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2018 1
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2023 3
2024 1

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14 results

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Page 1
Mutational Landscape of Autism Spectrum Disorder Brain Tissue.
Woodbury-Smith M, Lamoureux S, Begum G, Nassir N, Akter H, O'Rielly DD, Rahman P, Wintle RF, Scherer SW, Uddin M. Woodbury-Smith M, et al. Among authors: akter h. Genes (Basel). 2022 Jan 24;13(2):207. doi: 10.3390/genes13020207. Genes (Basel). 2022. PMID: 35205252 Free PMC article.
Analyzing single cell transcriptome data from severe COVID-19 patients.
Nassir N, Tambi R, Bankapur A, Karuvantevida N, Khansaheb HH, Zehra B, Begum G, Hameid RA, Ahmed A, Deesi Z, Alkhajeh A, Uddin KMF, Akter H, Safizadeh Shabestari SA, Gaudet M, Hachim MY, Alsheikh-Ali A, Berdiev BK, Al Heialy S, Uddin M. Nassir N, et al. Among authors: akter h. STAR Protoc. 2022 Apr 21;3(2):101379. doi: 10.1016/j.xpro.2022.101379. eCollection 2022 Jun 17. STAR Protoc. 2022. PMID: 35582459 Free PMC article.
Single-cell transcriptome identifies FCGR3B upregulated subtype of alveolar macrophages in patients with critical COVID-19.
Nassir N, Tambi R, Bankapur A, Al Heialy S, Karuvantevida N, Khansaheb HH, Zehra B, Begum G, Hameid RA, Ahmed A, Deesi Z, Alkhajeh A, Uddin KMF, Akter H, Safizadeh Shabestari SA, Almidani O, Islam A, Gaudet M, Kandasamy RK, Loney T, Tayoun AA, Nowotny N, Woodbury-Smith M, Rahman P, Kuebler WM, Yaseen Hachim M, Casanova JL, Berdiev BK, Alsheikh-Ali A, Uddin M. Nassir N, et al. Among authors: akter h. iScience. 2021 Sep 24;24(9):103030. doi: 10.1016/j.isci.2021.103030. Epub 2021 Aug 25. iScience. 2021. PMID: 34458692 Free PMC article.
Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi population.
Sarker S, Eshaque TB, Soorajkumar A, Nassir N, Zehra B, Kanta SI, Rahaman MA, Islam A, Akter S, Ali MK, Mim RA, Uddin KMF, Chowdhury MSJ, Shams N, Baqui MA, Lim ET, Akter H, Woodbury-Smith M, Uddin M. Sarker S, et al. Among authors: akter h. Sci Rep. 2023 Dec 6;13(1):21547. doi: 10.1038/s41598-023-48982-w. Sci Rep. 2023. PMID: 38057384 Free PMC article.
Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders.
Akter H, Rahman MM, Sarker S, Basiruzzaman M, Islam MM, Rahaman MA, Rahaman MA, Eshaque TB, Dity NJ, Sarker S, Amin MR, Hossain MM, Lopa M, Jahan N, Hossain S, Islam A, Mondol A, Faruk MO, Saha N, Kundu GK, Kanta SI, Kazal RK, Fatema K, Rahman MA, Hasan M, Hossain Mollah MA, Hosen MI, Karuvantevida N, Begum G, Zehra B, Nassir N, Nabi AHMN, Uddin KMF, Uddin M. Akter H, et al. Front Genet. 2023 Mar 7;14:955631. doi: 10.3389/fgene.2023.955631. eCollection 2023. Front Genet. 2023. PMID: 36959829 Free PMC article.
Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development.
Safizadeh Shabestari SA, Nassir N, Sopariwala S, Karimov I, Tambi R, Zehra B, Kosaji N, Akter H, Berdiev BK, Uddin M. Safizadeh Shabestari SA, et al. Among authors: akter h. Hum Genet. 2023 Aug;142(8):1201-1213. doi: 10.1007/s00439-022-02482-5. Epub 2022 Nov 16. Hum Genet. 2023. PMID: 36383254 Free PMC article.
Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome.
Begum G, Albanna A, Bankapur A, Nassir N, Tambi R, Berdiev BK, Akter H, Karuvantevida N, Kellam B, Alhashmi D, Sung WWL, Thiruvahindrapuram B, Alsheikh-Ali A, Scherer SW, Uddin M. Begum G, et al. Among authors: akter h. Int J Mol Sci. 2021 Feb 19;22(4):2060. doi: 10.3390/ijms22042060. Int J Mol Sci. 2021. PMID: 33669700 Free PMC article.
Novel mutations in actionable breast cancer genes by targeted sequencing in an ethnically homogenous cohort.
Akter H, Sultana N, Martuza N, Siddiqua A, Dity NJ, Rahaman MA, Samara B, Sayeed A, Basiruzzaman M, Rahman MM, Rashidul Hoq M, Amin MR, Baqui MA, Woodbury-Smith M, Uddin KMF, Islam SS, Awwal R, Berdiev BK, Uddin M. Akter H, et al. BMC Med Genet. 2019 Sep 2;20(1):150. doi: 10.1186/s12881-019-0881-0. BMC Med Genet. 2019. PMID: 31477031 Free PMC article.
14 results