Upadacitinib for Successful Treatment of Alopecia Universalis in a Child: A Case Report and Literature Review

por YU, Dianhe, REN, Yunqing
Publicado 2023

Systemic Analysis of the Prognosis-Related RNA Alternative Splicing Signals in Melanoma

por Xue, Dan, Cheng, Pu, Jiang, Jinxin, Ren, Yunqing, Wu, Dang, Chen, Wuzhen
Publicado 2020

Epigenomic and genomic analysis of transcriptome modulation in skin cutaneous melanoma

por Chen, Wuzhen, Cheng, Pu, Jiang, Jingxin, Ren, Yunqing, Wu, Dang, Xue, Dan
Publicado 2020

Discovery of Novel Genetic Risk Loci for Acute Central Serous Chorioretinopathy and Genetic Pleiotropic Effect With Age-Related Macular Degeneration

por Feng, Lei, Chen, Si, Dai, Huatuo, Dorajoo, Rajkumar, Liu, Jianjun, Kong, Jinfeng, Yin, Xianyong, Ren, Yunqing
Publicado 2021

Clinical Characteristics and In Silico Analysis of Cystinuria Caused by a Novel SLC3A1 Mutation

por Liu, Lexin, Xu, Zihao, Guan, Yuelin, Zhang, Ying, Li, Xue, Ren, Yunqing, Hu, Lidan, Yan, Xiang
Publicado 2022

Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy

por Ren, Yunqing, Liu, Jipeng, Yao, Dianyi, Hua, Huixia, Guo, Xiaoxuan, Dai, Huatuo, Dang, Nan, Huang, Yan, Yu, Dianhe
Publicado 2022

Causal Associations between Vitamin D Levels and Psoriasis, Atopic Dermatitis, and Vitiligo: A Bidirectional Two-Sample Mendelian Randomization Analysis

por Ren, Yunqing, Liu, Jipeng, Li, Wei, Zheng, Huiwen, Dai, Huatuo, Qiu, Guiying, Yu, Dianhe, Yao, Dianyi, Yin, Xianyong
Publicado 2022

Anti-TNF- αtreatment-related pathways and biomarkers revealed by transcriptome analysis in Chinese psoriasis patients

por Liu, Lunfei, Liu, Wenting, Zheng, Yuxin, Chen, Jisu, Zhou, Jiong, Dai, Huatuo, Cai, Suiqing, Liu, Jianjun, Zheng, Min, Ren, Yunqing
Publicado 2019

Genome-wide association analysis of anti-TNF-α treatment response in Chinese patients with psoriasis

por Ren, Yunqing, Wang, Ling, Dai, Huatuo, Qiu, Guiying, Liu, Jipeng, Yu, Dianhe, Liu, Jianjun, Lyu, Cheng-Zhi, Liu, Lunfei, Zheng, Min
Publicado 2022

A missense variant of the ABCC11 gene is associated with Axillary Osmidrosis susceptibility and clinical phenotypes in the Chinese Han Population

por Ren, Yunqing, Liu, Wenting, Chen, Jisu, Wang, Jianyou, Wang, Ke, Zhou, Jiong, Cai, Suiqing, Zheng, Min, Liu, Jianjun, Liu, Lunfei, Xue, Dan
Publicado 2017

Genetic Variation of Promoter Sequence Modulates XBP1 Expression and Genetic Risk for Vitiligo

por Ren, Yunqing, Yang, Sen, Xu, Shengxin, Gao, Min, Huang, Wei, Gao, Tianwen, Fang, Qiaoyun, Quan, Cheng, Zhang, Chi, Sun, Liangdan, Liang, Yanhua, Han, Jianwen, Wang, Zhimin, Zhang, Fengyu, Zhou, Youwen, Liu, Jianjun, Zhang, Xuejun
Publicado 2009