Yaguang Zhao
Changsha, 410078, China
Last Updated: 09/26/2026
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Found 11 publications
A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism.
Journal: Human molecular genetics
Published: October 08, 2022
SLIT2 Rare Sequencing Variants Identified in Idiopathic Hypogonadotropic Hypogonadism.
Journal: Hormone research in paediatrics
Published: November 25, 2021
Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism.
Journal: European journal of endocrinology
Published: December 14, 2019
Phenotypic Spectrum of Idiopathic Hypogonadotropic Hypogonadism Patients With CHD7 Variants From a Large Chinese Cohort.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 23, 2019
Genotypic and phenotypic spectra of FGFR1, FGF8, and FGF17 mutations in a Chinese cohort with idiopathic hypogonadotropic hypogonadism.
Journal: Fertility and sterility
Published: May 14, 2019
Prokineticins and their G protein-coupled receptors in health and disease.
Journal: Progress in molecular biology and translational science
Published: February 04, 2019
Functional analysis of SOX10 mutations identified in Chinese patients with Kallmann syndrome.
Journal: Gene
Published: December 21, 2018
Effect of cisplatin on the clock genes expression in the liver, heart and kidney.
Journal: Biochemical and biophysical research communications
Published: May 07, 2018
A novel PNPLA6 compound heterozygous mutation identified in a Chinese patient with Boucher‑Neuhäuser syndrome.
Journal: Molecular medicine reports
Published: October 28, 2017
A dominant negative FGFR1 mutation identified in a Kallmann syndrome patient.
Journal: Gene
Published: February 15, 2017
Showing 1-11 of 11
Last Updated: 09/26/2026