Jianjiang Zhu
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Explore the profile of Jianjiang Zhu including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
31
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Recent Articles
1.
Jia R, Zhu J, Zhang F, Sun Y, Zhang B, Du Y, et al.
Front Genet
. 2025 Mar;
16:1527884.
PMID: 40061129
Cell-free DNA (cfDNA) is a dynamic biomarker reflecting the physiological state of the body. Its unique physical and biochemical properties, inherited from the tissue of origin, enable a wide range...
2.
Zeng W, Zhu J, Qi H, Cai L, Wen X, Luo Y, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
. 2024 Jul;
41(7):797-802.
PMID: 38946360
Objective: To assess the efficiency of modified enrichment method for cell-free fetal DNA (cffDNA) through purified superparamagnetic beads during non-invasive prenatal testing (NIPT). Methods: A total of 26 252 pregnant...
3.
Zeng W, Qi H, Du Y, Cai L, Wen X, Wan Q, et al.
Heliyon
. 2023 Aug;
9(8):e18868.
PMID: 37593615
Background: Copy number variation sequencing (CNV-seq) was proven to be a highly effective tool in studying of chromosomal copy number variations (CNVs) in prenatal diagnosis and post-natal cases with developmental...
4.
Wen X, Xing H, Qi K, Wang H, Li X, Zhu J, et al.
Dis Markers
. 2023 Jun;
2022:5487452.
PMID: 37284664
Copy number variations (CNVs) at the chromosomal 1q21.1 region represent a group of hot-spot recurrent rearrangements in human genome, which have been detected in hundreds of patients with variable clinical...
5.
Zhu J, Meng R, Zhao H, Cai L, Wen X, Zeng W, et al.
DNA Cell Biol
. 2022 Nov;
41(11):996-1006.
PMID: 36322898
This study aims to conduct a comprehensive clinical and genetic investigation on a large family with members having various phenotypes, including acromesomelic dysplasia, type Maroteaux (AMDM), idiopathic short stature (ISS),...
6.
Wen X, Zhu J, Cai L, Tang G, Zeng W, Luo Y, et al.
Am J Transl Res
. 2022 Apr;
14(3):1663-1671.
PMID: 35422908
The 3q29 duplication syndrome is an uncommon imbalanced chromosomal disorder with highly variable manifestations, mainly characterized by a mild mental anomaly, eye abnormalities, and developmental delay. Only a few such...
7.
Zhang S, Zhu J, Qi H, Xu L, Cai L, Meng R
Mol Cytogenet
. 2021 Dec;
14(1):55.
PMID: 34863242
Introduction: De novo balanced reciprocal translocations mosaicism in fetus conceived using preimplantation genetic testing from a different balanced translocation carrier parent has been rarely reported. Methods: Chromosomal microarray analysis, karyotype...
8.
Shi L, Li M, Qi H, Zhu J, Yang J, Tang J, et al.
Ann Transl Med
. 2021 Jul;
9(9):807.
PMID: 34268420
Background: Genetic mutations in genes related to the production, migration, or differentiation of cortical neurons can result in malformations of cortical development (MCDs). However, a large number of MCD-related pathogenetic...
9.
Zhu J, Hui F, Mao X, Zhang S, Qi H, Du Y
Hum Genomics
. 2021 Feb;
15(1):14.
PMID: 33622405
Cell-free DNA is known to be a mixture of DNA fragments originating from various tissue types and organs of the human body and can be utilized for several clinical applications...
10.
Zhu J, Li W, Huang H, Qi H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
. 2020 May;
37(6):599-602.
PMID: 32472532
With the development of high-throughput sequencing technology, non-invasive prenatal testing (NIPT) has been rapidly used for fetal chromosomal aneuploidy screening and gradually become a first-line test. With the increase of...