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Endocrine Journal|July 20, 2018
Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidismWei Long, Guanting Lu, Wenbai Zhou, et al.
Biomedicines|December 30, 2025
Tissue-Resident Memory T Cells in Rheumatoid Immune Diseases: Pathogenic Mechanisms and Therapeutic StrategiesYu Tian, Jie Zhang, Lianying Wu, et al.
BMC Gastroenterology|February 2, 2019
Elevated D-dimer is associated with increased 28-day mortality in acute-on-chronic liver failure in China: a retrospective studyTingting Qi, Congyan Zhu, Guanting Lu, et al.
Frontiers in Molecular Neuroscience|December 26, 2022
Identification of a de novo mutation of the FOXG1 gene and comprehensive analysis for molecular factors in Chinese FOXG1-related encephalopathiesGuanting Lu, Yan Zhang, Huiyun Xia, et al.
Metabolites|April 25, 2025
Metabolomics Insights into Gut Microbiota and Functional ConstipationFan Zheng, Yong Yang, Guanting Lu, et al.
Medicine|May 14, 2016
Association of IL12A Expression Quantitative Trait Loci (eQTL) With Primary Biliary Cirrhosis in a Chinese Han PopulationPing Li, Guanting Lu, Ying Cui, et al.
Frontiers in Genetics|April 18, 2022
A de Novo ZMIZ1 Pathogenic Variant for Neurodevelopmental Disorder With Dysmorphic Facies and Distal Skeletal AnomaliesGuanting Lu, Liya Ma, Pei Xu, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|April 6, 2016
A rare nonsynonymous variant in the lipid metabolic gene HELZ2 related to primary biliary cirrhosis in Chinese HanPing Li, Guanting Lu, Li Wang, et al.
Frontiers in Nutrition|August 1, 2026
Lactiplantibacillus plantarum Probio87 supplementation improves functional constipation and is associated with peripheral gene-expression responses related to inflammation and the gut-brain axis: a randomized, double-blind, placebo-controlled trialFan Zheng, Yong Yang, Yu Zhan, et al.
Frontiers in Molecular Neuroscience|November 17, 2022
A synonymous variant contributes to a rare Wiedemann-Rautenstrauch syndrome complicated with mild anemia via affecting pre-mRNA splicingQiongling Peng, Yan Zhang, Binqiang Xian, et al.
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