Cargando…
De novo mutations identified by whole-genome sequencing implicate chromatin modifications in obsessive-compulsive disorder
Obsessive-compulsive disorder (OCD) is a chronic anxiety disorder with a substantial genetic basis and a broadly undiscovered etiology. Recent studies of de novo mutation (DNM) exome-sequencing studies for OCD have reinforced the hypothesis that rare variation contributes to the risk. We performed,...
Autores principales: | Lin, Guan Ning, Song, Weichen, Wang, Weidi, Wang, Pei, Yu, Huan, Cai, Wenxiang, Jiang, Xue, Huang, Wu, Qian, Wei, Chen, Yucan, Chen, Miao, Yu, Shunying, Xu, Tingting, Jiao, Yumei, Liu, Qiang, Zhang, Chen, Yi, Zhenghui, Fan, Qing, Chen, Jue, Wang, Zhen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8754407/ https://www.ncbi.nlm.nih.gov/pubmed/35020433 http://dx.doi.org/10.1126/sciadv.abi6180 |
Ejemplares similares
-
Dissection of the Genetic Association between Anorexia Nervosa and Obsessive–Compulsive Disorder at the Network and Cellular Levels
por: Song, Weichen, et al.
Publicado: (2021) -
A Comprehensive Study of De Novo Mutations on the Protein-Protein Interaction Interfaces Provides New Insights into Developmental Delay
por: Maharjan, Dhruba Tara, et al.
Publicado: (2022) -
A Comprehensive Evaluation of Cross-Omics Blood-Based Biomarkers for Neuropsychiatric Disorders
por: Song, Weichen, et al.
Publicado: (2021) -
Untargeted metabolomics analysis in drug-naïve patients with severe obsessive–compulsive disorder
por: Li, Zheqin, et al.
Publicado: (2023) -
PsyMuKB: An Integrative De Novo Variant Knowledge Base for Developmental Disorders
por: Lin, Guan Ning, et al.
Publicado: (2019)