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Mutation analysis of the NRXN1 gene in a Chinese autism cohort.
Liu Y, Hu Z, Xun G, Peng Y, Lu L, Xu X, Xiong Z, Xia L, Liu D, Li W, Zhao J, Xia K. Liu Y, et al. J Psychiatr Res. 2012 May;46(5):630-4. doi: 10.1016/j.jpsychires.2011.10.015. Epub 2012 Mar 9. J Psychiatr Res. 2012. PMID: 22405623
Abnormal regional spontaneous neural activity in first-episode, treatment-naive patients with late-life depression: a resting-state fMRI study.
Liu F, Hu M, Wang S, Guo W, Zhao J, Li J, Xun G, Long Z, Zhang J, Wang Y, Zeng L, Gao Q, Wooderson SC, Chen J, Chen H. Liu F, et al. Prog Neuropsychopharmacol Biol Psychiatry. 2012 Dec 3;39(2):326-31. doi: 10.1016/j.pnpbp.2012.07.004. Epub 2012 Jul 10. Prog Neuropsychopharmacol Biol Psychiatry. 2012. PMID: 22796277
Common genetic variants on 1p13.2 associate with risk of autism.
Xia K, Guo H, Hu Z, Xun G, Zuo L, Peng Y, Wang K, He Y, Xiong Z, Sun L, Pan Q, Long Z, Zou X, Li X, Li W, Xu X, Lu L, Liu Y, Hu Y, Tian D, Long L, Ou J, Liu Y, Li X, Zhang L, Pan Y, Chen J, Peng H, Liu Q, Luo X, Su W, Wu L, Liang D, Dai H, Yan X, Feng Y, Tang B, Li J, Miedzybrodzka Z, Xia J, Zhang Z, Luo X, Zhang X, St Clair D, Zhao J, Zhang F. Xia K, et al. Mol Psychiatry. 2014 Nov;19(11):1212-9. doi: 10.1038/mp.2013.146. Epub 2013 Nov 5. Mol Psychiatry. 2014. PMID: 24189344
40 results