Min Nie
17PUBLICATIONS
25CO-AUTHORS
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Publications (17)
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|Apr 01, 2026
Clinical and Genetic Profile of Chinese Familial Hypocalciuric Hypercalcemia Type 1 (FHH1): A Retrospective Study.Liyuan Kou, An Song, Min Nie
|Mar 20, 2026
Novel CYP17A1 variants and functional validation in a large Chinese cohort of complete 17α-hydroxylase deficiency.Yaqing Cao, Lin Lu, Ming Li
|Feb 25, 2026
Congenital Hypogonadotropic Hypogonadism Caused by Prokineticin Receptor 2 Rare Sequence Variants: Molecular Genetics, Clinical Phenotypes and Therapeutic Outcomes From a Single-center Cohort.Yuhan Wang, Wei Zhang, Jiangfeng Mao
|May 28, 2025
The Efficacy of Semaglutide on Hypothalamic Obesity Caused by Craniopharyngioma Surgery.Xi Wang, Hailu Ma, Fang Wang
|Feb 04, 2025
Chimeric CYP21A1P/CYP21A2 Genes in 21-Hydroxylase Deficiency Detected by Long-Read Sequencing and Phenotypes Correlation.Xiaoxia Zhang, Yinjie Gao, Lin Lu
|Jan 27, 2025
MYRF Variants in Patients With 46,XY Differences/Disorders of Sex Development and Literature Review.Wei Zhang, Xi Wang, Jiangfeng Mao
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