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Journal of Neurochemistry|May 14, 2022
Protein interactome and cell-type expression analyses reveal that cytoplasmic FMR1-interacting protein 1 (CYFIP1), but not CYFIP2, associates with astrocytic focal adhesionRuiying Ma, Kaifang Pang, Hyojin Kang, et al.
Molecular Psychiatry|May 9, 2026
Homozygous CHD8 mutation intensifies ASD phenotypes and attenuates sex differencesJinkyeong Kim, Seungjoon Lee, Eunkyu Hwang, et al.
Nature Communications|June 15, 2023
Kv7/KCNQ potassium channels in cortical hyperexcitability and juvenile seizure-related death in Ank2-mutant miceHyoseon Oh, Suho Lee, Yusang Oh, et al.
Plos Biology|May 8, 2024
Loss of Katnal2 leads to ependymal ciliary hyperfunction and autism-related phenotypes in miceRyeonghwa Kang, Kyungdeok Kim, Yewon Jung, et al.
EMBO Molecular Medicine|January 11, 2021
SLC6A20 transporter: a novel regulator of brain glycine homeostasis and NMDAR functionMihyun Bae, Junyeop Daniel Roh, Youjoung Kim, et al.
Nature|May 31, 2013
RAS-MAPK-MSK1 pathway modulates ataxin 1 protein levels and toxicity in SCA1Jeehye Park, Ismael Al-Ramahi, Qiumin Tan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 26, 2018
A Druggable Genome Screen Identifies Modifiers of α-Synuclein Levels via a Tiered Cross-Species Validation ApproachMaxime W C Rousseaux, Gabriel E Vázquez-Vélez, Ismael Al-Ramahi, et al.
Annals of Neurology|June 21, 2020
Haploinsufficiency of Cyfip2 Causes Lithium-Responsive Prefrontal DysfunctionSeung-Hyun Lee, Yinhua Zhang, Jina Park, et al.
Nature Neuroscience|August 15, 2018
Sexually dimorphic behavior, neuronal activity, and gene expression in Chd8-mutant miceHwajin Jung, Haram Park, Yeonsoo Choi, et al.
Plos Biology|October 9, 2025
Seizure evolution in a mouse model of West syndrome involves complex and time-dependent synapse remodeling, gliosis and alterations in lipid metabolismRuiying Ma, Muwon Kang, Gyu Hyun Kim, et al.
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