Jiang Wei

1997 8 ---2000 9 2003 9 ---2006 8 2006 8 ---2010 8 2010 8 ---2015 8 2015 8 --- (1)2005 “ ” “ ” 1. (2)2008 “ ” “ ” 3. (3)2003 -2010 985 “ ”I、II、III. 9.8. (4)2011 10-2012 9 “ AD ”“ - DQ ” 8. (5)2011 11 -2012 10 “ ”“ - ” 5. (6)2012 “SCCA1 ”, 23. (7)2014 “ ”. (8)2015 5.;;;;;;; (2005 ); (2008 ); (2010 、2018 ); (2011 、2017 ); (2019 ) (2019 ) 50,SCI 9.: (1)Duyi Guo, Hua Zhang, Shiyuan Yang, Shi Yan, Xiangbo Wei, Jiangang Hu, Xiulian Zhang, Xueyan Lu, Chunlei,Zhang, Wei Jiang*. Prevalence, clinical and biochemical characteristics of female acne patients with insulin resistance[J]. Journal of Cosmetic Dermatology. 2021, 00:1–3. (IF:1.62) (2)Pei-Qiu Zhu, Hui-Min Yan, Hui-Juan Zhao, Du-Yi Guo, Wei Jiang*. A novel nonsense mutation in FDPS in a Chinese family with disseminated superficial actinic porokeratosis. British Journal of Dermatology 2018;12. (IF:6.129) (3)Hui-Juan Zhao1, Xin Zeng2, Peng-cheng Lei1, Xiao-Dan Jiang3, Xue-Min Li3, Jian-Ying Liu4, Hui-Min Yan1, Du-Yi Guo1, Xue-yan Lu1, Wei-Jiang1*. A Chinese family with autosomal recessive congenital ichthyosis and Leber congenital amaurosis due to mutations in PNPLA1 and LCA5. European Journal of Dermatology 2018; 28(2):244-246. (4)Hui-Min Yan, Hui-Juan Zhao, Du-Yi Guo, Pei-Qiu Zhu, Chun-Lei Zhang, Wei-Jiang*. Gut microbiome alterations in moderate-severe acne patients. Journal of Dermatology 2018;8(13):1-6. (5)WeiJiang,Ting-tingSun, Peng-chengLei, Xue-junZhu. Genotype-Phenotype Correlation in Chinese Patients with Dystrophic Epidermolysis Bullosa Pruriginosa. Acta dermato veneral. 2012:92:50-53. (6)YanhongZheng,CuncaiZhou, YongchuHuang, DingfangBu, XuejunZhu and WeiJiang*. A Novel Missence Mutationin SLC6A19 gene in A Chinese family with Hartnup disorder. Intern J Dermatol. 2009;48:388-392. (7)Y.Wang,J.Y.Zhao,P.Tu,W.Jiang*,X.J.Zhu.A novel missense mutation in COL7A1 in a Chinese predigree with epidermolysis bullosa pruriginosa. J Dermatol Science 2007; 46(3):211-213. (8)W.Jiang, Y.Sun, S.Li, X.X.Chen, D.F.Bu, X.J.Zhu. Two novel heterozygous mutations in COL7A1 in a Chinese patient with recessive dystrophic epidermolysis bullosa of Hallopeau-Siemens type. BrJDermatol2005;152(6):1357-1360. (9)WeiJiang, DingfangBu, YongYang and XuejunZhu. A Novel Splice Site Mutation in Collagen TypeVII Gene in a Chinese Family with Dominant Dystrophic Epidermolysis Bullosa Pruriginosa.Actadermatoveneral.2002;82:187-191. (10) 、 、 、 、 、.. 2013;27:17-19. (11) 、 、 、 、 、.. 2013:29:164-167. (12),,,,,. PTCH1. 2014;47(12):860-863. (13) 、 、 、. 8. 2015;44(11):743-745. (14) 、 、.. 2016;(10):991-994. (15) 、 、 、 、.. 2016;(10):601-604. (16) 、 、 、. OSMR. 2017;50(2):15-18. (17),,,,,. PNPLA1. 2017;50(6):408-411. (18),,,,.. 2017;50(3):172-176. (19);. 2020;37(2)158-164 (20),,,,;524.. 2021,37(8):490-493. 《 》2008 、《 》2006 《 》2017.