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Page 1
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.
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.
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 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.
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.
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.
Genomic insights from a deeply phenotyped highly consanguineous neurodevelopmental disorders cohort.
Akter H, Rahaman MA, Eshaque TB, Mohamed N, Islam A, Morshed M, Shahin Z, Muhaimin A, Foyzullah AM, Mim RA, Omar FB, Hasan MN, Satsangi D, Ahmed N, Al Saba A, Jahan N, Hossen MA, Mondol MA, Sakib AS, Kabir R, Jahan Chowdhury MS, Shams N, Afroz S, Kanta SI, Bhuiyan SJ, Biswas R, Hanif S, Tambi R, Nassir N, Rahman MM, Duan J, D Børglum A, Amin R, Basiruzzaman M, Kamruzzaman M, Sarker S, Woodbury-Smith M, Uddin KMF, Nabi AHMN, Uddin M. Akter H, et al. Among authors: nassir n. Genet Med. 2024 Sep 26;27(1):101282. doi: 10.1016/j.gim.2024.101282. Online ahead of print. Genet Med. 2024. PMID: 39342494 Free article.
24 results