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Genetics and Molecular Biology|February 1, 2018
Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformationAsmat Ullah, Ajab Gul, Muhammad Umair, et al.Molecular Neurobiology|July 21, 2019
Deciphering the Role of WNT Signaling in Metabolic Syndrome-Linked Alzheimer's DiseaseAbuzer Ali, Amena Ali, Wasim Ahmad, et al.Plos One|June 27, 2015
A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31Rabia Habib, Muhammad Ansar, Manuel Mattheisen, et al.Annals of Human Genetics|January 12, 2018
A novel homozygous variant in BMPR1B underlies acromesomelic dysplasia Hunter-Thompson typeAsmat Ullah, Muhammad Umair, Dost Muhammad, et al.Annals of Human Genetics|August 30, 2022
A splice site variant in TCTN3 underlies an atypical form of orofaciodigital syndrome IVShabir Hussain, Shoaib Nawaz, Hammal Khan, et al.Journal of Pharmacy & Bioallied Sciences|October 18, 2019
<i>Tamarindus indica</i> Fruit: Pharmacognostical Standardization, Detection of Contaminant, and <i>In Vitro</i> Antioxidant ActivityMohd Amir, Niyaz Ahmad, Md Sarfaroz, et al.CNS & Neurological Disorders Drug Targets|January 11, 2021
Experimental Rodent Models of Vascular Dementia: A Systematic ReviewNidhi Tiwari, Jyoti Upadhyay, Mohammad Nazam Ansari, et al.3 Biotech|August 29, 2023
Formulation of lemongrass oil (<i>Cymbopogon citratus</i>)-loaded solid lipid nanoparticles: an in vitro assessment studyAbuzer Ali, Amena Ali, Musarrat Husain Warsi, et al.Bone|March 5, 2026
HOXD12 a candidate gene for a novel form of synpolydactylyHammal Khan, Muhammad Bilal, Thashi Bharadwaj, et al.Molecular Genetics & Genomic Medicine|May 23, 2019
Exome sequencing revealed a novel loss-of-function variant in the GLI3 transcriptional activator 2 domain underlies nonsyndromic postaxial polydactylyMuhammad Umair, Naveed Wasif, Alia M Albalawi, et al.Pageof 34