ZFIN Person: Shen, Yan

ZFIN ID: ZDB-PERS-110923-2

Shen, Yan

Email:	yshen@pku.edu.cn
URL:
Affiliation:	PKU Zebrafish Functional Genomics Group
Address:	No 5 YiHeYuan Rd. Haidian District College of Life Sciences Peking University Beijing, 100871 China
Country:	China
Phone:
Fax:
ORCID ID:

BIOGRAPHY AND RESEARCH INTERESTS

PUBLICATIONS

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

NON-ZEBRAFISH PUBLICATIONS