91. Novel FOXL2 mutations cause blepharophimosis‐ptosis‐epicanthus inversus syndrome with premature ovarian insufficiency. Issue 2 (29th January 2018) Authors: Yang, Xiao‐Wen; He, Wen‐Bin; Gong, Fei; Li, Wen; Li, Xiu‐Rong; Zhong, Chang‐Gao; Lu, Guang‐Xiu; Lin, Ge; Du, Juan; Tan, Yue‐Qiu Journal: Molecular genetics & genomic medicine Issue: Volume 6:Issue 2(2018) Page Start: 261 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
92. Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility. Issue 1 (15th November 2020) Authors: Hu, Tong‐Yao; Zhang, Huan; Meng, Lan‐Lan; Yuan, Shi‐Min; Tu, Chao‐Feng; Du, Juan; Lu, Guang‐Xiu; Lin, Ge; Nie, Hong‐Chuan; Tan, Yue‐Qiu Journal: Human mutation Issue: Volume 42:Issue 1(2021) Page Start: 31 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
93. Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Issue 4 (3rd January 2023) Authors: 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 Journal: Clinical genetics Issue: Volume 103:Issue 4(2023) Page Start: 495 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
94. Novel homozygous variations in PLCZ1 lead to poor or failed fertilization characterized by abnormal localization patterns of PLCζ in sperm. Issue 2 (8th September 2019) Authors: Dai, Jing; Dai, Can; Guo, Jing; Zheng, Wei; Zhang, Tianlei; Li, Yuan; Lu, Changfu; Gong, Fei; Lu, Guangxiu; Lin, Ge Journal: Clinical genetics Issue: Volume 97:Issue 2(2020) Page Start: 347 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
95. Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome. Issue 3 (March 2019) Authors: He, Wen-Bin; Du, Juan; Yang, Xiao-Wen; Li, Wen; Tang, Wei-Lin; Dai, Can; Chen, Yong-Zhe; Zhang, Ya-Xin; Lu, Guang-Xiu; Lin, Ge; Gong, Fei; Tan, Yue-Qiu Journal: Reproductive biomedicine online Issue: Volume 38:Issue 3(2019) Page Start: 397 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
96. Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency. Issue 4 (11th February 2020) Authors: Zhang, Ya‐Xin; He, Wen‐Bin; Xiao, Wen‐Juan; Meng, Lan‐Lan; Tan, Chen; Du, Juan; Lu, Guang‐Xiu; Lin, Ge; Tan, Yue‐Qiu Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 4(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
97. Novel mutation in TTC21A triggers partial nonsense‐mediated mRNA decay and causes male infertility with MMAF. Issue 5 (3rd August 2022) Authors: Liu, Gang; Yin, Xinyu; Xing, Xiaowei; Yin, Silu; Shen, Yuehan; Zhang, Huan; Lin, Ge; Lu, Guangxiu; Li, Weina Journal: Clinical genetics Issue: Volume 102:Issue 5(2022) Page Start: 459 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
98. Novel mutations in PMFBP1, TSGA10 and SUN5: Expanding the spectrum of mutations that may cause acephalic spermatozoa. Issue 6 (13th April 2020) Authors: Liu, Gang; Wang, Ni; Zhang, Huan; Yin, Silu; Dai, Haibo; Lin, Ge; Li, Weina Journal: Clinical genetics Issue: Volume 97:Issue 6(2020) Page Start: 938 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
99. Parkinson's Disease and Pesticides Exposure: New Findings From a Comprehensive Study in Nebraska, USA. Issue 3 (30th October 2015) Authors: Wan, Neng; Lin, Ge Journal: Journal of rural health Issue: Volume 32:Issue 3(2016:Summer) Page Start: 303 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
100. Pathogenic variant in ACTL7A causes severe teratozoospermia characterized by bubble-shaped acrosomes and male infertility. (21st July 2022) Authors: Dai, Jing; Chen, Yongzhe; Li, Qi; Zhang, Tianlei; Zhou, Qinwei; Gong, Fei; Lu, Guangxiu; Zheng, Wei; Lin, Ge Journal: Molecular human reproduction Issue: Volume 28:Number 8(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗