YearNumberAuthors / Title / Journal
2019162Kim IB*, Lee T*, Lee J*, Kim J, Lee H, Kim WK, Ju YS, Cho Y, Yu SJ, Kim SA, Oh M, Kwak TH, Hali S, Han DW, Kim E#, Choi JK#, Yoo HJ#, and Lee JH#. (2019).
Noncoding de novo mutations contribute to autism spectrum disorder via chromatin interactions.
BioRxiv. (doi:
161Choi Y*, Park H*, Kang S,  Jung H, Kweon H, Kim S, Choi l, Lee SY, Choi YE, Lee SH and Kim E. (2019).
NGL-1/LRRC4C-mutant mice display hyperactivity and anxiolytic-like behavior associated with widespread suppression of neuronal activity.
Front Mol Neurosci 12:250. (abstract)
160Yoo T, Cho H, Park H, Lee J, and Kim E. (2019).
Shank3 exons 14–16 deletion in glutamatergic neurons leads to social and repetitive behavioral deficits associated with increased cortical layer 2/3 neuronal excitability.
Front Cell Neurosci 13:458. (abstract)
159Yook C, Kim K, Kim D, Kang H, Kim SG, Kim E#, and Kim SY#. (2019).
A TBR1-K228E mutation induces Tbr1 upregulation, altered cortical distribution of interneurons, increased inhibitory synaptic transmission, and autistic-like behavioral deficits in mice.
Front Mol Neurosci 12:241. (abstract)
158Koopmans F, van Nierop P, Andres-Alonso M, Byrnes A, Cijsouw T, Coba MP, Cornelisse LN, Farrell RJ, Goldschmidt HL, Howrigan DP, Hussain NK, Imig C, de Jong APH, Jung H, Kohansalnodehi M, Kramarz B, Lipstein N, Lovering RC, MacGillavry H, Mariano V, Mi H, Ninov M, Osumi-Sutherland D, Pielot R, Smalla KH, Tang H, Tashman K, Toonen RFG, Verpelli C, Reig-Viader R, Watanabe K, van Weering J, Achsel T, Ashrafi G, Asi N, Brown TC, De Camilli P, Feuermann M, Foulger RE, Gaudet P, Joglekar A, Kanellopoulos A, Malenka R, Nicoll RA, Pulido C, de Juan-Sanz J, Sheng M, Südhof TC, Tilgner HU, Bagni C, Bayés À, Biederer T, Brose N, Chua JJE, Dieterich DC, Gundelfinger ED, Hoogenraad C, Huganir RL, Jahn R, Kaeser PS, Kim E, Kreutz MR, McPherson PS, Neale BM, O'Connor V, Posthuma D, Ryan TA, Sala C, Feng G, Hyman SE, Thomas PD, Smit AB, Verhage M. (2019).
SynGO: an evidence-based, expert-curated resource for synapse function and gene enrichment studies.
Neuron 103:217-234. (abstract)
157Kim DY, Park JA, Kim Y, Noh M, Park S, Lie E, Kim E, Kim YM, and Kwon YG. (2019).
SALM4 regulates angiogenic functions in endothelial cells through VEGFR2 phosphorylation at Tyr1175.
FASEB J 33:9842-9857. (abstract)
156Yoo YE, Yoo T, Lee S, Lee J, Kim D, Han HM, Bae YC, Kim E. (2019).
Shank3 mice carrying the human Q321R mutation display enhanced self-grooming, abnormal electroencephalogram patterns, and suppressed neuronal excitability and seizure susceptibility.
Front Mol Neurosci 12:155. (abstract)
155Shin W*, Kweon H*, Kang R*, Kim D, Kim K, Kang M, Kim SY, Hwang SN, Kim JY, Yang E, Kim H, and Kim E. (2019).
Scn2a haploinsufficiency in mice suppresses hippocampal neuronal excitability, excitatory synaptic drive, and long-term potentiation, and spatial learning and memory.
Front Mol Neurosci 12:145. (abstract)
154Lee H*, Shin W*, Kim K*, Lee S, Lee EJ, Kim J, Kweon H, Lee E, Park H, Kang M, Yang E, Kim H, and Kim E. (2019).
NGL-3 in the regulation of brain development, Akt/GSK3b signaling, long-term depression, and locomotive and cognitive behaviors.
PLoS Biol 17:e2005326. (abstract)
153Choi Y*, Park H*, Jung H, Kweon H, Kim S, Lee SY, Han H, Cho Y, Kim S, Sim WS, Kim J, Bae Y, and Kim E. (2019).
NGL-1/LRRC4C deletion moderately suppresses hippocampal excitatory synapse development and function in an input-independent manner.
Front Mol Neurosci 12:119. (abstract)
152Chung C*, Ha S*, Kang H, Lee J, Um SM, Yan H, Yoo YE, Yoo T, Jung H, Lee D, Lee E, Lee S, Kim J, Kim R, Kwon Y, Kim W, Kim H, Duffney L, Kim D, Mah W, Won H, Mo S, Kim JY, Lim CS, Kaang BK, Boeckers TM, Chung Y, Kim H, Jiang YH, and Kim E. (2019).
Early correction of NMDAR function improves autistic-like behaviors in adult Shank2–/– mice.
Biol Psychiatry 85:534-543. (abstract)