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Year | Number of Results |
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2021 | 4 |
2022 | 2 |
2023 | 1 |
2024 | 0 |
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Page 1
Mutational Landscape of Autism Spectrum Disorder Brain Tissue.
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: begum g.
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.
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Single-cell transcriptomics trajectory and molecular convergence of clinically relevant mutations in Brugada syndrome.
Tambi R, Abdel Hameid R, Bankapur A, Nassir N, Begum G, Alsheikh-Ali A, Uddin M, Berdiev BK.
Tambi R, et al. Among authors: begum g.
Am J Physiol Heart Circ Physiol. 2021 May 1;320(5):H1935-H1948. doi: 10.1152/ajpheart.00061.2021. Epub 2021 Apr 2.
Am J Physiol Heart Circ Physiol. 2021.
PMID: 33797273
Free article.
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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: begum g.
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.
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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: begum g.
Front Genet. 2023 Mar 7;14:955631. doi: 10.3389/fgene.2023.955631. eCollection 2023.
Front Genet. 2023.
PMID: 36959829
Free PMC article.
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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.
Int J Mol Sci. 2021 Feb 19;22(4):2060. doi: 10.3390/ijms22042060.
Int J Mol Sci. 2021.
PMID: 33669700
Free PMC article.
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Whole exome sequencing uncovered highly penetrant recessive mutations for a spectrum of rare genetic pediatric diseases in Bangladesh.
Akter H, Hossain MS, Dity NJ, Rahaman MA, Furkan Uddin KM, Nassir N, Begum G, Hameid RA, Islam MS, Tusty TA, Basiruzzaman M, Sarkar S, Islam M, Jahan S, Lim ET, Woodbury-Smith M, Stavropoulos DJ, O'Rielly DD, Berdeiv BK, Nurun Nabi AHM, Ahsan MN, Scherer SW, Uddin M.
Akter H, et al. Among authors: begum g.
NPJ Genom Med. 2021 Feb 16;6(1):14. doi: 10.1038/s41525-021-00173-0.
NPJ Genom Med. 2021.
PMID: 33594065
Free PMC article.
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