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Huawei Mao

ResearcherPublications, citations & collaboration network

Huawei Mao is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Huawei Mao have?

ScholarIQindexed works

Huawei Mao has 21 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Huawei Mao have?

ScholarIQcitation count

Huawei Mao has 112 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Huawei Mao?

ScholarIQh-index

Huawei Mao has an h-index of 7 in OpenAlex.

What is the i10-index of Huawei Mao?

ScholarIQi10-index

Huawei Mao has an i10-index of 4 in OpenAlex.

What is the OpenAlex record for Huawei Mao?

ScholarIQopenalex

The OpenAlex for Huawei Mao is on the source record.

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
Cell Death and Differentiation. 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
Cellular Immunology. 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

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