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Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|November 17, 2025
Early Versus Delayed Decompression in Cauda Equina Syndrome: Neurological and Functional OutcomesGohar Ali, Waseem Sajjad, Muhammad Zeeshan Ali, et al.Heliyon|October 29, 2021
Pharmacological evaluation of Euphorbia hirta, Fagonia indica and Capparis decidua in hypertension through in-vivo and in vitro-assaysMuhammad Zeeshan Ali, Malik Hassan Mehmood, Muhammad Saleem, et al.Nucleosides, Nucleotides & Nucleic Acids|May 8, 2024
Current updates on genetic spectrum of usher syndromeFarman Ullah, Muhammad Zeeshan Ali, Safeer Ahmad, et al.Frontiers in Genetics|September 16, 2024
Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosisJamil Amjad Hashmi, Muhammad Latif, Reham M Balahmar, et al.JPMA. the Journal of the Pakistan Medical Association|May 17, 2017
Ophthalmo-genetic analysis of Pakistani patients with nonsyndromic oculocutaneous albinism through whole exome sequencingHadia Gul, Muhammad Zeeshan Ali, Ejazullah Khan, et al.JPMA. the Journal of the Pakistan Medical Association|January 2, 2022
The molecular genetics of UV-Sensitive syndrome: A rare dermal anomalyMuhammad Muzammal, Muhammad Zeeshan Ali, Safeer Ahmad, et al.Current Medicinal Chemistry|March 27, 2025
Identification of a Protein-truncating Variant in SCAPER Gene Causing Syndromic form of Intellectual DisabilityMonis Bilal Shamsi, Muhammad Zeeshan Ali, Safeer Ahmad, et al.Bone Reports|November 14, 2024
A clinical and molecular characterization of a Pakistani family with multicentric osteolysis, nodulosis and arthropathy (MONA) syndromeSafeer Ahmad, Mari Muurinen, Petra Loid, et al.Pakistan Journal of Pharmaceutical Sciences|March 4, 2020
A flavonoid driven phyto-pharmacological effects of Capparis decidua Edgew. in rodentsMuhammad Zeeshan Ali, Malik Hassan Mehmood, Muhammad Haneef, et al.Journal of Genetics|July 5, 2017
Molecular genetic analysis of consanguineous families with primary microcephaly identified pathogenic variants in the ASPM geneMuzammil Ahmad Khan, Christian Windpassinger, Muhammad Zeeshan Ali, et al.Pageof 4