| Single-cell transcriptome identifies molecular subtype of autism spectrum disorder impacted by de novo loss-of-function variants regulating glial cells N Nassir, A Bankapur, B Samara, A Ali, A Ahmed, IM Inuwa, M Zarrei, ... Human Genomics 15, 1-16, 2021 | 19 | 2021 |
| Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome MU Ghausia Begum ,Ammar Albanna ,Asma Bankapur ,Nasna Nassir ,Richa Tambi ... International journal of molecular sciences 22 (4), 2021 | 19 | 2021 |
| Single-cell transcriptome identifies FCGR3B upregulated subtype of alveolar macrophages in patients with critical COVID-19 N Nassir, R Tambi, A Bankapur, S Al Heialy, N Karuvantevida, ... Iscience 24 (9), 2021 | 12 | 2021 |
| Whole exome sequencing uncovered highly penetrant recessive mutations for a spectrum of rare genetic pediatric diseases in Bangladesh npj genomic medicine 6 (14), 2021 | 12 | 2021 |
| Mutational landscape of autism spectrum disorder brain tissue M Woodbury-Smith, S Lamoureux, G Begum, N Nassir, H Akter, ... Genes 13 (2), 207, 2022 | 10 | 2022 |
| A telomerase with novel non-canonical roles: TERT controls cellular aggregation and tissue size in Dictyostelium N Nassir, GJ Hyde, R Baskar PLoS genetics 15 (6), e1008188, 2019 | 10 | 2019 |
| Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development SA Safizadeh Shabestari, N Nassir, S Sopariwala, I Karimov, R Tambi, ... Human Genetics 142 (8), 1201-1213, 2023 | 7 | 2023 |
| Single-cell transcriptomics trajectory and molecular convergence of clinically relevant mutations in Brugada syndrome R Tambi, R Abdel Hameid, A Bankapur, N Nassir, G Begum, ... American Journal of Physiology-Heart and Circulatory Physiology 320 (5 …, 2021 | 7 | 2021 |
| Cell-specific MAPT gene expression is preserved in neuronal and glial tau cytopathologies in progressive supranuclear palsy SL Forrest, S Lee, N Nassir, I Martinez-Valbuena, V Sackmann, J Li, ... Acta Neuropathologica 146 (3), 395-414, 2023 | 5 | 2023 |
| Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders H Akter, MR Amin, MA Rahman, MI Hosen, N Karuvantevida, AHM Nabi, ... Frontiers in Genetics 14, 955631, 2023 | 4 | 2023 |
| Neuronal SNCA transcription during Lewy body formation T Kon, SL Forrest, S Lee, I Martinez‑Valbuena, J Li, N Nassir, MJ Uddin, ... Acta neuropathologica communications 11 (1), 185, 2023 | 3 | 2023 |
| Lack of ethnic diversity in single-cell transcriptomics hinders cell type detection and precision medicine inclusivity N Kosaji, B Zehra, N Nassir, R Tambi, AR Orszulak, ET Lim, BK Berdiev, ... Med 4 (4), 217-219, 2023 | 2 | 2023 |
| Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi population S Sarker, TB Eshaque, A Soorajkumar, N Nassir, B Zehra, SI Kanta, ... Scientific Reports 13 (1), 21547, 2023 | 1 | 2023 |
| A draft Arab pangenome reference M Uddin, N Nassir, M Almarri, M Kumail, N Mohamed, B Balan, S Hanif, ... | 1 | 2023 |
| Analyzing single cell transcriptome data from severe COVID-19 patients N Nassir, R Tambi, A Bankapur, N Karuvantevida, HH Khansaheb, ... STAR protocols 3 (2), 101379, 2022 | 1 | 2022 |
| Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohort N Nassir, I Sati, S Al Shaibani, A Ahmed, O Almidani, H Akter, ... neurogenetics 23 (2), 137-149, 2022 | 1 | 2022 |
| SARS‐CoV‐2 May Hijack GPCR Signaling Pathways to Compromise Lung Ion and Fluid Transport R Abdel Hameid, R Tambi, N Nassir, G Begum, B Zehra, H Akter, ... The FASEB Journal 35, 2021 | 1 | 2021 |
| Single-cell reconstruction and mutation enrichment analysis identifies dysregulated cardiomyocyte and endothelial cells in congenital heart disease R Tambi, B Zehra, S Nandkishore, S Sharafat, F Kader, N Nassir, ... Physiological Genomics 55 (12), 634-646, 2023 | | 2023 |
| Cell‑specifc MAPT gene expression is preserved in neuronal and glial tau cytopathologies in progressive supranuclear palsy N Nassir, A Ahmed, M Uddin | | 2023 |
| Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders. N Karuvantevida, G Begum, B Zehra, N Nassir, M Uddin | | 2023 |
Mohammed Uddin (Dafil)Associate Professor, MBRU, Dubai Health, UAE; Scientist, GenomeArc Inc, TorontoVerified email at mbru.ac.ae
