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Theriogenology|September 11, 2020
Effect of photoperiodicity and methods of follicular wave emergence on follicle turn-over, recovery and quality of oocytes, and early in-vitro developmental competence of embryos using ovum pick-up in Nili-Ravi buffaloes: Preliminary evidenceMasroor Sagheer, Farid Ullah, Usman Arshad, et al.
The International Journal of Neuroscience|March 21, 2019
A novel in-frame mutation in CLN3 leads to Juvenile neuronal ceroid lipofuscinosis in a large Pakistani familyMuhammad Sher, Muhammad Farooq, Uzma Abdullah, et al.
Pharmaceuticals (Basel, Switzerland)|October 27, 2022
Anti-Alzheimer and Antioxidant Effects of Nelumbo nucifera L. Alkaloids, Nuciferine and Norcoclaurine in Alloxan-Induced Diabetic Albino RatsShahnaz Khan, Hidayat Ullah Khan, Farman Ali Khan, et al.
Frontiers in Oral Health|May 8, 2025
Odontogenic carcinosarcoma: a comprehensive review of clinical and therapeutic insightsMuhammad Osama, Cyril Kocherry, Farid Ullah, et al.
Vaccines|March 27, 2026
From Estimated Targets to Verified Coverage: Implementation of a Community Health Worker-Based Tracking Intervention to Address Denominator Inaccuracies in High-Risk Urban Settings of Balochistan, PakistanRubab Kamran, Maliha Fatima, Babar Shahid, et al.
European Journal of Medical Genetics|April 19, 2021
A GDF5 frameshift mutation segregating with Grebe type chondrodysplasia and brachydactyly type C+ in a 6 generations family: Clinical report and mini reviewSanam Faryal, Muhammad Farooq, Uzma Abdullah, et al.
Human Genetics|October 14, 2021
A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing lossFarid Ullah, Waqar Rauf, Kamal Khan, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Pathogenic variants in TMEM184B cause a neurodevelopmental syndrome via alteration of metabolic signalingKimberly A Chapman, Farid Ullah, Zachary A Yahiku, et al.
American Journal of Human Genetics|May 14, 2019
Bi-allelic Variants in DYNC1I2 Cause Syndromic Microcephaly with Intellectual Disability, Cerebral Malformations, and Dysmorphic Facial FeaturesMuhammad Ansar, Farid Ullah, Sohail A Paracha, et al.
Annals of Neurology|September 12, 2017
Mutations of KIF14 cause primary microcephaly by impairing cytokinesisAbubakar Moawia, Ranad Shaheen, Sajida Rasool, et al.
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