Jonathan Andrews on Muck Rack

Jonathan Andrews

As seen in: BBC, Wiley Online Library, JAMA Dermatology, HuffPost UK, The American Journal of Human Genetics, KPHO-TV (Phoenix, AZ), WXIX-TV (Cincinnati, OH), JD Supra, KGMB-TV (Honolulu, HI), WANF-TV (Atlanta, GA) and
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Articles

Florida lawmakers urged to take up bill targeting third-party litigation financing

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By Jonathan Andrews
| Florida's Voice
TALLAHASSEE, Fla. – Once the special session for redistricting is over, we get a short break, and then the legislature is at it again, this time for another special session to finalize and approve the state budget. This could be the last special session of 2026, and it is important that one agenda item be added for discussion: Passing legislation to stop third-party financing of lawsuits.
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De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms

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By Ali H. Bereshneh, Jonathan Andrews, Daniel F Eberl, Guney Bademci, Nicholas A. Borja, Stephanie A. Bivona, Wendy Chung, Shinya Yamamoto, Michael F. Wangler, Shane McKee, Mustafa Tekin, Hugo J. Bellen, Oguz Kanca
| The American Journal of Human Genetics
Keywords CDKL2 CDKL1 CDKL5 Drosophila Cdkl CG7236 epilepsy peripheral nervous system developmental delay Get full text access Log in, subscribe or purchase for full access. References 1. Malumbres, M. ∙ Harlow, E. ∙ Hunt, T. ... Cyclin-dependent kinases: a family portrait Nat. Cell Biol. 2009; 11:1275-1276 2. Canning, P. ∙ Park, K. ∙ Gonçalves, J. ... CDKL Family Kinases Have Evolved Distinct Structural Features and Ciliary Function Cell Rep. 2018; 22:885-894 3. Park, K. ∙ Li, C. ∙ Tsiropoulou, S. ...
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A De Novo Missense Variant in EZH1 Associated With Developmental Delay Exhibits Functional Deficits in Drosophila melanogaster

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By Sharayu Jangam, Lauren C. Briere, Kristy L Jay, Jonathan Andrews
| Texas Medical Center
10.1093/genetics/iyad110 Post-print yes Abnormalities, Multiple, Enhancer of Zeste Homolog 2 Protein, Drosophila melanogaster, Craniofacial Abnormalities, Drosophila, Humans, Histones, Congenital Hypothyroidism, Animals, Hand Deformities, Congenital, Polycomb Repressive Complex 2, Drosophila melanogaster, EZH1, E(z), H3K27-trimethylation, rare undiagnosed disease, polycomb repressive complex 2, patterning defect, missense, developmental delay
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