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Retrospective identification of patients with SRRM2-related neurodevelopmental disorder in a single tertiary children's hospital.
Am J Med Genet A. 2023 Aug;191(8):2149-2155. doi: 10.1002/ajmg.a.63302. Epub 2023 May 22.
Am J Med Genet A. 2023.
PMID: 37212523
Nuclear speckleopathies: developmental disorders caused by variants in genes encoding nuclear speckle proteins.
Regan-Fendt KE, Izumi K.
Regan-Fendt KE, et al.
Hum Genet. 2024 Apr;143(4):529-544. doi: 10.1007/s00439-023-02540-6. Epub 2023 Mar 16.
Hum Genet. 2024.
PMID: 36929417
Review.
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Synergy from gene expression and network mining (SynGeNet) method predicts synergistic drug combinations for diverse melanoma genomic subtypes.
Regan-Fendt KE, Xu J, DiVincenzo M, Duggan MC, Shakya R, Na R, Carson WE 3rd, Payne PRO, Li F.
Regan-Fendt KE, et al.
NPJ Syst Biol Appl. 2019 Feb 26;5:6. doi: 10.1038/s41540-019-0085-4. eCollection 2019.
NPJ Syst Biol Appl. 2019.
PMID: 30820351
Free PMC article.
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