6584.

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Rapid molecular diagnosis in pediatric cataract using gene panel testing

Clinical and molecular characterization of foveal hypoplasia

Genotype and Phenotypic investigation of a New Zealand Cohort of Inherited Optic neuropathies

Characterising the natural history of retinal degeneration progression associated with a founder mutation in the PDE6B gene.

Lamination of the outer plexiform layer in dominant Wolfram disease

Collagen hydrogels covalently crosslinked by bioorthogonal click chemistry resist cell-induced contraction while preserving encapsulated corneal stromal cell phenotype

Phenotypic variability of WFS1 related eye disease

Bio-orthogonally Crosslinked Matrix Therapies for Corneal Defect Repair

Harboyan Syndrome with biallelic SLC4A11 pathogenic variants misdiagnosed as congenital CMV infection

Molecular and phenotypic investigation of a New Zealand cohort of childhood-onset retinal dystrophy

Detailed characterization of an inherited optic atrophy cohort demonstrates highly variable phenotypes and uncommon molecular associations

Bioengineered, In Situ-Crosslinked Collagen Gels for Suture-Free Stromal Defect Reconstruction of the Cornea

Biophysical characterization of a simultaneous interpenetrating polymer network composed of crosslinked collagen and hyaluronic acid

Characterization of bioorthogonally crosslinked collagen gels with encapsulated corneal stromal stem cells

Effects of mesenchymal stem cells encapsulated within crosslinked collagen carrier gels on alkali burns in a corneal organ culture model

Leber Congenital Amaurosis associated with GUCY2D variants: A Retrospective Natural History Study in preparation for future Therapies.

Effects of engineered cellular microenvironments on the secretome of human mesenchymal stem cells

Mutations in AGBL5 , Encoding α-Tubulin Deglutamylase, Are Associated With Autosomal Recessive Retinitis Pigmentosa

Survey of ophthalmic and systemic features in patients with PNPLA6 -related disorders

Molecular study of the MFRP gene in patients with posterior microphthalmia (MCOP) supports its role in autosomal recessive MCOP pathogenesis

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