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Association of DISC1 Polymorphisms with Late-Onset Alzheimer’s Disease in Northern Han Chinese

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Abstract

The disrupted-in-schizophrenia-1 (DISC1) is a candidate gene for psychiatric diseases and plays various roles in brain development. It has been reported as a candidate gene for Alzheimer's disease (AD) in a recent large genome-wide association study in Caucasians. To explore the associations between DISC1 and AD, we performed a case–control study including 2318 subjects in Northern Han Chinese. We found that one single nucleotide polymorphism (rs6675281) was associated with the risk of late-onset Alzheimer’s disease (LOAD) in northern Han Chinese population. As for rs821616 and rs3738401, no association was detected with LOAD. In conclusion, DISC1 increased the risk for LOAD in northern Han Chinese population.

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Acknowledgments

This work was supported by grants from the National Natural Science Foundation of China (81471309, 81371406, 81571245, and 81501103), the Shandong Provincial Outstanding Medical Academic Professional Program, Qingdao Key Health Discipline Development Fund, Qingdao Outstanding Health Professional Development Fund, and Shandong Provincial Collaborative Innovation Center for Neurodegenerative Disorders.

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Correspondence to Lan Tan or Jin-Tai Yu.

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The authors declare that they no conflicts of interest.

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Xiao-Yan Zhang and Hui-Fu Wang are both co-first authors.

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Zhang, XY., Wang, HF., Tan, MS. et al. Association of DISC1 Polymorphisms with Late-Onset Alzheimer’s Disease in Northern Han Chinese. Mol Neurobiol 54, 2922–2927 (2017). https://doi.org/10.1007/s12035-016-9881-7

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  • DOI: https://doi.org/10.1007/s12035-016-9881-7

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