Leila K. Myrick

Age-associated DNA methylation in pediatric populations

Reid S. Alisch, Benjamin G. Barwick, Pankaj Chopra et al. · Genome Research · 2012 · 388 citations · Full text

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

Leila K. Myrick, Pan‐Yue Deng, Hideharu Hashimoto et al. · Proceedings of the National Academy of Sciences · 2015 · 123 citations · Full text

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

Leila K. Myrick, Hideharu Hashimoto, Xiaodong Cheng et al. · Human Molecular Genetics · 2014 · 112 citations · Full text

Amino Terminal Domain, Genetics, Genomic Mechanism +20

Fragile X syndrome due to a missense mutation

Leila K. Myrick, Mika Nakamoto-Kinoshita, Noralane M. Lindor et al. · European Journal of Human Genetics · 2014 · 93 citations · Full text

Developmental Anomaly, Fragile X Syndrome, Mendelian Disorder +6

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

Pan‐Yue Deng, Dan Carlin, Young Mi Oh et al. · Journal of Neuroscience · 2018 · 67 citations · Full text