Author

Kamron N. Khan

Observed names: K Khan, K N Khan, K. Khan, K. N. Khan, K.N. Khan, Kamron Khan, Kamron N Khan, Kamron Nasser Khan, Khan, K, Khan, Kamron, Khan, Kamron N

Institution: Tufts University

Observed institutions: Tufts University, University of Leeds, Moorfields Eye Hospital NHS Foundation Trust, Harvard University, University of Cambridge, Leeds Teaching Hospitals NHS Trust, Calderdale Royal Hospital, Hull University Teaching Hospitals NHS Trust, Bradford Royal Infirmary, Aberdeen Royal Infirmary, St James's University Hospital, Cork University Hospital, Calderdale and Huddersfield NHS Foundation Trust, St Mary's Hospital, Manchester University NHS Foundation Trust, Queen's Medical Centre, Moorfields Eye Hospital, University College London

ORCID: 0000-0001-8654-1323

Observed ORCID: 0000-0001-8654-1323

OpenAlex ID: A5085805504

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

Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options

2019 · Najiha Rahman, Michalis Georgiou, et al. · British Journal of Ophthalmology · 139

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Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa

2016 · Gavin Arno, Smriti A. Agrawal, et al. · The American Journal of Human Genetics · 124

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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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Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy

2018 · Kamron N. Khan, Melissa Kasilian, et al. · Ophthalmology · 83

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Clinical and Genetic Features of Choroideremia in Childhood

2016 · Kamron N. Khan, Farrah Islam, et al. · Ophthalmology · 82

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

A clinical and molecular characterisation of CRB1-associated maculopathy

2018 · Kamron N. Khan, Anthony Robson, et al. · European Journal of Human Genetics · 74

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Changes in Retinal Sensitivity Associated With Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa With RPGR Gene Variations

2023 · Lenore von Krusenstiern, Jiajun Liu, et al. · JAMA Ophthalmology · 67

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Autosomal Recessive Bestrophinopathy

2020 · Giuseppe Casalino, Kamron N. Khan, et al. · Ophthalmology · 55

Specific Alleles of CLN7 / MFSD8 , a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy

2017 · Kamron N. Khan, Mohammed E. El-Asrag, et al. · Investigative Ophthalmology & Visual Science · 53

Association of Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation With Early-Onset Retinal Dystrophy

2017 · Rachel L. Taylor, Gavin Arno, et al. · JAMA Ophthalmology · 51

DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration

2020 · Anjali Vig, James A. Poulter, et al. · Genetics in Medicine · 47

Functional and Anatomical Outcomes of Choroidal Neovascularization Complicating Best1-related Retinopathy

2016 · Kamron N. Khan, Omar A. Mahroo, et al. · Retina · 41

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Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.

2010 · Manir Ali, Beatriz Buentello-Volante, et al. · PubMed · 41

Loss-of-Function Mutations in the CFH Gene Affecting Alternatively Encoded Factor H-like 1 Protein Cause Dominant Early-Onset Macular Drusen

2019 · Rachel L. Taylor, James A. Poulter, et al. · Ophthalmology · 37

Systemic lipid dysregulation is a risk factor for macular neurodegenerative disease

2020 · Roberto Bonelli, Sasha M. Woods, et al. · Scientific Reports · 36

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Unilateral BEST1-Associated Retinopathy

2016 · Rashi Arora, Kamron Khan, et al. · American Journal of Ophthalmology · 36

Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

2017 · Gavin Arno, Keren J. Carss, et al. · The American Journal of Human Genetics · 34

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Panel‐based genetic testing for inherited retinal disease screening 176 genes

2021 · Leo H. N. Sheck, Simona D. Esposti, et al. · Molecular Genetics & Genomic Medicine · 33

Outcomes of sulfur hexafluoride (SF6) versus perfluoroethane (C2F6) gas tamponade for non-posturing macular-hole surgery

2011 · Rubina Rahman, Indira Madgula, et al. · British Journal of Ophthalmology · 33

Outcome of Cataract Surgery in Patients With Retinitis Pigmentosa

2022 · Xuan-Thanh-An Nguyen, Alberta A.H.J. Thiadens, et al. · American Journal of Ophthalmology · 30

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Optical Coherence Tomographic Pattern May Predict Visual Outcome after Intravitreal Triamcinolone for Diabetic Macular Edema

2007 · S.K. Gibran, K. Khan, et al. · Ophthalmology · 30

Phenotype and genotype of 197 British patients with McArdle disease: An observational single‐centre study

2021 · Chiara Pizzamiglio, Omar A. Mahroo, et al. · Journal of Inherited Metabolic Disease · 26

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Works count: 93

Citation count: 2,061

H-index: 26

I10-index: 45