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Xp22.31 copy number variations in 87 fetuses: refined genotype–phenotype correlations by prenatal and postnatal follow-up.
Published in:
BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01493-z
By:
- Hu, Huamei;
- Huang, Yulin;
- Hou, Renke;
- Xu, Huanhuan;
- Liu, Yalan;
- Liao, Xueqian;
- Xu, Juchun;
- Jiang, Lupin;
- Wang, Dan
Publication type:
Article
Prenatal Diagnosis and Genetic Analysis of 21q21.1–q21.2 Aberrations in Seven Chinese Pedigrees.
Published in:
Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.731815
By:
- Hu, Huamei;
- Zhang, Rong;
- Ma, Yongyi;
- Luo, Yanmei;
- Pan, Yan;
- Xu, Juchun;
- Jiang, Lupin;
- Wang, Dan
Publication type:
Article
Genome-wide detection of additional fetal chromosomal abnormalities by cell-free DNA testing of 15,626 consecutive pregnant women.
Published in:
SCIENCE CHINA Life Sciences, 2019, v. 62, n. 2, p. 215, doi. 10.1007/s11427-017-9344-7
By:
- Yao, Hong;
- Gao, Ya;
- Zhao, Jia;
- Zhang, Rong;
- Xu, Huixin;
- Hu, Huamei;
- Luo, Yanmei;
- Yuan, Yuying;
- Fu, Meili;
- Zhang, Hongyun;
- Jiang, Hui;
- Wang, Wei;
- Yang, Huanming;
- Wang, Jian;
- Liang, Zhiqing;
- Chen, Fang
Publication type:
Article
Detection of fetal trisomy and single gene disease by massively parallel sequencing of extracellular vesicle DNA in maternal plasma: a proof-of-concept validation.
Published in:
BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0590-8
By:
- Zhang, Weiting;
- Lu, Sen;
- Pu, Dandan;
- Zhang, Haiping;
- Yang, Lin;
- Zeng, Peng;
- Su, Fengxia;
- Chen, Zhichao;
- Guo, Mei;
- Gu, Ying;
- Luo, Yanmei;
- Hu, Huamei;
- Lu, Yanping;
- Chen, Fang;
- Gao, Ya
Publication type:
Article
A functional varient in microRNA-146a is associated with risk of esophageal squamous cell carcinoma in Chinese Han.
Published in:
Familial Cancer, 2010, v. 9, n. 4, p. 599, doi. 10.1007/s10689-010-9370-5
By:
- Guo, Hong;
- Wang, Kai;
- Xiong, Gang;
- Hu, Huamei;
- Wang, Dongmei;
- Xu, Xueqing;
- Guan, Xingying;
- Yang, Kang;
- Bai, Yun
Publication type:
Article
An assessment of the analytical performance of non‐invasive prenatal testing (NIPT) in detecting sex chromosome aneuploidies: 34,717‐patient sample in a single prenatal diagnosis Centre in China.
Published in:
Journal of Gene Medicine, 2021, v. 23, n. 9, p. 1, doi. 10.1002/jgm.3362
By:
- Luo, Yanmei;
- Hu, Huamei;
- Zhang, Rong;
- Ma, Yongyi;
- Pan, Yan;
- Long, Yang;
- Hu, Bin;
- Yao, Hong;
- Liang, Zhiqing
Publication type:
Article
A Robust Approach for Blind Detection of Balanced Chromosomal Rearrangements with Whole-Genome Low-Coverage Sequencing.
Published in:
Human Mutation, 2014, v. 35, n. 5, p. 625, doi. 10.1002/humu.22541
By:
- Dong, Zirui;
- Jiang, Lupin;
- Yang, Chuanchun;
- Hu, Hua;
- Wang, Xiuhua;
- Chen, Haixiao;
- Choy, Kwong Wai;
- Hu, Huamei;
- Dong, Yanling;
- Hu, Bin;
- Xu, Juchun;
- Long, Yang;
- Cao, Sujie;
- Chen, Hui;
- Wang, Wen ‐ Jing;
- Jiang, Hui;
- Xu, Fengping;
- Yao, Hong;
- Xu, Xun;
- Liang, Zhiqing
Publication type:
Article
Targeted next-generation sequencing identification of mutations in patients with disorders of sex development.
Published in:
BMC Medical Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12881-016-0286-2
By:
- Yanling Dong;
- Yuting Yi;
- Hong Yao;
- Ziying Yang;
- Huamei Hu;
- Jiucheng Liu;
- Changxin Gao;
- Ming Zhang;
- Liying Zhou;
- Asan;
- Xin Yi;
- Zhiqing Liang
Publication type:
Article
CpG island methylation status of miRNAs in esophageal squamous cell carcinoma.
Published in:
International Journal of Cancer, 2012, v. 130, n. 7, p. 1607, doi. 10.1002/ijc.26171
By:
- Chen, Xuedan;
- Hu, Huamei;
- Guan, Xingying;
- Xiong, Gang;
- Wang, Yan;
- Wang, Kai;
- Li, Juan;
- Xu, Xueqing;
- Yang, Kang;
- Bai, Yun
Publication type:
Article

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