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Environmental Monitoring and Assessment|June 25, 2025
A comparative study of fully automatic and semi-automatic methods for oil spill detection using Sentinel-1 dataMuhammad Iqbal Habibie, Hariyanto, Robby Arifandri, et al.
Frontiers in Neurology|June 12, 2023
Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanismsNazif Muhammad, Syeda Iqra Hussain, Zia Ur Rehman, et al.
Biotechnology and Applied Biochemistry|November 26, 2021
Mutation screening of multiple Pakistani MCPH families revealed novel and recurrent protein-truncating mutations of ASPMSadam Hussain, Amjad Nawaz, Malaika Hamid, et al.
BMC Neurology|October 4, 2023
Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disabilitySyeda Iqra Hussain, Nazif Muhammad, Salah Ud Din Shah, et al.
Genes|May 27, 2023
Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl SyndromeHamed Nawaz, Mujahid, Sher Alam Khan, et al.
International Journal of Molecular Sciences|October 27, 2019
Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics SimulationsAsia Parveen, Sher Alam Khan, Muhammad Usman Mirza, et al.
Genes|November 14, 2020
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani FamiliesJulia Doll, Barbara Vona, Linda Schnapp, et al.
Human Mutation|July 11, 2022
Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory functionSheng-Jia Lin, Barbara Vona, Hillary M Porter, et al.
Genome Medicine|May 8, 2026
The contribution of rare germline variants to the immune landscape of breast cancerFelipe Rojas-Rodríguez, Sander Canisius, Renske Keeman, et al.
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