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Human genetics and molecular genomics of Chiari malformation type 1.
Mekbib KY, Muñoz W, Allington G, McGee S, Mehta NH, Shofi JP, Fortes C, Le HT, Nelson-Williams C, Nanda P, Dennis E, Kundishora AJ, Khanna A, Smith H, Ocken J, Greenberg ABW, Wu R, Moreno-De-Luca A, DeSpenza T Jr, Zhao S, Marlier A, Jin SC, Alper SL, Butler WE, Kahle KT. Mekbib KY, et al. Among authors: kundishora aj. Trends Mol Med. 2023 Dec;29(12):1059-1075. doi: 10.1016/j.molmed.2023.08.013. Epub 2023 Oct 4. Trends Mol Med. 2023. PMID: 37802664 Review.
Novel EWSR1-VGLL1 fusion in a pediatric neuroepithelial neoplasm.
Kundishora AJ, Reeves BC, Nelson-Williams C, Hong CS, Gopal PP, Snuderl M, Kahle KT, Erson-Omay EZ. Kundishora AJ, et al. Clin Genet. 2020 May;97(5):791-792. doi: 10.1111/cge.13703. Epub 2020 Jan 16. Clin Genet. 2020. PMID: 31925773 No abstract available.
Risk Factors for the Development of Post-Traumatic Hydrocephalus in Children.
Elsamadicy AA, Koo AB, Lee V, David WB, Zogg CK, Kundishora AJ, Hong CS, DeSpenza T, Reeve BC, DiLuna M, Kahle KT. Elsamadicy AA, et al. Among authors: kundishora aj. World Neurosurg. 2020 Sep;141:e105-e111. doi: 10.1016/j.wneu.2020.04.216. Epub 2020 May 7. World Neurosurg. 2020. PMID: 32389871 Free PMC article.
Persistent STAG2 mutation despite multimodal therapy in recurrent pediatric glioblastoma.
Hong CS, Vasquez JC, Kundishora AJ, Elsamadicy AA, Beckta JM, Sule A, Marks AM, Leelatian N, Huttner A, Bindra RS, DiLuna ML, Kahle KT, Erson-Omay EZ. Hong CS, et al. Among authors: kundishora aj. NPJ Genom Med. 2020 Jun 1;5:23. doi: 10.1038/s41525-020-0130-7. eCollection 2020. NPJ Genom Med. 2020. PMID: 32528726 Free PMC article.
68 results