Whole exome sequencing analysis of 167 men with primary infertility
Zhou, Haiyan, Yin, Zhaochu, Ni, Bin, Lin, Jiwu, Luo, Shuwei, Xie, Wanqin
Published in BMC medical genomics (12.09.2024)
Published in BMC medical genomics (12.09.2024)
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Journal Article
The Role of Probiotics in the Prevention and Treatment of Atopic Dermatitis in Children: An Updated Systematic Review and Meta-Analysis of Randomized Controlled Trials
Jiang, Wen, Ni, Bin, Liu, Zhiyu, Liu, Xuan, Xie, Wanqin, Wu, Irene X. Y., Li, Xingli
Published in Paediatric drugs (01.10.2020)
Published in Paediatric drugs (01.10.2020)
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Journal Article
Novel CH25H + and OASL + microglia subclusters play distinct roles in cerebral ischemic stroke
Zhang, Yueman, Guo, Yunlu, Li, Ruqi, Huang, Tingting, Li, Yan, Xie, Wanqin, Chen, Chen, Chen, Weijie, Wan, Jieqing, Yu, Weifeng, Li, Peiying
Published in Journal of neuroinflammation (15.05.2023)
Published in Journal of neuroinflammation (15.05.2023)
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Journal Article
A novel frameshift deletion variant of ARSL associated with X-linked recessive chondrodysplasia punctata 1: a case report and literature review of prenatal, confirmed cases
Zhou, Lin, Peng, Ying, Chen, Jing, Xi, Hui, Wang, Si, Kang, Gehua, Tang, Wanglan, Xie, Wanqin
Published in BMC medical genomics (18.10.2024)
Published in BMC medical genomics (18.10.2024)
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Journal Article
First trimester exposure to ambient gaseous air pollutants and risk of orofacial clefts: a case–control study in Changsha, China
Jiang, Wen, Xie, Wanqin, Ni, Bin, Zhou, Haiyan, Liu, Zhiyu, Li, Xingli
Published in BMC oral health (15.10.2021)
Published in BMC oral health (15.10.2021)
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Journal Article
Clinical features and genetic analysis of a case series of skeletal ciliopathies in a prenatal setting
Peng, Ying, Zhou, Lin, Chen, Jing, Huang, Xiaoliang, Pang, Jialun, Liu, Jing, Tang, Wanglan, Yang, Shuting, Liang, Changbiao, Xie, Wanqin
Published in BMC medical genomics (07.12.2023)
Published in BMC medical genomics (07.12.2023)
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Journal Article
Clinical features and genetic analysis of two Chinese families with X-linked ichthyosis
Xie, Wanqin, Zhou, Haiyan, Zhou, Lin, Gong, Yun, Lin, Jiwu, Chen, Yong
Published in Journal of international medical research (01.10.2020)
Published in Journal of international medical research (01.10.2020)
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Journal Article
Adipose stem cells control obesity-induced T cell infiltration into adipose tissue
Liao, Xiyan, Zeng, Qin, Xie, Limin, Zhang, Haowei, Hu, Wanyu, Xiao, Liuling, Zhou, Hui, Wang, Fanqi, Xie, Wanqin, Song, Jianfeng, Sun, Xiaoxiao, Wang, Dandan, Ding, Yujin, Jiao, Yayi, Mai, Wuqian, Aini, Wufuer, Hui, Xiaoyan, Liu, Wei, Hsueh, Willa A., Deng, Tuo
Published in Cell reports (Cambridge) (26.03.2024)
Published in Cell reports (Cambridge) (26.03.2024)
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Journal Article
HIF-1α promotes kidney organoid vascularization and applications in disease modeling
Peng, Kexin, Xie, Wanqin, Wang, Tingting, Li, Yamei, de Dieu Habimana, Jean, Amissah, Obed Boadi, Huang, Jufang, Chen, Yong, Ni, Bin, Li, Zhiyuan
Published in Stem cell research & therapy (19.11.2023)
Published in Stem cell research & therapy (19.11.2023)
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Journal Article
Wave In in auditory brainstem response suggests a high possibility of a high jugular bulb
Liu, Jia, Xie, Wanqin, Ding, Yan, Hu, Ya, Lai, Ruosha, Hu, Peng, Zhu, Ganghua
Published in Frontiers in pediatrics (06.11.2023)
Published in Frontiers in pediatrics (06.11.2023)
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Journal Article
Case Report: A Novel Missense Variant in the SIPA1L3 Gene Associated With Cataracts in a Chinese Family
Yang, Duo, Zhou, Haiyan, Lin, Jiwu, Zhao, Shuangxi, Zhou, Hao, Yin, Zhaochu, Ni, Bin, Chen, Yong, Xie, Wanqin
Published in Frontiers in genetics (16.09.2021)
Published in Frontiers in genetics (16.09.2021)
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Journal Article
Compound heterozygous B3GALNT2 mutations in a fetus with encephalocele: A case report
Ling, Dandan, Xie, Wanqin, Mao, Xiao, Yang, Shengzhi, Pang, Haiyan, Yang, Ping, Shen, Ping, Tang, Yabing
Published in Clinical case reports (01.04.2024)
Published in Clinical case reports (01.04.2024)
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Journal Article
Novel Mutations of PAX6 and WFS1 Associated With Congenital Cataract in a Chinese Family
Sheng, Dan, Yang, Duo, Xie, Wanqin, Li, Mojiang, Zhong, Liqin, Zhao, Shuangxi, Liang, Hao
Published in Curēus (Palo Alto, CA) (25.01.2023)
Published in Curēus (Palo Alto, CA) (25.01.2023)
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Journal Article
Case Report: Novel NIPBL Variants Cause Cornelia de Lange Syndrome in Chinese Patients
Peng, Ying, Liang, Changbiao, Xi, Hui, Yang, Shuting, Hu, Jiancheng, Pang, Jialun, Liu, Jing, Luo, Yingchun, Tang, Chengyuan, Xie, Wanqin, Wang, Hua
Published in Frontiers in genetics (30.07.2021)
Published in Frontiers in genetics (30.07.2021)
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Journal Article
A chromosome 1q22 microdeletion including ASH1L is associated with intellectual disability in a Chinese family
Xi, Hui, Peng, Ying, Xie, Wanqin, Pang, Jialun, Ma, Na, Yang, Shuting, Peng, Jinping, Wang, Hua
Published in Molecular cytogenetics (04.06.2020)
Published in Molecular cytogenetics (04.06.2020)
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Journal Article
Genetic variations rs11892031 and rs401681 are associated with bladder cancer risk in a Chinese population
Zhang, Yu, Sun, Yan, Chen, Tao, Hu, Hailong, Xie, Wanqin, Qiao, Zhihui, Ding, Na, Xie, Linguo, Li, Sheng, Wang, Wenlong, Xing, Chen, Wang, Yihan, Qie, Yunkai, Wu, Changli
Published in International journal of molecular sciences (24.10.2014)
Published in International journal of molecular sciences (24.10.2014)
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