Noor FA, Sultana N, Bhuyan GS, Islam MT, Hossain M, Sarker SK et al. Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population. Orphanet Journal of Rare Diseases. 2020; doi.org/10.1186/s13023-020-1294-z

Sarker SK, Islam MT, Hasib SH, Sultana N, Hossain SR, Biswas A et al. A novel missense mutation of Isovaleryl-CoA dehydrogenase gene associated with chronic intermittent Isovaleric acidemia in a Bangladeshi patient. Meta Gene. 2019; doi.org/10.1016/j.mgene.2019.100557

Sarker SK, Islam MT, Biswas A, Bhuyan GS, Sultana R, Sultana N et al. Age-Specific Cut-off Values of Amino Acids and Acylcarnitines for Diagnosis of Inborn Errors of Metabolism Using Liquid Chromatography Tandem Mass Spectrometry. BioMed Research International. 2019; 10.1155/2019/3460902

Sarker SK, Islam MT, Bhuyan GS, Sultana N, Begum MN, Al Mahmud-Un-Nabi M et al. Impaired acylcarnitine profile in transfusion-dependent beta-thalassemia major patients in Bangladesh. J. Adv. Res. 2018;12:55-66.

Islam MT, Sarker SK, Sultana N, Begum MN, Bhuyan GS, et al. (2018) High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh. BMC Genetics 19:1 doi:10.1186/s12863-017-0594-3

Bhuyan GS, Hossain MA, Sarker SK, Rahat A, Islam MT, et al. (2017) Bacterial and viral pathogen spectra of acute respiratory infections in under-5 children in hospital settings in Dhaka city. PLOS ONE 12(3): e0174488. doi: 10.1371/journal.pone.0174488