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Fluoxetine FDA Label
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The association of myelin oligodendrocyte glycoprotein gene and white matter volume in obsessive-compulsive disorder.J Affect Disord. 2010 Aug;124(3):309-13. doi: 10.1016/j.jad.2010.03.027. Epub 2010 May 7.
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The functional coding variant Asn107Ile of the neuropeptide S receptor gene (NPSR1) influences age at onset of obsessive-compulsive disorder.Int J Neuropsychopharmacol. 2013 Oct;16(9):1951-8. doi: 10.1017/S1461145713000382. Epub 2013 May 17.
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Randomized, Double-Blind, Placebo-Controlled Trial of N-Acetylcysteine Augmentation for Treatment-Resistant Obsessive-Compulsive Disorder.J Clin Psychiatry. 2017 Jul;78(7):e766-e773. doi: 10.4088/JCP.16m11101.
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Obsessive-compulsive disorder is not a clinical manifestation of the DYT1 dystonia gene.Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 5;144B(3):361-4. doi: 10.1002/ajmg.b.30431.
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Psychological Characteristics of Inflammatory Bowel Disease Patients: A Comparison Between Active and Nonactive Patients.Inflamm Bowel Dis. 2019 Jul 17;25(8):1399-1407. doi: 10.1093/ibd/izy400.
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OLIG2 gene polymorphisms are associated with nasty, unpleasant and uncontrollable thoughts in obsessive-compulsive disorder.J Clin Neurosci. 2019 Dec;70:202-207. doi: 10.1016/j.jocn.2019.08.050. Epub 2019 Aug 17.
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Psychiatric symptoms in myoclonus-dystonia syndrome are just concomitant features regardless of the SGCE gene mutation.Parkinsonism Relat Disord. 2017 Sep;42:73-77. doi: 10.1016/j.parkreldis.2017.06.014. Epub 2017 Jun 23.
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Gene variations in PBX1, LMX1A and SLITRK1 are associated with obsessive-compulsive disorder and its clinical features.J Clin Neurosci. 2019 Mar;61:180-185. doi: 10.1016/j.jocn.2018.10.042. Epub 2018 Oct 28.
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Mice deficient in AKAP13 (BRX) develop compulsive-like behavior and increased body weight.Brain Res Bull. 2018 Jun;140:72-79. doi: 10.1016/j.brainresbull.2018.04.005. Epub 2018 Apr 10.
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DRD4 gene and obsessive compulsive disorder: do symptom dimensions have specific genetic correlates?.Prog Neuropsychopharmacol Biol Psychiatry. 2013 Mar 5;41:18-23. doi: 10.1016/j.pnpbp.2012.10.023. Epub 2012 Nov 2.
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Attenuation of compulsive-like behavior by fluvoxamine in a non-induced mouse model of obsessive-compulsive disorder.Behav Pharmacol. 2018 Jun;29(4):299-305. doi: 10.1097/FBP.0000000000000348.
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Neuropsychological, electrophysiological and neurological impairments in patients with obsessive compulsive disorder, their healthy siblings and healthy controls: Identifying potential endophenotype(s).Psychiatry Res. 2016 Jun 30;240:110-117. doi: 10.1016/j.psychres.2016.04.013. Epub 2016 Apr 7.
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Activation of the orbitofrontal and anterior cingulate cortices during the expression of a naturalistic compulsive-like behavior in the rabbit.Behav Brain Res. 2017 Mar 1;320:67-74. doi: 10.1016/j.bbr.2016.11.022. Epub 2016 Nov 19.
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Association of intronic variants of the BTBD9 gene with Tourette syndrome.Arch Neurol. 2009 Oct;66(10):1267-72. doi: 10.1001/archneurol.2009.213.
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Abnormalities of the serotonergic system in diacylglycerol kinase -deficient mouse brain.Biochem Biophys Res Commun. 2018 Mar 18;497(4):1031-1037. doi: 10.1016/j.bbrc.2018.02.165. Epub 2018 Feb 24.
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Dlgap1 knockout mice exhibit alterations of the postsynaptic density and selective reductions in sociability.Sci Rep. 2018 Feb 2;8(1):2281. doi: 10.1038/s41598-018-20610-y.
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Lateral orbitofrontal dysfunction in the Sapap3 knockout mouse model of obsessivecompulsive disorder.J Psychiatry Neurosci. 2019 Mar 1;44(2):120-131. doi: 10.1503/jpn.180032.
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DNA hypermethylation of serotonin transporter gene promoter in drug nave patients with schizophrenia.Schizophr Res. 2014 Feb;152(2-3):373-80. doi: 10.1016/j.schres.2013.12.007. Epub 2014 Jan 8.
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Evidence for the gamma-amino-butyric acid type B receptor 1 (GABBR1) gene as a susceptibility factor in obsessive-compulsive disorder.Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):25-9. doi: 10.1002/ajmg.b.30152.
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5-HT3 receptor influences the washing phenotype and visual organization in obsessive-compulsive disorder supporting 5-HT3 receptor antagonists as novel treatment option.Eur Neuropsychopharmacol. 2014 Jan;24(1):86-94. doi: 10.1016/j.euroneuro.2013.07.003. Epub 2013 Aug 6.
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Early maladaptive schemas and suicidal risk in an Iranian sample of patients with obsessive-compulsive disorder.Psychiatry Res. 2017 Sep;255:441-448. doi: 10.1016/j.psychres.2017.06.080. Epub 2017 Jun 27.
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Homeobox genes in obsessive-compulsive disorder.Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):53-60. doi: 10.1002/ajmg.b.32001. Epub 2011 Nov 16.
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Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls.BMC Med Genet. 2010 Jul 5;11:108. doi: 10.1186/1471-2350-11-108.
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A genetic family-based association study of OLIG2 in obsessive-compulsive disorder.Arch Gen Psychiatry. 2007 Feb;64(2):209-14. doi: 10.1001/archpsyc.64.2.209.
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Reduced 3-O-methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):542-548.
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The association of spinophilin with disks large-associated protein 3 (SAPAP3) is regulated by metabotropic glutamate receptor (mGluR) 5.Mol Cell Neurosci. 2018 Jun 14;90:60-69. doi: 10.1016/j.mcn.2018.06.001. Online ahead of print.
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Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD.Hum Genet. 2011 Dec;130(6):795-805. doi: 10.1007/s00439-011-1033-6. Epub 2011 Jun 21.
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Integrative analysis of shared genetic pathogenesis by autism spectrum disorder and obsessive-compulsive disorder.Biosci Rep. 2019 Dec 20;39(12):BSR20191942. doi: 10.1042/BSR20191942.
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Amelioration of obsessive-compulsive disorder in three mouse models treated with one epigenetic drug: unraveling the underlying mechanism.Sci Rep. 2019 Jun 19;9(1):8741. doi: 10.1038/s41598-019-45325-6.
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OCD-like behavior is caused by dysfunction of thalamo-amygdala circuits and upregulated TrkB/ERK-MAPK signaling as a result of SPRED2 deficiency.Mol Psychiatry. 2018 Feb;23(2):444-458. doi: 10.1038/mp.2016.232. Epub 2017 Jan 10.
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Detrimental effect of clomipramine on hippocampus-dependent learning in an animal model of obsessive-compulsive disorder induced by sensitization with d2/d3 agonist quinpirole.Behav Brain Res. 2017 Jan 15;317:210-217. doi: 10.1016/j.bbr.2016.09.042. Epub 2016 Sep 19.
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The role of spatial store and executive strategy in spatial working memory: a comparison between patients with obsessive-compulsive disorder and controls.Cogn Neuropsychiatry. 2019 Jan;24(1):14-27. doi: 10.1080/13546805.2018.1544888. Epub 2018 Nov 21.
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De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case report.BMC Med Genet. 2018 Nov 13;19(1):197. doi: 10.1186/s12881-018-0711-9.
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Sex differences in the genetic architecture of obsessive-compulsive disorder.Am J Med Genet B Neuropsychiatr Genet. 2019 Sep;180(6):351-364. doi: 10.1002/ajmg.b.32687. Epub 2018 Nov 20.
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Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder.Mol Psychiatry. 2020 Sep;25(9):2036-2046. doi: 10.1038/s41380-018-0115-4. Epub 2018 Aug 7.
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Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.Am J Psychiatry. 2015 Jan;172(1):82-93. doi: 10.1176/appi.ajp.2014.13101306. Epub 2014 Oct 31.
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Comparison of neurocognitive domains in patients with schizophrenia with and without co-morbid obsessive compulsive disorder.Schizophr Res. 2018 Nov;201:151-158. doi: 10.1016/j.schres.2018.05.029. Epub 2018 May 29.
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