ZFIN ID: ZDB-PERS-110923-2
Shen, Yan
Email: yshen@pku.edu.cn
Affiliation: PKU Zebrafish Functional Genomics Group
Address: No 5 YiHeYuan Rd. Haidian District College of Life Sciences Peking University Beijing, 100871 China
Country: China


Pang, L., Zhang, Z., Shen, Y., Cheng, Z., Gao, X., Zhang, B., Wang, X., Tian, H. (2020) Mutant dlx3b disturbs normal tooth mineralization and bone formation in zebrafish. PeerJ. 8:e8515
Wang, L., Ren, A., Tian, T., Li, N., Cao, X., Zhang, P., Jin, L., Li, Z., Shen, Y., Zhang, B., Finnell, R.H., Lei, Y. (2019) Whole-Exome Sequencing Identifies Damaging de novo Variants in Anencephalic Cases. Frontiers in neuroscience. 13:1285
Wang, K., Zhao, S., Liu, B., Zhang, Q., Li, Y., Liu, J., Shen, Y., Ding, X., Lin, J., Wu, Y., Yan, Z., Chen, J., Li, X., Song, X., Niu, Y., Liu, J., Chen, W., Ming, Y., Du, R., Chen, C., Long, B., Zhang, Y., Tong, X., Zhang, S., Posey, J.E., Zhang, B., Wu, Z., Wythe, J.D., Liu, P., Lupski, J.R., Yang, X., Wu, N. (2018) Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM). Journal of Medical Genetics. 55(10):675-684
Tian, T., Wang, L., Shen, Y., Zhang, B., Finnell, R.H., Ren, A. (2018) Hypomethylation of GRHL3 gene is associated with the occurrence of neural tube defects. Epigenomics. 10(7):891-901
Zhang, J., Wang, C., Shen, Y., Chen, N., Wang, L., Liang, L., Guo, T., Yin, X., Ma, Z., Zhang, B., Yang, L. (2016) A mutation in ADIPOR1 causes nonsyndromic autosomal dominant retinitis pigmentosa. Human genetics. 135(12):1375-1387
Shen, Y., Xiao, A., Huang, P., Wang, W.Y., Zhu, Z.Y., and Zhang, B. (2013) TALE nuclease engineering and targeted genome modification. Yi chuan = Hereditas. 35(4):395-409
Shen, Y., Huang, P., and Zhang, B. (2013) A protocol for TALEN construction and gene targeting in zebrafish. Yi chuan = Hereditas. 35(4):533-544