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YearNumberAuthors / Title / Journal
2026227Kim J*, Lee S*, Hwang E*, Jung H, Lee C, Choi SH, Lee S, Kim S, Moon H, Kim J, Lee G, Kim YG, Shin S, Kang H, Kim SJ, Gee HY, Kim SG, Lee E**, Kim E**. (2026).
Homozygous CHD8 mutation intensifies ASD phenotypes and attenuates sex differences.
Mol Psych, in press.
2026226Lee H, Ko K, Kim S, Lee G, Kim S, Lee J, Song DY, Bong G, Han JH, Lee J, Kim YR, Lee Y, Kim E, Børglum AD, Grove J, Kim SH, Sun W, Yoo HJ, An JY. (2026).
Co-occurrence of rare variants implicates gene pairs in cytoskeletal pathways and is associated with increased severity in autism spectrum disorder.
Genome Biol, in press. (abstract)
2026225Farsi Z*, Nicolella A, Simmons SK, Shin W, Kang M, Lee G, Kwon MJ, Brenner KS, Picard I, Shepard N, Misri D, Mandell KAP, Levin JZ, Kim E, Sheng M. (2026).
Aberrant mRNA Splicing and Impaired Hippocampal Neurogenesis in Grin2b Mutant Mice.
iScience 29:114700. (abstract)
2026224Kim E. (2026).
The traffic controller: GARLH4 dictates neuroligin synapse-type preference.
J Cell Biol 225:e202512185. (abstract)