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H

Hui Guo

Central South University
H指数:35
被引数:4,657

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MSL2 orchestrates oligodendrocyte precursor cell cycle via H3K4me3 to prevent white matter defects in neurodevelopmental disorders

MSL2通过H3K4me3调控少突胶质祖细胞周期以防止神经发育障碍中的白质缺陷

2026-10-060
OAAI
Genomic landscape of rare variants in a Chinese autism cohort and discovery of novel risk genes

中国自闭症队列中稀有变异的基因组景观及新型风险基因的发现

2026-07-160
PRE
Haplotype-resolved methylomes reveal parent-of-origin DNA methylation imbalance in autism spectrum disorder

单倍型解析的甲基组揭示自闭症谱系障碍中亲源特异性DNA甲基化失衡

2026-06-170
OA
Evidence supporting the role of GIGYF2 in synapse development and autism

支持GIGYF2在突触发育和自闭症中作用的证据

2026-06-150
PRE
Disrupting integrator complex subunit INTS6 causes neurodevelopmental disorders and impairs neurogenesis and synapse development

彭X.; 贾X.; 王H.; 陈J.; 张X.; 谭S.; 段X.; 丘C.; 胡M.; 侯H.; 等. 破坏整合器复合物亚基INTS6会导致神经发育障碍并损害神经发生和突触发育。J. Clin. Investig. 2025, 18, e191729. [Google Scholar] [CrossRef]

2025-11-171
OA
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis (Vol 135, e200195, 2025)
2025-11-031
PRE
Exploring resistance mechanisms and identifying QTLs for brown planthopper in tropical and subtropical rice (Oryza sativa L.) germplasm

探索热带和亚热带水稻(Oryza sativa L.)种质资源中褐飞虱的抗性机制及QTL定位

2025-02-200
PRE
KCTD10 p.C124W variant contributes to schizophrenia by attenuating LLPS- mediated synapse formation

KCTD10 p.C124W变体通过减弱LLPS介导的突触形成而导致精神分裂症

2024-11-200
PRE
Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay
2024-10-290
PRE