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BMC Pediatrics|August 29, 2025
Association of early hyperglycemia with morbidity and mortality in very low birth weight infantsJingwen Zhu, Xiyu He, Ming Guo
Frontiers in Genetics|September 2, 2022
Case Report: Aarskog-scott syndrome caused by FGD1 gene variation: A family studyYijia Liang, Honglin Wu, Xiumei He, et al.
Lung|January 17, 2026
Stratified Comparison of Risk Factors for Mild Versus Moderate-to-Severe Bronchopulmonary Dysplasia in Very Preterm Infants (< 32 Weeks Gestational Age)Jingwen Zhu, Ming Guo, Xiyu He, et al.
Gene|March 7, 2013
Four novel GALC gene mutations in two Chinese patients with Krabbe diseaseYao Yang, Xiaotun Ren, Quangang Xu, et al.
Gene|May 5, 2012
Novel chromosomal translocation t(11;9)(p15;p23) involving deletion and duplication of 9p in a girl associated with autism and mental retardationYao Yang, Chunzhi Wang, Fang Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 9, 2014
[Analysis of clinical features, metabolic profiling and gene mutations of patients with ornithine transcarbamylase deficiency]Yan Wang, Xin Liu, Honglin Wu, et al.
Chemical Society Reviews|June 2, 2025
Correction: DNA-mediated precise regulation of SERS hotspots for biosensing and bioimagingJingjing Zhang, Chunyuan Song, Xiyu He, et al.
Chemical Society Reviews|May 16, 2025
DNA-mediated precise regulation of SERS hotspots for biosensing and bioimagingJingjing Zhang, Chunyuan Song, Xiyu He, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 3, 2009
[Detection of the genetic abnormalities in patients with mental retardation using multiplex ligation-dependent probe amplification assay]Lina Zhu, Chunzhi Wang, Xiao Yang, et al.
Genomics|June 19, 2013
Two homozygous nonsense mutations of GNPTAB gene in two Chinese families with mucolipidosis II alpha/beta using targeted next-generation sequencingYao Yang, Jian Wu, Haihong Liu, et al.
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