Wenjuan Qiu
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Explore the profile of Wenjuan Qiu including associated specialties, affiliations and a list of published articles.
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Articles
122
Citations
832
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Recent Articles
1.
Gong Z, Xia Y, Sun C, Zheng W, Du T, Liang L, et al.
J Clin Lipidol
. 2025 Mar;
18(6):e1086-e1095.
PMID: 40023655
Background: Familial chylomicronemia syndrome (FCS) comprises a group of ultrarare disorders caused by biallelic variants in LPL or, less frequently, by GPIHBP1, APOC2, APOA5, or LMF1. Objectives: To evaluate the...
2.
Xia Y, Sun Y, Du T, Sun C, Xu Y, Ge W, et al.
JAMA Netw Open
. 2025 Feb;
8(2):e2461888.
PMID: 40009380
Importance: Glycogen storage disease type Ib (GSDIb) is a rare metabolic disorder characterized by impaired glucose-6-phosphate transporter function with limited descriptions. Objective: To describe the genetic and clinical features of...
3.
Ding J, Zhang L, Li X, Qiu W, Zhu Q, Luo G, et al.
J Colloid Interface Sci
. 2025 Jan;
685:153-164.
PMID: 39837250
Sodium-ion batteries (SIBs) have the advantages of abundant resources and low cost, making them potential candidates for the next-generation large-scale energy storage technology. However, the capacity fade during cycling used...
4.
Qiu W, Wang R, Liang L, Sun Y, Zhou R, Wang X, et al.
Infect Drug Resist
. 2024 Dec;
17:5675-5684.
PMID: 39720618
Introduction: Growth hormone (GH) is crucial for immune system development and regulation, potentially benefiting COVID-19 outcomes. However, there are limited studies on the role of GH treatment in COVID-19 in...
5.
Zhang X, Yan D, Qiu W, Chen S, Hu Y, Jin J, et al.
Int J Biol Macromol
. 2024 Nov;
284(Pt 1):138184.
PMID: 39615307
No abstract available.
6.
Zhang X, Yan D, Qiu W, Chen S, Hu Y, Jin J, et al.
Int J Biol Macromol
. 2024 Nov;
283(Pt 4):137874.
PMID: 39571849
The parameters for ultrasound and pH shift co-modification of peanut proteins (PP) were optimized, and the functional properties, structures of PP were investigated. The results showed that under the optimum...
7.
Luo X, Hou L, Zhong Y, Zhao S, Chen X, Dong Q, et al.
Clin Endocrinol (Oxf)
. 2024 Nov;
102(2):136-146.
PMID: 39513569
Objective: Children born small for gestational age (SGA) are at increased risk of health issues. This study evaluated the efficacy, safety and optimal dose of PEGylated-recombinant human growth hormone (PEG-rhGH)...
8.
Hao L, Ling S, Ding S, Qiu W, Zhang H, Zhang K, et al.
Pediatr Res
. 2024 Sep;
PMID: 39306609
Background: Methylmalonic acidemia (MMA) is the most common organic acidemia in China, with cblC (cblC-MMA) and mut (mut-MMA) being the predominant subtypes. The present study aimed to investigate the prognostic...
9.
Ling S, Wu S, Shuai R, Yu Y, Qiu W, Wei H, et al.
Hum Genomics
. 2024 Jul;
18(1):84.
PMID: 39075538
Background: Isolated methylmalonic acidemia, an autosomal recessive disorder of propionate metabolism, is usually caused by mutations in the methylmalonyl-CoA mutase gene (mut-type). Because no universal consensus was made on whether...
10.
Long-Read Sequencing Solves Complex Structure of CYP21A2 in a Large 21-Hydroxylase Deficiency Cohort
Wang R, Luo X, Sun Y, Liang L, Mao A, Lu D, et al.
J Clin Endocrinol Metab
. 2024 Jul;
110(2):406-416.
PMID: 39049755
Context: Genetic testing for 21-hydroxylase deficiency (21-OHD) is always challenging. The current approaches of short-read sequencing and multiplex ligation-dependent probe amplification (MLPA) are insufficient for the detection of chimeric genes...