Fang L. Jiang - Publications

A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism.

Journal: Human molecular genetics

Published: October 08, 2022

ANOS1 variants in a large cohort of Chinese patients with congenital hypogonadotropic hypogonadism.

Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences

Published: August 30, 2022

SLIT2 Rare Sequencing Variants Identified in Idiopathic Hypogonadotropic Hypogonadism.

Journal: Hormone research in paediatrics

Published: November 25, 2021

Discovery of a Novel Variant of SEMA3A in a Chinese Patient with Isolated Hypogonadotropic Hypogonadism.

Journal: International journal of endocrinology

Published: August 05, 2021

Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadism.

Journal: Molecular genetics & genomic medicine

Published: June 03, 2021

An investigation of insulin injection-related needlestick injuries among clinical nurses in Hunan, China

Journal: Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases

Published: July 07, 2020

Prevalence and associated phenotypes of DUSP6, IL17RD and SPRY4 variants in a large Chinese cohort with isolated hypogonadotropic hypogonadism.

Journal: Journal of medical genetics

Published: December 17, 2019

Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism.

Journal: European journal of endocrinology

Published: December 14, 2019

Functional analysis of SEMA3A variants identified in Chinese patients with isolated hypogonadotropic hypogonadism.

Journal: Clinical genetics

Published: December 09, 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

Functional analysis of SOX10 mutations identified in Chinese patients with Kallmann syndrome.

Journal: Gene

Published: December 21, 2018