Rong Qiang
Overview
Explore the profile of Rong Qiang including associated specialties, affiliations and a list of published articles.
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Articles
37
Citations
342
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Recent Articles
1.
Zhang R, Li H, Qiang R, Gao X, Guo J, Chen G, et al.
Mol Genet Genomics
. 2025 Mar;
300(1):28.
PMID: 40047934
Congenital chloride diarrhea (CCD) is an autosomal recessive disease, characterized by watery diarrhea, hypochloremia and metabolic alkalosis. It is associated with defects in solute carrier family 26 member 3 (SLC26A3)...
2.
Liu W, Zhu J, Ren K, Xiao D, Qiang R, Rabouhi N, et al.
Curr Osteoporos Rep
. 2025 Feb;
23(1):9.
PMID: 39945916
Purpose Of Review: The purpose of this review is to explore the multifaceted roles of the ERI1 exoribonuclease, particularly in RNA metabolism and bone development, and to address the genotype-phenotype...
3.
Ren K, Pirmarzdashti N, Pakdel F, Zhu J, Liu W, Wang L, et al.
J Hum Genet
. 2025 Feb;
70(4):195-198.
PMID: 39901041
Craniotubular dysplasia, Ikegawa type (CTDI) is a rare autosomal recessive skeletal dysplasia characterized by hyperostosis of the calvaria and skull base, metadiaphyseal undermodeling of the long tubular bones, and mild...
4.
Wang L, Mizumoto S, Zhang R, Zhang Y, Liu Y, Cheng W, et al.
J Hum Genet
. 2024 Apr;
69(7):321-327.
PMID: 38565611
Spondylocostal dysostosis (SCDO) encompasses a group of skeletal disorders characterized by multiple segmentation defects in the vertebrae and ribs. SCDO has a complex genetic etiology. This study aimed to analyze...
5.
Zhang R, Cui D, Song C, Ma X, Cai N, Zhang Y, et al.
Clin Chim Acta
. 2024 Feb;
555:117820.
PMID: 38307397
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders predominantly characterized by impaired corticosteroid synthesis. Clinical phenotypes include hypoadrenocorticism, electrolyte disturbances, abnormal gonadal development, and short stature, of...
6.
Cao Z, He X, Wang D, Gu M, Suo F, Qiang R, et al.
Mol Genet Genomic Med
. 2024 Jan;
12(1):e2357.
PMID: 38284445
Background: Newborn screening (NBS) aims to detect congenital anomalies, and next-generation sequencing (NGS) has shown promise in this aspect. However, the NBS strategy for monogenic inherited diseases in China remains...
7.
Ma Q, Qiang R, Shao Y, Yang X, Xue R, Chen B, et al.
J Colloid Interface Sci
. 2023 Aug;
651:106-116.
PMID: 37542886
The demand of microwave absorption materials (MAMs) with unique morphologies and electromagnetic (EM) balance has become necessary in recent years. Due to the ease of synthesis and tunable structure, metal-organic...
8.
Bu Q, Qiang R, Fang L, Peng X, Zhang H, Cheng H
Front Pharmacol
. 2023 Mar;
14:1156249.
PMID: 36909179
The study aimed to quantify the global trends of the incidence rates of multidrug-resistant (MDR) tuberculosis (MDR-TB) and extensively drug-resistant (XDR) tuberculosis (XDR-TB). Cases, age-standardized rates (ASRs), and incidence rates...
9.
Guo L, Qiang R, Zhang Y, Simsek-Kiper P
Front Genet
. 2023 Feb;
14:1139228.
PMID: 36777736
No abstract available.
10.
Lou C, Qiang R, Wu H, Zhang L, Li W, Jia T, et al.
Medicine (Baltimore)
. 2023 Jan;
101(49):e31964.
PMID: 36626466
Background: The aim of this study is to investigate a new mechanism that may affect spontaneous abortions (SA): Can long interspersed nuclear element-1 (LINE-1) insertions in embryo cells lead to...