Yongyi Zou
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Explore the profile of Yongyi Zou including associated specialties, affiliations and a list of published articles.
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30
Citations
153
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Recent Articles
1.
Zeng B, Yu Y, Liu C, Li X, Lu Q, Chen Z, et al.
Sci Rep
. 2025 Mar;
15(1):8135.
PMID: 40057613
Alport syndrome (AS) is the second-most frequent monogenic kidney disease and 85% of cases are caused by mutations in the genes of the α5 chains of collagen type IV (COL4A5)....
2.
Tan L, Huang T, Luo L, Ma P, Liu J, Zou J, et al.
Hemoglobin
. 2024 Dec;
48(6):369-374.
PMID: 39659024
Hemoglobin disorders are highly prevalent inherited hematological defects in Southern China. The identification of novel variants in globin genes and accurate assessment of hematological parameters play a crucial role in...
3.
You X, Zhang Z, Xu Y, Yang B, Huang S, Zou Y, et al.
Biomark Med
. 2024 Sep;
18(17-18):749-758.
PMID: 39254332
To investigate the association between serum homocysteine (HCY) levels, red blood cell folate (RCF) levels, methylenetetrahydrofolate reductase (MTHFR) gene polymorphism and infertility. Serum HCY and RCF levels and C677T polymorphism...
4.
Lu Q, Luo L, Zeng B, Luo H, Wang X, Qiu L, et al.
Orphanet J Rare Dis
. 2024 Aug;
19(1):307.
PMID: 39175064
Background And Objectives: Congenital heart defect (CHD) is one of the most common birth defects. The aim of this cohort study was to evaluate the prevalence of chromosomal abnormalities and...
5.
Yang Y, Luo H, Pan L, Feng C, Guo Z, Zou Y, et al.
Hum Mol Genet
. 2024 Apr;
PMID: 38676628
Purpose: The aim of this study was to determine the genetic cause of early onset autosomal dominant hearing loss segregating in five-generation kindred of Chinese descent and provide preimplantation genetic...
6.
Wang X, Li H, Luo H, Zou Y, Li H, Qin Y, et al.
Eur J Med Genet
. 2024 Jan;
67:104909.
PMID: 38199457
Background: The 2015 American College of Medical Genetics and Genomics (ACMG) and Association for Molecular Pathology (AMP) guidelines articulates that the effects of certain types of variants on gene function...
7.
Huang C, Luo H, Zeng B, Feng C, Chen J, Yuan H, et al.
Front Genet
. 2024 Jan;
14:1290949.
PMID: 38179410
Intellectual disability-7 (MRD7) is a subtype disorder of intellectual disability (MRD) involving feeding difficulties, hypoactivity, and febrile seizures at an age of early onset, then progressive intellectual and physical development...
8.
Zeng B, Zhang H, Lu Q, Fu Q, Yan Y, Lu W, et al.
Front Behav Neurosci
. 2023 Nov;
17:1272748.
PMID: 38025388
Background: Epilepsy is characterized by recurrent unprovoked seizures. Mutations in the voltage-gated sodium channel alpha subunit 1 () gene are the main monogenic cause of epilepsy. Type and location of...
9.
Rao H, Zhang H, Zou Y, Ma P, Huang T, Yuan H, et al.
Front Genet
. 2023 Sep;
14:1248755.
PMID: 37732322
Certain chromosomal structural variations (SVs) in biological parents can lead to recurrent spontaneous abortions (RSAs). Unequal crossing over during meiosis can result in the unbalanced rearrangement of gamete chromosomes such...
10.
Zeng B, Lu Q, Chen S, Guan H, Xu X, Zou Y, et al.
Front Genet
. 2023 Feb;
14:1049816.
PMID: 36845377
Phenylalanine hydroxylase deficiency (PAHD) is an autosomal recessive disorder of amino acid metabolism and caused by mutations in the phenylalanine hydroxylase () gene. Without timely and appropriate dietary management, the...