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Journal of Genetics|September 2, 2021
Homozygosity mapping coupled with whole-exome sequencing and protein modelling identified a novel missense mutation in GUCY2D in a consanguineous Pakistani family with Leber congenital amaurosisHadia Gul, Abdul Haleem Shah, Ricardo Harripaul, et al.
Evolutionary Bioinformatics Online|April 27, 2019
Evolutionary Analysis of Makorin Ring Finger Protein 3 Reveals Positive Selection in MammalsMuhammad Jamil Ahmad, Hafiz Ishfaq Ahmad, Muhammad Muzammal Adeel, et al.
Molecules (Basel, Switzerland)|May 28, 2022
Preparation and Characterization of Controlled-Release Floating Bilayer Tablets of Esomeprazole and ClarithromycinMuhammad Israr, Nicola Pugliese, Arshad Farid, et al.
Polymers|July 27, 2022
Preparation and In Vitro Evaluation of Controlled-Release Matrices of Losartan Potassium Using Ethocel Grade 10 and Carbopol 934P NF as Rate-Controlling PolymersKamran Ahmad Khan, Claudia Zizzadoro, Alessandro Di Cerbo, et al.
International Journal of Ophthalmology|October 29, 2025
Protein truncating splice site variant in ALDH1A3 associated with bilateral anophthalmia identified in a multiplex consanguineous Pakistani familyKashmala Samad, Khalid J Alzahrani, Khalaf F Alsharif, et al.
Molecules (Basel, Switzerland)|May 28, 2022
In Silico Analysis and Functional Characterization of Antimicrobial and Insecticidal Vicilin from Moth Bean (Vigna aconitifolia (Jacq.) Marechal) SeedsMuhammad Ateeq, Muhammad Muzammal Adeel, Ayesha Kanwal, et al.
Molecules (Basel, Switzerland)|February 15, 2022
Preparation of Losartan Potassium Controlled Release Matrices and In-Vitro Investigation Using Rate Controlling AgentsKamran Ahmad Khan, Gul Majid Khan, Muhammad Muzammal, et al.
Metabolic Brain Disease|November 1, 2021
A novel protein truncating mutation in L2HGDH causes L-2-hydroxyglutaric aciduria in a consanguineous Pakistani familyMuhammad Muzammal, Muhammad Zeeshan Ali, Beatrice Brugger, et al.
Frontiers in Genetics|November 7, 2022
Transcriptome analysis reveals pathogenesis-related gene 1 pathway against salicylic acid treatment in grapevine (Vitis vinifera L)Faiz Ur Rahman, Irshad Ahmad Khan, Ali Aslam, et al.
Genetics and Molecular Biology|February 13, 2026
A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani familySana Fatima, Dong Sun, Jianguo Han, et al.
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