Fatao Li
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Explore the profile of Fatao Li including associated specialties, affiliations and a list of published articles.
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15
Citations
78
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Recent Articles
1.
Zhang L, Huang R, Zhou H, Lin X, Guo F, Jing X, et al.
Mol Cytogenet
. 2024 Sep;
17(1):22.
PMID: 39334424
Background: Right aortic arch (RAA) is a common congenital aortic arch abnormality. Fetuses with RAA frequently have good outcomes after birth. However, chromosomal abnormalities and genetic syndromes suggest poor prognosis...
2.
Huang Q, Zhang Y, Jing X, Li F, Qin J, Li F, et al.
Int J Gynaecol Obstet
. 2023 Aug;
164(2):770-777.
PMID: 37565521
Objective: To systematically evaluate the association of prenatal thoracic ultrasound abnormalities with copy number variants (CNVs). Methods: Chromosomal microarray (CMA) data and clinical characteristics from fetuses with thoracic ultrasound abnormalities...
3.
Jiang F, Zhou J, Zuo L, Tang X, Li J, Li F, et al.
Front Genet
. 2023 Aug;
14:1208102.
PMID: 37529778
Thalassemia is the most prevalent monogenic disorder caused by an imbalance between the α- and β-globin chains as a result of pathogenic variants in the α- or β-globin genes. Novel...
4.
Fu F, Li R, Yu Q, Wang D, Deng Q, Li L, et al.
Genome Med
. 2022 Oct;
14(1):123.
PMID: 36307859
Background: Exome sequencing (ES) is becoming more widely available in prenatal diagnosis. However, data on its clinical utility and integration into clinical management remain limited in practice. Herein, we report...
5.
Fu F, Li R, Dang X, Yu Q, Xu K, Gu W, et al.
Front Genet
. 2022 Oct;
13:951829.
PMID: 36186435
Balanced chromosomal abnormalities (BCAs) are the most common chromosomal abnormalities and the frequency of congenital abnormalities is approximately twice as high in newborns with a BCA, but a prenatal diagnosis...
6.
Wan J, Li R, Li F, Yu Q, Wang D, Sun X, et al.
J Matern Fetal Neonatal Med
. 2022 Mar;
35(25):9647-9653.
PMID: 35282756
Objective: To report the frequency of maternal mosaicism contributing to false-positive chromosome X loss associated with noninvasive prenatal testing (NIPT) at a single center. Methods: Pregnancies undergone NIPT using massively...
7.
Li R, Fu F, Yu Q, Wang D, Jing X, Zhang Y, et al.
Clin Genet
. 2020 May;
98(3):215-230.
PMID: 32410215
The genetic diagnosis of congenital heart defects (CHDs) is challenging because of genetic and phenotypic heterogeneity. The aim of our study was to evaluate the clinical value of whole exome...
8.
Deng Q, Huang L, Liu J, Fang F, Liu Z, Zhang Y, et al.
J Matern Fetal Neonatal Med
. 2019 Oct;
34(16):2623-2629.
PMID: 31581877
Objectives: To explore the copy number variations (CNVs) of fetal congenital cystic adenomatoid malformation (CCAM). Methods: Fetuses with CCAM were investigated by karyotypes and chromosomal microarray analysis (CMA). The cases...
9.
Li D, Lin Y, Huang Y, Zhang W, Jiang M, Li X, et al.
Prenat Diagn
. 2019 Jan;
39(1):57.
PMID: 30632198
No abstract available.
10.
Sun X, Jin Y, Liang Q, Tang J, Chen J, Yu Q, et al.
J Clin Lab Anal
. 2018 Nov;
33(3):e22825.
PMID: 30485544
Background: Hypoxic preconditioning alters the biological properties of mesenchymal stem cells (MSCs). It is not known whether this process has an effect on circular RNAs (circRNAs) in MSCs. Methods: Human...