Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Yunsheng, Ge"'
Autor:
Yunsheng Ge, Jiayan Chen, Yanru Huang, Di Shao, Wenbo Wang, Meijiao Cai, Meihua Tan, Jian Zhang
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Fetal chromosomal abnormalities are the main cause of adverse pregnancy outcomes and are the focus of invasive prenatal diagnosis. Recent studies have demonstrated that various techniques have distinct advantages. Achieving high-resolution and effect
Externí odkaz:
https://doaj.org/article/81aee62e5a1c4754b05a2e0eb128a48f
Autor:
Xingmei Yao, Qing Li, Yu Chen, Zhuowen Du, Yanru Huang, Yixi Zhou, Jian Zhang, Wenbo Wang, Lutan Zhang, Jieqiong Xie, Chao Xu, Yunsheng Ge, Yulin Zhou
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
BackgroundCervical cancer is primarily caused by HPV infection. The epidemiology of HPV infection in specific areas is of great meaning of guide cervical cancer screening and formulating HPV vaccination strategies. Here, we evaluated the epidemiologi
Externí odkaz:
https://doaj.org/article/df38351972794dc38debaa7103298a3f
Autor:
Ye Shen, Yanru Huang, Wenbo Wang, Jian Zhang, Xiaolu Chen, Lutan Zhang, Xiaomei Huang, Yunsheng Ge
Publikováno v:
Frontiers in Microbiology, Vol 14 (2023)
ObjectiveThis study aimed to evaluate the prevalence of HPV and genotype distribution among female populations in Xiamen, Fujian Province, China, which can be conducive for local governments to formulate cervical cancer screening and HPV vaccine stra
Externí odkaz:
https://doaj.org/article/de14ae90e11343c59067f77cb4fd8a44
Autor:
Zhongmin Xia, Xudong Wang, Huiming Ye, Chunliu Gao, Xiaoman Zhou, Jing Chen, Yunsheng Ge, Juan Li, Yulin Zhou, Qiwei Guo
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency, which is caused by pathogenic variants of G6PD that result in decreased G6PD activity, is an X-linked inherited inborn error of metabolism that occurs worldwide. Individuals with G6PD deficiency an
Externí odkaz:
https://doaj.org/article/81ccf8766b2f40b7befa8356efd794ea
Autor:
Yun-e Chen, Jingfang Chen, Wenxing Guo, Yanhong Zhang, Jialing Li, Hui Xie, Tong Shen, Yunsheng Ge, Yanru Huang, Wenying Zheng, Mei Lu
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
We aimed to explore the genotypic and phenotypic characteristics of neonatal-onset inflammatory bowel disease (IBD) with combined immunodeficiency due to TTC7A mutation. We examined the clinical manifestations, imaging results, endoscopic and histolo
Externí odkaz:
https://doaj.org/article/b492a6bf2cfa454cac2cdc93f709ed21
Autor:
Yunsheng Ge, Jia Li, Jianlong Zhuang, Jian Zhang, Yanru Huang, Meihua Tan, Wei Li, Jiayan Chen, Yulin Zhou
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-12 (2021)
Abstract Background Noninvasive prenatal testing (NIPT) has been wildly used to screen for common aneuplodies. In recent years, the test has been expanded to detect rare autosomal aneuploidies (RATs) and copy number variations (CNVs). This study was
Externí odkaz:
https://doaj.org/article/9a43c7f444474e8fa0c3434c47eaa3a4
Autor:
Jia Li, Jia Ju, Qiang Zhao, Weiqiang Liu, Yuying Yuan, Qiang Liu, Lijun Zhou, Yuan Han, Wen Yuan, Yonghua Huang, Yingjun Xie, Zhihua Li, Jingsi Chen, Shuyu Huang, Rufang Chen, Wei Li, Meihua Tan, Danchen Wang, Si Zhou, Jian Zhang, Fanwei Zeng, Nan Yu, Fengxia Su, Min Chen, Yunsheng Ge, Yanming Huang, Xin Jin
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: The existence of maternal malignancy may cause false-positive results or failed tests of NIPT. Though recent studies have shown multiple chromosomal aneuploidies (MCA) are associated with malignancy, there is still no effective solution t
Externí odkaz:
https://doaj.org/article/3f1dd22efc8b44e28cb1e493ece82cac
Autor:
Xudong Wang, Zhongmin Xia, Ying He, Xiaoman Zhou, Haixia Zhang, Chunliu Gao, Yunsheng Ge, Xiaofang Cai, Yulin Zhou, Qiwei Guo
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common inherited enzymatic defect. The purpose of this study was to evaluate the profile of G6PD deficiency and investigate the factors associated with the accuracy of newborn scree
Externí odkaz:
https://doaj.org/article/c72187336f69430ca2bc5bd57aa87c27
Autor:
Yanru Huang, Libin Mei, Yangdan Wang, Huiming Ye, Xiaomin Ma, Jian Zhang, Meijiao Cai, Ping Li, Yunsheng Ge, Yulin Zhou
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
ObjectiveGlobal developmental delay has markedly high phenotypic and genetic heterogeneity, and is a great challenge for clinical diagnosis. Hypotonia, ataxia, and delayed development syndrome (HADDS), first reported in 2017, is one type of global de
Externí odkaz:
https://doaj.org/article/0077f7668c884639a5f4153518a43d81
Publikováno v:
Cytogenetic and Genome Research. :1-11
Fetal cystic hygroma (CH) is associated with poor prognosis and chromosomal anomalies. Recent studies have suggested that the genetic background of affected fetuses is essential for predicting pregnancy outcomes. However, the detection performance of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29e2c73a90e6d0026e0c5ecd8bbd6234
https://doi.org/10.1159/000528600
https://doi.org/10.1159/000528600