1. An M1AP homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family. Issue 5 (10th February 2020) Authors: 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 Journal: Clinical genetics Issue: Volume 97:Issue 5(2020) Page Start: 741 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice. (29th April 2022) Authors: 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 Journal: Molecular human reproduction Issue: Volume 28:Number 6(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia. Issue 2 (6th April 2022) Authors: Hu, Tongyao; Meng, Lanlan; Tan, Chen; Luo, Chen; He, Wen-Bin; Tu, Chaofeng; Zhang, Huan; Du, Juan; Nie, Hongchuan; Lu, Guang-Xiu; Lin, Ge; Tan, Yue-Qiu Journal: Journal of medical genetics Issue: Volume 60:Issue 2(2023) Page Start: 144 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations. Issue 11 (14th August 2019) Authors: Wang, Weili; Tu, Chaofeng; Nie, Hongchuan; Meng, Lanlan; Li, Yong; Yuan, Shimin; Zhang, Qianjun; Du, Juan; Wang, Junpu; Gong, Fei; Fan, Liqing; Lu, Guang-Xiu; Lin, Ge; Tan, Yue-Qiu Journal: Journal of medical genetics Issue: Volume 56:Issue 11(2019) Page Start: 750 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis. Issue 23 (7th July 2021) Authors: 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 Journal: Human molecular genetics Issue: Volume 30:Issue 23(2021) Page Start: 2240 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Front Cover. Issue 3 (18th February 2019) Authors: Zhang, Ya‐Xin; Li, Hai‐Yu; He, Wen‐Bin; Tu, Chaofeng; Du, Juan; Li, Wen; Lu, Guang‐Xiu; Lin, Ge; Yang, Yongjia; Tan, Yue‐Qiu Journal: Clinical genetics Issue: Volume 95:Issue 3(2019) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Front Cover. Issue 5 (19th April 2020) Authors: 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 Journal: Clinical genetics Issue: Volume 97:Issue 5(2020) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genetic underpinnings of asthenozoospermia. Issue 6 (December 2020) Authors: Tu, Chaofeng; Wang, Weili; Hu, Tongyao; Lu, Guangxiu; Lin, Ge; Tan, Yue-Qiu Journal: Best practice & research Issue: Volume 34:Issue 6(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Identification of genomic alterations in nasopharyngeal carcinoma and nasopharyngeal carcinoma-derived Epstein–Barr virus by whole-genome sequencing. (9th August 2018) Authors: 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 Journal: Carcinogenesis Issue: Volume 39:Number 12(2018) Page Start: 1517 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Loss-of-function missense variant of AKAP4 induced male infertility through reduced interaction with QRICH2 during sperm flagella development. Issue 2 (20th August 2021) Authors: 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 Journal: Human molecular genetics Issue: Volume 31:Issue 2(2022) Page Start: 219 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗