Author

Asad Munir

Observed name: Munir, Asad

Institution: Hazara University

Observed institution: Hazara University

ORCID: 0000-0001-5461-3599

Observed ORCID: 0000-0001-5461-3599

OpenAlex ID: A5075891849

A systematic review of inherited retinal dystrophies in Pakistan: updates from 1999 to April 2023

2024 · Asad Munir, Salma Afsar, et al. · BMC Ophthalmology · 17

A comprehensive genetic landscape of inherited retinal diseases in a large Pakistani cohort

2025 · Mukhtar Ullah, Atta Ur Rehman, et al. · npj Genomic Medicine · 14

Early-Onset Retinopathy in Patients With Variants in SLC6A6 Leading to Impaired Taurine Transport

2025 · Mukhtar Ullah, Atta Ur Rehman, et al. · JAMA Ophthalmology · 2

Exome sequencing identifies a homozygous splice site variant in RP1 as the underlying cause of autosomal recessive retinitis pigmentosa in a Pakistani family

2025 · Abdur Rashid, Asad Munir, et al. · Annals of Medicine · 2

A novel homozygous missense variant in POC1B causes cone dystrophy in a consanguineous Pakistani family

2024 · Asad Munir, Inam Ullah Khan, et al. · Ophthalmic Genetics · 1

The genetic architecture of monogenic neurodevelopmental disorders in Pakistan: a systematic review, 2006–2024

2026 · Fareeza Anwar, Shah Zainab, et al. · Research Square

Duplication of 4-bp in SACS leads to autosomal recessive spastic ataxia of Charlevoix–Saguenay type in two Pakistani patients

2026 · Saba Bibi, Asad Munir, et al. · Human Genome Variation

Uncovering the Novel Genetic Determinants of Primary Congenital Glaucoma in Pakistani Families

2026 · Hamza Khan, Sadia Bukhari, et al. · Human Mutation

A novel homozygous DST variant causes hereditary sensory and autonomic neuropathy in a Pakistani family

2025 · Asad Munir, Helen Nabiryo Frederiksen, et al. · Human Genome Variation

Works count: 13

Citation count: 36

H-index: 2

I10-index: 2