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Scientific Reports|August 4, 2015
Support of positive association in family-based genetic analysis between COL27A1 and Tourette syndromeShiguo Liu, Xiaoxia Yu, Quanchen Xu, et al.
Hematology (Amsterdam, Netherlands)|November 4, 2017
Identification of a de novo ANK1 mutation in a Chinese family with hereditary spherocytosisHongzai Guan, Xinping Liang, Rong Zhang, et al.
Plos One|August 17, 2016
Investigation of a Possible Role for the Histidine Decarboxylase Gene in Tourette Syndrome in the Chinese Han Population: A Family-Based StudyHe Dong, Wenmiao Liu, Meixin Liu, et al.
Optics Letters|March 19, 2010
Increased optical-damage resistance in tin-doped lithium niobateLizhong Wang, Shiguo Liu, Yongfa Kong, et al.
Asia-Pacific Psychiatry : Official Journal of the Pacific Rim College of Psychiatrists|April 11, 2015
Lack of genetic association of 5-HTR2A 102 T/C and -1438A/G polymorphisms with Tourette syndrome in a family-based association study in a Chinese Han populationLongqiang Xu, Lanlan Zheng, Jianhua Ma, et al.
Genetic Testing and Molecular Biomarkers|July 14, 2012
Polymorphisms -1082 G/A and -819 C/T in the interleukin-10 gene are not associated with gout susceptibility in the Chinese Han male populationShiguo Liu, Kun Zhang, Congcong Yin, et al.
Cancer Cell International|August 28, 2012
Stromal proteome expression profile and muscle-invasive bladder cancer researchHaitao Niu, Haiping Jiang, Bo Cheng, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|July 13, 2012
Clinical and genetic analysis of a compound heterozygous mutation in the thyroglobulin gene in a Chinese twin family with congenital goiter and hypothyroidismShiguo Liu, Shasha Zhang, Wenjie Li, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 28, 2021
Molecular and clinical characteristics of congenital hypothyroidism in a large cohort study based on comprehensive thyroid transcription factor mutation screening in HenanLiangshan Li, Chenlu Jia, Xiaole Li, et al.
Immunogenetics|April 8, 2024
A novel hemizygous CD40L mutation of X-linked hyper IgM syndromes and compound heterozygous DOCK8 mutations of hyper IgE syndromes in two Chinese familiesMingzhen Guo, Yuanxuan Ma, Kangxi Cai, et al.
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