Chaofeng Tu

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 20

Top Topics

Intellectual Disability

Genome Wide Analysis

Monoclonal Antibody

Top Venues

Journal of assisted reproduction and genetics

Clinical genetics

Molecular human reproduction

Human reproduction (Oxford, England)

This page only lists publications with an associated author ORCID identifier.

Publications

Siyi Zhao, Qiong Liu, Lilan Su, Lanlan Meng, Chen Tan, Chunjia Wei, Huan Zhang, Tao Luo, Qianjun Zhang, Yue-Qiu Tan, Chaofeng Tu, Houyang Chen, Xingcheng Gao
Identification of novel homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagella. Journal of assisted reproduction and genetics 41 (5) (2024)
Sibing Yi, Weili Wang, Lilan Su, Lanlan Meng, Yong Li, Chen Tan, Qiang Liu, Huan Zhang, Liqing Fan, Guangxiu Lu, Liang Hu, Juan Du, Ge Lin, Yue-Qiu Tan, Chaofeng Tu, Qianjun Zhang
Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia. Molecular human reproduction (2024)
Chen Luo, Zixu Chen, Lanlan Meng, Chen Tan, Wenbin He, Chaofeng Tu, Juan Du, Guang-Xiu Lu, Ge Lin, Yue-Qiu Tan, Tong-Yao Hu
A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia. Clinical genetics 106 (1) (2024)
Siyi Zhao, Qiong Liu, Lilan Su, Lanlan Meng, Chen Tan, Chunjia Wei, Huan Zhang, Tao Luo, Qianjun Zhang, Yue-Qiu Tan, Chaofeng Tu, Houyang Chen, Xingcheng Gao
Identification of novel homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagella. Journal of assisted reproduction and genetics (2024)
Sibing Yi, Weili Wang, Lilan Su, Lanlan Meng, Yong Li, Chen Tan, Qiang Liu, Huan Zhang, Liqing Fan, Guangxiu Lu, Liang Hu, Juan Du, Ge Lin, Yue-Qiu Tan, Chaofeng Tu, Qianjun Zhang
Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia. Molecular human reproduction 30 (2) (2024)
Sibing Yi, Weili Wang, Lilan Su, Lanlan Meng, Yong Li, Chen Tan, Qiang Liu, Huan Zhang, Liqing Fan, Guangxiu Lu, Liang Hu, Juan Du, Ge Lin, Yue-Qiu Tan, Chaofeng Tu, Qianjun Zhang
Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia. Molecular human reproduction 30 (2) (2024)
Chen Luo, Zixu Chen, Lanlan Meng, Chen Tan, Wenbin He, Chaofeng Tu, Juan Du, Guang-Xiu Lu, Ge Lin, Yue-Qiu Tan, Tong-Yao Hu
A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia. Clinical genetics (2024)
Siyi Zhao, Qiong Liu, Lilan Su, Lanlan Meng, Chen Tan, Chunjia Wei, Huan Zhang, Tao Luo, Qianjun Zhang, Yue-Qiu Tan, Chaofeng Tu, Houyang Chen, Xingcheng Gao
Identification of novel homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagella. Journal of assisted reproduction and genetics 41 (5) (2024)
Jiaxin He, Qiang Liu, Weili Wang, Lilan Su, Lanlan Meng, Chen Tan, Huan Zhang, Qianjun Zhang, Guangxiu Lu, Juan Du, Ge Lin, Chaofeng Tu, Yue-Qiu Tan
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clinical genetics 103 (4) (2023)
Jiaxin He, Qiang Liu, Weili Wang, Lilan Su, Lanlan Meng, Chen Tan, Huan Zhang, Qianjun Zhang, Guangxiu Lu, Juan Du, Ge Lin, Chaofeng Tu, Yue-Qiu Tan
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clinical genetics 103 (4) (2023)
Weili Wang, Lilan Su, Lanlan Meng, Jiaxin He, Chen Tan, Duo Yi, Dehua Cheng, Huan Zhang, Guangxiu Lu, Juan Du, Ge Lin, Qianjun Zhang, Chaofeng Tu, Yue-Qiu Tan
Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia. Human reproduction (Oxford, England) (2023)
Jiaxin He, Qiang Liu, Weili Wang, Lilan Su, Lanlan Meng, Chen Tan, Huan Zhang, Qianjun Zhang, Guangxiu Lu, Juan Du, Ge Lin, Chaofeng Tu, Yue-Qiu Tan
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clinical genetics 103 (4) (2023)
Yunhao Li, Yong Li, Ying Wang, Lanlan Meng, Chen Tan, Juan Du, Yue-Qiu Tan, Hongchuan Nie, Qianjun Zhang, Guangxiu Lu, Ge Lin, Huanzhu Li, Huan Zhang, Chaofeng Tu
Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility. Journal of assisted reproduction and genetics 40 (1) (2022)
Yunhao Li, Yong Li, Ying Wang, Lanlan Meng, Chen Tan, Juan Du, Yue-Qiu Tan, Hongchuan Nie, Qianjun Zhang, Guangxiu Lu, Ge Lin, Huanzhu Li, Huan Zhang, Chaofeng Tu
Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility. Journal of assisted reproduction and genetics 40 (1) (2022)
Weili Wang, Lanlan Meng, Jiaxin He, Lilan Su, Yong Li, Chen Tan, Xilin Xu, Hongchuan Nie, Huan Zhang, Juan Du, Guangxiu Lu, Mengcheng Luo, Ge Lin, Chaofeng Tu, Yue-Qiu Tan
Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice. Molecular human reproduction 28 (6) (2022)
Jiaxin He, Qiang Liu, Weili Wang, Lilan Su, Lanlan Meng, Chen Tan, Huan Zhang, Qianjun Zhang, Guangxiu Lu, Juan Du, Ge Lin, Chaofeng Tu, Yue-Qiu Tan
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clinical genetics (2022)
Yunhao Li, Yong Li, Ying Wang, Lanlan Meng, Chen Tan, Juan Du, Yue-Qiu Tan, Hongchuan Nie, Qianjun Zhang, Guangxiu Lu, Ge Lin, Huanzhu Li, Huan Zhang, Chaofeng Tu
Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility. Journal of assisted reproduction and genetics 40 (1) (2022)
Yunhao Li, Yong Li, Ying Wang, Lanlan Meng, Chen Tan, Juan Du, Yue-Qiu Tan, Hongchuan Nie, Qianjun Zhang, Guangxiu Lu, Ge Lin, Huanzhu Li, Huan Zhang, Chaofeng Tu
Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility. Journal of assisted reproduction and genetics 40 (1) (2022)
Yunhao Li, Yong Li, Ying Wang, Lanlan Meng, Chen Tan, Juan Du, Yue-Qiu Tan, Hongchuan Nie, Qianjun Zhang, Guangxiu Lu, Ge Lin, Huanzhu Li, Huan Zhang, Chaofeng Tu
Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility. Journal of assisted reproduction and genetics (2022)
Jiaxin He, Qiang Liu, Weili Wang, Lilan Su, Lanlan Meng, Chen Tan, Huan Zhang, Qianjun Zhang, Guangxiu Lu, Juan Du, Ge Lin, Chaofeng Tu, Yue-Qiu Tan
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clinical genetics (2022)