| Antibody-drug conjugate T-DM1 treatment for HER2+ breast cancer induces ROR1 and confers resistance through activation of Hippo transcriptional coactivator YAP1 SS Islam, M Uddin, ASM Noman, H Akter, NJ Dity, M Basiruzzman, ... EBioMedicine 43, 211-224, 2019 | 31 | 2019 |
| The complete Spectrum of beta (β) thalassemia mutations in Bangladeshi population GNN Sultana, R Begum, H Akhter, Z Shamim, MA Rahim, G Chubey Austin Biomark Diagn 3 (1), 1024, 2016 | 25 | 2016 |
| Long-read sequencing improves the detection of structural variations impacting complex non-coding elements of the genome G Begum, A Albanna, A Bankapur, N Nassir, R Tambi, BK Berdiev, ... International Journal of Molecular Sciences 22 (4), 2060, 2021 | 21 | 2021 |
| Mutational Landscape of Autism Spectrum Disorder Brain Tissue Marc Woodbury-Smith1, Sylvia Lamoureux2, Ghausia Begum3, Nasna Nassir3 ... Genes 13 (2), 207, 2022 | 16 | 2022 |
| 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 | 15 | 2021 |
| Whole exome sequencing uncovered highly penetrant recessive mutations for a spectrum of rare genetic pediatric diseases in Bangladesh H Akter, MS Hossain, NJ Dity, MA Rahaman, KM Furkan Uddin, N Nassir, ... NPJ Genomic Medicine 6 (1), 14, 2021 | 14 | 2021 |
| An ANKRD26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome) KMF Uddin, MR Amin, SN Majumder, MA Aleem, MA Rahaman, NJ Dity, ... Clinical case reports 6 (8), 1426, 2018 | 11 | 2018 |
| 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 | 10 | 2023 |
| Novel mutations in actionable breast cancer genes by targeted sequencing in an ethnically homogenous cohort H Akter, N Sultana, N Martuza, A Siddiqua, NJ Dity, MA Rahaman, ... BMC medical genetics 20, 1-8, 2019 | 10 | 2019 |
| Gonadal mosaicism of large terminal de novo duplication and deletion in siblings with variable intellectual disability phenotypes MM Rahman, KMF Uddin, NK Al Jezawi, N Karuvantevida, H Akter, ... Molecular genetics & genomic medicine 7 (10), e00954, 2019 | 10 | 2019 |
| Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders H Akter, MM Rahman, S Sarker, M Basiruzzaman, MM Islam, ... Frontiers in Genetics 14, 955631, 2023 | 6 | 2023 |
| Mutational landscape of mitochondrial cytochrome b and its flanking tRNA genes associated with increased mitochondrial DNA copy number and disease risk in children with autism M Adiba, M Rahman, H Akter, MM Rahman, M Uddin, A Ebihara, ... Gene Reports 35, 101895, 2024 | 4 | 2024 |
| Detection of clinically relevant copy number variation of SEZ6L2 gene in a Bangladeshi autism spectrum disorder cohort KMF Uddin, MR Amin, N Sultana, MA Aleem, SK Sarker, LA Banu, MS Ali, ... Bangladesh Journal of Medicine 30 (1), 24-29, 2019 | 3 | 2019 |
| 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 | 2 | 2023 |
| 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 | 2 | 2022 |
| Life cycle emissions and unit production cost of sustainable aviation fuel from logging residues in Georgia, United States HA Akter, FH Masum, P Dwivedi Renewable Energy 228, 120611, 2024 | 1 | 2024 |
| Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11–q13 imprinting region RA Mim, A Soorajkumar, N Kosaji, MM Rahman, S Sarker, ... Brain and Behavior 14 (4), e3437, 2024 | 1 | 2024 |
| 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 |
| 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 |
| Precision Therapies in Neurodevelopmental Disorders: Update on Gene Therapies M Uddin, AN Abou Tayoun, RK Jan, H Akter, DM Andrade, C Boelman Advances in Molecular Pathology 3, 21-27, 2020 | 1 | 2020 |
