Human FMRP contains an integral tandem Agenet (Tudor) and KH motif in the amino terminal domain

od Myrick, Leila K., Hashimoto, Hideharu, Cheng, Xiaodong, Warren, Stephen T.
Izdano u Hum Mol Genet (2015)

Fragile X syndrome due to a missense mutation

od Myrick, Leila K, Nakamoto-Kinoshita, Mika, Lindor, Noralane M, Kirmani, Salman, Cheng, Xiaodong, Warren, Stephen T
Izdano 2014

Age-associated DNA methylation in pediatric populations

od Alisch, Reid S., Barwick, Benjamin G., Chopra, Pankaj, Myrick, Leila K., Satten, Glen A., Conneely, Karen N., Warren, Stephen T.
Izdano 2012

Voltage-Independent SK-Channel Dysfunction Causes Neuronal Hyperexcitability in the Hippocampus of Fmr1 Knock-Out Mice

od Deng, Pan-Yue, Carlin, Dan, Oh, Young Mi, Myrick, Leila K., Warren, Stephen T., Cavalli, Valeria, Klyachko, Vitaly A.
Izdano u J Neurosci (2019)

Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures

od Myrick, Leila K., Deng, Pan-Yue, Hashimoto, Hideharu, Oh, Young Mi, Cho, Yongcheol, Poidevin, Mickael J., Suhl, Joshua A., Visootsak, Jeannie, Cavalli, Valeria, Jin, Peng, Cheng, Xiaodong, Warren, Stephen T., Klyachko, Vitaly A.
Izdano u Proc Natl Acad Sci U S A (2015)