Xiaorui Xie
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Explore the profile of Xiaorui Xie including associated specialties, affiliations and a list of published articles.
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Citations
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Recent Articles
11.
He K, Xie X, Duan X, Zhou Q, Wu J
Cerebrovasc Dis
. 2023 Apr;
52(6):692-699.
PMID: 37088074
Introduction: The red blood cell distribution width-to-platelet ratio (RPR), a novel inflammatory index, has already been proven as a prognostic factor in some other diseases, but its prognostic effect on...
12.
Xie X, Tong X, Li Z, Cheng Q, Wang X, Long Y, et al.
Cell Death Dis
. 2023 Jan;
14(1):15.
PMID: 36631452
Skin infections caused by drug-resistant Staphylococcus aureus occur at high rates nationwide. Mouse primary epidermal organoids (mPEOs) possess stratified histological and morphological characteristics of epidermis and are highly similar to...
13.
Cai M, Huang H, Su L, Wu X, Xie X, Li Y, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
. 2022 Dec;
39(12):1329-1333.
PMID: 36453953
Objective: To analyze the ultrasonographic phenotype and result of genetic testing in six fetuses carrying a 17q12 microdeletion. Methods: Chromosomal microarray analysis (CMA) was carried out for 6200 pregnant women...
14.
Cai M, Lin N, Su L, Wu X, Xie X, Xu S, et al.
J Transl Med
. 2022 Apr;
20(1):168.
PMID: 35397568
Background: The etiology of fetal growth restriction (FGR) is complex and currently, there is a paucity of research about the genetic etiology of fetal growth restriction. We investigated the genetic...
15.
Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios
Wu X, Li Y, Lin N, Su L, Xie X, Liang B, et al.
BMC Med Genomics
. 2022 Mar;
15(1):73.
PMID: 35354480
Background: Polyhydramnios, the excessive accumulation of amniotic fluid, is associated with an elevated risk of abnormal karyotype, particularly aneuploidy. Studies focusing on chromosomal microarray analysis (CMA) in pregnancies with polyhydramnios...
16.
Cai M, Huang H, Lin N, Su L, Wu X, Xie X, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
. 2022 Jan;
39(2):227-230.
PMID: 35076926
Objective: To analyze the intrauterine phenotype and genotype of eight fetuses carrying a 16p11.2 microdeletion. Methods: 5100 fetuses undergoing routine prenatal diagnosis were subjected to single nucleotide polymorphism-based microarray (SNP-array)...
17.
Yu Z, Wang H, Zhang X, Gong S, Liu Z, Zhao N, et al.
J Hazard Mater
. 2021 Dec;
425:127766.
PMID: 34916105
We established long-term surveillance sites in Jinan city to monitor PM particles (PM2.5) and PM2.5-bound PAHs (2014-2020). The range of PM2.5 was 15-230 µg/m. The average annual ƩPAH were 433 ...
18.
Wu X, Su L, Xie X, He D, Chen X, Wang M, et al.
Mol Cytogenet
. 2021 Dec;
14(1):56.
PMID: 34863241
Background: Pregnancy loss is one of the most common complications during pregnancy. Clinical consultation based on etiology analysis are critical for reducing anxiety and distress. This study aimed to perform...
19.
Su L, Wu X, Lin N, Xie X, Cai M, Wang M, et al.
Int J Gen Med
. 2021 Nov;
14:8437-8443.
PMID: 34819751
Introduction: Increased nuchal translucency (NT) is closely related to an increased risk of chromosomal abnormalities. However, the criterion of increased NT for invasive prenatal diagnosis remains controversial, as the cutoff...
20.
Cai M, Lin N, Su L, Wu X, Xie X, Li Y, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
. 2021 Sep;
38(9):853-856.
PMID: 34487529
Objective: To analyze the prenatal ultrasonic characteristics and genetic features of 14 fetuses with chromosome 22q11 microdeletion syndrome (22q11DS). Methods: 4989 fetuses were analyzed by using single nucleotide polymorphism array...