Asad Munir

4PUBLICATIONS

11CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesVision science

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Publications (4)

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|Sep 19, 2026

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

|Apr 27, 2026

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

|Nov 18, 2025

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

Asad Munir, Helen Nabiryo Frederiksen, Fawad Ali

|Nov 21, 2024

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

Asad Munir, Inam Ullah Khan, Abdur Rashid

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Frequent Collaborators

Atta Ur Rehman

Hamid Ur Rahman

Shahab Uddin

Mukhtar Ullah

Hamza Khan

Yousaf Jamal Mahsood

Muhammad Moeez Uddin

Syeda Hafiza Benish Ali

1 joint publications

Muhammad Ajmal

1 joint publications

Maleeha Azam

Frequent Collaborators

Atta Ur Rehman

Hamid Ur Rahman

Shahab Uddin

Mukhtar Ullah