Search details
1.
Pathogenic variations in MAML2 and MAMLD1 contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway.
J Med Genet
; 60(9): 874-884, 2023 09.
Article
in English
| MEDLINE | ID: mdl-36898841
2.
Large-scale forward genetic screening of zebrafish affecting thyroid development.
Biochem Biophys Res Commun
; 642: 21-26, 2023 01 29.
Article
in English
| MEDLINE | ID: mdl-36543020
3.
The mutation screening in candidate genes related to thyroid dysgenesis by targeted next-generation sequencing panel in the Chinese congenital hypothyroidism.
Clin Endocrinol (Oxf)
; 96(4): 617-626, 2022 04.
Article
in English
| MEDLINE | ID: mdl-34374102
4.
Tpo knockout in zebrafish partially recapitulates clinical manifestations of congenital hypothyroidism and reveals the involvement of TH in proper development of glucose homeostasis.
Gen Comp Endocrinol
; 323-324: 114033, 2022 07 01.
Article
in English
| MEDLINE | ID: mdl-35367205
5.
Upregulation of GBP1 in thyroid primordium is required for developmental thyroid morphogenesis.
Genet Med
; 23(10): 1944-1951, 2021 10.
Article
in English
| MEDLINE | ID: mdl-34194003
6.
Correlation of DUOX2 residual enzymatic activity with phenotype in congenital hypothyroidism caused by biallelic DUOX2 defects.
Clin Genet
; 100(6): 713-721, 2021 12.
Article
in English
| MEDLINE | ID: mdl-34564849
7.
The effect of radioiodine treatment on the characteristics of TRAb in Graves' disease.
BMC Endocr Disord
; 21(1): 238, 2021 Nov 30.
Article
in English
| MEDLINE | ID: mdl-34847904
8.
A five-gene panel refines differential diagnosis of thyroid nodules.
J Clin Lab Anal
; 35(9): e23920, 2021 Sep.
Article
in English
| MEDLINE | ID: mdl-34318534
9.
Fine mapping MHC associations in Graves' disease and its clinical subtypes in Han Chinese.
J Med Genet
; 55(10): 685-692, 2018 10.
Article
in English
| MEDLINE | ID: mdl-29987165
10.
A dense mapping study of six European AITD susceptibility regions in a large Chinese Han Cohort of Graves' disease.
Clin Endocrinol (Oxf)
; 89(6): 840-848, 2018 12.
Article
in English
| MEDLINE | ID: mdl-30176063
11.
Multiregion sequencing reveals the intratumor heterogeneity of driver mutations in TP53-driven non-small cell lung cancer.
Int J Cancer
; 140(1): 103-108, 2017 Jan 01.
Article
in English
| MEDLINE | ID: mdl-27646734
12.
Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations.
Hum Mol Genet
; 23(20): 5505-17, 2014 Oct 15.
Article
in English
| MEDLINE | ID: mdl-24852370
13.
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
Hum Mol Genet
; 22(16): 3347-62, 2013 Aug 15.
Article
in English
| MEDLINE | ID: mdl-23612905
14.
Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association study.
Hum Genet
; 133(5): 661-71, 2014 May.
Article
in English
| MEDLINE | ID: mdl-24346624
15.
An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.
J Med Genet
; 50(7): 479-85, 2013 Jul.
Article
in English
| MEDLINE | ID: mdl-23667180
16.
Contactin 6, A Novel Causative Gene for Congenital Hypothyroidism, Mediates Thyroid Hormone Biosynthesis Through Notch Signaling.
Thyroid
; 34(3): 324-335, 2024 Mar.
Article
in English
| MEDLINE | ID: mdl-38183624
17.
Deficiency of the HGF/Met pathway leads to thyroid dysgenesis by impeding late thyroid expansion.
Nat Commun
; 15(1): 3165, 2024 Apr 11.
Article
in English
| MEDLINE | ID: mdl-38605010
18.
Identification of Eukaryotic Translation Initiation Factor 4B as a Novel Candidate Gene for Congenital Hypothyroidism.
J Clin Endocrinol Metab
; 2024 Apr 24.
Article
in English
| MEDLINE | ID: mdl-38654471
19.
TSHR Variant Screening and Phenotype Analysis in 367 Chinese Patients With Congenital Hypothyroidism.
Ann Lab Med
; 44(4): 343-353, 2024 Jul 01.
Article
in English
| MEDLINE | ID: mdl-38433572
20.
Dense mapping of IL2RA shows no association with Graves' disease in Chinese Han population.
Clin Endocrinol (Oxf)
; 79(2): 267-74, 2013 Aug.
Article
in English
| MEDLINE | ID: mdl-23170961