{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T01:53:08Z","timestamp":1790733188673,"version":"4.1.0"},"reference-count":94,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2018,4,1]],"date-time":"2018-04-01T00:00:00Z","timestamp":1522540800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","medical-hypotheses.com","clinicalkey.com","clinicalkey.es","clinicalkey.fr","clinicalkey.com.au","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Medical Hypotheses"],"published-print":{"date-parts":[[2018,4]]},"DOI":"10.1016\/j.mehy.2018.02.009","type":"journal-article","created":{"date-parts":[[2018,2,15]],"date-time":"2018-02-15T18:18:26Z","timestamp":1518718706000},"page":"54-64","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":20,"special_numbering":"C","title":["Molecular hypotheses to explain the shared pathways and underlying pathobiological causes in catatonia and in catatonic presentations in neuropsychiatric disorders"],"prefix":"10.1016","volume":"113","author":[{"given":"E.M.","family":"Peter-Ross","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.mehy.2018.02.009_b0005","series-title":"The future of the brain: essays by the world\u2019s leading neuroscientists","first-page":"234","article-title":"The miswired brain, genes, and mental illness","author":"Kevin","year":"2015"},{"key":"10.1016\/j.mehy.2018.02.009_b0010","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1111\/acps.12038","article-title":"Rediscovering catatonia: the biography of a treatable syndrome","volume":"441","author":"Fink","year":"2013","journal-title":"Acta Psychiatr Scand Suppl"},{"key":"10.1016\/j.mehy.2018.02.009_b0015","doi-asserted-by":"crossref","first-page":"825","DOI":"10.1136\/jnnp-2014-309098","article-title":"Movement disorders in catatonia","volume":"86","author":"Wijemanne","year":"2015","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"10.1016\/j.mehy.2018.02.009_b0020","series-title":"Diagnostic and Statistical Manual of Mental Disorders (DSM-V)","author":"American Psychiatric Association","year":"2013"},{"issue":"4","key":"10.1016\/j.mehy.2018.02.009_b0025","doi-asserted-by":"crossref","first-page":"391","DOI":"10.5498\/wjp.v6.i4.391","article-title":"Catatonia: our current understanding of its diagnosis, treatment and pathophysiology","volume":"6","author":"Rasmussen","year":"2016","journal-title":"World J Psychiatr"},{"issue":"5","key":"10.1016\/j.mehy.2018.02.009_b0030","first-page":"1","article-title":"A clinical review of the treatment of catatonia","volume":"12","author":"Sienaert","year":"2014","journal-title":"Front Psychiatry"},{"issue":"7","key":"10.1016\/j.mehy.2018.02.009_b0035","doi-asserted-by":"crossref","first-page":"58","DOI":"10.1017\/S1092852900013419","article-title":"An analysis of 17 catatonic patients diagnosed with neuroleptic malignant syndrome","volume":"5","author":"White","year":"2000","journal-title":"CNS Spectr"},{"key":"10.1016\/j.mehy.2018.02.009_b0040","doi-asserted-by":"crossref","first-page":"1222","DOI":"10.4088\/JCP.10m06438","article-title":"An International consensus study of neuroleptic malignant syndrome diagnostic criteria using the Delphi method","volume":"72","author":"Gurrera","year":"2011","journal-title":"J Clin Psychiatry"},{"issue":"2","key":"10.1016\/j.mehy.2018.02.009_b0045","doi-asserted-by":"crossref","DOI":"10.1093\/schbul\/sbp105","article-title":"The catatonia conundrum: evidence of psychomotor phenomena as a symptom dimension in psychotic disorders","volume":"36","author":"Ungvari","year":"2010","journal-title":"Schizophr Bull"},{"issue":"157","key":"10.1016\/j.mehy.2018.02.009_b0050","first-page":"1","article-title":"Decalogue of catatonia in autism spectrum disorders","volume":"5","author":"Dhossche","year":"2014","journal-title":"Front Psychiatry"},{"issue":"255","key":"10.1016\/j.mehy.2018.02.009_b0055","doi-asserted-by":"crossref","first-page":"215","DOI":"10.1016\/j.psychres.2017.05.039","article-title":"Catatonia in an inpatient gerontopsychiatric population","volume":"9","author":"Takacs","year":"2017","journal-title":"Psychiatry Res"},{"key":"10.1016\/j.mehy.2018.02.009_b0060","doi-asserted-by":"crossref","first-page":"1201","DOI":"10.1016\/S0002-9297(07)62950-4","article-title":"Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15","volume":"67","author":"St\u00f6ber","year":"2000","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.mehy.2018.02.009_b0065","doi-asserted-by":"crossref","first-page":"323","DOI":"10.1007\/s00439-002-0805-4","article-title":"Periodic catatonia: confirmation of linkage to chromosome 15 and further genetic evidence for genetic heterogeneity","volume":"111","author":"St\u00f6ber","year":"2002","journal-title":"Hum Genet"},{"key":"10.1016\/j.mehy.2018.02.009_b0070","doi-asserted-by":"crossref","first-page":"421","DOI":"10.1038\/nature13595","article-title":"Biological insights from 108 schizophrenia-associated genetic loci","volume":"511","author":"Schizophrenia Working Group of the Psychiatric Genomics Consortium","year":"2014","journal-title":"Nature"},{"issue":"9","key":"10.1016\/j.mehy.2018.02.009_b0075","doi-asserted-by":"crossref","first-page":"436","DOI":"10.1016\/j.ejmg.2016.08.003","article-title":"Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing factor","volume":"59","author":"Breckpot","year":"2016","journal-title":"Eur J Med Genet"},{"key":"10.1016\/j.mehy.2018.02.009_b0080","doi-asserted-by":"crossref","first-page":"387","DOI":"10.1093\/hmg\/ddq471","article-title":"Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries","volume":"20","author":"Williams","year":"2011","journal-title":"Hum Mol Genet"},{"issue":"4","key":"10.1016\/j.mehy.2018.02.009_b0085","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1002\/wrna.1417","article-title":"Box C\/D small nucleolar RNA genes and the Prader-Willi syndrome: a complex interplay","volume":"8","author":"Cavaill\u00e9","year":"2017","journal-title":"Wiley Interdiscip Rev RNA"},{"key":"10.1016\/j.mehy.2018.02.009_b0090","doi-asserted-by":"crossref","first-page":"1153","DOI":"10.1093\/hmg\/ddp585","article-title":"The snoRNA MBII-52 (SNORD 115) is processed into smaller RNAs and regulates alternative splicing","volume":"19","author":"Kishore","year":"2010","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.mehy.2018.02.009_b0095","doi-asserted-by":"crossref","first-page":"230","DOI":"10.1126\/science.1118265","article-title":"The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C","volume":"311","author":"Kishore","year":"2006","journal-title":"Science"},{"issue":"5","key":"10.1016\/j.mehy.2018.02.009_b0100","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1371\/journal.pgen.1005993","article-title":"Parental origin of interstitial duplication at 15q11.2-q13.3 in schizophrenia and neurodevelopmental disorders","volume":"12","author":"Isles","year":"2016","journal-title":"PLoS Genet"},{"issue":"4","key":"10.1016\/j.mehy.2018.02.009_b0105","doi-asserted-by":"crossref","first-page":"247","DOI":"10.3109\/10401239709147805","article-title":"Catatonia with Prader-Willi Syndrome","volume":"9","author":"Dhossche","year":"1997","journal-title":"Ann Clin Psychiatry"},{"issue":"5","key":"10.1016\/j.mehy.2018.02.009_b0110","doi-asserted-by":"crossref","first-page":"545","DOI":"10.1002\/aur.1469","article-title":"Neuroanatomical phenotypes are consistent with autism-like behavioral phenotypes in the 15q11-13 duplication mouse models","volume":"8","author":"Ellegood","year":"2015","journal-title":"Autism Res"},{"key":"10.1016\/j.mehy.2018.02.009_b0115","doi-asserted-by":"crossref","first-page":"1235","DOI":"10.1016\/j.cell.2009.04.024","article-title":"Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism","volume":"137","author":"Nakatani","year":"2009","journal-title":"Cell"},{"issue":"12","key":"10.1016\/j.mehy.2018.02.009_b0120","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1371\/journal.pone.0015126","article-title":"Decreased exploratory activity in a mouse model of 15q duplication syndrome; implications for disturbance of serotonin signaling","volume":"5","author":"Tamada","year":"2010","journal-title":"PLoS One"},{"issue":"17","key":"10.1016\/j.mehy.2018.02.009_b0125","first-page":"1","article-title":"DNA methylation differences in monozygotic twin pairs discordant for schizophrenia identifies psychosis related genes and networks","volume":"8","author":"Castellani","year":"2015","journal-title":"BMC Med Genomics"},{"issue":"7","key":"10.1016\/j.mehy.2018.02.009_b0130","first-page":"1","article-title":"Insights into the origin of DNA methylation differences between monozygotic twins discordant for schizophrenia","volume":"3","author":"Melka","year":"2015","journal-title":"J Mol Psychiatry"},{"key":"10.1016\/j.mehy.2018.02.009_b0135","doi-asserted-by":"crossref","first-page":"827","DOI":"10.1038\/mp.2011.78","article-title":"Imprinted DLK1-DIO3 region of 14q32 defines a schizophrenia-associated miRNA signature in peripheral blood mononuclear cells","volume":"17","author":"Gardiner","year":"2012","journal-title":"Mol Psychiatry"},{"key":"10.1016\/j.mehy.2018.02.009_b0140","doi-asserted-by":"crossref","first-page":"551","DOI":"10.1038\/ng.2968","article-title":"The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome","volume":"46","author":"Stelzer","year":"2014","journal-title":"Nat Genet"},{"key":"10.1016\/j.mehy.2018.02.009_b0145","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1007\/s00406-013-0479-z","article-title":"Neuropathological changes in the substantia nigra in schizophrenia but not depression","volume":"264","author":"Williams","year":"2014","journal-title":"Eur Arch Psychiatry Clin Neurosci"},{"issue":"1","key":"10.1016\/j.mehy.2018.02.009_b0150","doi-asserted-by":"crossref","first-page":"38","DOI":"10.1111\/ahg.12135","article-title":"Practical experience of the application of a weighted burden test to whole exome sequence data for obesity and schizophrenia","volume":"80","author":"Curtis","year":"2016","journal-title":"Ann Hum Genet"},{"issue":"2","key":"10.1016\/j.mehy.2018.02.009_b0155","doi-asserted-by":"crossref","first-page":"220","DOI":"10.1038\/mp.2013.129","article-title":"HPA axis genetic variation, cortisol and psychosis in major depression","volume":"19","author":"Schatzberg","year":"2014","journal-title":"Mol Psychiatry"},{"key":"10.1016\/j.mehy.2018.02.009_b0160","doi-asserted-by":"crossref","first-page":"402","DOI":"10.1038\/nature11436","article-title":"Severe stress switches CRF action in the nucleus accumbens from appetitive to aversive","volume":"490","author":"Lemos","year":"2012","journal-title":"Nature"},{"issue":"7618","key":"10.1016\/j.mehy.2018.02.009_b0165","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1038\/nature19318","article-title":"Serotonin engages an anxiety and fear-promoting circuit in the extended amygdala","volume":"537","author":"Marcinkiewcz","year":"2016","journal-title":"Nature"},{"issue":"2","key":"10.1016\/j.mehy.2018.02.009_b0170","doi-asserted-by":"crossref","first-page":"744","DOI":"10.1016\/j.jad.2013.08.012","article-title":"Association between OPCRIT dimensions and polymorphisms of HPA axis genes in bipolar disorder","volume":"151","author":"Leszczy\u0144ska-Rodziewicz","year":"2013","journal-title":"J Affect Disord"},{"key":"10.1016\/j.mehy.2018.02.009_b0175","doi-asserted-by":"crossref","first-page":"1374","DOI":"10.1093\/schbul\/sbu027","article-title":"Reduced levels of vasopressin and reduced behavioral modulation of oxytocin in psychotic disorders","volume":"40","author":"Rubin","year":"2014","journal-title":"Schizophr Bull"},{"issue":"516","key":"10.1016\/j.mehy.2018.02.009_b0180","first-page":"1","article-title":"ASD and genetic associations with receptors for oxytocin and vasopressin-AVPR1A, AVPR1B, and OXTR","volume":"10","author":"Francis","year":"2016","journal-title":"Front Neurosci"},{"issue":"1","key":"10.1016\/j.mehy.2018.02.009_b0185","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1371\/journal.pone.0055119","article-title":"The spectrum of SWI\/SNF mutations, ubiquitous in human cancers","volume":"8","author":"Shain","year":"2013","journal-title":"PLoS One"},{"key":"10.1016\/j.mehy.2018.02.009_b0190","doi-asserted-by":"crossref","first-page":"128","DOI":"10.1038\/ng.523","article-title":"Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1","volume":"42","author":"MacMahon","year":"2010","journal-title":"Nat Genet"},{"key":"10.1016\/j.mehy.2018.02.009_b0195","doi-asserted-by":"crossref","first-page":"645","DOI":"10.1016\/j.biopsych.2012.02.040","article-title":"Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder","volume":"72","author":"Vassos","year":"2012","journal-title":"Biol Psychiatry"},{"issue":"12","key":"10.1016\/j.mehy.2018.02.009_b0200","doi-asserted-by":"crossref","first-page":"2324","DOI":"10.4161\/15548627.2014.984274","article-title":"New horizons in schizophrenia treatment: autophagy protection is coupled with behavioral improvements in a mouse model of schizophrenia","volume":"10","author":"Merenlender-Wagner","year":"2014","journal-title":"Autophagy"},{"issue":"4","key":"10.1016\/j.mehy.2018.02.009_b0205","doi-asserted-by":"crossref","first-page":"380","DOI":"10.1038\/ng.2899","article-title":"A SWI\/SNF-related autism syndrome caused by de novo mutations in ADNP","volume":"46","author":"Helsmoortel","year":"2014","journal-title":"Nat Genet"},{"key":"10.1016\/j.mehy.2018.02.009_b0210","doi-asserted-by":"crossref","first-page":"1275","DOI":"10.4161\/auto.21153","article-title":"Atg11: a Rab-dependent, coiled-coil membrane protein that acts as a tether for autophagy","volume":"8","author":"Backues","year":"2012","journal-title":"Autophagy"},{"key":"10.1016\/j.mehy.2018.02.009_b0215","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1016\/j.neubiorev.2014.11.005","article-title":"Mitochondrial dysfunction in schizophrenia: pathways, mechanisms and implications","volume":"48","author":"Rajasekaran","year":"2015","journal-title":"Neurosci Biobehav Rev"},{"key":"10.1016\/j.mehy.2018.02.009_b0220","doi-asserted-by":"crossref","first-page":"539","DOI":"10.1038\/nature09639","article-title":"Exome sequencing identifies frequent mutation of the SWI\/SNF complex gene PBRM1 in renal carcinoma","volume":"469","author":"Varela","year":"2011","journal-title":"Nature"},{"key":"10.1016\/j.mehy.2018.02.009_b0225","doi-asserted-by":"crossref","first-page":"309","DOI":"10.1016\/j.biochi.2008.10.019","article-title":"Polybromo-1: the chromatin targeting subunit of the PBAF complex","volume":"91","author":"Thompson","year":"2009","journal-title":"Biochimie"},{"key":"10.1016\/j.mehy.2018.02.009_b0230","doi-asserted-by":"crossref","first-page":"13246","DOI":"10.1523\/JNEUROSCI.2661-11.2011","article-title":"Corticotrophin-releasing hormone receptor type 1 (CRHR1) genetic variation and stress interact to influence reward learning","volume":"31","author":"Bogdan","year":"2011","journal-title":"J Neurosci"},{"key":"10.1016\/j.mehy.2018.02.009_b0235","doi-asserted-by":"crossref","first-page":"2483","DOI":"10.1093\/hmg\/ddp166","article-title":"Involvement of SMARCA2\/BRM in the SWI\/SNF chromatin-remodeling complex in schizophrenia","volume":"18","author":"Koga","year":"2009","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.mehy.2018.02.009_b0240","doi-asserted-by":"crossref","first-page":"2841","DOI":"10.1093\/hmg\/ddq184","article-title":"SMARCA2 and other genome-wide supported schizophrenia-associated genes: regulation by REST\/NRSF, network organization and primate-specific evolution","volume":"19","author":"Loe-Mie","year":"2010","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.mehy.2018.02.009_b0245","doi-asserted-by":"crossref","first-page":"92","DOI":"10.4161\/trns.19783","article-title":"A novel TBP-TAF complex on RNA polymerase II-transcribed snRNA genes","volume":"3","author":"Zaborowska","year":"2012","journal-title":"Transcription"},{"issue":"16","key":"10.1016\/j.mehy.2018.02.009_b0250","doi-asserted-by":"crossref","first-page":"3205","DOI":"10.1007\/s00018-016-2159-4","article-title":"Evidence of TAF1 dysfunction in peripheral models of x-linked dystonia-parkinsonism","volume":"73","author":"Domingo","year":"2016","journal-title":"Cell Mol Life Sci"},{"issue":"5","key":"10.1016\/j.mehy.2018.02.009_b0255","doi-asserted-by":"crossref","first-page":"680","DOI":"10.1111\/ene.13256","article-title":"Striatal dysfunction in X-linked dystonia-parkinsonism is associated with disease progression","volume":"24","author":"Br\u00fcggemann","year":"2017","journal-title":"Eur J Neurol"},{"issue":"1","key":"10.1016\/j.mehy.2018.02.009_b0260","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1002\/ana.20513","article-title":"Functional anatomy of the basal ganglia in X-linked recessive dystonia-parkinsonism","volume":"58","author":"Goto","year":"2005","journal-title":"Ann Neurol"},{"key":"10.1016\/j.mehy.2018.02.009_b0265","doi-asserted-by":"crossref","first-page":"2475","DOI":"10.1093\/emboj\/19.11.2475","article-title":"Human dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3","volume":"19","author":"Maeda","year":"2000","journal-title":"EMBO J"},{"key":"10.1016\/j.mehy.2018.02.009_b0270","doi-asserted-by":"crossref","first-page":"550","DOI":"10.1002\/ana.23632","article-title":"DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy","volume":"72","author":"Barone","year":"2012","journal-title":"Ann Neurol"},{"key":"10.1016\/j.mehy.2018.02.009_b0275","doi-asserted-by":"crossref","first-page":"157","DOI":"10.1007\/s10545-014-9760-1","article-title":"Genetic defects in dolichol metabolism","volume":"38","author":"Buczkowska","year":"2015","journal-title":"J Inherit Metab Dis"},{"key":"10.1016\/j.mehy.2018.02.009_b0280","doi-asserted-by":"crossref","first-page":"2976","DOI":"10.1016\/j.bbamcr.2014.09.004","article-title":"Ral small GTPase signaling and oncogenesis: More than just 15 minutes of fame","volume":"1843","author":"Gentry","year":"2014","journal-title":"Biochim Biophys Acta"},{"issue":"8","key":"10.1016\/j.mehy.2018.02.009_b0285","doi-asserted-by":"crossref","first-page":"2072","DOI":"10.1016\/j.bbamcr.2016.05.010","article-title":"RalA employs GRK2 and \u03b2-arrestins for the filamin A-mediated regulation of trafficking and signaling of dopamine D 2 and D 3 receptor","volume":"1863","author":"Zheng","year":"2016","journal-title":"Biochim Biophys Acta"},{"key":"10.1016\/j.mehy.2018.02.009_b0290","doi-asserted-by":"crossref","first-page":"424","DOI":"10.1038\/mp.2014.63","article-title":"Proteomic and genomic evidence implicates the postsynaptic density in schizophrenia","volume":"20","author":"F\u00f6cking","year":"2015","journal-title":"Mol Psychiatry"},{"key":"10.1016\/j.mehy.2018.02.009_b0295","doi-asserted-by":"crossref","first-page":"13406","DOI":"10.1074\/jbc.C000085200","article-title":"Identification and characterization of a new family of guanine nucleotide exchange factors for the ras-related GTPase Ral","volume":"275","author":"Rebhun","year":"2000","journal-title":"J Biol Chem"},{"issue":"10118","key":"10.1016\/j.mehy.2018.02.009_b0300","first-page":"1","article-title":"Interneuronal DISC1 regulates NRG1-ErbB4 signaling and excitatory\u2013inhibitory synapse formation in the mature cortex","volume":"6","author":"Seshadri","year":"2015","journal-title":"Nat Commun"},{"key":"10.1016\/j.mehy.2018.02.009_b0305","doi-asserted-by":"crossref","first-page":"157","DOI":"10.1097\/01.pra.0000428562.86705.cd","article-title":"Anti-NMDA receptor encephalitis: a cause of acute psychosis and catatonia","volume":"19","author":"Ryan","year":"2013","journal-title":"J Psychiatr Pract"},{"key":"10.1016\/j.mehy.2018.02.009_b0310","doi-asserted-by":"crossref","first-page":"206","DOI":"10.3389\/fimmu.2015.00206","article-title":"Neuroimmunology: an expanding frontier in autoimmunity","volume":"6","author":"H\u00f6ftberger","year":"2015","journal-title":"Front Immunol"},{"key":"10.1016\/j.mehy.2018.02.009_b0315","article-title":"The role of RalA in biology and therapy of ovarian cancer","author":"Wang","year":"2013","journal-title":"Oncotarget"},{"key":"10.1016\/j.mehy.2018.02.009_b0320","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1016\/S0165-4608(02)00855-5","article-title":"THY1 expression is associated with tumor suppression of human ovarian cancer","volume":"143","author":"Abeysinghe","year":"2003","journal-title":"Cancer Genet Cytogenet"},{"issue":"4","key":"10.1016\/j.mehy.2018.02.009_b0325","doi-asserted-by":"crossref","first-page":"307","DOI":"10.1016\/j.ymgme.2014.10.002","article-title":"Folinic acid treatment for schizophrenia associated with folate receptor autoantibodies","volume":"113","author":"Ramaekers","year":"2014","journal-title":"Mol Genet Metab"},{"key":"10.1016\/j.mehy.2018.02.009_b0330","doi-asserted-by":"crossref","first-page":"152","DOI":"10.1126\/science.1246886","article-title":"Association of the autoimmune disease scleroderma with an immunologic response to cancer","volume":"343","author":"Joseph","year":"2014","journal-title":"Science"},{"issue":"15","key":"10.1016\/j.mehy.2018.02.009_b0335","first-page":"1","article-title":"Lithium as a rescue therapy for regression and catatonia features in two SHANK3 patients with autism spectrum disorder: case reports","volume":"7","author":"Serret","year":"2015","journal-title":"BMC Psychiatry"},{"key":"10.1016\/j.mehy.2018.02.009_b0340","doi-asserted-by":"crossref","first-page":"403","DOI":"10.1016\/j.neubiorev.2015.05.012","article-title":"Bipolar disorder and antibodies against the N-methyl-d-aspartate receptor: a gate to the involvement of autoimmunity in the pathophysiology of bipolar illness","volume":"55","author":"Le\u00f3n-Caballero","year":"2015","journal-title":"Neurosci Behav Rev"},{"key":"10.1016\/j.mehy.2018.02.009_b0345","first-page":"533","article-title":"Serotonin Syndrome","volume":"13","author":"Volpi-Abadie","year":"2013","journal-title":"Ochsner J"},{"issue":"97","key":"10.1016\/j.mehy.2018.02.009_b0350","first-page":"1","article-title":"Conundrums in neurology: diagnosing serotonin syndrome\u2013a meta-analysis of cases","volume":"16","author":"Werneke","year":"2016","journal-title":"BMC Neurol"},{"key":"10.1016\/j.mehy.2018.02.009_b0355","doi-asserted-by":"crossref","first-page":"638","DOI":"10.1134\/S0006297913060096","article-title":"New functions of small nucleolar RNAs","volume":"78","author":"Makarova","year":"2013","journal-title":"Biochemistry (Mosc)"},{"key":"10.1016\/j.mehy.2018.02.009_b0360","doi-asserted-by":"crossref","first-page":"2140","DOI":"10.1093\/hmg\/ddp137","article-title":"Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behavior","volume":"18","author":"Doe","year":"2009","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.mehy.2018.02.009_b0365","doi-asserted-by":"crossref","first-page":"1293","DOI":"10.1261\/rna.2109710","article-title":"Identification of novel ribonucleo-protein complexes from the brain-specific snoRNA MBII-52","volume":"16","author":"Soeno","year":"2010","journal-title":"RNA"},{"issue":"7","key":"10.1016\/j.mehy.2018.02.009_b0370","first-page":"1","article-title":"Nop17 is a key R2TP factor for the assembly and maturation of box C\/D snoRNP complex","volume":"16","author":"Prieto","year":"2015","journal-title":"BMC Mol Biol"},{"key":"10.1016\/j.mehy.2018.02.009_b0375","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1016\/S0920-9964(00)00091-8","article-title":"Identification of antibodies to head shock proteins 90\u202fkDa and 70\u202fkDa in patients with schizophrenia","volume":"52","author":"Kim","year":"2001","journal-title":"Schizophr Res"},{"issue":"728605","key":"10.1016\/j.mehy.2018.02.009_b0380","first-page":"1","article-title":"Role of hsp90 in systemic lupus erythematosus and its clinical relevance","volume":"2012","author":"Shukla","year":"2012","journal-title":"Autoimmune Dis"},{"key":"10.1016\/j.mehy.2018.02.009_b0385","doi-asserted-by":"crossref","first-page":"120","DOI":"10.1016\/j.pnpbp.2015.12.006","article-title":"5-HT2C receptors in psychiatric disorders: a review","volume":"66","author":"Chagraoui","year":"2016","journal-title":"Prog Neuropsychopharmacol Biol Psychiatry"},{"key":"10.1016\/j.mehy.2018.02.009_b0390","doi-asserted-by":"crossref","first-page":"170","DOI":"10.1002\/ajmg.b.32292","article-title":"A preliminary analysis of microRNA as potential clinical biomarker for schizophrenia","volume":"168B","author":"Sun","year":"2015","journal-title":"Am J Med Genet B Neuropsychiatr Genet"},{"key":"10.1016\/j.mehy.2018.02.009_b0395","doi-asserted-by":"crossref","first-page":"134","DOI":"10.1016\/j.jpsychires.2014.03.008","article-title":"A preliminary analysis of association between the down-regulation of microRNA-181b expression and symptomatology improvement in schizophrenia patients before and after antipsychotic treatment","volume":"54","author":"Song","year":"2014","journal-title":"J Psychiatry Res"},{"key":"10.1016\/j.mehy.2018.02.009_b0400","doi-asserted-by":"crossref","first-page":"921","DOI":"10.1007\/s007020200075","article-title":"Exposure to prenatal infections, genetics and the risk of systematic and periodic catatonia","volume":"109","author":"St\u00f6ber","year":"2002","journal-title":"J Neural Transm (Vienna)"},{"key":"10.1016\/j.mehy.2018.02.009_b0405","doi-asserted-by":"crossref","first-page":"261","DOI":"10.1007\/s11910-012-0266-7","article-title":"Schizophrenia genetics: putting all the pieces together","volume":"12","author":"Girard","year":"2012","journal-title":"Curr Neurol Neurosci Rep"},{"key":"10.1016\/j.mehy.2018.02.009_b0410","doi-asserted-by":"crossref","first-page":"1365","DOI":"10.1038\/ng.2446","article-title":"De Novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia","volume":"44","author":"Xu","year":"2012","journal-title":"Nat Genet"},{"key":"10.1016\/j.mehy.2018.02.009_b0415","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1083\/jcb.200102142","article-title":"Human Vam6p promotes lysosome clustering and fusion in vivo","volume":"154","author":"Caplan","year":"2001","journal-title":"J Cell Biol"},{"key":"10.1016\/j.mehy.2018.02.009_b0420","doi-asserted-by":"crossref","first-page":"219","DOI":"10.1111\/tra.12027","article-title":"The HOPS proteins hVps41 and hVps39 are required for homotypic and heterotypic late endosome fusion","volume":"14","author":"Pols","year":"2013","journal-title":"Traffic"},{"key":"10.1016\/j.mehy.2018.02.009_b0425","doi-asserted-by":"crossref","first-page":"e281129","DOI":"10.4161\/cib.28129","article-title":"Vps 11, a subunit of the tethering complexes HOPS and CORVET, is involved in the regulation of glycolipid degradation and retrograde toxin transport","volume":"7","author":"Kvalvaag","year":"2014","journal-title":"Commun Integr Biol"},{"key":"10.1016\/j.mehy.2018.02.009_b0430","doi-asserted-by":"crossref","first-page":"30280","DOI":"10.1074\/jbc.M115.688440","article-title":"Characterization of the mammalian CORVET and HOPS complexes and their modular restructuring for endospecificity","volume":"290","author":"Van der Kant","year":"2015","journal-title":"J Biol Chem"},{"issue":"5","key":"10.1016\/j.mehy.2018.02.009_b0435","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1038\/nrn3229","article-title":"Impaired mitochondrial function in psychiatric disorders","volume":"13","author":"Manji","year":"2012","journal-title":"Nat Rev Neurosci"},{"issue":"10","key":"10.1016\/j.mehy.2018.02.009_b0440","doi-asserted-by":"crossref","first-page":"3219","DOI":"10.1083\/jcb.201610055","article-title":"Vps13-Mcp1 interacts at vacuole-mitochondria interfaces and bypasses ER-mitochondria contact sites","volume":"16","author":"John Peter","year":"2016","journal-title":"J Cell Biol"},{"key":"10.1016\/j.mehy.2018.02.009_b0445","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1007\/978-981-10-4567-7_9","article-title":"Role of intra- and inter-mitochondrial membrane contact sites in yeast phospholipids biogenesis","volume":"997","author":"Tamura","year":"2017","journal-title":"Adv Exp Med Biol"},{"issue":"1","key":"10.1016\/j.mehy.2018.02.009_b0450","doi-asserted-by":"crossref","first-page":"95","DOI":"10.1016\/j.devcel.2014.06.007","article-title":"A dynamic interface between vacuoles and mitochondria in yeast","volume":"30","author":"Elbaz-Alon","year":"2014","journal-title":"Dev Cell"},{"issue":"1","key":"10.1016\/j.mehy.2018.02.009_b0455","doi-asserted-by":"crossref","first-page":"86","DOI":"10.1016\/j.devcel.2014.06.006","article-title":"Cellular metabolism regulates contact sites between vacuoles and mitochondria","volume":"30","author":"H\u00f6nscher","year":"2014","journal-title":"Dev Cell"},{"issue":"32","key":"10.1016\/j.mehy.2018.02.009_b0460","doi-asserted-by":"crossref","first-page":"13197","DOI":"10.1074\/jbc.M117.784249","article-title":"Endoplasmic reticulum-mitochondria junction is required for iron homeostasis","volume":"292","author":"Xue","year":"2017","journal-title":"J Biol Chem"},{"issue":"6","key":"10.1016\/j.mehy.2018.02.009_b0465","doi-asserted-by":"crossref","first-page":"499","DOI":"10.1016\/S0006-3223(98)00109-7","article-title":"Serum iron in catatonia and neuroleptic malignant syndrome","volume":"44","author":"Lee","year":"1998","journal-title":"Biol Psychiatry"},{"key":"10.1016\/j.mehy.2018.02.009_b0470","doi-asserted-by":"crossref","first-page":"348","DOI":"10.1038\/cdd.2013.187","article-title":"Regulation of autophagy by the Rab GTPase network","volume":"21","author":"Ao","year":"2014","journal-title":"Cell Death Differ"}],"container-title":["Medical Hypotheses"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0306987717309015?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0306987717309015?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,10,11]],"date-time":"2019-10-11T01:57:44Z","timestamp":1570759064000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0306987717309015"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,4]]},"references-count":94,"alternative-id":["S0306987717309015"],"URL":"https:\/\/doi.org\/10.1016\/j.mehy.2018.02.009","relation":{},"ISSN":["0306-9877"],"issn-type":[{"value":"0306-9877","type":"print"}],"subject":[],"published":{"date-parts":[[2018,4]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Molecular hypotheses to explain the shared pathways and underlying pathobiological causes in catatonia and in catatonic presentations in neuropsychiatric disorders","name":"articletitle","label":"Article Title"},{"value":"Medical Hypotheses","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.mehy.2018.02.009","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}