姓名：郭俊 性别：女 职称：研究员、副教授 招生院所：附属儿童医院 招生类型：科学学位(硕) 招生专业：遗传学(硕) 研究方向名称：遗传性心血管疾病分子病因学研究 电子信箱：guojunbjmu@hotmail.com


社会任职
个人简历
1. 199609-200107:山东大学临床医学系 本科
2. 200109-200407:北京大学医学部 硕士
3. 200410-200510:北京大学医学部天士力微循环研究中心 助理研究员
4. 200510-200703:日本庆应大学内科学系 访问研究员
5. 200704-201003:日本庆应大学内科学系 博士
6. 201005-201410:首都医科大学附属北京安贞医院 助理研究员
7. 201410-201703:首都医科大学附属北京安贞医院 副研究员
8. 201703-201912:首都医科大学附属北京儿童医院 副研究员，副教授
9. 201912-:首都医科大学附属北京儿童医院 研究员，副教授
重要学术论文
1. Boliang Fang#, Jun Guo#, Chanjuan Hao, Ruolan Guo, Suyun Qian, Wei Li*, Xinlei Jia*.Whole-exome sequencing identifies a novel compound heterozygous mutation of ANKS6 gene in a Chinese nephronophthisis patient. Clinica Chimica Acta. 2020,501:131-135.SCI
2. Qiqing Sun#, Jun Guo#, Chanjuan Hao, Ruolan Guo, Xuyun Hu, Yuanying Chen, Weili Yang, Wei Li*, Yingjun Feng*.Whole-exome sequencing reveals two de novo variants in the RBM20 gene in two Chinese patients with left ventricular noncompaction cardiomyopathy. Pediatric Investigation. 2020,4(1):11-16.
3. Jun Guo#, Zheng Li#, Chanjuan Hao, Ruolan Guo, Xuyun Hu, Suyun Qian, Jiansheng Zeng, Hengmiao Gao*, Wei Li*.A novel de novo CASZ1 heterozygous frameshift variant causes dilated cardiomyopathy and left ventricular noncompaction cardiomyopathy. Molecular Genetics & Genomic Medicine. 2019,7(8):e828.SCI
4. Xin Chen#, Jun Guo#, Tao Cai, Fengshan Zhang, Shengfa Pan, Li Zhang, Shaobo Wang, Feifei Zhou, Yinze Diao, Yanbin Zhao, Zhen Chen, Xiaoguang Liu, Zhongqiang Chen, Zhongjun Liu, Yu Sun* and Jie Du*.Targeted next-generation sequencing reveals multiple deleterious variants in OPLL-associated genes. Scientific Reports. 2016,6:26962.SCI
5. Jinrui Chang#, Jun Guo#, Yue Wang, Yuelong Hou, Weiwei Lu, Jinsheng Zhang, Yanrong Yu, Mingjiang Xu, Xiuying Liu, Xiujie Wang, Youfei Guan, Yi Zhu, Jie Du, Chaoshu Tang and Yongfen Qi*.Intermedin1-53 attenuates vascular calcification in rats with chronic kidney disease by upregulation of α-Klotho. Kidney International. 2016,89(3):586-600.SCI
6. Jun Guo, Lun Cai, Lixin Jia, Xiaoyan Li, Xin Xi, Shuai Zheng, Xuxia Liu, Chunmei Piao, Tingting Liu, Zhongsheng Sun, Tao Cai and Jie Du*.Wide mutation spectrum and frequent variant Ala27Thr of FBN1 identified in a large cohort of Chinese patients with sporadic TAAD. Scientific Reports. 2015,5:13115.SCI
主编或副主编的著作/译著
重要奖项