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dc.contributor.authorHall, Nicola A
dc.contributor.authorTunbridge, Elizabeth
dc.date.accessioned2021-08-24T10:05:54Z
dc.date.available2021-08-24T10:05:54Z
dc.date.issued2021-08
dc.identifier.citationArne W. Mould, Nicola A. Hall, Ira Milosevic, Elizabeth M. Tunbridge, Targeting synaptic plasticity in schizophrenia: insights from genomic studies, Trends in Molecular Medicine, 2021en
dc.identifier.urihttps://oxfordhealth-nhs.archive.knowledgearc.net/handle/123456789/935
dc.descriptionContact the library for a copy of this articleen
dc.description.abstractRecent genomic findings identify many hundreds of genomic loci that are associated with schizophrenia. Consistent with data from the pregenomic era, genomic findings implicate synaptic function and plasticity as a tractable therapeutic target for the cognitive dysfunction and negative symptoms that patients experience. Genomic findings have the potential to provide insights into the nature of synaptic dysfunction in schizophrenia, and to identify novel therapeutic targets, but identifying the most promising candidates remains a challenge. We propose an integrated approach to triaging the long list of potential genomic targets and provide six practical criteria that we use to prioritise putative candidates.en
dc.description.sponsorshipSupported by the NIHRen
dc.description.urihttps://doi.org/10.1016/j.molmed.2021.07.014en
dc.language.isoenen
dc.subjectSchizophreniaen
dc.titleTargeting synaptic plasticity in schizophrenia: insights from genomic studiesen
dc.typeArticleen


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