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Journal of Personalized Medicine|August 26, 2022
Pharmacological Efficacy of Probiotics in Respiratory Viral Infections: A Comprehensive ReviewShadma Wahab, Dalia Almaghaslah, Syed Esam Mahmood, et al.Journal of Infection and Public Health|July 31, 2023
Deciphering the emerging role of phytocompounds: Implications in the management of drug-resistant tuberculosis and ATDs-induced hepatic damageMohammad Azam Ansari, Shoaib Shoaib, Mohammad N Alomary, et al.Human Mutation|September 1, 2005
Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairmentRegie Lyn P Santos, Muhammad Wajid, Mohammad Nasim Khan, et al.Journal of Medical Genetics|July 11, 2015
A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hairMuhammad Ansar, Syed Irfan Raza, Kwanghyuk Lee, et al.Journal of Human Genetics|September 5, 2018
Novel missense and 3'-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairmentKhurram Liaqat, Ilene Chiu, Kwanghyuk Lee, et al.Journal of Human Genetics|April 21, 2021
Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13Anushree Acharya, Syed Irfan Raza, Muhammad Zeeshan Anwar, et al.Antibiotics (Basel, Switzerland)|March 4, 2020
Biogenic Gold Nanoparticles as Potent Antibacterial and Antibiofilm Nano-Antibiotics against <i>Pseudomonas aeruginosa</i>Syed Ghazanfar Ali, Mohammad Azam Ansari, Mohammad A Alzohairy, et al.The Journal of Dermatology|June 26, 2024
Novel pathogenic variants in HR underlie atrichia with papular lesions in a cohort of 10 familiesKifayat Ullah, Sohail Ahmed, Nicole Cesarato, et al.European Journal of Medical Genetics|May 16, 2020
Biallelic variants in four genes underlying recessive osteogenesis imperfectaAmir Hayat, Shabir Hussain, Muhammad Bilal, et al.Journal of Human Genetics|December 1, 2018
Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significanceKhurram Liaqat, Isabelle Schrauwen, Syed Irfan Raza, et al.Pageof 34