1.2009.07–2013.06, 中国科学技术大学, 遗传学, 博士

2.2007.09–2009.06, 中国科学技术大学, 遗传学, 硕士直接攻读博士

1.国家自然科学基金-青年项目， 82101685，中心粒蛋白POC1B纯合移码突变导致少弱畸精子症的分子机制研究，2022.01-2025.01，主持；

2.安徽医科大学基础与临床合作研究提升计划，2020xkjT014，WDR12纯合错义突变导致锥形头部精子的分子机制研究， 2021.01-2023.12，主持；

3.安徽省自然科学基金青年项目，1608085QH174，SOD1调节原始卵泡形成的分子机制，2016.06-2018.06，主持。

1. Juan Hua^#, Bo Xu^#, Wenjing Liu, JingTian Shi, Hui Jiang, XiaoJun Zha^*, Xiansheng Zhang^*, Yangyang Wan^*. Homozygous frameshift variant in POC1B cause male infertility with oligoasthenoteratozoospermia in human and mice. Hum Mol Genet. 2023 Apr 18;ddad061. doi: 10.1093/hmg/ddad061. 

2. Yang-Yang Wan^#, Wenjing Liu, Bo Xu*, Xiaohua Jiang*, Juan Hua*. Association of paternal MTHFR polymorphisms (C677T) with clinical outcomes in ICSI treatment. Frontiers in Endocrinology, 2022 Dec 22;13:1084463.

3. Juan Hua^#, Lan Guo, Yao Yao, Wen Hu, Yang-Yang Wan, Bo Xu. Biallelic mutations in WDR12 are associated with male infertility with tapered-head sperm. Asian J Androl. 2022 Sep 30. doi: 10.4103/aja202269.

4. Yao Yao^#, Yangyang Wan^#, Xiaoyun Shi^#, Lan Guo, Hui Jiang; Xiansheng Zhang, Bo Xu*, Juan Hua*. Letrozole protects against cadmium-induced inhibition of spermatogenesis via LHCGR and Hsd3b6 to activate testosterone synthesis in mice. Reproductive Biology and Endocrinology, 2022, 20(1).

5. Yang-Yang Wan^#, Lan Guo, Yao Yao, Xiao-Yun Shi, Hui Jiang, Bo Xu, Juan Hua*, Xian-Sheng Zhang*. MBOAT1 homozygous missense variant causes nonobstructive azoospermia. Asian Journal of Andrology, 2022, 24(2): 186–190.

6. Juan Hua^#, Yang-yang Wan*. Whole-exome sequencing identified a novel mutation of AURKC in a Chinese family with macrozoospermia. Journal of Assisted Reproduction and Genetics, 2019, 36(3): 529-534.

7. Hua J^#, Xu B, Yang Y, Ban R, Iqbal F, Cooke HJ, Zhang Y, Shi Q. Follicle Online: an integrated database of follicle assembly, development and ovulation. Database (Oxford).2015 Apr 29; 2015: bav036.