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

Runx2 mutation plays a key role in the development of scoliosis

Runx2基因突变在脊柱侧弯的发生发展中起着关键作用。

Lu, Ke; Wei, Guizheng; Li, Guozhuang; Zhao, Lina; Hsu, Yu-Ching; Qin, Ling; Xiao, Guozhi; Wu, Zhihong; Wang, Huaiyu; Chen, Jianquan; Shen, Jianxiong; Wu, Nan; Chen, Di

Chromoanagenesis in Osteosarcoma

骨肉瘤中的染色质新生

Li, Guozhuang; Wu, Nan; Ghabrial, Jen; Stinnett, Victoria; Klausner, Melanie; Morsberger, Laura; Long, Patty; Baraban, Ezra; Gross, John M; Zou, Ying S

Shaping the future of care for patients with Ehlers-Danlos syndromes: from multidisciplinary management to precision medicine

塑造埃勒斯-当洛斯综合征患者护理的未来:从多学科管理到精准医疗

Xu, Kexin; Li, Guozhuang; Zhang, Terry Jianguo; Wu, Nan

Selecting the Substantially Touched Vertebra as the Lowest Instrumented Vertebra in Spinal Surgeries for B3GALT6 -Related Disorders: Clinical Experience and Literature Review

在B3GALT6相关疾病的脊柱手术中,选择受累最严重的椎体作为最低位固定椎体:临床经验和文献综述

Maheshati, Aoran; Xu, Kexin; Li, Ziquan; Li, Guozhuang; Yin, Xiangjie; Li, Qing; Liu, Di; Wang, Shengru; Wu, Zhihong; Qiu, Guixing; Zhang, Baozhong; Zhang, Terry Jianguo; Wang, Yu; Wu, Nan

The Smallest Worthwhile Effect as a Promising Alternative to the MCID in Estimating PROMs for Adult Idiopathic Scoliosis

最小有效效应作为评估成人特发性脊柱侧弯患者报告结局指标的一种有前景的替代最小临床重要差异(MCID)的方法

Liu, Di; Zhao, Zhengye; Li, Guozhuang; Yin, Xiangjie; Zhu, Yuanpeng; Liu, Ze; Han, Jialuo; Zhang, Terry Jianguo; Wu, Nan

Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine

揭示先天性椎体畸形的遗传结构及其与脊柱发育的关系

Zhao, Sen; Zhao, Hengqiang; Zhao, Lina; Cheng, Xi; Zheng, Zhifa; Wu, Mengfan; Wen, Wen; Wang, Shengru; Zhou, Zixiang; Xie, Haibo; Ruan, Dengfeng; Li, Qing; Liu, Xinquan; Ou, Chengzhu; Li, Guozhuang; Zhao, Zhengye; Chen, Guilin; Niu, Yuchen; Yin, Xiangjie; Hu, Yuhong; Zhang, Xiaochen; Liu, Pengfei; Qiu, Guixing; Liu, Wanlu; Zhao, Chengtian; Wu, Zhihong; Zhang, Jianguo; Wu, Nan

Core planar cell polarity genes VANGL1 and VANGL2 in predisposition to congenital vertebral malformations

核心平面细胞极性基因VANGL1和VANGL2与先天性椎体畸形的易感性

Feng, Xin; Ye, Yongyu; Zhang, Jianan; Zhang, Yuanqiang; Zhao, Sen; Mak, Judith C W; Otomo, Nao; Zhao, Zhengye; Niu, Yuchen; Yonezawa, Yoshiro; Li, Guozhuang; Lin, Mao; Li, Xiaoxin; Cheung, Prudence Wing Hang; Xu, Kexin; Takeda, Kazuki; Wang, Shengru; Xie, Junjie; Kotani, Toshiaki; Choi, Vanessa N T; Song, You-Qiang; Yang, Yang; Luk, Keith Dip Kei; Lee, Kin Shing; Li, Ziquan; Li, Pik Shan; Leung, Connie Y H; Lin, Xiaochen; Wang, Xiaolu; Qiu, Guixing; Watanabe, Kota; Wu, Zhihong; Posey, Jennifer E; Ikegawa, Shiro; Lupski, James R; Cheung, Jason Pui Yin; Zhang, Terry Jianguo; Gao, Bo; Wu, Nan

SIGMA leverages protein structural information to predict the pathogenicity of missense variants.

SIGMA 利用蛋白质结构信息来预测错义变异的致病性

Zhao Hengqiang, Du Huakang, Zhao Sen, Chen Zefu, Li Yaqi, Xu Kexin, Liu Bowen, Cheng Xi, Wen Wen, Li Guozhuang, Chen Guilin, Zhao Zhengye, Qiu Guixing, Liu Pengfei, Zhang Terry Jianguo, Wu Zhihong, Wu Nan

Diagnosis and treatment of the Ehlers-Danlos syndromes in China: synopsis of the first guidelines

中国埃勒斯-当洛斯综合征的诊断和治疗:首版指南概要

Xu, Kexin; Li, Guozhuang; Wu, Zhihong; Zhang, Terry Jianguo; Wu, Nan

Integrating deep phenotyping with genetic analysis: a comprehensive workflow for diagnosis and management of rare bone diseases

将深度表型分析与基因分析相结合:罕见骨病诊断和管理的综合工作流程

Li, Guozhuang; Xu, Kexin; Yin, Xiangjie; Yang, Jianle; Cai, Jihao; Yang, Xinyu; Li, Qing; Wang, Jie; Zhao, Zhengye; Mahesahti, Aoran; Zhang, Ning; Zhang, Terry Jianguo; Wu, Nan