Works by Tu, Chaofeng

Results: 34

Novel mutations in ZMYND15 are associated with male infertility with oligozoospermia/azoospermia.

Published in:

Journal of Assisted Reproduction & Genetics, 2025, v. 42, n. 5, p. 1601, doi. 10.1007/s10815-025-03480-y

By:

Wei, Chunjia;
Lu, Yingchi;
Yi, Sibing;
Liang, Yaoqiong;
Meng, Lanlan;
Tan, Chen;
Du, Juan;
Lin, Ge;
Tan, Yue-Qiu;
Gan, Xianyou;
Tu, Chaofeng;
Qin, Zailong

Publication type:

Article

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 homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagella.

Published in:

Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 5, p. 1297, doi. 10.1007/s10815-024-03087-9

By:

Zhao, Siyi;
Liu, Qiong;
Su, Lilan;
Meng, Lanlan;
Tan, Chen;
Wei, Chunjia;
Zhang, Huan;
Luo, Tao;
Zhang, Qianjun;
Tan, Yue-Qiu;
Tu, Chaofeng;
Chen, Houyang;
Gao, Xingcheng

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

XRCC2 driven homologous recombination subtypes and therapeutic targeting in lung adenocarcinoma metastasis.

Published in:

NPJ Precision Oncology, 2024, v. 8, n. 1, p. 1, doi. 10.1038/s41698-024-00658-y

By:

Gong, Han;
Zhang, Peihe;
Liu, Qiang;
Tian, Yuxuan;
Chen, Fuxin;
Qian, Siyi;
Tu, Chaofeng;
Tan, Yueqiu;
Hu, Xingming;
Zhang, Bin

Publication type:

Article

Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice.

Published in:

Human Reproduction Open, 2024, v. 2024, n. 1, p. 1, doi. 10.1093/hropen/hoae003

By:

Meng, Gui-Quan;
Wang, Yaling;
Luo, Chen;
Tan, Yu-Mei;
Li, Yong;
Tan, Chen;
Tu, Chaofeng;
Zhang, Qian-Jun;
Hu, Liang;
Zhang, Huan;
Meng, Lan-Lan;
Liu, Chun-Yu;
Deng, Leiyu;
Lu, Guang-Xiu;
Lin, Ge;
Du, Juan;
Tan, Yue-Qiu;
Sha, Yanwei;
Wang, Lingbo;
He, Wen-Bin

Publication type:

Article

Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature.

Published in:

2018

By:

Li, Haiyu;
Du, Juan;
Li, Wen;
Cheng, Dehua;
He, Wenbin;
Yi, Duo;
Xiong, Bo;
Yuan, Shimin;
Tu, Chaofeng;
Meng, Lanlan;
Luo, Aixiang;
Lin, Ge;
Lu, Guangxiu;
Tan, Yue-Qiu

Publication type:

Case Study

Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia.

Published in:

2022

By:

Xie, Chunbo;
Wang, Weili;
Tu, Chaofeng;
Meng, Lanlan;
Lu, Guangxiu;
Lin, Ge;
Lu, Lin-Yu;
Tan, Yue-Qiu

Publication type:

journal article

Identification of genomic alterations in nasopharyngeal carcinoma and nasopharyngeal carcinoma-derived Epstein–Barr virus by whole-genome sequencing.

Published in:

Carcinogenesis, 2018, v. 39, n. 12, p. 1517, doi. 10.1093/carcin/bgy108

By:

Tu, Chaofeng;
Zeng, Zhaoyang;
Qi, Peng;
Li, Xiayu;
Guo, Can;
Xiong, Fang;
Xiang, Bo;
Zhou, Ming;
Liao, Qianjin;
Yu, Jianjun;
Li, Yong;
Li, Xiaoling;
Li, Guiyuan;
Xiong, Wei

Publication type:

Article

Homozygous deleterious variants in MYCBPAP induce asthenoteratozoospermia involving abnormal acrosome biogenesis, manchette structure and sperm tail assembly in humans and mice.

Published in:

SCIENCE CHINA Life Sciences, 2025, v. 68, n. 3, p. 777, doi. 10.1007/s11427-024-2757-7

By:

Zhou, Yiling;
Tu, Chaofeng;
Coutton, Charles;
Tang, Jianan;
Tian, Shixiong;
Tang, Shuyan;
Martinez, Guillaume;
Zhou, Dapeng;
Tebbakh, Célia;
Wang, Jiaxiong;
Zouari, Raoudha;
Zhou, Xuehai;
Ben Mustapha, Selima Fourati;
Wang, Xuemei;
Wu, Bangguo;
Geng, Xinyan;
Liu, Shuang;
Jin, Li;
Shi, Huijuan;
Tan, Yue-Qiu

Publication type:

Article

Novel biallelic PCNT deletion causing microcephalic osteodysplastic primordial dwarfism type II with congenital heart defect.

Published in:

SCIENCE CHINA Life Sciences, 2019, v. 62, n. 1, p. 144, doi. 10.1007/s11427-018-9329-3

By:

Meng, Lanlan;
Tu, Chaofeng;
Lu, Guangxiu;
Lin, Ge;
Tan, Yueqiu

Publication type:

Article

SHARED DECISION-MAKING IN GENETIC COUNSELING: A SCOPING REVIEW.

Published in:

Acta Bioéthica, 2022, v. 28, n. 2, p. 227

By:

Peng Chenyang;
Ning Ni;
Li Yiyu;
Tan Xiangmin;
Tu Chaofeng;
Sun Mei

Publication type:

Article

Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia.

Published in:

Human Reproduction, 2023, v. 38, n. 7, p. 1399, doi. 10.1093/humrep/dead095

By:

Wang, Weili;
Su, Lilan;
Meng, Lanlan;
He, Jiaxin;
Tan, Chen;
Yi, Duo;
Cheng, Dehua;
Zhang, Huan;
Lu, Guangxiu;
Du, Juan;
Lin, Ge;
Zhang, Qianjun;
Tu, Chaofeng;
Tan, Yue-Qiu

Publication type:

Article

Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression.

Published in:

Cell Discovery, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41421-023-00580-w

By:

Tu, Chaofeng;
Wen, Junfei;
Wang, Weili;
Zhu, Qifan;
Chen, Ying;
Cheng, Jianglu;
Li, Zeye;
Meng, Lanlan;
Li, Yong;
He, Wenbin;
Tan, Chen;
Xie, Chunbo;
Fu, Shao-Mei;
Du, Juan;
Lu, Guangxiu;
Lin, Ge;
Gou, Lan-Tao;
Tan, Yue-Qiu

Publication type:

Article

Loss-of-function missense variant of AKAP4 induced male infertility through reduced interaction with QRICH2 during sperm flagella development.

Published in:

Human Molecular Genetics, 2022, v. 31, n. 2, p. 219, doi. 10.1093/hmg/ddab234

By:

Zhang, Guohui;
Li, Dongyan;
Tu, Chaofeng;
Meng, Lanlan;
Tan, Yueqiu;
Ji, Zhiliang;
Cheng, Jiao;
Lu, Guangxiu;
Lin, Ge;
Zhang, Huan;
Sun, Jinpeng;
Wang, Mingwei;
Du, Juan;
Xu, Wenming

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

A hemizygous loss‐of‐function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia.

Published in:

Clinical Genetics, 2024, v. 106, n. 1, p. 27, doi. 10.1111/cge.14500

By:

Luo, Chen;
Chen, Zixu;
Meng, Lanlan;
Tan, Chen;
He, Wenbin;
Tu, Chaofeng;
Du, Juan;
Lu, Guang‐Xiu;
Lin, Ge;
Tan, Yue‐Qiu;
Hu, Tong‐Yao

Publication type:

Article

Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype.

Published in:

Clinical Genetics, 2023, v. 103, n. 4, p. 495, doi. 10.1111/cge.14281

By:

He, Jiaxin;
Liu, Qiang;
Wang, Weili;
Su, Lilan;
Meng, Lanlan;
Tan, Chen;
Zhang, Huan;
Zhang, Qianjun;
Lu, Guangxiu;
Du, Juan;
Lin, Ge;
Tu, Chaofeng;
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

XRCC2 mutation causes premature ovarian insufficiency as well as non‐obstructive azoospermia in humans.

Published in:

Clinical Genetics, 2019, v. 95, n. 3, p. 442, doi. 10.1111/cge.13475

By:

Zhang, Ya‐Xin;
Li, Hai‐Yu;
Tu, Chaofeng;
He, Wen‐Bin;
Du, Juan;
Li, Wen;
Lu, Guang‐Xiu;
Lin, Ge;
Tan, Yue‐Qiu;
Yang, Yongjia

Publication type:

Article

Front Cover.

Published in:

Clinical Genetics, 2019, v. 95, n. 3, p. i, doi. 10.1111/cge.13520

By:

Zhang, Ya‐Xin;
Li, Hai‐Yu;
Tu, Chaofeng;
He, Wen‐Bin;
Du, Juan;
Li, Wen;
Lu, Guang‐Xiu;
Lin, Ge;
Tan, Yue‐Qiu;
Yang, Yongjia

Publication type:

Article

TDRD7 participates in lens development and spermiogenesis by mediating autophagosome maturation.

Published in:

Autophagy, 2021, v. 17, n. 11, p. 3848, doi. 10.1080/15548627.2021.1894058

By:

Tu, Chaofeng;
Li, Haiyu;
Liu, Xuyang;
Wang, Ying;
Li, Wei;
Meng, Lanlan;
Wang, Weili;
Li, Yong;
Li, Dongyan;
Du, Juan;
Lu, Guangxiu;
Lin, Ge;
Tan, Yue-Qiu

Publication type:

Article

Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and mice.

Published in:

Frontiers of Medicine, 2023, v. 17, n. 5, p. 957, doi. 10.1007/s11684-023-0988-8

By:

Wang, Rongchun;
Yang, Danhui;
Tu, Chaofeng;
Lei, Cheng;
Ding, Shuizi;
Guo, Ting;
Wang, Lin;
Liu, Ying;
Lu, Chenyang;
Yang, Binyi;
Ouyang, Shi;
Gong, Ke;
Tan, Zhiping;
Deng, Yun;
Tan, Yueqiu;
Qing, Jie;
Luo, Hong

Publication type:

Article

Telomerase insufficiency induced telomere erosion accumulation in successive generations in dyskeratosis congenita family.

Published in:

Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 7, p. N.PAG, doi. 10.1002/mgg3.709

By:

He, Caixia;
Jing, Shuang;
Dai, Congling;
Tu, Chaofeng;
Tan, Zhenhua;
Du, Juan;
Lu, Guang‐Xiu;
Lin, Ge;
Zeng, Sicong

Publication type:

Article

Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia.

Published in:

Molecular Human Reproduction, 2024, v. 30, n. 2, p. 1, doi. 10.1093/molehr/gaae002

By:

Yi, Sibing;
Wang, Weili;
Su, Lilan;
Meng, Lanlan;
Li, Yong;
Tan, Chen;
Liu, Qiang;
Zhang, Huan;
Fan, Liqing;
Lu, Guangxiu;
Hu, Liang;
Du, Juan;
Lin, Ge;
Tan, Yue-Qiu;
Tu, Chaofeng;
Zhang, Qianjun

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

Estimation for volunteer web survey samples using a model-averaging approach.

Published in:

Journal of Applied Statistics, 2023, v. 50, n. 16, p. 3251, doi. 10.1080/02664763.2022.2107187

By:

Zhan Liu;
Junbo Zheng;
Chaofeng Tu;
Yingli Pan

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

Model-assisted calibration with SCAD to estimated control for non-probability samples.

Published in:

Statistical Methods & Applications, 2022, v. 31, n. 4, p. 849, doi. 10.1007/s10260-021-00615-0

By:

Liu, Zhan;
Tu, Chaofeng;
Pan, Yingli

Publication type:

Article

LRRC4 haplotypes are associated with pituitary adenoma in a Chinese population.

Published in:

Medical Oncology, 2014, v. 31, n. 4, p. 1, doi. 10.1007/s12032-014-0888-5

By:

Xiao, Lan;
Tu, Chaofeng;
Chen, Shuai;
Yu, Zhibin;
Lei, Qianqian;
Wang, Zeyou;
Xu, Gang;
Wu, Minghua;
Li, Guiyuan

Publication type:

Article