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Year Number of Results
2019 1
2021 5
2022 4
2023 7
2024 0

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16 results

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Page 1
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: nassir n. Sci Rep. 2023 Dec 6;13(1):21547. doi: 10.1038/s41598-023-48982-w. Sci Rep. 2023. PMID: 38057384 Free PMC article.
Neuronal SNCA transcription during Lewy body formation.
Kon T, Forrest SL, Lee S, Martinez-Valbuena I, Li J, Nassir N, Uddin MJ, Lang AE, Kovacs GG. Kon T, et al. Among authors: nassir n. Acta Neuropathol Commun. 2023 Nov 23;11(1):185. doi: 10.1186/s40478-023-01687-7. Acta Neuropathol Commun. 2023. PMID: 37996943 Free PMC article.
Single-cell reconstruction and mutation enrichment analysis identifies dysregulated cardiomyocyte and endothelial cells in congenital heart disease.
Tambi R, Zehra B, Nandkishore S, Sharafat S, Kader F, Nassir N, Mohamed N, Ahmed A, Abdel Hameid R, Alasrawi S, Brueckner M, Kuebler WM, Chung WK, Alsheikh-Ali A, Di Donato RM, Uddin M, Berdiev BK. Tambi R, et al. Among authors: nassir n. Physiol Genomics. 2023 Dec 1;55(12):634-646. doi: 10.1152/physiolgenomics.00070.2023. Epub 2023 Oct 9. Physiol Genomics. 2023. PMID: 37811720 Free 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. Among authors: nassir n. 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: nassir n. 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.
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. 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.
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: nassir n. Genes (Basel). 2022 Jan 24;13(2):207. doi: 10.3390/genes13020207. Genes (Basel). 2022. PMID: 35205252 Free PMC article.
16 results