Muhammad Imran Khan

Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides

Riccardo Sangermano, Alejandro Garanto, Mubeen Khan et al. · Genetics in Medicine · 2019 · 192 citations · Full text

A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)

Dror Sharon, Tamar Ben‐Yosef, Nitza Goldenberg‐Cohen et al. · Human Mutation · 2019 · 119 citations

Ocular Disease, Genetics, Genetic Epidemiology +17

Mutations in IMPG2, Encoding Interphotoreceptor Matrix Proteoglycan 2, Cause Autosomal-Recessive Retinitis Pigmentosa

Dikla Bandah‐Rozenfeld, Rob W.J. Collin, Eyal Banin et al. · The American Journal of Human Genetics · 2010 · 104 citations · Full text

Genome Instability, Mendelian Disorder, Genetic Disorder +6

Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts.

Humaira Ayub, Muhammad Imran Khan, Shazia Micheal et al. · PubMed · 2010 · 66 citations

MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma.

Shazia Micheal, Raheel Qamar, Farah Akhtar et al. · PubMed · 2009 · 65 citations · Full text