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Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes.
Liu N, Zhang L, Tian T, Cheng J, Zhang B, Qiu S, Geng Z, Cui G, Zhang Q, Liao W, Yu Y, Zhang H, Gao B, Xu X, Han T, Yao Z, Qin W, Liu F, Liang M, Xu Q, Fu J, Xu J, Zhu W, Zhang P, Li W, Shi D, Wang C, Lui S, Yan Z, Chen F, Li J, Zhang J, Wang D, Shen W, Miao Y, Xian J, Gao JH, Zhang X, Li MJ, Xu K, Zuo XN, Wang M, Ye Z, Yu C; CHIMGEN Consortium. Liu N, et al. Among authors: qin w. Nat Genet. 2023 Jul;55(7):1126-1137. doi: 10.1038/s41588-023-01425-8. Epub 2023 Jun 19. Nat Genet. 2023. PMID: 37337106
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
5,270 results