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Weihua Meng

Queen's University Belfast

19

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319

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Rare CFH mutations and early-onset age-related macular degeneration

2016 Acta Ophthalmologica
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Citations (9)
Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

2013 Journal of Medical Genetics
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A novel GUCY2D mutation, V933A, causes central areolar choroidal dystrophy.

2012 Investigative Ophthalmology & Visual Science
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A linear regression model to differentiate axial myopia from non-axial myopia

2012 Ophthalmic Genetics
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Genetic Factors for Choroidal Neovascularization Associated with High Myopia

2012 Investigative Ophthalmology & Visual Science
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Macular Degeneration Genetics

2012 Ophthalmology
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Myopia and iris colour: A possible connection?

2012 Medical Hypotheses
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Axial Length of Myopia: A Review of Current Research

2011 Ophthalmologica
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Article originalCaractérisation du profil biométrique oculaire d’une population myope fort : la myopie forte correspond-elle à un phénotype homogène ?Characterization of the biometric eye profile of a high myopic population: Does high myopia correspond to a homogenous phenotype?

2011 Journal Francais D Ophtalmologie
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Variants in the Nestin Gene and Coronary Heart Disease

2008 Circulation
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Citations (5)