Show simple item record

dc.contributor.authorFalk, A
dc.contributor.authorHeine, V M
dc.contributor.authorHarwood, A J
dc.contributor.authorSullivan, P F
dc.contributor.authorPeitz, M
dc.contributor.authorBrüstle, O
dc.contributor.authorShen, S
dc.contributor.authorSun, Y-M
dc.contributor.authorGlover, J C
dc.contributor.authorPosthuma, D
dc.contributor.authorDjurovic, S
dc.date.accessioned2018-09-20T16:07:32Z
dc.date.available2018-09-20T16:07:32Z
dc.date.issued2016-05-31
dc.identifier.citationFalk, A; Heine, V M; Harwood, A J; Sullivan, P F; Peitz, M; Brüstle, O; Shen, S; Sun, Y-M; Glover, J C; Posthuma, D; Djurovic, S (2016). Modeling psychiatric disorders: from genomic findings to cellular phenotypes. Molecular Psychiatry 21 (9), 1167-1179
dc.identifier.issn1359-4184,1476-5578
dc.identifier.urihttp://hdl.handle.net/10379/11398
dc.description.abstractMajor programs in psychiatric genetics have identified 4150 risk loci for psychiatric disorders. These loci converge on a small number of functional pathways, which span conventional diagnostic criteria, suggesting a partly common biology underlying schizophrenia, autism and other psychiatric disorders. Nevertheless, the cellular phenotypes that capture the fundamental features of psychiatric disorders have not yet been determined. Recent advances in genetics and stem cell biology offer new prospects for cell-based modeling of psychiatric disorders. The advent of cell reprogramming and induced pluripotent stem cells (iPSC) provides an opportunity to translate genetic findings into patient-specific in vitro models. iPSC technology is less than a decade old but holds great promise for bridging the gaps between patients, genetics and biology. Despite many obvious advantages, iPSC studies still present multiple challenges. In this expert review, we critically review the challenges for modeling of psychiatric disorders, potential solutions and how iPSC technology can be used to develop an analytical framework for the evaluation and therapeutic manipulation of fundamental disease processes.
dc.publisherSpringer Nature
dc.relation.ispartofMolecular Psychiatry
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/ie/
dc.subjectpluripotent stem-cells
dc.subjectipsc-derived neurons
dc.subjectheterozygous reeler mouse
dc.subjectautism spectrum disorders
dc.subjectfibrillary acidic protein
dc.subjectde-novo mutations
dc.subjectgene-expression
dc.subjectrett-syndrome
dc.subjectneural development
dc.subjectmental-disorders
dc.titleModeling psychiatric disorders: from genomic findings to cellular phenotypes
dc.typeArticle
dc.identifier.doi10.1038/mp.2016.89
dc.local.publishedsourcehttp://doi.org/10.1038/mp.2016.89
nui.item.downloads0


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

Attribution-NonCommercial-NoDerivs 3.0 Ireland
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Ireland