Zhiyu Peng
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Explore the profile of Zhiyu Peng including associated specialties, affiliations and a list of published articles.
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117
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Recent Articles
11.
Chen T, Fan C, Huang Y, Feng J, Zhang Y, Miao J, et al.
JAMA Netw Open
. 2023 Sep;
6(9):e2331162.
PMID: 37656460
Importance: Newborn screening via biochemical tests is in use worldwide. The availability of genetic sequencing has allowed rapid screening for a substantial number of monogenic disorders. However, the outcomes of...
12.
Chen Y, Zhong R, Guo X, Chen S, Wang Y, Li J, et al.
J Med Screen
. 2023 Jul;
31(1):53-57.
PMID: 37439030
Objectives: As one of the most common hereditary diseases, thalassemia affects a large number of people in China. The aim of this study was to investigate the feasibility of a...
13.
Xiang J, Peng J, Sun X, Lin Z, Li D, Ye H, et al.
Clin Chem
. 2023 May;
69(7):763-770.
PMID: 37207672
Background: Deafness, autosomal recessive 16 (DFNB16) is caused by compound heterozygous or homozygous variants in STRC and is the second most common form of genetic hearing loss. Due to the...
14.
Yang Z, Yang X, Sun Y, Wang Y, Song L, Qiao Z, et al.
BMC Med Genomics
. 2023 Apr;
16(1):74.
PMID: 37020281
Background: With advances in massive parallel sequencing (MPS) technology, whole-genome sequencing (WGS) has gradually evolved into the first-tier diagnostic test for genetic disorders. However, deployment practice and pipeline testing for...
15.
Qian Y, Sun Y, Guo X, Song L, Sun Y, Gao X, et al.
J Med Genet
. 2023 Apr;
60(10):933-938.
PMID: 37012053
Background: Low-pass genome sequencing (LP GS) is an alternative to chromosomal microarray analysis (CMA). However, validations of LP GS as a prenatal diagnostic test for amniotic fluid are rare. Moreover,...
16.
Qi T, Hu Y, Liu M, Tian L, Peng Z, Xu H, et al.
Int J Gynaecol Obstet
. 2023 Apr;
162(3):913-921.
PMID: 37010882
Objectives: To explore the effect of abnormally elevated serum alanine aminotransferase (ALT) on pregnancy outcomes in patients with moderate and severe ovarian hyperstimulation syndrome (OHSS) at disease onset. Methods: This...
17.
Xiang J, Li R, He J, Wang X, Yao L, Song N, et al.
Am J Obstet Gynecol MFM
. 2022 Nov;
5(1):100790.
PMID: 36377092
Background: Genome-wide noninvasive prenatal testing identifies several rare autosomal trisomies in the general obstetrical population, but its use is questioned by its low positive predictive value. Furthermore, the origin of...
18.
19.
Ma R, Li X, Peng Z, Guo J, Qian J, Zhang Y
Graefes Arch Clin Exp Ophthalmol
. 2022 Nov;
261(4):1151-1158.
PMID: 36322213
Purpose: Our study aims to develop a diagnostic model using 24-h intraocular pressure (IOP) patterns to differentiate between open-angle glaucoma (OAG) and dysthyroid optic neuropathy (DON) in thyroid eye disease...
20.
Jin Y, Liu X, Chen S, Xiang J, Peng Z, Sun Y
J Clin Med
. 2022 Sep;
11(18).
PMID: 36142981
To improve the etiological diagnosis of congenital hearing loss by combining whole-exome sequencing (WES) with cytomegalovirus (CMV) testing and to explore the potential benefits of adding CMV screening to newborn...