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Leila Myrick - Publications

Affiliations: 
2009-2013 Emory University School of Medicine, Atlanta, GA, United States 
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5 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Deng PY, Carlin D, Mi Oh Y, Myrick LK, Warren ST, Cavalli V, Klyachko VA. Voltage-Independent SK Channel Dysfunction Causes Neuronal Hyperexcitability in the Hippocampus of KO mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 30389838 DOI: 10.1523/Jneurosci.1593-18.2018  0.504
2015 Myrick LK, Deng PY, Hashimoto H, Oh YM, Cho Y, Poidevin MJ, Suhl JA, Visootsak J, Cavalli V, Jin P, Cheng X, Warren ST, Klyachko VA. Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures. Proceedings of the National Academy of Sciences of the United States of America. 112: 949-56. PMID 25561520 DOI: 10.1073/Pnas.1423094112  0.424
2015 Myrick LK, Hashimoto H, Cheng X, Warren ST. Human FMRP contains an integral tandem Agenet (Tudor) and KH motif in the amino terminal domain. Human Molecular Genetics. 24: 1733-40. PMID 25416280 DOI: 10.1093/Hmg/Ddu586  0.581
2014 Myrick LK, Nakamoto-Kinoshita M, Lindor NM, Kirmani S, Cheng X, Warren ST. Fragile X syndrome due to a missense mutation. European Journal of Human Genetics : Ejhg. 22: 1185-9. PMID 24448548 DOI: 10.1038/Ejhg.2013.311  0.613
2012 Alisch RS, Barwick BG, Chopra P, Myrick LK, Satten GA, Conneely KN, Warren ST. Age-associated DNA methylation in pediatric populations. Genome Research. 22: 623-32. PMID 22300631 DOI: 10.1101/Gr.125187.111  0.529
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