杨勇，长聘教授，主任医师，博士研究生导师，中国医学科学院皮肤病医院副院所长，江苏省皮肤医学重点实验室主任。曾获北京市科学技术奖（2009和2016，均为第一完成人），第六届国之名医·优秀风范奖（2023）。获得国家杰出青年科学基金和国自然重点项目（2018，2021和2023）等资助。 中国足球彩票：引进人才，2018年加入中国足球彩票：，曾在北京大学第一医院任主任医师。

长期从事遗传性皮肤病、离子通道病、疼痛及瘙痒的研究，带领课题组首次探明7种遗传病的致病基因和发病机制，其中4种是离子通道病，首次提出皮肤离子通道病的概念，揭示了两种与疼痛和瘙痒密切相关的离子通道。先后主持8项国家自然科学基金，包括国家杰出青年科学基金（2014），国自然重点项目（2017，2021和2023）等。已发表SCI论文70余篇，被他引千余次，部分成果系列发表于Nat Genet，Nat Chem Biol，Am J Hum Genet，J Clin Invest等杂志。

中国足球彩票

1. Chen Z*#, Liu Y, Yu H, Li J, Huang X, Xiang R, Mo R, Chen H*, Yang Y*. Safety and efficacy of topical simvastatin plus cholesterol cream versus topical simvastatin cream alone for porokeratosis ptychotropica: A randomized, single-blind, split-body, placebo-controlled, investigator-initiated trial. J Am Acad Dermatol. 2025 Oct;93(4):980-987. (IF=11.8)

2. Xu F#, Cui YZ, Yang XY, Zheng YX, Chen XB, Zhou H, Wang ZY, Zhou Y, Lu Y, Li YY, Ye LR, Fu NC, Chen SQ, Chen XY, Zheng M, Yang Y*, Man XY*. CXCL10 secreted by SPRY1-deficient epidermal keratinocytes fuels joint inflammation in psoriatic arthritis via CD14 signaling. J Clin Invest. 2025 Jun 5;135(15):e186135. (IF=13.6)

3. Fan J#, Hu L#, Yue Z#, Liao D#, Guo F, Ke H, Jiang D*, Yang Y*, Lei X*. Structural basis of TRPV3 inhibition by an antagonist. Nat Chem Biol. 2023 Jan;19(1):81-90. (IF=13.0)

4. Zhao J#, Munanairi A#, Liu XY, Zhang J, Hu L, Hu M, Bu D, Liu L, Xie Z, Kim BS, Yang Y*, Chen ZF*. PAR2 Mediates Itch via TRPV3 Signaling in Keratinocytes. J Invest Dermatol. 2020 Aug;140(8):1524-1532. (IF=8.551)

5. Lin Z#, Li S, Feng C, Yang S, Wang H, Ma D, Zhang J, Gou M, Bu D, Zhang T, Kong X, Wang X, Sarig O, Ren Y, Dai L, Liu H, Zhang J, Li F, Hu Y, Padalon-Brauch G, Vodo D, Zhou F, Chen T, Deng H, Sprecher E, Yang Y*, Tan X*. Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility. Nat Genet. 2016 Dec;48(12):1508-1516. (IF=27.959, C100)

6. Lin Z#, Zhao J#, Nitoiu D#, Scott CA#, Plagnol V, Smith FJ, Wilson NJ, Cole C, Schwartz ME, McLean WH, Wang H, Feng C, Duo L, Zhou EY, Ren Y, Dai L, Chen Y, Zhang J, Xu X, O'Toole EA, Kelsell DP*, Yang Y*. Loss-of-function mutations in CAST cause peeling skin, leukonychia, acral punctate keratoses, cheilitis, and knuckle pads. Am J Hum Genet. 2015 Mar 5;96(3):440-447. (IF=10.794)

7. Lin Z#, Chen Q#, Shi L, Lee M, Giehl KA, Tang Z, Wang H, Zhang J, Yin J, Wu L, Xiao R, Liu X, Dai L, Zhu X, Li R, Betz RC, Zhang X*, Yang Y*. Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia. Am J Hum Genet. 2012 Nov 2;91(5):906-911. (IF=11.202)

8. Lin Z#, Chen Q#, Lee M#, Cao X#, Zhang J, Ma D, Chen L, Hu X, Wang H, Wang X, Zhang P, Liu X, Guan L, Tang Y, Yang H, Tu P, Bu D, Zhu X, Wang K, Li R*, Yang Y*. Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome. Am J Hum Genet. 2012;90(3):558-564. (IF=11.202, C100)

9. Han C#, Rush AM, Dib-Hajj SD, Li S, Xu Z, Wang Y, Tyrrell L, Wang X, Yang Y*, Waxman SG*. Sporadic onset of erythermalgia: a gain-of-function mutation in Nav1.7. Ann Neurol. 2006 Mar;59(3):553-558. (IF=8.051, C100)

10. Yang Y#, Wang Y#, Li S#, Xu Z, Li H, Ma L, Fan J, Bu D, Liu B, Fan Z, Wu G, Jin J, Ding B, Zhu X*, Shen Y*. Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia. J Med Genet. 2004 Mar;41(3):171-174. (IF=4.112, C100)