Guan-Qi Gao
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Explore the profile of Guan-Qi Gao including associated specialties, affiliations and a list of published articles.
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20
Citations
394
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Recent Articles
1.
Yang R, Song S, Wu F, Yang R, Shen Y, Tu P, et al.
Nat Commun
. 2023 Dec;
14(1):8082.
PMID: 38057310
The pathogenesis of thyroid dysgenesis (TD) is not well understood. Here, using a combination of single-cell RNA and spatial transcriptome sequencing, we identify a subgroup of NF-κB-activated thyrocytes located at...
2.
Fang Y, Du W, Zhang C, Zhao S, Song H, Gao G, et al.
BMC Endocr Disord
. 2021 Dec;
21(1):238.
PMID: 34847904
Background: Graves' disease (GD) is one of the most common autoimmune thyroid diseases (AITDs) in humans, and thyrotropin receptor antibody (TRAb) is a characterized autoantibody in GD. The use of...
3.
Zhang Q, Liu W, Li L, Du W, Zuo C, Ye X, et al.
J Clin Endocrinol Metab
. 2020 Jul;
105(10).
PMID: 32671382
No abstract available.
4.
Zhang Q, Liu W, Li L, Du W, Zuo C, Ye X, et al.
J Clin Endocrinol Metab
. 2020 Apr;
105(7).
PMID: 32246145
Context: Hashimoto's thyroiditis (HT) and Graves' disease (GD) are the 2 main autoimmune thyroid diseases that have both similarities and differences. Determining the genetic basis that distinguishes HT from GD...
5.
Zhao S, Liu W, Liang J, Gao G, Zhang X, Yao Y, et al.
JAMA Netw Open
. 2019 May;
2(5):e193348.
PMID: 31050781
Importance: Thyrotoxic periodic paralysis (TPP) is a potentially lethal complication of hyperthyroidism. However, only 1 specific susceptibility locus for TPP has been identified. Additional genetic determinants should be detected so...
6.
Liu W, Zhang Q, Yuan F, Wang H, Zhang L, Ma Y, et al.
Clin Endocrinol (Oxf)
. 2018 Sep;
89(6):840-848.
PMID: 30176063
Objective: We aimed to investigate the six susceptibility loci of GD identified from European population in Chinese Han population and further to estimate the genetic heterogeneity of them in stratification...
7.
Sun F, Zhang J, Yang C, Gao G, Zhu W, Han B, et al.
Eur J Endocrinol
. 2018 Apr;
178(6):623-633.
PMID: 29650690
Objective: Congenital hypothyroidism (CH), the most common neonatal metabolic disorder, is characterized by impaired neurodevelopment. Although several candidate genes have been associated with CH, comprehensive screening of causative genes has...
8.
Gao G, Heng X, Wang Y, Li W, Dong Q, Liang C, et al.
Exp Ther Med
. 2014 Sep;
8(4):1191-1196.
PMID: 25187822
The purpose of this study was to evaluate and compare multiple daily injection (MDI) therapy of bolus insulin aspart and basal insulin glargine with continuous subcutaneous insulin infusion (CSII) with...
9.
Zhan M, Chen G, Pan C, Gu Z, Zhao S, Liu W, et al.
Hum Mol Genet
. 2014 May;
23(20):5505-17.
PMID: 24852370
Thyroid-stimulating hormone (TSH) is a sensitive indicator of thyroid function. High and low TSH levels reflect hypothyroidism and hyperthyroidism, respectively. Even within the normal range, small differences in TSH levels,...
10.
Liu W, Wang H, Gu Z, Yang S, Ye X, Pan C, et al.
Hum Genet
. 2013 Dec;
133(5):661-71.
PMID: 24346624
The BACH2 gene regulates B cell differentiation and function and has been reported to be a shared susceptibility gene for several autoimmune diseases. Our previous genome-wide association study (GWAS) indicated...