Ghausia Begum

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

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

Single-cell transcriptome identifies FCGR3B upregulated subtype of alveolar macrophages in patients with critical COVID-19

Asma R. Bankapur, J. Casanova, W. Kuebler, 2021, iScience.

Analyzing single cell transcriptome data from severe COVID-19 patients

Asma R. Bankapur, A. Alsheikh-Ali, M. Hachim, 2022, STAR Protocols.

Whole exome sequencing uncovered highly penetrant recessive mutations for a spectrum of rare genetic pediatric diseases in Bangladesh

S. Scherer, D. Stavropoulos, M. Uddin, 2021, NPJ genomic medicine.

Mutational Landscape of Autism Spectrum Disorder Brain Tissue

S. Scherer, P. Rahman, M. Uddin, 2022, Genes.

Single Cell Transcriptomics Trajectory and Molecular Convergence of Clinically Relevant Mutations in Brugada Syndrome.

Asma R. Bankapur, A. Alsheikh-Ali, M. Uddin, 2021, American journal of physiology. Heart and circulatory physiology.

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.

Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome

Asma R. Bankapur, S. Scherer, B. Thiruvahindrapuram, 2021, International journal of molecular sciences.