Works by Nie, Hongchuan

Results: 12

Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesia.

Published in:

Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 6, p. 1485, doi. 10.1007/s10815-024-03106-9

By:

Lu, Wenqing;
Li, Yong;
Meng, Lanlan;
Tan, Chen;
Nie, Hongchuan;
Zhang, Qianjun;
Song, Yuying;
Zhang, Huan;
Tan, Yue-Qiu;
Tu, Chaofeng;
Guo, Haichun;
Wu, Longxiang;
Du, Juan

Publication type:

Article

Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility.

Published in:

2023

By:

Li, Yunhao;
Li, Yong;
Wang, Ying;
Meng, Lanlan;
Tan, Chen;
Du, Juan;
Tan, Yue-Qiu;
Nie, Hongchuan;
Zhang, Qianjun;
Lu, Guangxiu;
Lin, Ge;
Li, Huanzhu;
Zhang, Huan;
Tu, Chaofeng

Publication type:

Case Study

Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 4, p. 811, doi. 10.1007/s10815-020-01735-4

By:

Wang, Ying;
Tu, Chaofeng;
Nie, Hongchuan;
Meng, Lanlan;
Li, Dongyan;
Wang, Weili;
Zhang, Huan;
Lu, Guangxiu;
Lin, Ge;
Tan, Yue-Qiu;
Du, Juan

Publication type:

Article

Long Y chromosome is not a fetal loss risk.

Published in:

Journal of Assisted Reproduction & Genetics, 2011, v. 28, n. 2, p. 151, doi. 10.1007/s10815-010-9497-1

By:

Nie, Hongchuan;
Lu, Guangxiu

Publication type:

Article

CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 24, p. 2240, doi. 10.1093/hmg/ddab185

By:

Wang, Weili;
Tian, Shixong;
Nie, Hongchuan;
Tu, Chaofeng;
Liu, Chunyu;
Li, Yong;
Li, Dongyan;
Yang, Xiaoxuan;
Meng, Lanlan;
Hu, Tongyao;
Zhang, Qianjun;
Du, Juan;
Fan, Liqing;
Lu, Guangxiu;
Lin, Ge;
Zhang, Feng;
Tan, Yue-Qiu

Publication type:

Article

CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 23, p. 2240, doi. 10.1093/hmg/ddab185

By:

Wang, Weili;
Tian, Shixong;
Nie, Hongchuan;
Tu, Chaofeng;
Liu, Chunyu;
Li, Yong;
Li, Dongyan;
Yang, Xiaoxuan;
Meng, Lanlan;
Hu, Tongyao;
Zhang, Qianjun;
Du, Juan;
Fan, Liqing;
Lu, Guangxiu;
Lin, Ge;
Zhang, Feng;
Tan, Yue-Qiu

Publication type:

Article

Front Cover.

Published in:

Clinical Genetics, 2020, v. 97, n. 5, p. i, doi. 10.1111/cge.13758

By:

Tu, Chaofeng;
Wang, Ying;
Nie, Hongchuan;
Meng, Lanlan;
Wang, Weili;
Li, Yong;
Li, Dongyan;
Zhang, Huan;
Lu, Guangxiu;
Lin, Ge;
Tan, Yue‐Qiu;
Du, Juan

Publication type:

Article

An M1AP homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family.

Published in:

Clinical Genetics, 2020, v. 97, n. 5, p. 741, doi. 10.1111/cge.13712

By:

Tu, Chaofeng;
Wang, Ying;
Nie, Hongchuan;
Meng, Lanlan;
Wang, Weili;
Li, Yong;
Li, Dongyan;
Zhang, Huan;
Lu, Guangxiu;
Lin, Ge;
Tan, Yue‐Qiu;
Du, Juan

Publication type:

Article

Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.936264

By:

Yurong Wang;
Ling Liu;
Chen Tan;
Guiquan Meng;
Lanlan Meng;
Hongchuan Nie;
Juan Du;
Guang-Xiu Lu;
Ge Lin;
Wen-Bin He;
Yue-Qiu Tan

Publication type:

Article

Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice.

Published in:

Molecular Human Reproduction, 2022, v. 28, n. 6, p. 1, doi. 10.1093/molehr/gaac015

By:

Wang, Weili;
Meng, Lanlan;
He, Jiaxin;
Su, Lilan;
Li, Yong;
Tan, Chen;
Xu, Xilin;
Nie, Hongchuan;
Zhang, Huan;
Du, Juan;
Lu, Guangxiu;
Luo, Mengcheng;
Lin, Ge;
Tu, Chaofeng;
Tan, Yue-Qiu

Publication type:

Article

Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella.

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-52436-7

By:

Tu, Chaofeng;
Nie, Hongchuan;
Meng, Lanlan;
Yuan, Shimin;
He, Wenbin;
Luo, Aixiang;
Li, Haiyu;
Li, Wen;
Du, Juan;
Lu, Guangxiu;
Lin, Ge;
Tan, Yue-Qiu

Publication type:

Article

Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD.

Published in:

Human Genetics, 2020, v. 139, n. 2, p. 257, doi. 10.1007/s00439-020-02110-0

By:

Tu, Chaofeng;
Nie, Hongchuan;
Meng, Lanlan;
Wang, Weili;
Li, Haiyu;
Yuan, Shimin;
Cheng, Dehua;
He, Wenbin;
Liu, Gang;
Du, Juan;
Gong, Fei;
Lu, Guangxiu;
Lin, Ge;
Zhang, Qianjun;
Tan, Yue-Qiu

Publication type:

Article