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Cross-ancestry genome-wide association studies of brain imaging phenotypes.
Fu J, Zhang Q, Wang J, Wang M, Zhang B, Zhu W, Qiu S, Geng Z, Cui G, Yu Y, Liao W, Zhang H, Gao B, Xu X, Han T, Yao Z, Qin W, Liu F, Liang M, Wang S, Xu Q, Xu J, Zhang P, Li W, Shi D, Wang C, Lui S, Yan Z, Chen F, Zhang J, Li J, Shen W, Miao Y, Wang D, Xian J, Gao JH, Zhang X, Xu K, Zuo XN, Zhang L, Ye Z, Cheng J, Li MJ, Yu C; CHIMGEN Consortium. Fu J, et al. Among authors: qin w. Nat Genet. 2024 Jun;56(6):1110-1120. doi: 10.1038/s41588-024-01766-y. Epub 2024 May 29. Nat Genet. 2024. PMID: 38811844
MPZL1/PZR, a novel candidate predisposing schizophrenia in Han Chinese.
He G, Liu X, Qin W, Chen Q, Wang X, Yang Y, Zhou J, Xu Y, Gu N, Feng G, Sang H, Wang P, He L. He G, et al. Among authors: qin w. Mol Psychiatry. 2006 Aug;11(8):748-51. doi: 10.1038/sj.mp.4001841. Epub 2006 May 9. Mol Psychiatry. 2006. PMID: 16702974
Whole brain functional connectivity in the early blind.
Liu Y, Yu C, Liang M, Li J, Tian L, Zhou Y, Qin W, Li K, Jiang T. Liu Y, et al. Among authors: qin w. Brain. 2007 Aug;130(Pt 8):2085-96. doi: 10.1093/brain/awm121. Epub 2007 May 28. Brain. 2007. PMID: 17533167
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family.
Cheng J, Han DY, Dai P, Sun HJ, Tao R, Sun Q, Yan D, Qin W, Wang HY, Ouyang XM, Yang SZ, Cao JY, Feng GY, Du LL, Zhang YZ, Zhai SQ, Yang WY, Liu XZ, He L, Yuan HJ. Cheng J, et al. Among authors: qin w. Clin Genet. 2007 Nov;72(5):471-7. doi: 10.1111/j.1399-0004.2007.00889.x. Epub 2007 Sep 14. Clin Genet. 2007. PMID: 17868390
Brain anatomical network and intelligence.
Li Y, Liu Y, Li J, Qin W, Li K, Yu C, Jiang T. Li Y, et al. Among authors: qin w. PLoS Comput Biol. 2009 May;5(5):e1000395. doi: 10.1371/journal.pcbi.1000395. Epub 2009 May 29. PLoS Comput Biol. 2009. PMID: 19492086 Free PMC article.
5,332 results