Muhammad Asif Naeem
University of the Punjab(PK)Centre of Excellence in Molecular Biology(PK)
Publications by Year
Research Areas
Retinal Development and Disorders, Retinal Diseases and Treatments, Connexins and lens biology, RNA regulation and disease, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease(2013)238 cited
- → GNAT1Associated with Autosomal Recessive Congenital Stationary Night Blindness(2011)73 cited
- → Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening(2017)59 cited
- → Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families(2017)48 cited
- → Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa(2018)44 cited
- → Investigating the Molecular Basis of Retinal Degeneration in a Familial Cohort of Pakistani Decent by Exome Sequencing(2015)39 cited
- → A mutation in IFT43 causes non-syndromic recessive retinal degeneration(2017)37 cited
- → Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts(2016)26 cited
- → A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent(2016)24 cited
- → exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels(2014)24 cited