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 · 198 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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 · 130 citations

Life Sciences, Genetics, Ophthalmology +15

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 · 106 citations · Full text

Medicine, Genetics, Molecular Genetics +13

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 · Full text

Life Sciences, Genetics, Molecular Genetics +13

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

Life Sciences, Genetics, Ophthalmology +14