Publications by authors named "Fatao Li"

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First Reported Case of Hemoglobin H Disease Caused by the Rare α-Globin Gene Mutation ( c.244delT) in a Chinese Family.
Jian-Ying Zhou, Chen-Yu Wang, Jian Li, Gui-Lan Chen, Xue-Wei Tang, Fa-Tao Li

Hemoglobin· January 2025

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Prenatal diagnosis in fetal right aortic arch using chromosomal microarray analysis and whole exome sequencing: a Chinese single-center retrospective study.
Lu Zhang, Ruibin Huang, Hang Zhou, Xiaomei Lin, Fei Guo, Yongling Zhang, Fucheng Li, Fatao Li, Dongzhi Li, Ru Li

Mol Cytogenet· September 2024

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Association of prenatal thoracic ultrasound abnormalities with copy number variants at a single Chinese tertiary center.
Qiong Huang, Yongling Zhang, Xiangyi Jing, Fucheng Li, Jiachun Qin, Fatao Li, Dongzhi Li, Ru Li, Can Liao

Int J Gynaecol Obstet· February 2024

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Application of real-time PCR-based multicolor melting curve with automatic analysis system in pregestational and prenatal thalassemia diagnoses.
Xue-Wei Tang, Fan Jiang, Jian Li, Xiao-Mei Lin, Jian-Ying Zhou, Lian-Dong Zuo, Fa-Tao Li, Dong-Zhi Li

Ann Hum Genet· November 2023

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Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants.
Fan Jiang, Jianying Zhou, Liandong Zuo, Xuewei Tang, Jian Li, Fatao Li, Can Liao, Dongzhi Li

Front Genet· July 2023

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Ndufa4 Regulates the Proliferation and Apoptosis of Neurons via miR-145a-5p/Homer1/Ccnd2.
Fang Fu, Chen Chen, Kun Du, Lu-Shan Li, Ru Li, Li Zhen, Li-Na Zhang, Jian Li, Fa-Tao Li, Yong-Ling Zhang, Fu-Cheng Li, Dong-Zhi Li, Can Liao

Mol Neurobiol· June 2023

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Contribution of maternal mosaicism to false-positive chromosome X loss associated with noninvasive prenatal testing.
Junhui Wan, Ru Li, Fatao Li, Qiuxia Yu, Dan Wang, Yongling Zhang, Fucheng Li, Yan Li, Lina Zhang, Jian Li, Dongzhi Li, Can Liao

J Matern Fetal Neonatal Med· December 2022

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Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses.
Fang Fu, Ru Li, Qiuxia Yu, Dan Wang, Qiong Deng, Lushan Li, Li Zhen, Yongling Zhang, Fucheng Li, Fatao Li, Lina Zhang, Yingsi Li, Jian Li, Lina Xiang, Dongzhi Li, Can Liao

Genome Med· October 2022

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Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing.
Fang Fu, Ru Li, Xiao Dang, Qiuxia Yu, Ke Xu, Li Zhen, Yongling Zhang, Fatao Li, Fucheng Li, Dongzhi Li, Can Liao

Front Genet· September 2022

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Detection of rare thalassemia mutations using long-read single-molecule real-time sequencing.
Fan Jiang, Ai-Ping Mao, Yin-Yin Liu, Feng-Zhi Liu, Yan-Lin Li, Jian Li, Fa-Tao Li, Lian-Dong Zuo, Dong-Zhi Li

Gene· May 2022

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A novel SPTB frameshift deletion causing hereditary spherocytosis identified by next-generation sequencing in a Chinese family.
Ru-Qing Zhao, Fan Jiang, Jian Li, Jian-Ying Zhou, Xue-Wei Tang, Fa-Tao Li, Li-Qiong Chen, Dong-Zhi Li

Int J Lab Hematol· December 2021

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Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with congenital cystic adenomatoid malformation by chromosomal microarray analysis.
Qiong Deng, Lihua Huang, Juan Liu, Fu Fang, Zequn Liu, Yongling Zhang, Fatao Li, Can Liao

J Matern Fetal Neonatal Med· August 2021

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Insufficient fetal fraction of cell-free DNA in non-invasive prenatal testing: Not always true.
Jun-Hui Wan, Fa-Tao Li, Ru Li, Hui-Zhu Zhong, Dong-Zhi Li

Eur J Obstet Gynecol Reprod Biol· June 2021

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Evaluation of the Z-score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center.
Wan Junhui, Li Ru, Yu Qiuxia, Wang Dan, Sun Xiuhong, Zhang Yongling, Li Fatao, Li Fucheng, Li Yan, Zhang Lina, Li Jian, Li Dongzhi, Liao Can

Prenat Diagn· May 2021

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Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease.
Fang Fu, Ru Li, Ting-Ying Lei, Dan Wang, Xin Yang, Li Zhen, Jian Li, Fa-Tao Li, Dong-Zhi Li, Can Liao

Hum Genet· February 2021

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Prenatal exome sequencing in fetuses with congenital heart defects.
Ru Li, Fang Fu, Qiuxia Yu, Dan Wang, Xiangyi Jing, Yongling Zhang, Fucheng Li, Fatao Li, Li Zhen, Dongzhi Li, Can Liao

Clin Genet· September 2020

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Altered expression of circular RNAs in human placental chorionic plate-derived mesenchymal stem cells pretreated with hypoxia.
Xunsha Sun, Yulin Jin, Qihua Liang, Jie Tang, Jinsong Chen, Fatao Li, Yan Li

J Clin Lab Anal· March 2019

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Corrigendum for Li D, Lin Y, Huang Y, et al (2018) https://doi.org/10.1002/pd.5329.
Duan Li, Yunting Lin, Yonglan Huang, Wen Zhang, Minyan Jiang, Xiuzhen Li, Zongcai Liu, Dongzhi Li, Fatao Li, Can Liao, Li Liu

Prenat Diagn· January 2019

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Pregnancy outcome of autosomal aneuploidies other than common trisomies detected by noninvasive prenatal testing in routine clinical practice.
Junhui Wan, Ru Li, Yongling Zhang, Xiangyi Jing, Qiuxia Yu, Fatao Li, Yan Li, Lina Zhang, Jian Li, Dongzhi Li, Can Liao

Prenat Diagn· October 2018

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Early prenatal diagnosis of lysosomal storage disorders by enzymatic and molecular analysis.
Duan Li, Yunting Lin, Yonglan Huang, Wen Zhang, Minyan Jiang, Xiuzhen Li, Zongcai Liu, Dongzhi Li, Fatao Li, Can Liao, Li Liu

Prenat Diagn· September 2018

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Prenatal diagnosis of trisomy 18 rescue resulting in mosaic of two different diploid cell lines in a hydropic fetus.
Qiong Deng, Ru Li, Fang Fu, Fa-Tao Li, Xiang-Yi Jing, Can Liao

Eur J Obstet Gynecol Reprod Biol· May 2018

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Two homozygous mutations in the exon 5 of BCKDHB gene that may cause the classic form of maple syrup urine disease.
Ling Su, Zhikun Lu, Fatao Li, Yongxian Shao, Huiying Sheng, Li Liu

Metab Brain Dis· June 2017

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Chromosome microarray analysis in the investigation of children with congenital heart disease.
Xiao-Li Wu, Ru Li, Fang Fu, Min Pan, Jin Han, Yong-Ling Zhang, Fa-Tao Li, Can Liao

BMC Pediatr· May 2017

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[Deep sequencing of the T cell receptor Vb CDR3 repertoire of peripheral CD4+T cells in primary biliary cirrhosis].
Junjie Bao, Qihuan Xu, Yong Zou, Fei Gao, Fatao Li, Yan Li, Haiying Liu

Zhonghua Gan Zang Bing Za Zhi· August 2015

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[Clinical value of genome-wide high resolution chromosomal microarray analysis in etiological study of fetuses with congenital heart defects].
Xiaoli Wu, Fang Fu, Ru Li, Min Pan, Jin Han, Li Zhen, Yongling Zhang, Fatao Li, Can Liao

Zhonghua Fu Chan Ke Za Zhi· December 2014

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