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Moin D. Mohamed

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
2006 · Eranga N Vithana, Patricio Morgan, et al. · Nature Genetics · 292
Quantification of Homozygosity in Consanguineous Individuals with Autosomal Recessive Disease
2006 · C. Geoffrey Woods, James Cox, et al. · The American Journal of Human Genetics · 263
Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes
2016 · Kamron N. Khan, Omar A. Mahroo, et al. · Progress in Retinal and Eye Research · 224
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration
2012 · Robert K Koenekoop, Hui Wang, et al. · Nature Genetics · 205
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis
2007 · Anneke I den Hollander, Robert K Koenekoop, et al. · Nature Genetics · 200
Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy
2010 · James A. Poulter, Manir Ali, et al. · The American Journal of Human Genetics · 193
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Paracentral acute middle maculopathy and acute macular neuroretinopathy following SARS-CoV-2 infection
2020 · Jonathan Virgo, Moin Mohamed · Eye · 171
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The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies
2020 · Samantha R. De Silva, Gavin Arno, et al. · Progress in Retinal and Eye Research · 152
Ethnic Variations in the Prevalence of Diabetic Retinopathy in People with Diabetes Attending Screening in the United Kingdom (DRIVE UK)
2012 · Sobha Sivaprasad, Bhaskar Gupta, et al. · PLoS ONE · 141
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Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism
2013 · James A. Poulter, Musallam Al-Araimi, et al. · The American Journal of Human Genetics · 93
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Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects
2011 · Kamron Khan, Clare V. Logan, et al. · Human Molecular Genetics · 93
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Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma
2011 · Kamron Khan, Adam Rudkin, et al. · The American Journal of Human Genetics · 82
Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36
2003 · T Jeffrey Keen, Moin D Mohamed, et al. · European Journal of Human Genetics · 62
Spectral Domain Optical Coherence Tomography Findings in Long-term Silicone Oil–related Visual Loss
2014 · Zaid Shalchi, Omar A. Mahroo, et al. · Retina · 57
Poststreptococcal Syndrome Uveitis
2006 · Shafiq Ur Rehman, Seema Anand, et al. · Ophthalmology · 44
Anti‐vascular endothelial growth factor therapies in ophthalmology: current use, controversies and the future
2014 · Tsong Qiang Kwong, Moin Mohamed · British Journal of Clinical Pharmacology · 43
Progession of phenotype in Leber's congenital amaurosis with a mutation at the LCA5 locus
2003 · M D Mohamed · British Journal of Ophthalmology · 41
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Prevalence of vitreomacular interface abnormalities on spectral domain optical coherence tomography of patients undergoing macular photocoagulation for centre involving diabetic macular oedema
2015 · I Akbar Khan, M D Mohamed, et al. · British Journal of Ophthalmology · 40
Retina Rejuvenation Therapy for Diabetic Macular Edema
2012 · Lucia Pelosini, Robin Hamilton, et al. · Retina · 37
A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration.
2008 · Manir Ali, Vedam Lakshmi Ramprasad, et al. · PubMed · 37
Ultrasound biomicroscopy in the management of melanocytoma of the ciliary body with extrascleral extension
2004 · M D Mohamed · British Journal of Ophthalmology · 33
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Macular spectral domain optical coherence tomography findings in Tanzanian endemic optic neuropathy
2013 · John Kisimbi, Zaid Shalchi, et al. · Brain · 32
A new recessively inherited disorder composed of foveal hypoplasia, optic nerve decussation defects and anterior segment dysgenesis maps to chromosome 16q23.3-24.1.
2013 · Musallam Al-Araimi, Bishwanath Pal, et al. · PubMed · 32
Bietti crystalline dystrophy and choroidal neovascularisation
2010 · B. Gupta, S. Parvizi, et al. · International Ophthalmology · 28
A new phenotype of recessively inherited foveal hypoplasia and anterior segment dysgenesis maps to a locus on chromosome 16q23.2–24.2.
2004 · B Pal, M D Mohamed, et al. · Journal of Medical Genetics · 26
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Works count: 69
Citation count: 2,855
H-index: 25
I10-index: 36
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