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Frontiers in Immunology|March 30, 2026
Timing of coffee consumption and insulin resistance: evidence from human and animal studiesPeiyan Liu, Guixiang Yao, Yixia Wu, et al.Medicine|January 26, 2019
Identification of a novel mutation of FGFR3 gene in a large Chinese pedigree with hypochondroplasia by next-generation sequencing: A case report and brief literature reviewGuixiang Yao, Guangxin Wang, Dawei Wang, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 8, 2026
Timing of Coffee Intake Modifies Mortality Risk in Cardiovascular-Kidney-Metabolic Syndrome: A Cohort and Experimental StudyPeiyan Liu, Guixiang Yao, Yixia Wu, et al.Journal of Religion and Health|March 15, 2026
Global Research Across Countries on Moral Distress and Moral Injury Among Health Care Professionals (2006-2025): A Bibliometric Study of Ethical and Health-Related Research TrendsGuixiang Yao, Xu Jia, Ying Liu, et al.Plos One|October 26, 2022
An integrated multi-omics analysis of topoisomerase family in pan-cancer: Friend or foe?Xin Zhou, Guixiang Yao, Jin Zhang, et al.Journal of Religion and Health|July 6, 2026
The Marginalization of Spiritual Dimensions in Nursing Moral Injury Research: A Bibliometric Analysis, 2018-2025Ang Li, Hao Zhang, Hailong Liu, et al.Parasites & Vectors|November 7, 2023
A nanoparticle vaccine displaying the ookinete PSOP25 antigen elicits transmission-blocking antibody response against Plasmodium bergheiGuixiang Yao, Hui Min, Xinxin Yu, et al.Microbiology Spectrum|April 23, 2025
<i>Bacteroides fragilis</i> and propionate synergize with low-dose methimazole to treat Graves' diseaseXinjie Zhang, Qingxin Pan, Guixiang Yao, et al.Environmental Science and Pollution Research International|August 17, 2023
A colorimetric and fluorometric dual-mode probe for Cu<sup>2+</sup>detection based on functionalized silver nanoparticlesGuixiang Yao, Shuju Fang, Pengyuan Yin, et al.Medicine|April 22, 2020
Targeted next generation sequencing revealed a novel deletion-frameshift mutation of KCNH2 gene in a Chinese Han family with long QT syndrome: A case report and review of Chinese casesFengli Du, Guangxin Wang, Dawei Wang, et al.Pageof 3