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商璇 封面图

商璇 (Xuan Shang)

Shanxi Medical University教授
H指数:17
被引数:1,245

个人简介

任职于南方医科大学基础医学院医学遗传学教研室，教授、博士生导师，并担任教研室教学秘书。2002年至2007年在武汉大学攻读遗传学博士学位，1998年至2002年在中山大学获生物化学学士学位。2007年至2013年任南方医科大学基础医学院医学遗传学教研室讲师，2014年至2020年任该教研室副教授。

教育背景

  • 2002.09 – 2007.06

    武汉大学 博士 遗传学

  • 1998.09 – 2002.06

    中山大学 学士 生物化学

工作经历

  • 2020.07 – 至今

    南方医科大学

    教授

  • 2014.01 – 2020.06

    南方医科大学

    副教授

  • 2007.06 – 2013.12

    南方医科大学

    讲师

荣誉奖项

  1. 国家科技进步二等奖（2011）
  2. 全国妇幼健康科学技术二等奖（2015）
Semaphorin 3A protects against thoracic aortic aneurysm dissection by suppressing aortic angiogenesis

Semaphorin 3A通过抑制主动脉血管生成来保护 against 胸主动脉瘤破裂

Angiogenesis
IF9.2
2025-06-280
PRE
Li-Fei Wu; Jiao-Jiao Zhang; Xing Zhang; De-Ping Wang; Zhi-Fa Zheng; Jing Shen; Ying Zhou; Li-Juan Gao; Xuan Shang; Jun-Ya Ning; Qing-Hua Liu; Lan Zhou; Zhang-Rong Jia; Jia-Song Chang; Jian-Yun Shi; Shuang Wang; Teng Sun; Xue-Ning Wang; Zhi-Fang Wu; Si-Jin Li; Xin Zhou; Ji-Min Cao
Investigating genotype-phenotype correlation of limb-girdle muscular dystrophy R8: association of clinical severity, protein biological function and protein oligomerization (vol 13,47, 2025)

研究 limb-girdle muscular dystrophy R8 的基因型-表型相关性：临床严重程度、蛋白质生物学功能与蛋白质寡聚化的关联（卷 13, 47, 2025）

ACTA NEUROPATHOLOGICA COMMUNICATIONS
IF5.7
2025-05-060
OA
Liang, XD; Si, JM; Xie, HT; Guan, YQ; Lin, WY; Lin, ZZ; Zheng, GW; Wei, XF; Xiong, XB; Zhuang, ZF; Shang, X
Application value of long-read sequencing in full characterization of thalassemia-associated structural variations: identifying a novel large segmental duplication and literature review

长读测序在地中海贫血相关结构变异全面表征中的应用价值: 鉴定一种新的大节段重复和文献综述

ORPHANET JOURNAL OF RARE DISEASES
IF3.5
2025-04-020
OAAI
Zhong, Zeyan; Zheng, Ganwei; Zhu, Dina; Liu, Yongqiong; Lin, Zezhang; Guan, Zhiyang; Xiong, Fu; Chen, Jianhong; Shang, Xuan
NGS-based spinal muscular atrophy carrier screening of 10,585 diverse couples in China: a pan-ethnic study

基于NGS的脊髓性肌萎缩症携带者筛查中国10,585对不同种族的夫妇: 一项泛种族研究

EUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
2020-09-0322
OAAI
Zhao, Sumin; Wang, Wanyang; Wang, Yaoshen; Han, Rui; Fan, Chunna; Ni, Peixiang; Guo, Fengyu; Zeng, Fanwei; Yang, Qiaona; Yang, Yun; Sun, Yan; Zhang, Xinhua; Chen, Yan; Zhu, Baosheng; Cai, Wangwei; Chen, Shaoke; Cai, Ren; Guo, Xiaoling; Zhang, Chonglin; Zhou, Yuqiu; Huang, Shuodan; Liu, Yanhui; Chen, Biyan; Yan, Shanhuo; Chen, Yajun; Ding, Hongmei; Shang, Xuan; Xu, Xiangmin; Sun, Jun; Peng, Zhiyu
LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathies

Lovd-dash: 一个综合的LOVD数据库，结合诊断和血红蛋白病的风险评估系统

HUMAN MUTATION
IF3.7
2019-09-1113
OAAI
Zhang, Li; Zhang, Qianqian; Tang, Yaohua; Cong, Peikuan; Ye, Yuhua; Chen, Shiping; Zhang, Xinhua; Chen, Yan; Zhu, Baosheng; Cai, Wangwei; Chen, Shaoke; Cai, Ren; Guo, Xiaoling; Zhang, Chonglin; Zhou, Yuqiu; Zou, Jie; Liu, Yanhui; Chen, Biyan; Yan, Shanhuo; Chen, Yajun; Zhou, Yuehong; Ding, Hongmei; Li, Xiarong; Chen, Dianyu; Zhong, Jianmei; Shang, Xuan; Liu, Xuanzhu; Qi, Ming; Xu, Xiangmin
Pilot study of expanded carrier screening for 11 recessive diseases in China: results from 10,476 ethnically diverse couples

中国11种隐性遗传病扩展携带者筛查的试点研究：来自10,476对不同民族背景夫妇的结果

EUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
2018-10-0142
OAAI
Zhao, Sumin; Xiang, Jiale; Fan, Chunna; Asan; Shang, Xuan; Zhang, Xinhua; Chen, Yan; Zhu, Baosheng; Cai, Wangwei; Chen, Shaoke; Cai, Ren; Guo, Xiaoling; Zhang, Chonglin; Zhou, Yuqiu; Huang, Shuodan; Liu, Yanhui; Chen, Biyan; Yan, Shanhuo; Chen, Yajun; Ding, Hongmei; Guo, Fengyu; Wang, Yaoshen; Zhong, Wenwei; Zhu, Yaping; Wang, Yaling; Chen, Chao; Li, Yun; Huang, Hui; Mao, Mao; Yin, Ye; Wang, Jian; Yang, Huanming; Xu, Xiangmin; Sun, Jun; Peng, Zhiyu
Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies

用于血红蛋白病患者分子筛查和临床基因分型的快速靶向下一代测序平台

EBIOMEDICINE
IF10.8
2017-09-01162
OAAI
Shang, Xuan; Peng, Zhiyu; Ye, Yuhua; Asan; Zhang, Xinhua; Chen, Yan; Zhu, Baosheng; Cai, Wangwei; Chen, Shaoke; Cai, Ren; Guo, Xiaoling; Zhang, Chonglin; Zhou, Yuqiu; Huang, Shuodan; Liu, Yanhui; Chen, Biyan; Yan, Shanhuo; Chen, Yajun; Ding, Hongmei; Yin, Xiaolin; Wu, Liusong; He, Jing; Huang, Dongai; He, Sheng; Yan, Tizhen; Fan, Xin; Zhou, Yuehong; Wei, Xiaofeng; Zhao, Sumin; Cai, Decheng; Guo, Fengyu; Zhang, Qianqian; Li, Yun; Zhang, Xuelian; Lu, Haorong; Huang, Huajie; Guo, Junfu; Zhu, Fei; Yuan, Yuan; Zhang, Li; Liu, Na; Li, Zhiming; Jiang, Hui; Zhang, Qiang; Zhang, Yijia; Juhari, Wan Khairunnisa Wan; Hanafi, Sarifah; Zhou, Wanjun; Xiong, Fu; Yang, Huanming; Wang, Jian; Zilfalil, Bin Alwi; Qi, Ming; Yang, Yaping; Yin, Ye; Mao, Mao; Xu, Xiangmin
Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I
HUMAN MUTATION
IF3.7
2016-10-1936
OAAI
Xiong, Fu; Ji, Zhisong; Liu, Yanhui; Zhang, Yu; Hu, Lingling; Yang, Qi; Qiu, Qinwei; Zhao, Lingfeng; Chen, Dong; Tian, Zhihui; Shang, Xuan; Zhang, Leitao; Wei, Xiaofeng; Liu, Cuixian; Yu, Qiuxia; Zhang, Meichao; Cheng, Jing; Xiong, Jun; Li, Dongri; Wu, Xiuhua; Yuan, Huijun; Zhang, Wenqing; Xu, Xiangmin

研究方向

人类遗传病的分子基础、精准诊断和人群防控遗传性溶血性贫血、血红蛋白病、地中海贫血、精准诊断、人群预防遗传性溶血性贫血血红蛋白病地中海贫血精准诊断人群预防
X
Xiangmin Xu
H 指数:30论文数:136被引数:3,035
X
Xiaofeng Wei
H 指数:25论文数:85被引数:4,701
张新化 封面图
张新化
H 指数:41论文数:337被引数:6,193
陈
陈亚军
H 指数:38论文数:260被引数:5,134
B
Baosheng Zhu
H 指数:16论文数:88被引数:1,055
Y
Yuqiu Zhou
H 指数:15论文数:51被引数:1,505
蔡
蔡仁
H 指数:22论文数:111被引数:1,627
X
Xiangmin Xu
H 指数:15论文数:67被引数:794
C
Chonglin Zhang
H 指数:15论文数:56被引数:979
H
Hongmei Ding
H 指数:28论文数:167被引数:2,951