Chen-yan Yan
Shanghai, China
Last Updated: 09/26/2026
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Found 10 publications
Deficiency of the HGF/Met pathway leads to thyroid dysgenesis by impeding late thyroid expansion.
Journal: Nature communications
Published: June 17, 2023
Large-scale forward genetic screening of zebrafish affecting thyroid development.
Journal: Biochemical and biophysical research communications
Published: December 01, 2022
Pathogenic variations in MAML2 and MAMLD1 contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway.
Journal: Journal of medical genetics
Published: August 06, 2022
The isl2a transcription factor regulates pituitary development in zebrafish.
Journal: Frontiers in endocrinology
Published: April 19, 2022
Mutation Screening and Functional Study of SLC26A4 in Chinese Patients with Congenital Hypothyroidism
Journal: Journal of clinical research in pediatric endocrinology
Published: September 21, 2021
NUCB2 polymorphisms are associated with an increased risk for type 2 diabetes in the Chinese population.
Journal: Annals of translational medicine
Published: May 02, 2020
Candidate gene associations reveal sex-specific Graves' disease risk alleles among Chinese Han populations.
Journal: Molecular genetics & genomic medicine
Published: December 17, 2019
The TPO mutation screening and genotype-phenotype analysis in 230 Chinese patients with congenital hypothyroidism.
Journal: Molecular and cellular endocrinology
Published: December 04, 2019
Fine mapping of thyroglobulin gene identifies two independent risk loci for Graves' disease in Chinese Han population.
Journal: Annals of translational medicine
Published: November 09, 2019
Mutation screening of the TSHR gene in 220 Chinese patients with congenital hypothyroidism.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: May 13, 2019
Showing 1-10 of 10
Last Updated: 09/26/2026