Publications by authors named "Moin D Mohamed"

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Bifocal retinal degeneration observed on ultra-widefield autofluorescence in some cases of CRX-associated retinopathy.
Siying Lin, Gavin Arno, Anthony G Robson, Elena R Schiff, Moin D Mohamed

Eye (Lond)· April 2025

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Unusual OCT findings in a patient with CABP4-associated cone-rod synaptic disorder.
Jit Kai Tan, Gavin Arno, Dragana Josifova, Moin D Mohamed, Omar A Mahroo

Doc Ophthalmol· April 2024

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Impact of the ongoing worldwide shortage of verteporfin (Visudyne®) on the visual function of patients with chronic central serous chorioretinopathy.
Chrysanthi Tsika, Moin D Mohamed, Andrew J Lotery

Acta Ophthalmol· February 2024

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Novel homozygous mutations in the transcription factor cause non-syndromic retinitis pigmentosa.
Mohammed E El-Asrag, Marta Corton, Martin McKibbin, Almudena Avila-Fernandez, Moin D Mohamed

Mol Vis· June 2022

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The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies.
Samantha R De Silva, Gavin Arno, Anthony G Robson, Ana Fakin, Nikolas Pontikos, Moin D Mohamed

Prog Retin Eye Res· May 2021

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Clinical Features of a Retinopathy Associated With a Dominant Allele of the RGR Gene.
Rola Ba-Abbad, Monique Leys, Xinjing Wang, Christina Chakarova, Naushin Waseem, Moin D Mohamed

Invest Ophthalmol Vis Sci· October 2018

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Retinal thickness measurements in sickle cell patients with HbSS and HbSC genotype.
Wei S Lim, Tejal Magan, Omar A Mahroo, Pirro G Hysi, Juliana Helou, Moin D Mohamed

Can J Ophthalmol· August 2018

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Risk factors for visual impairment in patients with sickle cell disease in London.
Shohista Saidkasimova, Zaid Shalchi, Omar A Mahroo, Manoharan Shunmugam, D Alistair H Laidlaw, Moin D Mohamed

Eur J Ophthalmol· August 2016

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Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes.
Kamron N Khan, Omar A Mahroo, Rehna S Khan, Moin D Mohamed, Martin McKibbin

Prog Retin Eye Res· July 2016

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Cilioretinal Artery Territory Infarction Associated With Papilledema in a Patient With Neurofibromatosis Type 2.
Omar A Mahroo, Moin D Mohamed, Elizabeth M Graham, Samantha S Mann, Gordon T Plant

J Neuroophthalmol· March 2016

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Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy.
James A Poulter, Manir Ali, David F Gilmour, Aine Rice, Hiroyuki Kondo, Moin D Mohamed

Am J Hum Genet· March 2016

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Re: Abegg et al.: Microcystic macular edema: retrograde maculopathy caused by optic neuropathy (Ophthalmology 2014;121:142-9).
Omar A Mahroo, Zaid Shalchi, John Kisimbi, Anna J Sanyiwa, Moin D Mohamed

Ophthalmology· August 2014

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A new recessively inherited disorder composed of foveal hypoplasia, optic nerve decussation defects and anterior segment dysgenesis maps to chromosome 16q23.3-24.1.
Musallam Al-Araimi, Bishwanath Pal, James A Poulter, Maria M van Genderen, Ian Carr, Moin D Mohamed

Mol Vis· March 2014

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Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism.
James A Poulter, Musallam Al-Araimi, Ivan Conte, Maria M van Genderen, Eamonn Sheridan, Moin D Mohamed

Am J Hum Genet· December 2013

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Central visual disturbance associated with transient disruption of photoreceptor inner-outer segment junction.
Omar A R Mahroo, Elizabeth A Gavin, Samantha Mann, Moin D Mohamed

Can J Ophthalmol· October 2012

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Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration.
Robert K Koenekoop, Hui Wang, Jacek Majewski, Xia Wang, Irma Lopez, Moin D Mohamed

Nat Genet· September 2012

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Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects.
Kamron Khan, Clare V Logan, Martin McKibbin, Eamonn Sheridan, Nursel H Elçioglu, Moin D Mohamed

Hum Mol Genet· February 2012

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Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.
Kamron Khan, Adam Rudkin, David A Parry, Kathryn P Burdon, Martin McKibbin, Moin D Mohamed

Am J Hum Genet· September 2011

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Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.
James A Poulter, Manir Ali, David F Gilmour, Aine Rice, Hiroyuki Kondo, Moin D Mohamed

Am J Hum Genet· February 2010

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Genotype-phenotype correlation for leber congenital amaurosis in Northern Pakistan.
Martin McKibbin, Manir Ali, Moin D Mohamed, Adam P Booth, Fiona Bishop

Arch Ophthalmol· January 2010

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Further insight into West African crystalline maculopathy.
Saul N Rajak, Moin D Mohamed, Lucia Pelosini

Arch Ophthalmol· July 2009

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A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration.
Manir Ali, Vedam Lakshmi Ramprasad, Nagasamy Soumittra, Moin D Mohamed, Hussain Jafri

Mol Vis· March 2009

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Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.
Anneke I den Hollander, Robert K Koenekoop, Moin D Mohamed, Heleen H Arts, Karsten Boldt

Nat Genet· July 2007

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Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).
Eranga N Vithana, Patricio Morgan, Periasamy Sundaresan, Neil D Ebenezer, Donald T H Tan, Moin D Mohamed

Nat Genet· July 2006

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Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.
C Geoffrey Woods, James Cox, Kelly Springell, Daniel J Hampshire, Moin D Mohamed

Am J Hum Genet· May 2006

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