Fenxia Li
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Explore the profile of Fenxia Li including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
129
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0
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Recent Articles
1.
Zhang M, Li K, Huang X, Zhou H, Tan J, Guo Z, et al.
Placenta
. 2024 Dec;
159():84-92.
PMID: 39675128
Background: Pregnancy significantly alters the maternal immune system, affecting fetal development. The collection of tissues from the human placenta and fetus is not ethically or practically feasible at various gestational...
2.
Li K, Guo Z, Li F, Lu S, Zhang M, Gong Y, et al.
Gene
. 2024 Jul;
928:148789.
PMID: 39047956
Background: The expression profiles of placental genes are crucial for understanding the pathogenesis of fetal development and placental-origin pregnancy syndromes. However, owing to ethical limitations and the risks of puncture...
3.
Liu S, Xu Y, Chang Q, Jia B, Li F
Int J Gynaecol Obstet
. 2024 Apr;
167(1):273-280.
PMID: 38651210
Objective: To evaluate non-invasive prenatal testing (NIPT) and expanded non-invasive prenatal testing (NIPT-plus) for detecting aneuploidies at different sequencing depths and assess Z-score accuracy in predicting trisomies 21, 18, 13,...
4.
Liu S, Chang Q, Yang F, Xu Y, Jia B, Wu R, et al.
Arch Gynecol Obstet
. 2023 Jan;
308(3):787-795.
PMID: 36602559
Background: This paper evaluated the clinical utility of massively parallel sequencing-based non-invasive prenatal testing (NIPT) for detecting trisomy 21 (T21), T18, T13, sex chromosome aneuploidies (SCA), and rare chromosome aneuploidies...
5.
Zhang M, Li K, Qu S, Guo Z, Wang Y, Yang X, et al.
J Transl Med
. 2022 Nov;
20(1):536.
PMID: 36401256
Background: Chromosomal aneuploidy is the most common birth defect. However, the developmental mechanism and gene expression profile of fetuses with chromosomal aneuploidy are relatively unknown, and the maternal immune changes...
6.
Liu S, Yang F, Chang Q, Jia B, Xu Y, Wu R, et al.
Mol Cytogenet
. 2022 Jul;
15(1):29.
PMID: 35794576
Objective: Since 2011, noninvasive prenatal testing (NIPT) has undergone rapid expansion, with both utilization and coverage. However, conclusive data regarding the clinical validity and utility of this testing tool are...
7.
Zhou J, Ouyang G, Wu L, Zhang M, Weng R, Lin S, et al.
Prenat Diagn
. 2022 Apr;
42(8):1008-1014.
PMID: 35441712
Objective: To decrease the false-positive rate of NIPT using cell-free fetal DNA (cffDNA) fraction enrichment and the simulated confined placental mosaicism proportion (SCPMP) threshold application via cffDNA quantification. Method: Using...
8.
Li F, Liu S, Jia B, Wu R, Chang Q
Front Pediatr
. 2021 Nov;
9:691761.
PMID: 34746047
The Kagami-Ogata syndrome (KOS) is a rare imprinting disorder with a distinct clinical phenotype. In KOS, polyhydramnios is associated with a small bell-shaped thorax and coat-hanger ribs. The genetic etiology...
9.
Chen J, Li Q, Lin S, Li F, Huang L, Jin W, et al.
Thromb Res
. 2021 Mar;
202:8-13.
PMID: 33706050
Introduction: The reported variants of hemophilia A are mainly from European subjects and American subjects of European descent, and limited data are available from more diverse ethnic backgrounds. This study...
10.
Molecular analysis of 76 Chinese hemophilia B pedigrees and the identification of 10 novel mutations
Huang L, Li L, Lin S, Chen J, Li K, Fan D, et al.
Mol Genet Genomic Med
. 2020 Sep;
8(11):e1482.
PMID: 32875744
Background: Hemophilia B (HB) is an X-linked recessive inherited bleeding disorder caused by mutations in the F9 gene that lead to plasma factor IX deficiency. To identify the causative mutations...