Binte Zehra

Dubai, DU, United Arab Emirates

Last Updated: 09/26/2026

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Found 12 publications

Multiomics approaches to cardiovascular disease: technological innovations and clinical translation.

Multiomics approaches to cardiovascular disease: technological innovations and clinical translation.

Journal: American journal of physiology. Heart and circulatory physiology
Published: April 21, 2026

Neurabin I haploinsufficiency disrupts ion channel regulation and synaptic maturation in human cortical neurons in neurodevelopmental disorders.

Neurabin I haploinsufficiency disrupts ion channel regulation and synaptic maturation in human cortical neurons in neurodevelopmental disorders.

Journal: Molecular psychiatry
Published: August 18, 2025

Genomic insights into Rett syndrome-like features in Bangladeshi participants.

Genomic insights into Rett syndrome-like features in Bangladeshi participants.

Journal: Genetics in medicine open
Published: October 31, 2024

Artificial intelligence and omics in malignant gliomas.

Artificial intelligence and omics in malignant gliomas.

Journal: Physiological genomics
Published: October 22, 2024

Integrative analysis of long isoform sequencing and functional data identifies distinct cortical layer neuronal subtypes derived from human iPSCs.

Integrative analysis of long isoform sequencing and functional data identifies distinct cortical layer neuronal subtypes derived from human iPSCs.

Journal: Journal of neurophysiology
Published: July 11, 2024

Single-cell reconstruction and mutation enrichment analysis identifies dysregulated cardiomyocyte and endothelial cells in congenital heart disease.

Single-cell reconstruction and mutation enrichment analysis identifies dysregulated cardiomyocyte and endothelial cells in congenital heart disease.

Journal: Physiological genomics
Published: October 09, 2023

Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi population.

Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi population.

Journal: Scientific reports
Published: July 06, 2023

Lack of ethnic diversity in single-cell transcriptomics hinders cell type detection and precision medicine inclusivity.

Lack of ethnic diversity in single-cell transcriptomics hinders cell type detection and precision medicine inclusivity.

Journal: Med (New York, N.Y.)
Published: November 11, 2022

Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development.

Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development.

Journal: Human genetics
Published: June 21, 2022

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

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
Showing 1-12 of 12

Last Updated: 09/26/2026