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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 1
2011 2
2012 3
2013 7
2014 11
2015 11
2016 12
2017 8
2018 8
2019 11
2020 5
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2022 9
2023 10
2024 1

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Page 1
Characterization of a loss-of-function NSF attachment protein beta mutation in monozygotic triplets affected with epilepsy and autism using cortical neurons from proband-derived and CRISPR-corrected induced pluripotent stem cell lines.
Ali G, Shin KC, Habbab W, Alkhadairi G, AbdelAleem A, AlShaban FA, Park Y, Stanton LW. Ali G, et al. Among authors: shin kc. Front Neurosci. 2024 Jan 8;17:1302470. doi: 10.3389/fnins.2023.1302470. eCollection 2023. Front Neurosci. 2024. PMID: 38260021 Free PMC article.
A rigorous in silico genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disorders.
Ben-Mahmoud A, Jun KR, Gupta V, Shastri P, de la Fuente A, Park Y, Shin KC, Kim CA, da Cruz AD, Pinto IP, Minasi LB, Silva da Cruz A, Faivre L, Callier P, Racine C, Layman LC, Kong IK, Kim CH, Kim WY, Kim HG. Ben-Mahmoud A, et al. Among authors: shin kc. Front Mol Neurosci. 2022 Oct 6;15:979061. doi: 10.3389/fnmol.2022.979061. eCollection 2022. Front Mol Neurosci. 2022. PMID: 36277487 Free PMC article.
84 results