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Genes|September 23, 2022
Exome Sequencing Identified Molecular Determinants of Retinal Dystrophies in Nine Consanguineous Pakistani FamiliesRaeesa Tehreem, Iris Chen, Mudassar Raza Shah, et al.
Congenital Anomalies|October 2, 2018
Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2Rabia Afzal, Sabika Firasat, Haiba Kaul, et al.
Acta Parasitologica|August 8, 2025
Effectiveness of Anthelmintic Therapy and Determinants of Ascaris lumbricoides Infection among School-Aged Children: A Community-Based Cross-Sectional Study in Rural Khyber Pakhtunkhwa, PakistanAmjad Ullah Khan, Shahzad Hussain, Majid Khan, et al.
Peerj|December 15, 2022
Screening of high-risk deleterious missense variations in the CYP1B1 gene implicated in the pathogenesis of primary congenital glaucoma: A comprehensive in silico approachMuhammad Shahid, Ahmad Azfaralariff, Muhammad Tufail, et al.
Molecular Biology Reports|October 12, 2021
SLC4A11 mutations causative of congenital hereditary endothelial dystrophy (CHED) progressing to Harboyan syndrome in consanguineous Pakistani familiesSabika Firasat, Dur-E-Shawar, Wajid Ali Khan, et al.
Plos One|August 29, 2022
Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, PakistanAfia Iqbal, Shagufta Naz, Haiba Kaul, et al.
Microscopy Research and Technique|June 17, 2024
Revealing tick diversity: Chemical profiling and dynamics in scanning microscopy and molecular phylogeneticsAyesha Malik, Kiran Afshan, Mohammad K Okla, et al.
Plos One|October 26, 2023
Correction: Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, PakistanAfia Iqbal, Shagufta Naz, Haiba Kaul, et al.
Molecular Vision|November 27, 2025
Mutations in retinal cyclic nucleotide-gated channels identified in familial cases of inherited retinal dystrophies from PakistanZainab Akhtar, Kiran Afshan, Yumei Li, et al.
Human Genome Variation|August 11, 2016
A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descentBushra Rauf, Bushra Irum, Firoz Kabir, et al.
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