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1. Shi, W. *, Louzada, S.*, Grigorova, M., Massaia, A., Arciero, E., Kibena, L., Ge, X.J., Chen, Y., Ayub, Q., Poolamets, O., Tyler-Smith, C., Punab, M., Laan, M., Yang, F., Hallast, P., and Xue, Y. (2019). Evolutionary and functional analysis of RBMY1 gene copy number variation on the human Y chromosome. Hum Mol Genet 28, 2785-2798. (Co-first author)
2. Pinotti, T., Bergstrom, A., Geppert, M., Bawn, M., Ohasi, D., Shi, W., Lacerda, D.R., Solli, A., Norstedt, J., Reed, K., Dawtry, K., Gonzalez-Andrade, F., Paz, Y.M.C., Revollo, S., Cuellar, C., Jota, M.S., Santos, J.E., Jr., Ayub, Q., Kivisild, T., Sandoval, J.R., Fujita, R., Xue, Y., Roewer, L., Santos, F.R., and Tyler-Smith, C. (2019). Y Chromosome Sequences Reveal a Short Beringian Standstill, Rapid Expansion, and early Population structure of Native American Founders. Curr Biol 29, 149-157 e143.
3. Shi, W. *, Massaia, A. *, Louzada, S. *, Banerjee, R., Hallast, P., Chen, Y., Bergstrom, A., Gu, Y., Leonard, S., Quail, M.A., Ayub, Q., Yang, F., Tyler-Smith, C., and Xue, Y. (2018). Copy number variation arising from gene conversion on the human Y chromosome. Hum Genet 137, 73-83. (Co-first author)
4. Zhang, Y., Wei, F., Chen, C., Cai, C., Zhang, K., Sun, N., Tian, J., Shi, W., Zhang, M., Zang, Y., Song, J., He, Y., Feng, J., Zhou, Q., Li, M., Bai, P., Feng, S., and Li, W.D. (2018). Higher triglyceride level predicts hyperuricemia: A prospective study of 6-year follow-up. J Clin Lipidol 12, 185-192.
5. Yang, F.*, Gong, Q.*, Shi, W.*, Zou, Y.*, Shi, J., Wei, F., Li, Q., Chen, J., Li, W. D. Aberrant DNA methylation of acute myeloid leukemia and colorectal cancer in a Chinese pedigree with a MLL3 germline mutation[J]. Tumour Biol, 2016, 37(9): 12609-12618. (Co-first author)
6. Wei, F., Sun, N., Cai, C., Feng, S., Tian, J., Shi, W., Xu, W., Wang, Y., Yang, X., Li, W. D. Associations between serum uric acid and the incidence of hypertension: a Chinese senior dynamic cohort study[J]. J Transl Med, 2016, 14(1): 110.
7. Wei, F., Cai, C., Feng, S., Lv, J., Li, S., Chang, B., Zhang, H., Shi, W., Han, H., Ling, C., Yu, P., Chen, Y., Sun, N., Tian, J., Jiao, H., Yang, F., Li, M., Wang, Y., Zou, L., Su, L., Li, J., Li, R., Qiu, H., Shi, J., Liu, S., Chang, M., Lin, J., Chen, L., Li, W. D. TOX and CDKN2A/B Gene Polymorphisms Are Associated with Type 2 Diabetes in Han Chinese[J]. Sci Rep, 2015, 5: 11900.
8. Shi, W.*#, Cai, C. Y.*, Li, M. S., Ling, C., Li, W. D#. Han Chinese patients with dopa-responsive dystonia exhibit a low frequency of exonic deletion in the GCH1 gene[J]. Genet Mol Res, 2015, 14(3): 11185-11190. (Co-corresponding author)
9. Cai, C.*, Shi, W.*, Zeng, Z.*, Zhang, M., Ling, C., Chen, L., Zhang, B., Li, W. D. GTP cyclohydrolase I and tyrosine hydroxylase gene mutations in familial and sporadic dopa-responsive dystonia patients[J]. PLoS One, 2013, 8(6): e65215. (Co-first author)
10. Cai, C. Y.*, Zhu, H.*, Shi, W.*, Su, L.*, Shi, O., Cai, C. Q., Ling, C., Li, W. D. A novel splicing site mutation of the GPR143 gene in a Chinese X-linked ocular albinism pedigree[J]. Genet Mol Res, 2013,12(4): 5673-5679. (Co-first author)
11. Shi, W*., Ayub, Q., Vermeulen, M., Shao, R. G., Zuniga, S., van der Gaag, K., de Knijff, P., Kayser, M., Xue, Y., Tyler-Smith, C. A worldwide survey of human male demographic history based on Y-SNP and Y-STR data from the HGDP-CEPH
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