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Shery Thomas

University of Leicester

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Abnormal retinal development associated with FRMD7 mutations

2014 Human Molecular Genetics
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Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation

2014 European Journal of Human Genetics
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The Genetics of Nystagmus and Associated Inherited Diseases

2012
- Shery Thomas
- Irene Gottlob
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Erratum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (Nature Genetics (2006) 38 (1242-1244))

2011 Nature Genetics
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Clinical and oculomotor characteristics of albinism compared to FRMD7 associated infantile nystagmus.

2011 Investigative Ophthalmology & Visual Science
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Table 2. [How the Infantile Nystagmus Waveform Evolves: An Example].

2011
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Figure 1. [Eye rotation can occur about...].

2011
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Figure 2. [The horizontal eye movement recordings...].

2011
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Erratum: Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography: A predictor of visual acuity? (Ophthalmology (2011) 118 (1653-1160))

2011 Ophthalmology
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Table 1. [Summary of Molecular Genetic Testing Used in FRMD7-Related Infantile Nystagmus].

2011
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