Xiao Feifan相关文献与解析，生知库 | 链接生命科学的每一步

日期影响因子

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

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

发表日期：2025

文献求助收藏

Neurosonography: Shaping the future of neuroprotection strategies in extremely preterm infants

神经超声：塑造极早产儿神经保护策略的未来

影响因子:3.6

doi:10.1016/j.heliyon.2024.e31742

Tang, Lukun; Li, Qi; Xiao, Feifan; Gao, Yanyan; Zhang, Peng; Cheng, Guoqiang; Wang, Laishuan; Lu, Chunmei; Ge, Mengmeng; Hu, Liyuan; Xiao, Tiantian; Yin, Zhaoqing; Yan, Kai; Zhou, Wenhao

发表日期：2024

文献求助收藏

Blautia Coccoides is a Newly Identified Bacterium Increased by Leucine Deprivation and has a Novel Function in Improving Metabolic Disorders

Blautia Coccoides 是一种新发现的细菌，因亮氨酸缺乏而增加，在改善代谢紊乱方面具有新功能

期刊:Advanced Science

doi:10.1002/advs.202309255

Yuguo Niu, Xiaoming Hu, Yali Song, Cunchuan Wang, Peixiang Luo, Shihong Ni, Fuxin Jiao, Ju Qiu, Weihong Jiang, Sheng Yang, Jun Chen, Rui Huang, Haizhou Jiang, Shanghai Chen, Qiwei Zhai, Jia Xiao, Feifan Guo

发表日期：2024

文献求助收藏

Comparison of Genetic Profiles of Neonates in Intensive Care Units Conceived With or Without Assisted Reproductive Technology

比较重症监护病房中通过辅助生殖技术受孕和未通过辅助生殖技术受孕的新生儿的基因谱

期刊:Jama Network Open

影响因子:9.7

doi:10.1001/jamanetworkopen.2023.6537

Huang, Zhongwen; Xiao, Feifan; Xiao, Hui; Lu, Yulan; Yang, Lin; Zhuang, Deyi; Chen, Liping; Wei, Qiufen; Jiang, Yinmo; Li, Gang; Wu, Bingbing; Liu, Zhiwei; Zhou, Wenhao; Wang, Huijun

发表日期：2023

文献求助收藏

Incidence of Neonatal Seizures in China Based on Electroencephalogram Monitoring in Neonatal Neurocritical Care Units

基于新生儿神经重症监护病房脑电图监测的中国新生儿癫痫发生率

期刊:Jama Network Open

影响因子:9.7

doi:10.1001/jamanetworkopen.2023.26301

Yan, Kai; Cheng, Guoqiang; Zhou, Wei; Xiao, Feifan; Zhang, Chongfan; Wang, Laishuan; Zhang, Peng; Lu, Chunmei; Kong, Yanting; Wang, Xinhua; Zhou, Yuanfeng; Lu, Weineng; Tang, Juan; Song, Xiaoyan; Wei, Qiufen; Meng, Danhua; Yao, Liping; Zhuang, Deyi; Qu, Liuhong; Xu, Qinghuo; Yin, Zhaoqing; Su, Le; Wan, Jing; Si, Yuan; Fujioka, Kazumichi; Mussap, Michele; Kanungo, Shibani; Bhandari, Vineet; Huang, Weimin; Pan, Xinnian; Zhou, Wenhao

发表日期：2023

文献求助收藏

Fourteen cases of cerebral creatine deficiency syndrome in children: a cohort study in China

中国14例儿童脑肌酸缺乏症病例队列研究

期刊:Translational Pediatrics

影响因子:1.7

doi:10.21037/tp-23-164

Sun, Weihua; Wang, Yi; Wu, Mengyuan; Wu, Hongjiang; Peng, Xiaomin; Shi, Yingyan; Xiao, Feifan; Wu, Bingbing; Zhou, Wenhao; Lu, Wei

发表日期：2023

文献求助收藏

Systematic estimation of cystic fibrosis prevalence in Chinese and genetic spectrum comparison to Caucasians

对中国人囊性纤维化患病率进行系统估计，并与高加索人进行遗传谱比较

期刊:Orphanet Journal of Rare Diseases

影响因子:3.5

doi:10.1186/s13023-022-02279-9

Ni, Qi; Chen, Xiang; Zhang, Ping; Yang, Lin; Lu, Yulan; Xiao, Feifan; Wu, Bingbing; Wang, Huijun; Zhou, Wenhao; Dong, Xinran

发表日期：2022

文献求助收藏

Combining Metagenomic Sequencing With Whole Exome Sequencing to Optimize Clinical Strategies in Neonates With a Suspected Central Nervous System Infection

结合宏基因组测序和全外显子组测序优化疑似中枢神经系统感染新生儿的临床策略

期刊:Frontiers in Cellular and Infection Microbiology

影响因子:4.8

doi:10.3389/fcimb.2021.671109

Ge, Mengmeng; Gan, Mingyu; Yan, Kai; Xiao, Feifan; Yang, Lin; Wu, Bingbing; Xiao, Mili; Ba, Yin; Zhang, Rong; Wang, Jin; Cheng, Guoqiang; Wang, Laishuan; Cao, Yun; Zhou, Wenhao; Hu, Liyuan

发表日期：2021

文献求助收藏

High-Frequency Exon Deletion of DNA Cross-Link Repair 1C Accounting for Severe Combined Immunodeficiency May Be Missed by Whole-Exome Sequencing

全外显子组测序可能漏检导致重症联合免疫缺陷的DNA交联修复1C基因高频外显子缺失

期刊:Frontiers in Genetics

影响因子:2.8

doi:10.3389/fgene.2021.677748

Xiao, Feifan; Lu, Yulan; Wu, Bingbing; Liu, Bo; Li, Gang; Zhang, Ping; Zhou, Qinhua; Sun, Jinqiao; Wang, Huijun; Zhou, Wenhao

免疫/内分泌

发表日期：2021

文献求助收藏

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

发表日期：2021

文献求助收藏