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서울대학교 의과대학

최종업데이트 2026.03.24.

Co-occurrence of rare variants implicates gene pairs in cytoskeletal pathways and is associated with increased severity in autism spectrum disorder
- Genome Biol., 23 March 2026 | https://doi.org/10.1186/s13059-026-04041-x
- 2026-03
- 생명과학
- 한빛사논문
Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism
- Genome Med., Aug 20 2025, 17 (1) | https://doi.org/10.1186/s13073-025-01532-7
- 2025-08
- 생명과학
- 한빛사논문
Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism
- Genome Med., Sep 27 2024, 16 (1) 114 | https://doi.org/10.1186/s13073-024-01385-6
- 2024-09
- 의약학
- 한빛사논문
Short tandem repeat expansions in cortical layer-specific genes implicate in phenotypic severity and adaptability of autism spectrum disorder
- Psychiatry Clin. Neurosci., 15 May 2024 | https://doi.org/10.1111/pcn.13676
- 2024-05
- 생명과학
- 한빛사논문
Improving adaptive behaviors for autistic adults without intellectual disability through executive function training
- Asian J. Psychiatr., Volume 84, June 2023, 103579 | https://doi.org/10.1016/j.ajp.2023.103579
- 2023-06
- 의약학
- 한빛사논문
Non-coding de novo mutations in chromatin interactions are implicated in autism spectrum disorder
- Mol. Psychiatr., Published 15 July 2022 | https://doi.org/10.1038/s41380-022-01697-2
- 2022-07
- 의약학
- 한빛사논문

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