Muhammad Imran Khan
International Islamic University, Islamabad(PK)University of Toronto(CA)University of Balochistan(PK)Combined Military Hospital(PK)Hayatabad Medical Complex(PK)Government of Khyber Pakhtunkhwa(PK)
Publications by Year
Research Areas
Retinal Development and Disorders, Retinal Diseases and Treatments, Glaucoma and retinal disorders, Ocular Disorders and Treatments, Corneal surgery and disorders
Most-Cited Works
- → Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides(2019)195 cited
- → A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)(2019)121 cited
- → Mutations in IMPG2, Encoding Interphotoreceptor Matrix Proteoglycan 2, Cause Autosomal-Recessive Retinitis Pigmentosa(2010)104 cited
- Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts.(2010)
- MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma.(2009)
- → Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects(2016)58 cited
- → A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular coloboma