郑颖春｜西安科技大学｜学者主页

2026

The PHEX deletion variant (p.Thr605MetfsTer14) causes X-linked hypophosphatemic rickets by reducing protein expression and promoting mineralization

Zhongzhi Gan, Meiyu Zheng, Chenzhao Guo, Fei He, Yingchun Zheng, Jiayi Li, Chen Li, Fang Yang, Qi Song, Qingxian Chang, Qian Liu, Fu Xiong, Hairui Xie

Orphanet Journal of Rare Diseases

DOI

2026

Identification of a rare missense variant in the gene SPATA31H1 associated with hereditary gingival fibromatosis in a large Chinese family

Wanqing Wang, Jialin Xu, Shu-Ning Du, Zhi-Lu Yuan, Jianfan Chen, Yingchun Zheng, Yuhua Pan, Fei He, Gu Wei, Zhihan Kelvin Yang, Leitao Zhang, Guo-Fang Wang, Jian Zhang, Fu Xiong, Dong-Miao Chen

BMC Oral Health

DOI

2025

直觉犹豫模糊软专家集及其在决策中的应用

郑颖春，周婉婷

《山东大学学报(理学版)》

2025

一种改进的基于知识粒度的增量属性约简算法

郑颖春，郭玲

《小型微型计算机系统》

DOI

2025

A missense variant in the SOX5 gene (c.221C > T) is associated with intellectual disability

Xiu-Juan Yang, Zhongzhi Gan, Xiao-Ling Guo, Xiang Huang, Juan Liu, Yingchun Zheng, Xiaoqiang Zhou, Jingli Lian, Yue Liu, Tingting Yang, Chao Li, Fenying Chen, Fei He, Xiang-Min Xu, Ya-Si Zhou, Qian Liu, Xing-Kun Yang, Fu Xiong

Orphanet Journal of Rare Diseases

DOI

2025

Case Report: A novel germline donor splicing site mutation of RB1 gene in a Chinese Tibetan pedigree with familial retinoblastoma

Guo-Qian He, Yingchun Zheng, Lin-jun Tan, Cheng-Qi Shen, Ju Gao, Fu Xiong, Xia Guo

Frontiers in Oncology

DOI

2025

Identification of an IL17RC missense variant in a Chinese family with multiple osteochondromas and ankylosing spondylitis

Yingchun Zheng, Xuewu Wei, Zhongzhi Gan, Mingming Zhang, Zongrui Shen, Shunfei Ma, Yihao Huang, Fei He, Jian Wang, Fu Xiong

Journal of Human Genetics

DOI

2024

数据驱动多粒序贯三支分类模型

郑颖春，卢昕云

《模糊系统与数学》

2024

A large deletion in TSC2 causes tuberous sclerosis complex by dysregulating PI3K/AKT/mTOR signaling pathway.

Jiahui Fu, Peili Liang, Yingchun Zheng, Cailing Xu, Fu Xiong, Fang Yang

Gene

DOI

2024

Loss-of-function SLC25A20 mutation causes carnitine-acylcarnitine translocase deficiency by reducing SLC25A20 protein stability.

Zhongzhi Gan, Xiao-Feng Wei, Yingchun Zheng, Qiqi Zheng, Shushu Fan, Fu Xiong

Gene

DOI

2024

Single-cell RNA-seq analysis of rat molars reveals cell identity and driver genes associated with dental mesenchymal cell differentiation

Yingchun Zheng, Ting Lu, Leitao Zhang, Zhongzhi Gan, A. Li, Chuandong He, Fei He, Shan He, Jian Zhang, Fu Xiong

BMC Biology

DOI

2024

Corrigendum to "A large deletion in TSC2 causes tuberous sclerosis complex by dysregulating PI3K_AKT_mTOR signaling pathway" [GENE909 (2024) 148312/D-23-04187].

Jiahui Fu, Peili Liang, Yingchun Zheng, Cailing Xu, Fu Xiong, Fang Yang

Gene

DOI

2024

Second transplantation after kidney graft loss in primary hyperoxaluria type 2: a pedigree study and mutation analysis

Yushi Peng, Yingchun Zheng, Fu Xiong, Mingming Zhang, Yuchen Wang, Jiayi Luo, Wenli Zeng, Jia-Liang Hui, Wenfeng Deng, Jian Xu, Y. Miao, R. Xia, Yiling Fang

Renal Failure

DOI

2023

Plasma-derived exosomal miRNA profiles reveal potential epigenetic pathogenesis of premature ovarian failure

Jia-Qiong Lin, Zhihong Wu, Yingchun Zheng, Zongrui Shen, Zhongzhi Gan, Shunfei Ma, Yan-Hui Liu, Fu Xiong

Human Genetics

DOI

2023

The loss of function GBA1 c.231C > G mutation associated with Parkinson disease

Dejie Chen, Yingchun Zheng, Gui-Lian Zhang, Yuan-Bing Huang, Boyang Zheng, Jian Zhang, F. Xiong, Quan-Xi Su

Journal of neural transmission

DOI

2023

Intravenous Administration of an AAV9 Vector Ubiquitously Expressing C1orf194 Gene Improved CMT-Like Neuropathy in C1orf194-/- Mice

Zongrui Shen, Meiyi Li, Fei He, Cheng Huang, Yingchun Zheng, Zhi-Kui Wang, Shunfei Ma, Li Chen, Zhengshan Liu, Hui Zheng, Fu Xiong

Neurotherapeutics

DOI

2022

弱标记不完备决策系统的启发式增量约简算法

郑颖春，金莎

《模糊系统与数学》

2022

基于区分对的混合型弱标记数据增量约简算法

金莎，郑颖春

《河南科技大学学报(自然科学版)》

2022

A Novel Mutation in ATRX Causes Alpha-Thalassemia X-Linked Intellectual Disability Syndrome in a Han Chinese Family

Shao-Yen Wu, Yingchun Zheng, Cailing Xu, Jiahui Fu, F. Xiong, Fang Yang

Frontiers in Pediatrics

DOI

2022

A Rare Heterozygous TINF2 Deletional Frameshift Mutation in a Chinese Pedigree With a Spectrum of TBDs Phenotypes

H. Ren, Yingchun Zheng, Guo-Qian He, Ju Gao, Xia Guo

Frontiers in Genetics

DOI

2022

A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia

Da-yun Guo, Yingchun Zheng, Zhong-Yan Gan, Yingying Guo, Sijie Jiang, Fang Yang, F. Xiong, Hua Zheng

Frontiers in Genetics

DOI

2021

Global optimal solution on blending problem

Yingchun Zheng

Journal of Physics Conference Series

DOI

2020

基于SPOC的“线性代数”课程教学模式的探索

郑颖春

《牡丹江教育学院学报》

2020

The gain-of-function FAM83H mutation caused hypocalcification amelogenesis imperfecta in a Chinese family

Yingchun Zheng, Ting Lu, Jianfan Chen, Meiyi Li, J. Xiong, Fei He, Zhongzhi Gan, Yingying Guo, Leitao Zhang, F. Xiong

Clinical Oral Investigations

DOI

2020

C1orf194 deficiency leads to incomplete early embryonic lethality and dominant intermediate Charcot-Marie-Tooth disease in a knockout mouse model.

Cheng Huang, Zongrui Shen, Jin Huang, Shun-Chang Sun, Di Ma, Meiyi Li, Zhi-Kui Wang, Yingchun Zheng, Zhuojun Zheng, Fei He, Xiao-Yuan Xu, Ziang Li, Boyang Zheng, Yue-Mao Li, Xiang-Min Xu, F. Xiong

Human Molecular Genetics

DOI

2019

[Structural characteristics of the deciduous teeth of Tibetan miniature pigs].

Ting Lu, Yingchun Zheng, Haiying Yang, Bu-Ling Wu, J. Xiong, Cheng Huang, Yuhua Pan, Meiyi Li, Fei He, F. Xiong

Nan fang yi ke da xue xue bao = Journal of Southern Medical University

DOI

2017

不确定条件下的均衡市场

郑颖春，杨云锋

《郑州大学学报(理学版)》

2017

完备市场下的均衡和财富优化

郑颖春，杨云锋

《数学的实践与认识》

2016

支付红利时的财富优化模型

郑颖春，杨云锋

《宝鸡文理学院学报(自然科学版)》

2015

高等数学课程教学的几点思考

郑颖春

《读与写(教育教学刊)》

2013

一类求解极小极大问题的算法

郑颖春

《西安科技大学学报》

2013

一类不可微规划算法的线性收敛性

郑颖春，王雪峰

《陕西科技大学学报》

2008

一类不可微优化算法及在线性分类问题中的应用

郑颖春

《西安科技大学》

郑颖春

精选作品

期刊论文

The PHEX deletion variant (p.Thr605MetfsTer14) causes X-linked hypophosphatemic rickets by reducing protein expression and promoting mineralization

Identification of a rare missense variant in the gene SPATA31H1 associated with hereditary gingival fibromatosis in a large Chinese family

直觉犹豫模糊软专家集及其在决策中的应用

一种改进的基于知识粒度的增量属性约简算法

A missense variant in the SOX5 gene (c.221C > T) is associated with intellectual disability

Case Report: A novel germline donor splicing site mutation of RB1 gene in a Chinese Tibetan pedigree with familial retinoblastoma

Identification of an IL17RC missense variant in a Chinese family with multiple osteochondromas and ankylosing spondylitis

数据驱动多粒序贯三支分类模型

A large deletion in TSC2 causes tuberous sclerosis complex by dysregulating PI3K/AKT/mTOR signaling pathway.

Loss-of-function SLC25A20 mutation causes carnitine-acylcarnitine translocase deficiency by reducing SLC25A20 protein stability.

Single-cell RNA-seq analysis of rat molars reveals cell identity and driver genes associated with dental mesenchymal cell differentiation

Corrigendum to "A large deletion in TSC2 causes tuberous sclerosis complex by dysregulating PI3K_AKT_mTOR signaling pathway" [GENE909 (2024) 148312/D-23-04187].

Second transplantation after kidney graft loss in primary hyperoxaluria type 2: a pedigree study and mutation analysis

Plasma-derived exosomal miRNA profiles reveal potential epigenetic pathogenesis of premature ovarian failure

The loss of function GBA1 c.231C > G mutation associated with Parkinson disease

Intravenous Administration of an AAV9 Vector Ubiquitously Expressing C1orf194 Gene Improved CMT-Like Neuropathy in C1orf194-/- Mice

弱标记不完备决策系统的启发式增量约简算法

基于区分对的混合型弱标记数据增量约简算法

A Novel Mutation in ATRX Causes Alpha-Thalassemia X-Linked Intellectual Disability Syndrome in a Han Chinese Family

A Rare Heterozygous TINF2 Deletional Frameshift Mutation in a Chinese Pedigree With a Spectrum of TBDs Phenotypes

A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia

Global optimal solution on blending problem

基于SPOC的“线性代数”课程教学模式的探索

The gain-of-function FAM83H mutation caused hypocalcification amelogenesis imperfecta in a Chinese family

C1orf194 deficiency leads to incomplete early embryonic lethality and dominant intermediate Charcot-Marie-Tooth disease in a knockout mouse model.

[Structural characteristics of the deciduous teeth of Tibetan miniature pigs].

不确定条件下的均衡市场

完备市场下的均衡和财富优化

支付红利时的财富优化模型

高等数学课程教学的几点思考

一类求解极小极大问题的算法

一类不可微规划算法的线性收敛性

一类不可微优化算法及在线性分类问题中的应用

会议论文

The Value of European Option