{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,26]],"date-time":"2026-09-26T21:56:35Z","timestamp":1790459795035,"version":"4.1.0"},"reference-count":19,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2024,5,1]],"date-time":"2024-05-01T00:00:00Z","timestamp":1714521600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2024,5,1]],"date-time":"2024-05-01T00:00:00Z","timestamp":1714521600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2023,10,25]],"date-time":"2023-10-25T00:00:00Z","timestamp":1698192000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Schizophrenia Research"],"published-print":{"date-parts":[[2024,5]]},"DOI":"10.1016\/j.schres.2023.10.024","type":"journal-article","created":{"date-parts":[[2023,10,31]],"date-time":"2023-10-31T19:51:31Z","timestamp":1698781891000},"page":"470-472","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":9,"special_numbering":"C","title":["The translation of psychiatric genetic findings to the clinic"],"prefix":"10.1016","volume":"267","author":[{"given":"Kimberley Marie","family":"Kendall","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Donna","family":"Duffin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Joanne","family":"Doherty","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rachel","family":"Irving","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Annie","family":"Procter","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"James Tynan Rhys","family":"Walters","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"issue":"6","key":"10.1016\/j.schres.2023.10.024_bb0005","doi-asserted-by":"crossref","DOI":"10.1101\/cshperspect.a036608","article-title":"Evidence-based genetic counseling for psychiatric disorders: a road map","volume":"10","author":"Austin","year":"2020","journal-title":"Cold Spring Harb. Perspect. Med."},{"issue":"1","key":"10.1016\/j.schres.2023.10.024_bb0010","article-title":"P112: updated clinical practice guidelines for managing children and adults with 22q11.2 deletion syndrome","volume":"1","author":"Bassett","year":"2023","journal-title":"Genet. Med. Open"},{"issue":"1","key":"10.1016\/j.schres.2023.10.024_bb0015","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1001\/jamapsychiatry.2021.3392","article-title":"Comparing copy number variations in a Danish case cohort of individuals with psychiatric disorders","volume":"79","author":"Calle S\u00e1nchez","year":"2022","journal-title":"JAMA Psychiatry"},{"issue":"2","key":"10.1016\/j.schres.2023.10.024_bb0020","doi-asserted-by":"crossref","first-page":"110","DOI":"10.1016\/j.biopsych.2018.12.009","article-title":"Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases","volume":"86","author":"Charney","year":"2019","journal-title":"Biol. Psychiatry"},{"issue":"10","key":"10.1016\/j.schres.2023.10.024_bb0025","doi-asserted-by":"crossref","first-page":"1063","DOI":"10.1038\/ng.3092","article-title":"Refining analyses of copy number variation identifies specific genes associated with developmental delay","volume":"46","author":"Coe","year":"2014","journal-title":"Nat. Genet."},{"issue":"8","key":"10.1016\/j.schres.2023.10.024_bb0030","doi-asserted-by":"crossref","first-page":"599","DOI":"10.1038\/gim.2014.175","article-title":"Practical guidelines for managing adults with 22q11.2 deletion syndrome","volume":"17","author":"Fung","year":"2015","journal-title":"Genet. Med."},{"issue":"11","key":"10.1016\/j.schres.2023.10.024_bb0035","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pgen.1002334","article-title":"Relative burden of large CNVs on a range of neurodevelopmental phenotypes","volume":"7","author":"Girirajan","year":"2011","journal-title":"PLoS Genet."},{"issue":"6","key":"10.1016\/j.schres.2023.10.024_bb0040","doi-asserted-by":"crossref","first-page":"782","DOI":"10.1038\/nn.3708","article-title":"Large-scale genomics unveils the genetic architecture of psychiatric disorders","volume":"17","author":"Gratten","year":"2014","journal-title":"Nat. Neurosci."},{"issue":"6","key":"10.1016\/j.schres.2023.10.024_bb0045","doi-asserted-by":"crossref","first-page":"492","DOI":"10.1016\/j.biopsych.2017.08.017","article-title":"Heritability of schizophrenia and schizophrenia spectrum based on the Nationwide Danish Twin Register","volume":"83","author":"Hilker","year":"2018","journal-title":"Biol. Psychiatry"},{"key":"10.1016\/j.schres.2023.10.024_bb0050","doi-asserted-by":"crossref","DOI":"10.1001\/jamapsychiatry.2019.0566","article-title":"Association of rare copy number variants with risk of depression","author":"Kendall","year":"2019","journal-title":"JAMA Psychiatry"},{"issue":"7","key":"10.1016\/j.schres.2023.10.024_bb0055","doi-asserted-by":"crossref","first-page":"954","DOI":"10.1038\/s41593-021-00860-2","article-title":"Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions","volume":"24","author":"Levey","year":"2021","journal-title":"Nat. Neurosci."},{"issue":"5","key":"10.1016\/j.schres.2023.10.024_bb0060","doi-asserted-by":"crossref","first-page":"413","DOI":"10.1111\/j.1399-0004.2011.01636.x","article-title":"The Genetic Counseling Outcome Scale: a new patient-reported outcome measure for clinical genetics services","volume":"79","author":"McAllister","year":"2011","journal-title":"Clin. Genet."},{"issue":"5","key":"10.1016\/j.schres.2023.10.024_bb0065","doi-asserted-by":"crossref","first-page":"497","DOI":"10.1001\/archpsyc.60.5.497","article-title":"The heritability of bipolar affective disorder and the genetic relationship to unipolar depression","volume":"60","author":"McGuffin","year":"2003","journal-title":"Arch. Gen. Psychiatry"},{"issue":"2","key":"10.1016\/j.schres.2023.10.024_bb0070","doi-asserted-by":"crossref","first-page":"108","DOI":"10.1192\/bjp.bp.113.131052","article-title":"Analysis of copy number variations at 15 schizophrenia-associated loci","volume":"204","author":"Rees","year":"2014","journal-title":"Br. J. Psychiatry"},{"issue":"9","key":"10.1016\/j.schres.2023.10.024_bb0075","doi-asserted-by":"crossref","first-page":"963","DOI":"10.1001\/jamapsychiatry.2016.1831","article-title":"Analysis of intellectual disability copy number variants for association with schizophrenia","volume":"73","author":"Rees","year":"2016","journal-title":"JAMA Psychiatry"},{"issue":"7906","key":"10.1016\/j.schres.2023.10.024_bb0080","doi-asserted-by":"crossref","first-page":"509","DOI":"10.1038\/s41586-022-04556-w","article-title":"Rare coding variants in ten genes confer substantial risk for schizophrenia","volume":"604","author":"Singh","year":"2022","journal-title":"Nature"},{"issue":"10","key":"10.1016\/j.schres.2023.10.024_bb0085","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1176\/appi.ajp.157.10.1552","article-title":"Genetic epidemiology of major depression: review and meta-analysis","volume":"157","author":"Sullivan","year":"2000","journal-title":"Am. J. Psychiatry"},{"issue":"7906","key":"10.1016\/j.schres.2023.10.024_bb0090","doi-asserted-by":"crossref","first-page":"502","DOI":"10.1038\/s41586-022-04434-5","article-title":"Mapping genomic loci implicates genes and synaptic biology in schizophrenia","volume":"604","author":"Trubetskoy","year":"2022","journal-title":"Nature"},{"issue":"2","key":"10.1016\/j.schres.2023.10.024_bb0095","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1176\/appi.ajp.2011.11060822","article-title":"Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3","volume":"169","author":"Williams","year":"2012","journal-title":"Am. J. Psychiatry"}],"container-title":["Schizophrenia Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0920996423003857?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0920996423003857?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2026,5,12]],"date-time":"2026-05-12T10:24:38Z","timestamp":1778581478000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0920996423003857"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,5]]},"references-count":19,"alternative-id":["S0920996423003857"],"URL":"https:\/\/doi.org\/10.1016\/j.schres.2023.10.024","relation":{},"ISSN":["0920-9964"],"issn-type":[{"value":"0920-9964","type":"print"}],"subject":[],"published":{"date-parts":[[2024,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"The translation of psychiatric genetic findings to the clinic","name":"articletitle","label":"Article Title"},{"value":"Schizophrenia Research","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.schres.2023.10.024","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2023 The Authors. Published by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}