副教授,硕士生导师。日本长崎大学药理学博士,曾任日本名古屋大学特任助教,入选广州医科
大学“南山学者”。广东省药学会罕见病呼吸学组委员,中华医学会变态反应学分会基础与转化学组
(筹)成员。目前为呼吸疾病国家重点实验室哮喘方向核心成员,从事哮喘基因组学以及呼吸系统罕
见疾病的分子诊断研究。搭建了哮喘大型样本库和数据库,建立了哮喘基因型 - 表型关联方法学,探
讨遗传因素在哮喘中的作用;建立半自动细胞检测平台,可快速检测免疫通路中的
DNA
损伤应答
.
炎
症反应
.
细胞凋亡等信号。在《
Nature Protocols
》
.
《
Journal of Allergy and Clinical Immunology
》
.
《 Cell 》. 《 DNA Repair 》. 《 Journal of Medical Genetics 》等国际知名期刊发表多篇学术论文;
主持日本国家青年基金 1 项,广东省青年基金 1 项,广州市院校联合基金 1 项,参与多项国家级和
省市级科研基金项目。参编奥马珠单抗治疗专家共识。
1. Jia Nan#; Nakazawa Yuka#; Guo Chaowan; Shimada Mayuko; Sethi Mieran; Takahashi Yoshito;
Ueda Hiroshi; Nagayama Yuji; Ogi Tomoo*. A rapid, comprehensive system for assaying DNA repair
activity and cytotoxic effects of DNA-damaging reagents. Nature Protocols, 2015, 10(1): 12-24. #co-first
author. (Q1, IF=17.021)
2. Nan Jia, Chaowan Guo, Yuka Nakazawa, Diana van den Heuvel, Martijn S. Luijsterburg, Tomoo
Ogi*. Ubiquitination of DNA damage-stalled RNAPII promotes transcription-coupled repair. DNA Repair,
2021, 103192, https://doi.org/10.1016/j.dnarep.2021.103192. (Q2, IF=4.354)
3. Ruchong Chen#; Ling Sang#; Mei Jiang#; Zhaowei Yang#; Nan Jia#; Wanyi Fu#; Jiaxing Xie;
Weijie Guan; Wenhua Liang; Zhengyi Ni; Yu Hu; Lei Liu; Hong Shan; Chunliang Lei; Yixiang Peng; Li
Wei; Yong Liu; Yahua Hu; Peng Peng; Jianming Wang; Jiyang Liu; Zhong Chen; Gang Li; Zhijian Zheng;
Shaoqin Qiu; Jie Luo; Changjiang Ye; Shaoyong Zhu; Jinping Zheng; Nuofu Zhang; Yimin Li; Jianxing He;
Jing Li*; Shiyue Li*; Nanshan Zhong*. Longitudinal hematologic and immunologic variations associated
with the progression of COVID-19 patients in China. Journal of Allergy and Clinical Immunology, 2020.
146(1) :89-100. #co-first author. (Q1, IF=14.290)
4. Calmels Nadege#; Botta Elena#; Jia Nan#; Fawcett Heather; Nardo Tiziana; Nakazawa Yuka;
Lanzafame Manuela; Moriwaki Shinichi; Sugita Katsuo; Kubota Masaya; Obringer Cathy; Spitz Marie
Aude; Stefanini Miria; Laugel Vincent; Orioli Donata; Ogi Tomoo; Lehmann Alan Robert*. Functional and
clinical relevance of novel mutations in a large cohort of patients with Cockayne syndrome. Journal of
Medical Genetics, 2018, 55(5): 329-343. #co-first author. (Q1, IF=5.941)
5. Wenjun Jiang#, Nan Jia#, Chaowan Guo#, Juan Wen, Lingqian Wu, Tomoo Ogi*, Huiwen Zhang*.
Predominant cellular mitochondrial dysfunction in the TOP3A gene-caused Bloom syndrome-like disorder.
BBA - Molecular Basis of Disease, 2021, 166106, https://doi.org/10.1016/j.bbadis.2021.166106 #co-first
author. (Q1, IF=6.633)
代表性成果: