Journal Publications

• [41]et al, Zuo LJ, Xun GL, Hu ZM, Guo H, Xia K.Common variants on 1p13.2 associate with risk of autism.Mol Psychiatr, 2014, 19 (11) : 1212-1219.
• [42]et al, Liu YL, Wang TY, Peng Y, Tong P, Guo H.Homozygous loss-of-function mutation of the LEPREL1 gene causes severe non-syndromic high myopia with early-onset cataract.Clin Genet., 2014, 86 (6) : 575-579.
• [43]et al, Zhu TF, Jin XM, Guo H.SLC39A5 mutations interfering BMP/TGF-β pathway in nonsyndromic high myopia.J Med Genet, 2014, 51 (8) : 518-525.
• [44]et al, Liu YL, Xun GL, Peng Y, Guo H, Lu LN.Common and rare variants of THBS1 gene associated with the risk of autism.Psychiat Genet, 2014, 24 (6) : 235-240.
• [45]et al, Lu L, Liu Y, Zhang L, Xiong Z, Xu X.Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.Mol Biol Rep, 2014, 41 (6) : 4133-4140.
• [46]et al, Xiong ZM, Xiang XY, Peng Y, Xun GL, Guo H.Disruption of Contactin 4 in two subjects with autism in Chinese population.Gene, 2012, 505 (2) : 201-205.
• [47]et al, Lu L, Xue J, Xu M, Peng D, Guo H.Report of two FOP cases with 617G>A mutation in the ACVR1 gene from Chinese population.Clin Dysmorphol, 2010, 19 (4) : 206-208.