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Familial Cancer|November 16, 2016
Identification of a rare germline NBN gene mutation by whole exome sequencing in a lung-cancer survivor from a large family with various types of cancerMakia J Marafie, Mohammed Dashti, Fahd Al-Mulla
Multiple Sclerosis and Related Disorders|September 29, 2019
Leptin rs7799039 polymorphism is associated with multiple sclerosis risk in KuwaitMohammed Dashti, Raed Alroughani, Sindhu Jacob, et al.
Frontiers in Allergy|August 27, 2025
Mitochondrial haplogroup M contributes to asthma risk in the Kuwaiti populationMohammed Dashti, Hussain Bahbahani, Hussain Alsaleh, et al.
International Journal of Biological Macromolecules|July 12, 2026
Variant-specific pharmacophoric shifts in glucagon-like peptide-1 receptor-orforglipron complexes revealed by Boltz-2 co-folding and membrane molecular dynamicsAnwar Mohammad, Mohammed Dashti, M D Zubbair Malik, et al.
Scientific Reports|September 1, 2022
Frequency of functional exonic single-nucleotide polymorphisms and haplotype distribution in the SLCO1B1 gene across genetic ancestry groups in the Qatari populationMohammed Dashti, Abdullah Al-Matrouk, Arshad Channanath, et al.
Frontiers in Genetics|June 11, 2024
Evaluation of HLA typing content of next-generation sequencing datasets from family trios and individuals of arab ethnicityMohammed Dashti, Md Zubbair Malik, Rasheeba Nizam, et al.
Frontiers in Pharmacology|August 25, 2022
Distribution of HLA-B Alleles and Haplotypes in Qatari: Recommendation for Establishing Pharmacogenomic Markers Screening for Drug HypersensitivityMohammed Dashti, Abdullah Al-Matrouk, Arshad Channanath, et al.
Scientific Reports|January 14, 2021
Mitochondrial haplogroup J associated with higher risk of obesity in the Qatari populationMohammed Dashti, Hussain Alsaleh, Juan L Rodriguez-Flores, et al.
Frontiers in Immunology|August 28, 2023
Association between alleles, haplotypes, and amino acid variations in HLA class II genes and type 1 diabetes in Kuwaiti childrenMohammed Dashti, Rasheeba Nizam, Sindhu Jacob, et al.
Journal of Hypertension|November 8, 2014
Identification of a common molecular pathway in hypertensive renal damage: comparison of rat and human gene expression profilesTrude Skogstrand, Sabine Leh, John McClure, et al.
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