Guan-qi L. Gao

Linyi, China

Last Updated: 09/26/2026

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Found 15 publications

A case of Van Wyk-Grumbach syndrome with inherited RET gene variation

A case of Van Wyk-Grumbach syndrome with inherited RET gene variation

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: July 23, 2024

Myeloid cells interact with a subset of thyrocytes to promote their migration and follicle formation through NF-κB.

Myeloid cells interact with a subset of thyrocytes to promote their migration and follicle formation through NF-κB.

Journal: Nature communications
Published: June 15, 2022

The effect of radioiodine treatment on the characteristics of TRAb in Graves' disease.

The effect of radioiodine treatment on the characteristics of TRAb in Graves' disease.

Journal: BMC endocrine disorders
Published: June 13, 2021

Response Letter to the Editor: "Genetic Study in a Large Cohort Supported Different Pathogenesis of Graves' Disease and Hashimoto's Hypothyroidism".

Response Letter to the Editor: "Genetic Study in a Large Cohort Supported Different Pathogenesis of Graves' Disease and Hashimoto's Hypothyroidism".

Journal: The Journal of clinical endocrinology and metabolism
Published: July 01, 2020

Genetic Study in a Large Cohort Supported Different Pathogenesis of Graves' Disease and Hashimoto's Hypothyroidism.

Genetic Study in a Large Cohort Supported Different Pathogenesis of Graves' Disease and Hashimoto's Hypothyroidism.

Journal: The Journal of clinical endocrinology and metabolism
Published: November 06, 2019

Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study.

Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study.

Journal: JAMA network open
Published: May 04, 2019

A dense mapping study of six European AITD susceptibility regions in a large Chinese Han Cohort of Graves' disease.

A dense mapping study of six European AITD susceptibility regions in a large Chinese Han Cohort of Graves' disease.

Journal: Clinical endocrinology
Published: July 04, 2018

The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes.

The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes.

Journal: European journal of endocrinology
Published: December 10, 2017

Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations.

Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations.

Journal: Human molecular genetics
Published: May 24, 2014

Comparison of continuous subcutaneous insulin infusion and insulin glargine-based multiple daily insulin aspart injections with preferential adjustment of basal insulin in patients with type 2 diabetes.

Comparison of continuous subcutaneous insulin infusion and insulin glargine-based multiple daily insulin aspart injections with preferential adjustment of basal insulin in patients with type 2 diabetes.

Journal: Experimental and therapeutic medicine
Published: November 21, 2013

Refined association of TSH receptor susceptibility locus to Graves' disease in the Chinese Han population.

Refined association of TSH receptor susceptibility locus to Graves' disease in the Chinese Han population.

Journal: European journal of endocrinology
Published: October 23, 2013

Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association study.

Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association study.

Journal: Human genetics
Published: August 14, 2013
Showing 1-12 of 15

Last Updated: 09/26/2026