第一作者（含共同第一作者）及通讯作者论文（#共同第一作者，*共同通讯作者）：
1.Chang H., Cai X., Yang Z.H, Xiao X., Li M*. (2021) Regulation of TRANK1 by GSK-3 in the brain: unexpected interactions. Mol Psychiatry. Online ahead of print.（中科院JCR分区：医学1区；当年影响因子：12.384）
2.Chang H.#, Cai X.#, Li H.J.#, Liu W.P., Zhao L.J., Zhang C.Y., Wang J.Y., Liu J.W., Ma X.L., Wang L., Yao Y.G., Luo X.J., Li M.*, Xiao X.* (2021) Functional genomics identify a regulatory risk variation rs4420550 in the 16p11.2 schizophrenia-associated locus. Biol Psychiatry 89, 246-255. DOI: 10.1016/j.biopsych.2020.09.016.（封面论文；中科院JCR分区：医学1区；当年影响因子：12.095）
3.Chang H.#, Hoshina N.#, Zhang C.#, Ma Y., Cao H., Wang Y., Wu D.D., Bergen S.E., Landen M., Hultman C.M., Preisig M., Kutalik Z., Castelao E., Grigoroiu-Serbanescu M., Forstner A.J., Strohmaier J., Hecker J., Schulze T.G., Muller-Myhsok B., Reif A., Mitchell P.B., Martin N.G., Schofield P.R., Cichon S., Nothen M.M., Swedish Bipolar Study G., Moo D.S.B.C., Walter H., Erk S., Heinz A., Amin N., van Duijn C.M., Meyer-Lindenberg A., Tost H., Xiao X., Yamamoto T.*, Rietschel M.*, Li M.* (2018). The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders. Mol Psychiatry 23, 400-412. DOI: 10.1038/mp.2016.231.（中科院JCR分区：医学1区；当年影响因子：11.973）
4.Chang H.#, Xiao X.#, Li M.* (2017). The schizophrenia risk gene ZNF804A: clinical associations, biological mechanisms and neuronal functions. Mol Psychiatry 22, 944-953. DOI: 10.1038/mp.2017.19.（中科院JCR分区：医学1区；当年影响因子：11.64）
5.Cai X.#, Yang Z.H.#, Li H.J., Xiao X., Li M.*, Chang H.* (2021). A Human-Specific Schizophrenia Risk Tandem Repeat Affects Alternative Splicing of a Human-Unique Isoform AS3MTd2d3 and Mushroom Dendritic Spine Density. Schizophr Bull 47, 219-227. DOI: 10.1093/schbul/sbaa098.（中科院JCR分区：医学1区；当年影响因子：7.958）
6.Li W.#, Cai X.#, Li H.J.#, Song M.#, Zhang C.Y., Yang Y., Zhang L., Zhao L., Liu W., Wang L., Shao M., Zhang Y., Zhang C., Cai J., Zhou D.S., Li X., Hui L., Jia Q.F., Qu N., Zhong B.L., Zhang S.F., Chen J., Xia B., Li Y., Song X., Fan W., Tang W., Tang W., Tang J., Chen X., Yue W., Zhang D., Fang Y., Xiao X., Li M.*, Lv L.*, Chang H.* (2021). Independent replications and integrative analyses confirm TRANK1 as a susceptibility gene for bipolar disorder. Neuropsychopharmacology 46, 1103-1112. DOI: 10.1038/s41386-020-00788-4.（中科院JCR分区：医学1区；当年影响因子：6.751）
7.Li H.#, Chang H.#, Song X.#, Liu W., Li L., Wang L., Yang Y., Zhang L., Li W., Zhang Y., Zhou D.S., Li X., Zhang C., Fang Y., Sun Y., Dai J.P., Luo X.J., Yao Y.G., Xiao X.*, Lv L.*, Li M.* (2019). Integrative analyses of major histocompatibility complex loci in the genome-wide association studies of major depressive disorder. Neuropsychopharmacology 44, 1552-1561. DOI: 10.1038/s41386-019-0346-3.（中科院JCR分区：医学1区；当年影响因子：6.751）
8.Zhao L.#, Chang H.#, Zhou D.S.#, Cai J., Fan W., Tang W., Tang W., Li X., Liu W., Liu F., He Y., Bai Y., Sun Y., Dai J., Li L., Xiao X.*, Zhang C.*, Li M.* (2018). Replicated associations of FADS1, MAD1L1, and a rare variant at 10q26.13 with bipolar disorder in Chinese population. Transl Psychiatry 8, 270. DOI: 10.1038/s41398-018-0337-x.（中科院JCR分区：医学2区；当年影响因子：5.182）
9.Chang H.#, Li L.#, Peng T.#, Grigoroiu-Serbanescu M., Bergen S.E., Landen M., Hultman C.M., Forstner A.J., Strohmaier J., Hecker J., Schulze T.G., Muller-Myhsok B., Reif A., Mitchell P.B., Martin N.G., Cichon S., Nothen M.M., Jamain S., Leboyer M., Bellivier F., Etain B., Kahn J.P., Henry C., Rietschel M., Swedish Bipolar Study G., Moo D.S.C., Xiao X.*, Li M.* (2017). Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1. Mol Neurobiol 54, 5166-5176. DOI: 10.1007/s12035-016-0041-x.（中科院JCR分区：医学2区；当年影响因子：5.076）
10.Xiao X.#, Luo X.J.#, Chang H.#, Liu Z., Li M.* (2017). Evaluation of European Schizophrenia GWAS Loci in Asian Populations via Comprehensive Meta-Analyses. Mol Neurobiol 54, 4071-4080. DOI: 10.1007/s12035-016-9990-3.（中科院JCR分区：医学2区；当年影响因子：5.076）
11.Chang H., Li L., Li M.*, Xiao X.* (2017). Rare and common variants at 16p11.2 are associated with schizophrenia. Schizophr Res 184, 105-108. DOI: 10.1016/j.schres.2016.11.031.（中科院JCR分区：医学2区；当年影响因子：3.958）
12.Li H.#, Zhou D.S.#, Chang H.#, Wang L., Liu W., Dai S.X., Zhang C., Cai J., Liu W., Li X., Fan W., Tang W., Tang W., Liu F., He Y., Bai Y., Hu Z., Xiao X., Gao L.*, Li M.* (2019). Interactome Analyses implicated CAMK2A in the genetic predisposition and pharmacological mechanism of Bipolar Disorder. J Psychiatr Res 115, 165-175. DOI: 10.1016/j.jpsychires.2019.05.024.（中科院JCR分区：医学2区；当年影响因子：3.745）
13.Chang H.#, Yi B.#, Ma R., Zhang X., Zhao H., Xi Y.* (2016). CRISPR/cas9, a novel genomic tool to knock down microRNA in vitro and in vivo. Sci Rep 6, 22312. DOI: 10.1038/srep22312.（中科院JCR分区：综合性期刊3区；当年影响因子：4.259）
14.Chang H.#, Li L.#, Peng T., Li M.*, Gao L.*, Xiao X.* (2016). Replication analyses of four chromosomal deletions with schizophrenia via independent large-scale meta-analyses. Am J Med Genet B Neuropsychiatr Genet 171, 1161-1169. DOI: 10.1002/ajmg.b.32502.（中科院JCR分区：医学3区；当年影响因子：3.258）
15.Chang H.#, Zhang C.*, Xiao X., Pu X., Liu Z., Wu L., Li M.* (2016). Further evidence of VRK2 rs2312147 associated with schizophrenia. World J Biol Psychiatry 17, 457-466. DOI: 10.1080/15622975.2016.1200746.（中科院JCR分区：医学3区；当年影响因子：3.658）
其他作者论文：
1.Li H.J., Qu N., Hui L., Cai X., Zhang C.Y., Zhong B.L., Zhang S.F., Chen J., Xia B., Wang L., Jia Q.F., Li W., Chang H., Xiao X., Li M., Li Y. (2020). Further confirmation of netrin 1 receptor (DCC) as a depression risk gene via integrations of multi-omics data. Transl Psychiatry 10, 98. DOI: 10.1038/s41398-020-0777-y.
2.Liu W., Li W., Cai X., Yang Z., Li H., Su X., Song M., Zhou D.S., Li X., Zhang C., Shao M., Zhang L., Yang Y., Zhang Y., Zhao J., Chang H., Yao Y.G., Fang Y., Lv L., Li M., Xiao X. (2020). Identification of a functional human-unique 351-bp Alu insertion polymorphism associated with major depressive disorder in the 1p31.1 GWAS risk loci. Neuropsychopharmacology 45, 1196-1206. DOI: 10.1038/s41386-020-0659-2.
3.Yang Z.H., Cai X., Qu N., Zhao L.J., Zhong B.L., Zhang S.F., Chen J., Xia B., Jiang H.Y., Zhou D.Y., Liu W.P., Chang H., Xiao X., Li Y., Li M. (2019). Identification of a functional 339-bp Alu insertion polymorphism in the schizophrenia-associated locus at 10q24.32. Zool Res, 1-7. DOI: 10.24272/j.issn.2095-8137.2020.014.
4.Yang Z., Zhou D., Li H., Cai X., Liu W., Wang L., Chang H., Li M., Xiao X. (2020). The genome-wide risk alleles for psychiatric disorders at 3p21.1 show convergent effects on mRNA expression, cognitive function, and mushroom dendritic spine. Mol Psychiatry 25, 48-66. DOI: 10.1038/s41380-019-0592-0.
5.Yang Y., Wang L., Li L., Li W., Zhang Y., Chang H., Xiao X., Li M., Lv L. (2018). Genetic association and meta-analysis of a schizophrenia GWAS variant rs10489202 in East Asian populations. Transl Psychiatry 8, 144. DOI: 10.1038/s41398-018-0211-x.
6.Xiao X., Zhang C., Grigoroiu-Serbanescu M., Wang L., Li L., Zhou D., Yuan T.F., Wang C., Chang H., Wu Y., Li Y., Wu D.D., Yao Y.G., Li M. (2018). The cAMP responsive element-binding (CREB)-1 gene increases risk of major psychiatric disorders. Mol Psychiatry 23, 1957-1967. DOI: 10.1038/mp.2017.243.
7.Xiao X., Zheng F., Chang H., Ma Y., Yao Y.G., Luo X.J., Li M. (2018). The Gene Encoding Protocadherin 9 (PCDH9), a Novel Risk Factor for Major Depressive Disorder. Neuropsychopharmacology 43, 1128-1137. DOI: 10.1038/npp.2017.241.
8.Xiao X., Yu H., Li J., Wang L., Li L., Chang H., Zhang D., Yue W., Li M. (2017). Further evidence for the association between LRP8 and schizophrenia. Schizophr Res. DOI: 10.1016/j.schres.2017.05.002.
