日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Discovery of AKT1 Inhibitors for Obesity and Metabolic Dysfunction-Associated Steatotic Liver Disease Using QSAR-Guided Virtual Screening and Gaussian Accelerated Molecular Dynamics

利用QSAR指导的虚拟筛选和高斯加速分子动力学方法发现用于治疗肥胖和代谢功能障碍相关脂肪肝疾病的AKT1抑制剂

Cao, Kun; Wang, Ruonan; Ou, Dong; Wu, Siyu; Chen, Yiyao; Li, Lianhai; Liu, Xinguang

Universal noninvasive prenatal diagnosis for monogenic disorders using cell-free plasma DNA

利用游离血浆DNA进行单基因疾病的普遍无创产前诊断

Zhang, Lanlan; Hua, Renyi; Wu, Yiming; Han, Xu; Wu, Yi; Fei, Hongjun; Zhao, Xinrong; Chang, Chunxin; Gao, Li; Chen, Yiyao; Xu, Hui; Li, Niu; Yang, Jingmin; Wang, Yanlin; Wang, Jian; Li, Shuyuan

Identification and functional analysis of a novel SMARCC2 splicing variant in a family with syndromic neurodevelopmental disorder

对一例患有综合征性神经发育障碍的家族中一种新型SMARCC2剪接变异体的鉴定和功能分析

Li, Ming; Lin, Jingqi; Fei, Hongjun; Liu, Jinyu; Chen, Yiyao; Han, Xu; Wang, Yanlin; Wang, Jian; Hua, Renyi; Li, Shuyuan; Li, Niu

Genetic analysis of 25 Chinese pedigrees with neurofibromatosis type 1 and genotype-phenotype study from an extended cohort

对25个中国1型神经纤维瘤病家系进行遗传分析,并开展来自扩展队列的基因型-表型研究

Fei, Hongjun; Han, Xu; Chen, Yiyao; Xu, Yan; Chang, Chunxin; Li, Ming; Wang, Yanlin; Wang, Jian; Li, Niu; Li, Shuyuan

scFTAT: a novel cell annotation method integrating FFT and transformer

scFTAT:一种融合了FFT和Transformer的新型细胞注释方法

Tang, Binhua; Chen, Yiyao

Prenatal diagnosis and clinical pregnancy outcome of fetuses with conotruncal defects in a Chinese cohort

中国人群中圆锥动脉干畸形胎儿的产前诊断和临床妊娠结局

Li, Min; Wu, Yi; Chen, Yiyao; Wang, Hui; Cheng, Weiwei; Ye, Baoying

Biallelic variants in RBM42 cause a multisystem disorder with neurological, facial, cardiac, and musculoskeletal involvement.

RBM42 的双等位基因变异会导致多系统疾病,累及神经系统、面部、心脏和肌肉骨骼系统

Chen Yiyao, Yang Bingxin, Zhang Xiaoyu Merlin, Chen Songchang, Wang Minhui, Hu Liya, Pan Nina, Li Shuyuan, Shi Weihui, Yang Zhenhua, Wang Li, Tan Yajing, Wang Jian, Wang Yanlin, Xing Qinghe, Ma Zhonghua, Li Jinsong, Huang He-Feng, Zhang Jinglan, Xu Chenming

Concurrent of compound heterozygous variant of a novel in-frame deletion and the common hypomorphic haplotype in TBX6 and inherited 17q12 microdeletion in a fetus

胎儿中同时存在TBX6基因新型框内缺失复合杂合变异体和常见低表达单倍型,以及遗传性17q12微缺失

Li, Guoqiang; Chen, Yiyao; Han, Xu; Li, Niu; Li, Shuyuan

Abdominal wall hernia repair: from prosthetic meshes to smart materials

腹壁疝修补术:从人工网片到智能材料

Saiding, Qimanguli; Chen, Yiyao; Wang, Juan; Pereira, Catarina Leite; Sarmento, Bruno; Cui, Wenguo; Chen, Xinliang

Early characterisation and prediction of liver diseases in pregnancy by plasma cell-free RNAs

利用血浆游离RNA对妊娠期肝脏疾病进行早期表征和预测

Sun, Jinghua; Wang, Wen-Jing; Zhou, Xuanyou; Yang, Tingyu; Ye, Mujin; Shi, Weihui; Liu, Zhongzhen; Zhang, Lanlan; Zhou, Qing; Qin, Yulong; Chen, Yiyao; Chen, Fang; Huang, Hefeng; Chen, Songchang; Xu, Chenming