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Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|March 6, 2026
Effect of Mesenchymal Stem Cell Infusion in Stage II-IV Diabetic NephropathySohail Sabir, Mohsin Shahzad, Umair Ijaz Malik, et al.
Sensors (Basel, Switzerland)|February 15, 2022
Towards Automatic License Plate DetectionZahid Mahmood, Khurram Khan, Uzair Khan, et al.
Genes|February 25, 2023
FRMD7 Gene Alterations in a Pakistani Family Associated with Congenital Idiopathic NystagmusMuhammad Waqar Arshad, Muhammad Imran Shabbir, Saaim Asif, et al.
RSC Advances|February 26, 2025
Tuning diffusion coefficient, ionic conductivity, and transference number in rGO/BaCoO3 electrode material for optimized supercapacitor energy storageMohsin Shahzad, Farooq Ahmad, M Ibraheem, et al.
Genes|August 27, 2020
Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing LossSaba Zafar, Mohsin Shahzad, Rafaqat Ishaq, et al.
Biochemical Genetics|November 1, 2017
Genetic Testing of Non-familial Deaf Patients for CIB2 and GJB2 Mutations: Phenotype and Genetic CounsellingHina Shaikh, Ali M Waryah, Ashok K Narsani, et al.
Arabian Journal of Chemistry|December 15, 2021
In silico screening, SAR and kinetic studies of naturally occurring flavonoids against SARS CoV-2 main proteaseMuhammad Imran, Sana Iqbal, Ajaz Hussain, et al.
Transboundary and Emerging Diseases|May 5, 2022
Genome sequencing and analysis of genomic diversity in the locally transmitted SARS-CoV-2 in PakistanMuhammad Shakeel, Muhammad Irfan, Zaib Un Nisa, et al.
European Journal of Human Genetics : EJHG|July 24, 2014
Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophyRehan S Shaikh, Peggy Reuter, Robert A Sisk, et al.
Genes|May 25, 2024
A Missense Variant in HACE1 Is Associated with Intellectual Disability, Epilepsy, Spasticity, and Psychomotor Impairment in a Pakistani KindredMuhammad A Usmani, Amama Ghaffar, Mohsin Shahzad, et al.
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