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Huawei Mao
ResearcherPublications, citations & collaboration network
Huawei Mao is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 21 works, 112 citations, an h-index of 7 and an i10-index of 4.
21
Works
112
Citations
7
h-index
4
i10-index
IDs:OpenAlex
How has Huawei Mao's publication output changed over time?
ScholarIQpublication output · 2021–2025
Output declined67% over the shown period — from 3 works in 2021 to 1 in 2025.
3
1
4
1
1
20212022202320242025
What are the most-cited papers on Huawei Mao?
ScholarIQmost cited works
A Novel Mutation in the NBD Domain of NLRC4 Causes Mild Autoinflammation With Recurrent Urticaria
Li Wang, Wen Wen, Mengyue Deng, Yue Li, Gan Sun, Xiaodong Zhao, Xuemei Tang, Huawei Mao
Frontiers in Immunology. 202123 CitationsOPEN ACCESS
FAAH served a key membrane-anchoring and stabilizing role for NLRP3 protein independently of the endocannabinoid system
Yangyang Zhu, Hao Zhang, Huawei Mao, Suqin Zhong, Yubing Huang, Sirong Chen, Kai Yan, Zhibin Zhao, Xiaohan Hao, Yue Zhang, Yue Zhang, Han Yao, Xiaowan Huang, Meimei Wang, Wenbin Zhang, Juan Li, Guangxun Meng, Xiao‐Hua Qin, Zhiming Ye, Jiani Shen, Yang Song, Youcui Xu, Liansheng Wang, Liansheng Wang, Yunjiao Zhang, Yunjiao Zhang, Longping Wen
S152938505. 202220 CitationsOPEN ACCESS
Efficacy and Safety of Anti-TNFα Therapy for Uveitis Associated with Juvenile Idiopathic Arthritis: A Systematic Review and Meta-Analysis
Yulu Li, Xiaolan Mao, Xuemei Tang, Huawei Mao
Rheumatology and Therapy. 202118 CitationsOPEN ACCESS
A novel missense mutation in TNFAIP3 causes haploinsufficiency of A20
Wei Jiang, Mengyue Deng, Chun Loo Gan, Li Wang, Huawei Mao, Qiu Li
S193466101. 202116 CitationsOPEN ACCESS
Progressive osseous heteroplasia in a 5-year-old boy with a novel mutation in exon 2 of GNAS: a case presentation and literature review
Jing Ma, Wenxiu Mo, Jiapeng Sun, Yan Li, Tongxin Han, Huawei Mao
BMC Musculoskeletal Disorders. 20239 CitationsOPEN ACCESS
Related on ScholarIQ
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Institution
A Novel Mutation in the NBD Domain of NLRC4 Causes Mild Autoinflammation With Recurrent Urticaria
Paper
FAAH served a key membrane-anchoring and stabilizing role for NLRP3 protein independently of the endocannabinoid system
Paper
Efficacy and Safety of Anti-TNFα Therapy for Uveitis Associated with Juvenile Idiopathic Arthritis: A Systematic Review and Meta-Analysis
Paper
A novel missense mutation in TNFAIP3 causes haploinsufficiency of A20
Paper
Progressive osseous heteroplasia in a 5-year-old boy with a novel mutation in exon 2 of GNAS: a case presentation and literature review
Paper