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Year Number of Results
2016 3
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2020 5
2021 3
2022 3
2023 2
2024 0

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Page 1
Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes.
Dunn P, Albury CL, Maksemous N, Benton MC, Sutherland HG, Smith RA, Haupt LM, Griffiths LR. Dunn P, et al. Among authors: maksemous n. Front Genet. 2018 Feb 7;9:20. doi: 10.3389/fgene.2018.00020. eCollection 2018. Front Genet. 2018. PMID: 29467791 Free PMC article. Review.
Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine.
Maksemous N, Blayney CD, Sutherland HG, Smith RA, Lea RA, Tran KN, Ibrahim O, McArthur JR, Haupt LM, Cader MZ, Finol-Urdaneta RK, Adams DJ, Griffiths LR. Maksemous N, et al. Front Mol Neurosci. 2022 Jul 19;15:892820. doi: 10.3389/fnmol.2022.892820. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35928792 Free PMC article.
Discriminating head trauma outcomes using machine learning and genomics.
Ibrahim O, Sutherland HG, Lea RA, Nasrallah F, Maksemous N, Smith RA, Haupt LM, Griffiths LR. Ibrahim O, et al. Among authors: maksemous n. J Mol Med (Berl). 2022 Feb;100(2):303-312. doi: 10.1007/s00109-021-02158-z. Epub 2021 Nov 19. J Mol Med (Berl). 2022. PMID: 34797388
Tiered analysis of whole-exome sequencing for epilepsy diagnosis.
Dunn PJ, Maher BH, Albury CL, Stuart S, Sutherland HG, Maksemous N, Benton MC, Smith RA, Haupt LM, Griffiths LR. Dunn PJ, et al. Among authors: maksemous n. Mol Genet Genomics. 2020 May;295(3):751-763. doi: 10.1007/s00438-020-01657-x. Epub 2020 Mar 7. Mol Genet Genomics. 2020. PMID: 32146541
19 results