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Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|June 10, 2021
Potential health benefits of carotenoid lutein: An updated reviewSaikat Mitra, Abdur Rauf, Abu Montakim Tareq, et al.
Open Access Journal of Contraception|June 24, 2026
Impact of The Challenge Initiative on Public-Sector Family Planning Service Provision in Pakistan: Evidence from a Difference-in-Differences AnalysisGhazunfer Abbas, Junaid-Ur-Rehman Siddiqui, Bushra Rahim Butt, et al.
Journal of the American Chemical Society|December 9, 2025
Electrochemical CO<sub>2</sub> Capture by a Quinone-Based Covalent Organic FrameworkMuhammad Abdullah Khan, Zhen Xu, Muhammad Muzammil, et al.
Oxidative Medicine and Cellular Longevity|January 31, 2022
Antioxidant and Cytotoxic Activity of a New Ferruginan A from <i>Olea ferruginea</i>: <i>In Vitro</i> and <i>In Silico</i> StudiesZafar Ali Shah, Adil A H Mujawah, Irfan Ullah, et al.
Brain : a Journal of Neurology|September 18, 2024
Biallelic EPB41L3 variants underlie a developmental disorder with seizures and myelination defectsElizabeth A Werren, Guillermo Rodriguez Bey, Purvi Majethia, et al.
American Journal of Human Genetics|March 12, 2021
Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsyAmbrin Fatima, Jan Hoeber, Jens Schuster, et al.
Genes|June 2, 2021
Modifier Genes in Microcephaly: A Report on <i>WDR62</i>, <i>CEP63</i>, <i>RAD50</i> and <i>PCNT</i> Variants Exacerbating Disease Caused by Biallelic Mutations of <i>ASPM</i> and <i>CENPJ</i>Ehtisham Ul Haq Makhdoom, Syeda Seema Waseem, Maria Iqbal, et al.
Annals of Neurology|September 12, 2017
Mutations of KIF14 cause primary microcephaly by impairing cytokinesisAbubakar Moawia, Ranad Shaheen, Sajida Rasool, et al.
Molecular Genetics & Genomic Medicine|July 18, 2020
An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from PakistanSajida Rasool, Jamshaid Mahmood Baig, Abubakar Moawia, et al.
Journal of Inherited Metabolic Disease|September 15, 2023
Biallelic missense variants in COG3 cause a congenital disorder of glycosylation with impairment of retrograde vesicular traffickingRuizhi Duan, Dana Marafi, Zhi-Jie Xia, et al.
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