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

Deep clinical and genetic analysis of 17p13.3 region: 38 pediatric patients diagnosed using next-generation sequencing and literature review

对17p13.3区域进行深入的临床和遗传分析：采用新一代测序技术诊断的38例儿科患者及文献回顾

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-025-02155-y
Ji, Xiaoshan; Xu, Qiong; Lu, Yulan; Liu, Bo; Xiao, Feifan; Ni, Qi; Xu, Suzhen; Liu, Renchao; Li, Gang; Wu, Bingbing; Zhou, Shuizhen; Wang, Huijun
Sequencing
发表日期：2025
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Effectiveness and safety of intraoperative intraperitoneal 5-Fu drug implantation in patients with colorectal cancer: a retrospective cohort study

术中腹腔内植入5-氟尿嘧啶药物治疗结直肠癌患者的有效性和安全性：一项回顾性队列研究

期刊:Journal of Cancer Research and Clinical Oncology
影响因子:2.8
doi:10.1007/s00432-023-05523-2
Liu, Renchao; Hu, Xianqin; Lai, Chen
肿瘤
肠癌
肿瘤免疫
发表日期：2024
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Staggered circular nanoporous graphene converts electromagnetic waves into electricity

交错圆形纳米多孔石墨烯将电磁波转化为电能

期刊:Nature Communications
影响因子:14.7
doi:10.1038/s41467-023-37436-6
Hualiang Lv, Yuxing Yao, Shucong Li, Guanglei Wu, Biao Zhao, Xiaodi Zhou, Robert L Dupont, Ufuoma I Kara, Yimin Zhou, Shibo Xi, Bo Liu, Renchao Che, Jincang Zhang, Hongbin Xu, Solomon Adera, Renbing Wu, Xiaoguang Wang
信号转导
发表日期：2023
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Genetic Spectrum of Congenital Anomalies of the Kidney and Urinary Tract in Chinese Newborn Genome Project

中国新生儿基因组计划中肾脏和泌尿系统先天性异常的遗传谱

期刊:Kidney International Reports
影响因子:5.7
doi:10.1016/j.ekir.2023.08.005
Huang, Zhelan; Shen, Qian; Wu, Bingbing; Wang, Huijun; Dong, Xinran; Lu, Yulan; Cheng, Guoqiang; Wang, Laishuan; Lu, Wei; Chen, Liping; Kang, Wenqing; Li, Long; Pan, Xinnian; Wei, Qiufen; Zhuang, Deyi; Chen, Dongmei; Yin, Zhaoqing; Yang, Ling; Ni, Qi; Liu, Renchao; Li, Gang; Zhang, Ping; Qian, Yanyan; Peng, Xiaomin; Wang, Yao; Cao, Yun; Xu, Hong; Hu, Liyuan; Yang, Lin; Zhou, Wenhao
发表日期：2023
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Flavor improving effects of cysteine in xylose-glycine-fish waste protein hydrolysates (FPHs) Maillard reaction system

半胱氨酸对木糖-甘氨酸-鱼渣蛋白水解物（FPHs）美拉德反应体系的增鲜作用

期刊:Bioresources and Bioprocessing
影响因子:4.3
doi:10.1186/s40643-023-00714-8
Yicheng Ding, Chen Yan, Wangli Dai, Yanbo Wang, Shulai Liu, Renchao Zheng, Xuxia Zhou
信号转导
发表日期：2023
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Further delineation of EBF3-related syndromic neurodevelopmental disorder in twelve Chinese patients

对12名中国患者EBF3相关综合征性神经发育障碍的进一步描述

期刊:Frontiers in Pediatrics
影响因子:2
doi:10.3389/fped.2023.1091532
Zhu, Jitao; Li, Wenhui; Yu, Sha; Lu, Wei; Xu, Qiong; Wang, Sujuan; Qian, Yanyan; Guo, Qiufang; Xu, Suzhen; Wang, Yao; Zhang, Ping; Zhao, Xuemei; Ni, Qi; Liu, Renchao; Li, Xu; Wu, Bingbing; Zhou, Shuizhen; Wang, Huijun
发育与干细胞
神经科学
发表日期：2023
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Overdosage of HNF1B Gene Associated With Annular Pancreas Detected in Neonate Patients With 17q12 Duplication.

在患有 17q12 重复的新生儿患者中检测到与环状胰腺相关的 HNF1B 基因过量表达

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2021.615072
Xiao Feifan, Liu Xiuyun, Lu Yulan, Wu Bingbing, Liu Renchao, Liu Bo, Yan Kai, Chen Huiyao, Cheng Guoqiang, Wang Laishuan, Ni Qi, Li Gang, Zhang Ping, Peng Xiaomin, Cao Yun, Shen Chun, Wang Huijun, Zhou Wenhao
NF1
发表日期：2021
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Genetic identification of pathogenic variations of the DMD gene: a retrospective study from 10,481 neonatal patients based on next-generation sequencing data

DMD基因致病变异的遗传鉴定：一项基于二代测序数据的回顾性研究，纳入10481例新生儿患者

期刊:Annals of Translational Medicine
影响因子:
doi:10.21037/atm-20-7102
Xiao, Tiantian; Wu, Bingbing; Cao, Yun; Liu, Renchao; Cheng, Guoqiang; Wang, Laishuan; Zhuang, Deyi; Zhao, Zhengyan; Wang, Huijun; Zhou, Wenhao
DMD
发表日期：2021
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A genomic copy number variant analysis implicates the MBD5 and HNRNPU genes in Chinese children with infantile spasms and expands the clinical spectrum of 2q23.1 deletion

基因组拷贝数变异分析表明，MBD5 和 HNRNPU 基因与中国婴儿痉挛症患儿相关，并扩展了 2q23.1 缺失的临床谱。

期刊:BMC Medical Genetics
影响因子:
doi:10.1186/1471-2350-15-62
Du, Xiaonan; An, Yu; Yu, Lifei; Liu, Renchao; Qin, Yanrong; Guo, Xiaohong; Sun, Daokan; Zhou, Shuizhen; Wu, Bailin; Jiang, Yong-Hui; Wang, Yi
发表日期：2014
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