Jia Wang, Jianhua Gong, Li Li, Yanlin Chen, Lingfei Liu, HuaiTing Gu, Xiu Luo, Fang Hou, Jiajia Zhang and Ranran Song*, Neurexin gene family variants as risk factors for autism spectrum disorder, Autism Research, 2018, 11(1):37-43
Shanshan Shao, Rui Kong, Li Zou, Rong Zhong, Jiao Lou, Jie Zhou, Shengnan Guo, Jia Wang, Xiaohui Zhang, Jiajia Zhang, and Ranran Song*, The Roles of Genes in the Neuronal Migration and Neurite Outgrowth Network in Developmental Dyslexia: Single- and Multiple Risk-Genetic Variants, Mol Neurobiol, 2016, 53(6):3967-3975
Rui Kong, Shanshan Shao, Jia Wang, Xiaohui Zhang, Shengna Guon, Li Zou, Rong Zhong, Jiao Lou, Jie Zhou, Jiajia Zhang, and Ranan Song*, Genetic variant in DIP2A gene is associated with developmental dyslexia in Chinese population, Am J Med Genet B Neuropsychiatr Genet, 2016, 171(2): 203-208
Lingfei Liu, Jia Wang, Shanshan Shao, Xiu Luo, Rui Kong, Xiaohui Zhang, Ranran Song*, Descriptive Epidemiology of Prenatal and Perinatal Risk Factors in a Chinese Population with Reading Disorder; Sci Rep, 6, 36697; doi: 10.1038/srep36697, 2016 Nov 7
Zhen He, Shanshan Shao, Jie Zhou, Juntao Ke, Rui Kong, Shengnan Guo, Jiajia Zhang, and Ranran Song*. Does long time spending on the electronic devices affect the reading abilities? A cross-sectional study among Chinese school-aged children. Res Dev Disabil, 2014, 35(12): 3645-3654
Shanshan Shao, Sanqing Xu, Jun Yang, Ti Zhang, Zhen He, Zhao Sun, and Ranran Song*, A commonly carried genetic variant, rs9616915, in SHANK3 gene is associated with a reduced risk of autism spectrum disorder: replication in a Chinese population. Mol Biol Rep, 2014, 41(3), 1591-1595
Ranran Song*, Jiajia Zhang, Bo Wang, Hui Zhang, and Hanrong Wu, A near-infrared brain function study of Chinese dyslexic children, Neurocase, 2013,19(4),382-389
Li Zou, Wei Chen, Shanshan Shao, Zhao Sun, Rong Zhong, Junxin Shi, Xiaoping Miao, and Ranran Song*, Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis, Am J Med Genet B Neuropsychiatr Genet, 2012, 159B(8), 970-976