S. Hossain

Dissecting the structural and functional impact of SNPs located in the spinal muscular atrophy associated gene SMN1 using in silico analysis

Md. Ismail Hosen, I. Hosen, S. Hossain, 2019, Gene Reports.

Detection of Clinically Relevant Copy Number Variations and Genes in a Bangladeshi Cohort of Neurodevelopmental Disorders

M. Uddin, Md. Ismail Hosen, O. Faruk, 2021 .

Loss‐of‐function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations

M. Dubé, D. Bowsher, E. Boltshauser, 2007, Clinical genetics.

Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders

Md. Mazharul Islam, Md Mazharul Islam, M. Uddin, 2023, Frontiers in Genetics.

Comprehensive Characterization of the Coding and Non-Coding Single Nucleotide Polymorphisms in the Tumor Protein p63 (TP63) Gene Using In Silico Tools

Md. Ismail Hosen, Md. Ackas Ali, S. Hossain, 2021, Biomolecules.