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Frontiers in Immunology|June 12, 2025
Corrigendum: Identification of hub genes and immune-related pathways in acute myeloid leukemia: insights from bioinformatics and experimental validationMingliang Shan, Li Xu, Wenzhe Yang, et al.
Frontiers in Immunology|April 3, 2024
Exploring the role of exosomal MicroRNAs as potential biomarkers in preeclampsiaYuping Shan, Bo Hou, Jingli Wang, et al.
European Child & Adolescent Psychiatry|April 18, 2024
Abnormal H3K4 enzyme catalytic activity and neuronal morphology caused by ASH1L mutations in individuals with Tourette syndromeCheng Zhang, Wenmiao Liu, Lulu Xu, et al.
Gynecologic and Obstetric Investigation|April 22, 2015
The Association of CARD8 rs2043211 Polymorphism with Preeclampsia in the Chinese Han PopulationXuefeng Wang, Mengchun Liu, Zhen Liu, et al.
Asia-Pacific Psychiatry : Official Journal of the Pacific Rim College of Psychiatrists|July 1, 2015
Association between the polymorphism of C861G (rs6296) in the serotonin 1B receptor gene and Tourette syndrome in Han Chinese peopleMingji Yi, Ying Zhang, Yujie Wang, et al.
European Journal of Medical Research|September 26, 2022
Two Chinese siblings of combined oxidative phosphorylation deficiency 14 caused by compound heterozygous variants in FARS2Liangshan Li, Jianhua Ma, Jingli Wang, et al.
Genetic Testing and Molecular Biomarkers|June 25, 2011
Lack of association between polymorphism -592A/C in the promoter region of the IL10 gene and Tourette's syndrome in a family-based association study in the Chinese Han populationShiguo Liu, Mingji Yi, Fengguang Qi, et al.
Revista Internacional De Andrologia|May 12, 2025
Meta-analysis of the efficacy and safety of L-carnitine and N-acetylcysteine monotherapy for male idiopathic infertilityXiaohong Ma, Yingying Yang, Shiguo Liu, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|April 22, 2025
A Novel De Novo KAT6B Mutation Causes Hypospadias in a Chinese Fetus at 29 Weeks GestationXue Zhong, Meixin Liu, Qun Gao, et al.
Acta Neuropsychiatrica|March 9, 2016
A case-control study of interleukin-12 1188A/C polymorphism in obsessive-compulsive disorder in Chinese populationShiguo Liu, Yanhui Liu, Yingying Yin, et al.
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