Former faculty

Dr. M. Asif Naeem

Assistant Professor (TTS) Genetic Diseases Research Lab

Former in-charge of the Vision Impairment Lab, whose research worked to prevent heritable blindness in Pakistan through genetic screening.

Former facultyCEMB · University of the Punjab
154Consanguineous families sampled
36Manuscripts published
2PhD students trained

Profile

Human Geneticist, Vision Researcher and Educator

Dr. Muhammad Asif Naeem earned his PhD in Molecular Biology from CEMB, University of the Punjab. At CEMB he served as in-charge of the Vision Impairment Lab, Assistant Professor (TTS), and Principal Investigator of the HEC NRPU project "Investigating the Molecular Basis of Retinitis Pigmentosa (RP)," combining traditional linkage analysis with next-generation sequencing.

He has established links with LRBT Eye Hospital, Allama Iqbal Medical College Research Centre and the Ophthalmology Department of Jinnah Hospital nationally, and international collaborations with the National Eye Institute (Bethesda, USA) and the Wilmer Eye Institute at Johns Hopkins University.

His goal is to prevent heritable blindness in Pakistan through screening, research and education. DNA samples from 154 consanguineous Pakistani families affected by retinitis pigmentosa and congenital cataract have been processed to identify pathogenic mutations, with genome-wide scan and exome sequencing data analysed and two PhD students trained in these techniques. His work has resulted in 36 published manuscripts in international peer-reviewed journals.

Selected contributions

Science translated into capability

01

Retinitis Pigmentosa research

Principal Investigator of an HEC NRPU project on the molecular basis of Retinitis Pigmentosa.

02

Large family cohort study

Processed DNA from 154 consanguineous Pakistani families affected by RP and congenital cataract.

03

International eye-research collaborations

Partnerships with the National Eye Institute (USA) and the Wilmer Eye Institute at Johns Hopkins University.

04

NIH training

Trained at NIH during the 2018 Summit, using the experience to revise CEMB's Medical Genetics course.

Research output

Selected publications

A selection of publications listed on the official CEMB faculty profile.

  1. 01
    2015 · Mol Vis

    AIPL1 is implicated in the pathogenesis of two autosomal recessive retinal degeneration cases

  2. 02
    2015 · PLoS One

    Investigating the Molecular Basis of Retinal Degeneration in a Familial Cohort of Pakistani Decent by Exome Sequencing

  3. 03
    2015 · Mol Vis

    Splice-site mutations identified in PDE6A are responsible for retinitis pigmentosa in consanguineous Pakistani families

  4. 04
    2015 · Ophthalmology

    Phenotypic Variability Associated with the D226N Allele of IMPDH1

  5. 05
    2014 · Genomics

    ExomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease-causing SNVs/indels

  6. 06
    2013 · Am J Hum Genet

    Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

  7. 07
    2013 · Mol Vis

    Novel Mutations in RPE65 Identified in Consanguineous Pakistani Families with Retinal Dystrophies

  8. 08
    2012 · Invest Ophthalmol Vis Sci

    GNAT1 Associated with Autosomal Recessive Congenital Stationary Night Blindness

  9. 09
    2011 · Arch Ophthalmol

    Pathogenic mutations in TULP1 are associated with Retinitis pigmentosa in consanguineous Pakistani families

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