Ghausia Begum

Dubai, DU, United Arab Emirates

Last Updated: 09/26/2026

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Found 8 publications

The ASPIRE Research Institute Dataset: Building a Foundation for Brain Health Research in the United Arab Emirates.

The ASPIRE Research Institute Dataset: Building a Foundation for Brain Health Research in the United Arab Emirates.

Journal: Scientific data

Published: May 15, 2025

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

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

Journal: Frontiers in genetics

Published: May 29, 2022

Analyzing single cell transcriptome data from severe COVID-19 patients.

Analyzing single cell transcriptome data from severe COVID-19 patients.

Journal: STAR protocols

Published: May 18, 2022

Mutational Landscape of Autism Spectrum Disorder Brain Tissue.

Mutational Landscape of Autism Spectrum Disorder Brain Tissue.

Journal: Genes

Published: December 30, 2021

Single-cell transcriptomics trajectory and molecular convergence of clinically relevant mutations in Brugada syndrome.

Single-cell transcriptomics trajectory and molecular convergence of clinically relevant mutations in Brugada syndrome.

Journal: American journal of physiology. Heart and circulatory physiology

Published: April 02, 2021

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

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

Journal: iScience

Published: March 19, 2021

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

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

Journal: International journal of molecular sciences

Published: December 16, 2020

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

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

Journal: NPJ genomic medicine

Published: May 31, 2020

Showing 1-8 of 8

Last Updated: 09/26/2026