Jing Wu

Immunology and Microbiology · Life Sciences

8h-index157citations13works0.02yr avg
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Research Topics

Psoriasis: Treatment and Pathogenesis(5), Asthma and respiratory diseases(3), Dermatology and Skin Diseases(2), Cytokine Signaling Pathways and Interactions(2), T-cell and B-cell Immunology(1)

Publications13 total

THE SAFETY AND EFFICIENCY OF SCISSOR-TYPE KNIVES IN COLORECTAL ESD:AN INTERNATIONAL MULTICENTER PROSPECTIVE OBSERVATIONAL STUDY
Gastrointestinal Endoscopy·2025
Polymorphisms in ERAP1 gene are associated with psoriasis
Meta Gene·2021· 1 cited
Genome-wide meta-analysis identifies ten new psoriasis susceptibility loci in the Chinese population
Journal of genetics and genomics/Journal of Genetics and Genomics·2021· 4 cited
Three novel structural variations at the major histocompatibility complex and <i>IL12B</i> predispose to psoriasis*
British Journal of Dermatology·2021· 9 citedOpen Access
Proteomic analysis of psoriatic skin lesions in a Chinese population
Journal of Proteomics·2021· 8 cited
Novel Mutation of the <i>NCSTN</i> Gene Identified in a Chinese Acne Inversa Family
Annals of Dermatology·2020· 12 citedOpen Access
Differential occurrence of lysine 2-hydroxyisobutyrylation in psoriasis skin lesions
Journal of Proteomics·2019· 27 cited
Genetic Study on Small Insertions and Deletions in Psoriasis Reveals a Role in Complex Human Diseases
Journal of Investigative Dermatology·2019· 32 cited
A novel insertion mutation of <i>CDSN</i> responsible for hypotrichosis simplex of scalp in a Chinese family
Clinical and Experimental Dermatology·2018· 3 cited
Correlation analysis of the <i>HLA‐DPB1*05:01</i> and <i>BTNL2</i> genes within the histocompatibility complex region with a clinical phenotype of psoriasis vulgaris in the Chinese Han population
The Journal of Gene Medicine·2017· 8 cited
The preoperative sensitive-modified Glasgow prognostic score is superior to the modified Glasgow prognostic score in predicting long-term survival for esophageal squamous cell carcinoma
Oncotarget·2016· 12 citedOpen Access
Combined <scp>FV</scp> and <scp>FVIII</scp> deficiency (F5F8D) in a Chinese family with a novel missense mutation in <scp>MCFD</scp>2 gene
Haemophilia·2014· 6 cited
Novel Compound Heterozygous TMC1 Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family
PLoS ONE·2013· 35 citedOpen Access

Frequent Co-authors

Liangdan Sun(8), Qi Zhen(7), Huiyao Ge(7), Wenjun Wang(6), Qiongqiong Xu(5), Bao Li(4), Huayang Tang(4), Jinping Gao(4), Yafen Yu(4), Hui Cheng(3), Bo Liang(3), Weiwei Chen(3), Shirui Chen(3), Hui Zhang(3), Yong Liang(3), Xiaodong Zheng(3), Ying Qiu(2), Yuyang Zhang(2), Wenjun Qian(2), Yan Lu(2)