Atta Ur Rehman

10PUBLICATIONS
14CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesEpidemiological methodsCancer geneticsNeurogenetics
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Publications (10)

|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

|Oct 14, 2025
Epidemiological patterns of cutaneous leishmaniasis in north-west Pakistan (2022-2023).

Shahab Uddin, Izharullah Khan, Atta Ur Rehman

|Sep 04, 2025
BRCA1 Exon 11 Mutations in Breast Cancer: A Study From Pakistan.

Murad Ali, Aziz Uddin, Sajid Ul Ghafoor

|Mar 03, 2025
Exome sequencing identifies a homozygous splice site variant in RP1 as the underlying cause of autosomal recessive retinitis pigmentosa in a Pakistani family.

Abdur Rashid, Asad Munir, Muhammad Zahid

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Frequent Collaborators

4 joint publications

Asad Munir

3 joint publications

Hamid Ur Rahman

2 joint publications

Shahab Uddin

1 joint publications

Sajid Malik