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Chest|February 12, 2021
Clinical and Genetic Spectrum of Children With Primary Ciliary Dyskinesia in ChinaYuhong Guan, Haiming Yang, Xingfeng Yao, et al.
Genomics, Proteomics & Bioinformatics|August 31, 2024
DVsc: An Automated Framework for Efficiently Detecting Viral Infection from Single-cell Transcriptomics DataFei Leng, Song Mei, Xiaolin Zhou, et al.
European Journal of Human Genetics : EJHG|October 24, 2024
Targeted gene sequencing and hearing follow-up in 7501 newborns reveals an improved strategy for newborn hearing screeningChanjuan Hao, Xuyun Hu, Ruolan Guo, et al.
BMJ Paediatrics Open|July 5, 2023
Behavioural deficits of autism spectrum disorder and associations with different gene clusters: a study with the whole-genome transmission disequilibrium testQi Guo, Lu Xia, Ruolan Guo, et al.
Frontiers in Genetics|April 10, 2023
Genetic diagnostic yields of 354 Chinese ASD children with rare mutations by a pipeline of genomic testsYue Zhang, Ying Li, Ruolan Guo, et al.
Frontiers in Immunology|January 3, 2022
A Novel Homozygous <i>TTC7A</i> Missense Mutation Results in Familial Multiple Intestinal Atresia and Combined ImmunodeficiencyWenjun Mou, Shen Yang, Ruolan Guo, et al.
Brain Communications|March 30, 2026
Ertugliflozin improves animal behaviours associated with oxidative stress and inflammation in a BTBR <i>T</i> + <i>Itpr3tf/J</i> mouse model of autismXiaona Wang, Zhengqin Zhao, Limin Sun, et al.
Human Mutation|May 4, 2021
Exome sequencing as the first-tier test for pediatric respiratory diseases: A single-center studyChanjuan Hao, Ruolan Guo, Jun Liu, et al.
Frontiers in Immunology|November 23, 2020
HPS1 Regulates the Maturation of Large Dense Core Vesicles and Lysozyme Secretion in Paneth CellsJiaying Yu, Xin He, Aihua Wei, et al.
Frontiers in Genetics|September 20, 2021
Clinical Application of Whole Exome Sequencing for Monogenic Disorders in PICU of ChinaYingchao Liu, Chanjuan Hao, Kechun Li, et al.
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