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Items: 14


Genome-wide differential expression of synaptic long noncoding RNAs in autism spectrum disorder.

Wang Y, Zhao X, Ju W, Flory M, Zhong J, Jiang S, Wang P, Dong X, Tao X, Chen Q, Shen C, Zhong M, Yu Y, Brown WT, Zhong N.

Transl Psychiatry. 2015 Oct 20;5:e660. doi: 10.1038/tp.2015.144.


The Impact of Neuroimmune Alterations in Autism Spectrum Disorder.

Gottfried C, Bambini-Junior V, Francis F, Riesgo R, Savino W.

Front Psychiatry. 2015 Sep 9;6:121. doi: 10.3389/fpsyt.2015.00121. Review.


Shared Pathways Among Autism Candidate Genes Determined by Co-expression Network Analysis of the Developing Human Brain Transcriptome.

Mahfouz A, Ziats MN, Rennert OM, Lelieveldt BP, Reinders MJ.

J Mol Neurosci. 2015 Dec;57(4):580-94. doi: 10.1007/s12031-015-0641-3.


A critical role of RBM8a in proliferation and differentiation of embryonic neural progenitors.

Zou D, McSweeney C, Sebastian A, Reynolds DJ, Dong F, Zhou Y, Deng D, Wang Y, Liu L, Zhu J, Zou J, Shi Y, Albert I, Mao Y.

Neural Dev. 2015 Jun 21;10:18. doi: 10.1186/s13064-015-0045-7.


Genomics in neurological disorders.

Han G, Sun J, Wang J, Bai Z, Song F, Lei H.

Genomics Proteomics Bioinformatics. 2014 Aug;12(4):156-63. doi: 10.1016/j.gpb.2014.07.002. Review.


Development of a versatile enrichment analysis tool reveals associations between the maternal brain and mental health disorders, including autism.

Eisinger BE, Saul MC, Driessen TM, Gammie SC.

BMC Neurosci. 2013 Nov 19;14:147. doi: 10.1186/1471-2202-14-147.


SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).

Abrahams BS, Arking DE, Campbell DB, Mefford HC, Morrow EM, Weiss LA, Menashe I, Wadkins T, Banerjee-Basu S, Packer A.

Mol Autism. 2013 Oct 3;4(1):36. doi: 10.1186/2040-2392-4-36.


Genetic studies of complex human diseases: characterizing SNP-disease associations using Bayesian networks.

Han B, Chen XW, Talebizadeh Z, Xu H.

BMC Syst Biol. 2012;6 Suppl 3:S14. doi: 10.1186/1752-0509-6-S3-S14.


Biological databases for behavioral neurobiology.

Baker EJ.

Int Rev Neurobiol. 2012;103:19-38. doi: 10.1016/B978-0-12-388408-4.00002-2. Review.


AutismKB: an evidence-based knowledgebase of autism genetics.

Xu LM, Li JR, Huang Y, Zhao M, Tang X, Wei L.

Nucleic Acids Res. 2012 Jan;40(Database issue):D1016-22. doi: 10.1093/nar/gkr1145.


ADHDgene: a genetic database for attention deficit hyperactivity disorder.

Zhang L, Chang S, Li Z, Zhang K, Du Y, Ott J, Wang J.

Nucleic Acids Res. 2012 Jan;40(Database issue):D1003-9. doi: 10.1093/nar/gkr992.


An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males.

Chung RH, Ma D, Wang K, Hedges DJ, Jaworski JM, Gilbert JR, Cuccaro ML, Wright HH, Abramson RK, Konidari I, Whitehead PL, Schellenberg GD, Hakonarson H, Haines JL, Pericak-Vance MA, Martin ER.

Mol Autism. 2011 Nov 4;2(1):18. doi: 10.1186/2040-2392-2-18.


Variability in the incidence of miRNAs and genes in fragile sites and the role of repeats and CpG islands in the distribution of genetic material.

Laganà A, Russo F, Sismeiro C, Giugno R, Pulvirenti A, Ferro A.

PLoS One. 2010 Jun 17;5(6):e11166. doi: 10.1371/journal.pone.0011166.

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