Eunjoon S. Kim

Daejeon, Republic of Korea

Last Updated: 09/26/2026

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Found 136 publications

The traffic controller: GARLH4 dictates neuroligin synapse-type preference.

The traffic controller: GARLH4 dictates neuroligin synapse-type preference.

Journal: The Journal of cell biology
Published: January 02, 2026

Grin2b-mutant mice exhibit heightened remote fear via suppressed extinction and chronic amygdalar synaptic and neuronal dysfunction.

Grin2b-mutant mice exhibit heightened remote fear via suppressed extinction and chronic amygdalar synaptic and neuronal dysfunction.

Journal: Science advances
Published: September 17, 2025

Aberrant mRNA splicing and impaired hippocampal neurogenesis in Grin2b mutant mice.

Aberrant mRNA splicing and impaired hippocampal neurogenesis in Grin2b mutant mice.

Journal: iScience
Published: September 08, 2025

Publisher Correction: Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism.

Publisher Correction: Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism.

Journal: Genome medicine
Published: September 04, 2025

Synaptic and Non-Synaptic Functions of PTPRD: A Receptor Tyrosine Phosphatase at the Crossroads of Neural Circuitry and Metabolism.

Synaptic and Non-Synaptic Functions of PTPRD: A Receptor Tyrosine Phosphatase at the Crossroads of Neural Circuitry and Metabolism.

Journal: Journal of neurochemistry
Published: July 22, 2025

Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental Disorders.

Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental Disorders.

Journal: bioRxiv : the preprint server for biology
Published: June 26, 2025

Co-occurrence of rare variants implicates gene pairs in cytoskeletal pathways and is associated with increased severity in autism spectrum disorder.

Co-occurrence of rare variants implicates gene pairs in cytoskeletal pathways and is associated with increased severity in autism spectrum disorder.

Journal: Genome biology
Published: May 14, 2025

Glycine-modulating Slc6a20a-ASO restores NMDA receptor function in SHANK2 and SHANK3-mutant mice and cortical organoids.

Glycine-modulating Slc6a20a-ASO restores NMDA receptor function in SHANK2 and SHANK3-mutant mice and cortical organoids.

Journal: Nature communications
Published: April 30, 2025

Seizure evolution in a mouse model of West syndrome involves complex and time-dependent synapse remodeling, gliosis and alterations in lipid metabolism.

Seizure evolution in a mouse model of West syndrome involves complex and time-dependent synapse remodeling, gliosis and alterations in lipid metabolism.

Journal: PLoS biology
Published: April 23, 2025

Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism.

Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism.

Journal: Genome medicine
Published: March 25, 2025

Aberrant excitatory neuronal ERBB4 promotes Alzheimer's disease pathology.

Aberrant excitatory neuronal ERBB4 promotes Alzheimer's disease pathology.

Journal: Nature
Published: March 10, 2025

Homozygous CHD8 mutation intensifies ASD phenotypes and attenuates sex differences.

Homozygous CHD8 mutation intensifies ASD phenotypes and attenuates sex differences.

Journal: Molecular psychiatry
Published: March 05, 2025
Showing 1-12 of 136

Last Updated: 09/26/2026