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Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS

https://doi.org/10.1038/mp.2014.43

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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A Haplotype Containing Quantitative Trait Loci for SLC1A1 Gene Expression and Its Association With Obsessive-Compulsive Disorder

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A Family Study of Obsessive-compulsive Disorder

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Glutamate Transporter Gene SLC1A1 Associated With Obsessive-compulsive Disorder

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Association Testing of the Positional and Functional Candidate Gene SLC1A1/EAAC1 in Early-Onset Obsessive-compulsive Disorder

inferredcites →https://doi.org/10.1001/archpsyc.64.2.209openalex-snapshot

A Genetic Family-Based Association Study of OLIG2 in Obsessive-compulsive Disorder

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Population-Based, Multigenerational Family Clustering Study of Obsessive-compulsive Disorder

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Genome‐wide linkage analysis of families with obsessive‐compulsive disorder ascertained through pediatric probands

inferredcites →https://doi.org/10.1002/ajmg.b.30914openalex-snapshot

A family‐based association study of the glutamate transporter gene SLC1A1 in obsessive–compulsive disorder in 378 families

inferredcites →https://doi.org/10.1002/ajmg.b.31001openalex-snapshot

A screen of SLC1A1 for OCD‐related alleles

inferredcites →https://doi.org/10.1002/ajmg.b.31184openalex-snapshot

Comprehensive family‐based association study of the glutamate transporter gene SLC1A1 in obsessive‐compulsive disorder

inferredcites →https://doi.org/10.1002/ajmg.b.32137openalex-snapshot

Meta‐analysis of association between obsessive‐compulsive disorder and the 3′ region of neuronal glutamate transporter gene SLC1A1

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Exome sequencing of a pedigree with tourette syndrome or chronic tic disorder

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Diagnostic and Statistical Manual of Mental Disorders (DSM-IV)

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On Genome-wide Association Studies for Family-Based Designs: An Integrative Analysis Approach Combining Ascertained Family Samples with Unselected Controls

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Common Genetic Variants and Gene-Expression Changes Associated with Bipolar Disorder Are Over-Represented in Brain Signaling Pathway Genes

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Forgetting What You Have Checked: A Link Between Working Memory Impairment and Checking Behaviors in Obsessive-Compulsive Disorder

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Common genetic background in anorexia nervosa and obsessive compulsive disorder: Preliminary results from an association study

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Postsynaptic TrkC and Presynaptic PTPσ Function as a Bidirectional Excitatory Synaptic Organizing Complex

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The role of glutamate signaling in the pathogenesis and treatment of obsessive–compulsive disorder

inferredcites →https://doi.org/10.1016/j.pharmthera.2011.09.006openalex-snapshot

Glutamate abnormalities in obsessive compulsive disorder: Neurobiology, pathophysiology, and treatment

inferredcites →https://doi.org/10.1016/j.psc.2009.11.001openalex-snapshot

Genetics of Obsessive-Compulsive Disorder

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Obsessive-compulsive disorder

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Cross-National Epidemiology of Obsessive-Compulsive Disorder

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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

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A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa

inferredcites →https://doi.org/10.1038/mp.2011.80openalex-snapshot

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

inferredcites →https://doi.org/10.1038/mp.2012.85openalex-snapshot

Genome-wide association study of obsessive-compulsive disorder

inferredcites →https://doi.org/10.1038/nature02168openalex-snapshot

The International HapMap Project

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Cortico-striatal synaptic defects and OCD-like behaviours in Sapap3-mutant mice

inferredcites →https://doi.org/10.1038/nature07999openalex-snapshot

Common genetic variants on 5p14.1 associate with autism spectrum disorders

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Common variants conferring risk of schizophrenia

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A map of human genome variation from population-scale sequencing

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PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

inferredcites →https://doi.org/10.1038/ng.201openalex-snapshot

Identification of loci associated with schizophrenia by genome-wide association and follow-up

inferredcites →https://doi.org/10.1038/ng.642openalex-snapshot

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease

inferredcites →https://doi.org/10.1038/ng.940openalex-snapshot

Genome-wide association study identifies five new schizophrenia loci

inferredcites →https://doi.org/10.1038/ng1007-1181openalex-snapshot

The NCBI dbGaP database of genotypes and phenotypes

inferredcites →https://doi.org/10.1038/nm.2125openalex-snapshot

Slitrk5 deficiency impairs corticostriatal circuitry and leads to obsessive-compulsive–like behaviors in mice

inferredcites →https://doi.org/10.1038/nn.2279openalex-snapshot

Trans-synaptic adhesion between NGL-3 and LAR regulates the formation of excitatory synapses

inferredcites →https://doi.org/10.1038/nn.3040openalex-snapshot

Selective control of inhibitory synapse development by Slitrk3-PTPδ trans-synaptic interaction

inferredcites →https://doi.org/10.1038/nn1416openalex-snapshot

LAR receptor protein tyrosine phosphatases in the development and maintenance of excitatory synapses

inferredcites →https://doi.org/10.1038/sj.mp.4001847openalex-snapshot

Genomewide linkage scan for obsessive-compulsive disorder: evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q

inferredcites →https://doi.org/10.1073/pnas.0701361104openalex-snapshot

The human disease network

inferredcites →https://doi.org/10.1074/jbc.m109.061127openalex-snapshot

Trans-synaptic Adhesions between Netrin-G Ligand-3 (NGL-3) and Receptor Tyrosine Phosphatases LAR, Protein-tyrosine Phosphatase δ (PTPδ), and PTPσ via Specific Domains Regulate Excitatory Synapse Formation

inferredcites →https://doi.org/10.1086/381563openalex-snapshot

PBAT: Tools for Family-Based Association Studies

inferredcites →https://doi.org/10.1086/423899openalex-snapshot

Replication Study Supports Evidence for Linkage to 9p24 in Obsessive-Compulsive Disorder

inferredcites →https://doi.org/10.1086/519795openalex-snapshot

PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses

inferredcites →https://doi.org/10.1093/bioinformatics/btn564openalex-snapshot

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

inferredcites →https://doi.org/10.1093/bioinformatics/btq330openalex-snapshot

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

inferredcites →https://doi.org/10.1093/bioinformatics/btq340openalex-snapshot

METAL: fast and efficient meta-analysis of genomewide association scans

inferredcites →https://doi.org/10.1093/emboj/19.12.2775openalex-snapshot

Impaired learning with enhanced hippocampal long‐term potentiation in PTPδ‐deficient mice

inferredcites →https://doi.org/10.1093/nar/gkr1062openalex-snapshot

Comparative interactomics with Funcoup 2.0

inferredcites →https://doi.org/10.1097/00004583-199009000-00015openalex-snapshot

Obsessive Compulsive Disorder in Children and Adolescents: Phenomenology and Family History

inferredcites →https://doi.org/10.1101/pdb.top065581openalex-snapshot

Gene Set Analysis and Network Analysis for Genome-Wide Association Studies

inferredcites →https://doi.org/10.1126/science.1116502openalex-snapshot

Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome

inferredcites →https://doi.org/10.1139/o04-120openalex-snapshot

Functional significance of the LAR receptor protein tyrosine phosphatase family in development and diseases

inferredcites →https://doi.org/10.5860/choice.28-5931openalex-snapshot

Psychiatric disorders in America: the epidemiologic catchment area study

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Association analyses reveal gender-specific associations of DAT1 40-bp VNTR and -839C/T polymorphisms with obsessive–compulsive disorder and obsessive–compulsive symptoms

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C9orf72 hexanucleotide repeat expansions are not a common cause of obsessive-compulsive disorder

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Glutamate transporter gene polymorphisms and obsessive-compulsive disorder: A case-control association study

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OLIG2 gene polymorphisms are associated with nasty, unpleasant and uncontrollable thoughts in obsessive-compulsive disorder

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Hoarding in children and adolescents with obsessive–compulsive disorder

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A preliminary candidate gene study in body dysmorphic disorder

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ADHD and executive functioning deficits in OCD youths who hoard

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Genetic and epigenetic architecture of Obsessive-Compulsive Disorder: In search of possible diagnostic and prognostic biomarkers

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Prevalence and correlates of lifetime suicide attempt in obsessive-compulsive disorder with major depression

inferred← citeshttps://doi.org/10.1016/j.jpsychires.2025.03.050openalex-snapshot

Pediatric early-onset neuropsychiatric obsessive compulsive disorders

inferred← citeshttps://doi.org/10.1016/j.jpsychires.2026.04.003openalex-snapshot

A study of alcohol dependence in obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1016/j.mocell.2026.100323openalex-snapshot

A decade of progress in understanding LRRTM and Slitrk synaptic cell-adhesion molecules

inferred← citeshttps://doi.org/10.1016/j.molmed.2015.01.004openalex-snapshot

The balancing act of GABAergic synapse organizers

inferred← citeshttps://doi.org/10.1016/j.nbd.2023.106223openalex-snapshot

Mechanisms of pathogenesis and environmental moderators in preclinical models of compulsive-like behaviours

inferred← citeshttps://doi.org/10.1016/j.nbd.2025.107226openalex-snapshot

Pathological gain-of-function human variants in the GRIK2 kainate receptor gene cause wide-ranging behavioral dysfunction and seizures in mouse models

inferred← citeshttps://doi.org/10.1016/j.neubiorev.2016.03.011openalex-snapshot

Systematic review of environmental risk factors for Obsessive-Compulsive Disorder: A proposed roadmap from association to causation

inferred← citeshttps://doi.org/10.1016/j.neubiorev.2016.09.025openalex-snapshot

The link between autoimmune diseases and obsessive-compulsive and tic disorders: A systematic review

inferred← citeshttps://doi.org/10.1016/j.neubiorev.2017.05.029openalex-snapshot

A review of the role of serotonin system genes in obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1016/j.neubiorev.2020.08.008openalex-snapshot

Diagnostic biomarkers for obsessive-compulsive disorder: A reasonable quest or ignis fatuus?

inferred← citeshttps://doi.org/10.1016/j.neubiorev.2024.105715openalex-snapshot

Towards zebrafish models to unravel translational insights of obsessive-compulsive disorder: A neurobehavioral perspective

inferred← citeshttps://doi.org/10.1016/j.neuron.2019.01.046openalex-snapshot

Obsessive-Compulsive Disorder: Puzzles and Prospects

inferred← citeshttps://doi.org/10.1016/j.neuron.2019.05.002openalex-snapshot

SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse

inferred← citeshttps://doi.org/10.1016/j.neuropharm.2021.108585openalex-snapshot

Kainate receptors in the developing neuronal networks

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2015.11.009openalex-snapshot

Using mice to model Obsessive Compulsive Disorder: From genes to circuits

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2016.09.012openalex-snapshot

Rodent models of obsessive compulsive disorder: Evaluating validity to interpret emerging neurobiology

inferred← citeshttps://doi.org/10.1016/j.nlm.2023.107837openalex-snapshot

Behavioral and genetic architecture of fear conditioning and related phenotypes

inferred← citeshttps://doi.org/10.1016/j.pmip.2018.10.001openalex-snapshot

SCL6A4 polymorphisms rs25533 and I425V: Association with obsessive–compulsive disorder and its treatment response in Iranian patients

inferred← citeshttps://doi.org/10.1016/j.pmip.2020.100058openalex-snapshot

Integrating genetic variation with DNA methylation at SKA2 rs7208505 in analyses of obsessive-compulsive disorder disease risk and symptom severity

inferred← citeshttps://doi.org/10.1016/j.pnpbp.2016.01.012openalex-snapshot

The need for inclusion of sex and age of onset variables in genetic association studies of obsessive–compulsive disorder: Overview

inferred← citeshttps://doi.org/10.1016/j.pnpbp.2017.06.037openalex-snapshot

Quantifying dimensional severity of obsessive-compulsive disorder for neurobiological research

inferred← citeshttps://doi.org/10.1016/j.pnpbp.2025.111315openalex-snapshot

Pharmacogenetics of obsessive-compulsive disorder: Investigations of intragenic and regulatory region genetic variations

inferred← citeshttps://doi.org/10.1016/j.psc.2014.06.002openalex-snapshot

Genetics of Obsessive-Compulsive Disorder and Related Disorders

inferred← citeshttps://doi.org/10.1016/j.psc.2018.10.007openalex-snapshot

Genetics of Eating Disorders

inferred← citeshttps://doi.org/10.1016/j.psc.2022.10.002openalex-snapshot

Childhood Obsessive–Compulsive Disorder

inferred← citeshttps://doi.org/10.1016/j.psc.2022.11.003openalex-snapshot

Genomics of Obsessive-Compulsive Disorder and Related Disorders

inferred← citeshttps://doi.org/10.1016/j.psychres.2020.113332openalex-snapshot

Postpartum depression biomarkers predict exacerbation of OCD symptoms during pregnancy

inferred← citeshttps://doi.org/10.1016/j.psychres.2021.113853openalex-snapshot

Specialty knowledge and competency standards for pharmacotherapy for adult obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1016/j.psychres.2026.116977openalex-snapshot

Polygenic risk scores for pediatric obsessive-compulsive symptoms: Mediating effects in samples clinically diagnosed with mental disorders

inferred← citeshttps://doi.org/10.1016/j.psychres.2026.117135openalex-snapshot

Early life adversity, inhibitory control, and behavioral dysregulation among individuals with OCD

inferred← citeshttps://doi.org/10.1016/j.ssmph.2025.101814openalex-snapshot

Shadows in the Air: Mental health vulnerabilities under PM10 and PM2.5, before and after COVID-19

inferred← citeshttps://doi.org/10.1016/j.xgen.2022.100107openalex-snapshot

Single nucleus multi-omics identifies human cortical cell regulatory genome diversity

inferred← citeshttps://doi.org/10.1017/9781108164313.005openalex-snapshot

The Molecular Genetics of Obsessive-Compulsive and Related Disorders

inferred← citeshttps://doi.org/10.1017/s0033291718000375openalex-snapshot

Prevalence and heritability of body dysmorphic symptoms in adolescents and young adults: a population-based nationwide twin study

inferred← citeshttps://doi.org/10.1017/s0033291721001744openalex-snapshot

Genetics of obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1038/jhg.2017.61openalex-snapshot

Meta-analysis of genome-wide SNP- and pathway-based associations for facets of neuroticism

inferred← citeshttps://doi.org/10.1038/mp.2015.197openalex-snapshot

Meta-analysis of genome-wide association studies of anxiety disorders

inferred← citeshttps://doi.org/10.1038/mp.2015.32openalex-snapshot

Whole-genome association analysis of treatment response in obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1038/mp.2016.11openalex-snapshot

Erratum: Meta-analysis of genome-wide association studies of anxiety disorders

inferred← citeshttps://doi.org/10.1038/mp.2017.154openalex-snapshot

Revealing the complex genetic architecture of obsessive–compulsive disorder using meta-analysis

inferred← citeshttps://doi.org/10.1038/mp.2017.20openalex-snapshot

Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies

inferred← citeshttps://doi.org/10.1038/mp.2017.215openalex-snapshot

A total-population multigenerational family clustering study of autoimmune diseases in obsessive–compulsive disorder and Tourette’s/chronic tic disorders

inferred← citeshttps://doi.org/10.1038/mp.2017.248openalex-snapshot

Polygenic prediction of obsessive compulsive symptoms

inferred← citeshttps://doi.org/10.1038/nn.4594openalex-snapshot

Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders

inferred← citeshttps://doi.org/10.1038/nrn3746openalex-snapshot

Obsessive–compulsive disorder: an integrative genetic and neurobiological perspective

inferred← citeshttps://doi.org/10.1038/s41380-018-0115-4openalex-snapshot

Examination of the shared genetic basis of anorexia nervosa and obsessive–compulsive disorder

inferred← citeshttps://doi.org/10.1038/s41380-019-0431-3openalex-snapshot

Lower excitatory synaptic gene expression in orbitofrontal cortex and striatum in an initial study of subjects with obsessive compulsive disorder

inferred← citeshttps://doi.org/10.1038/s41380-021-01424-3openalex-snapshot

Developmental impact of glutamate transporter overexpression on dopaminergic neuron activity and stereotypic behavior

inferred← citeshttps://doi.org/10.1038/s41380-024-02811-2openalex-snapshot

Genome-wide copy number variation association study in anorexia nervosa

inferred← citeshttps://doi.org/10.1038/s41386-018-0302-7openalex-snapshot

Behavioral and synaptic alterations relevant to obsessive-compulsive disorder in mice with increased EAAT3 expression

inferred← citeshttps://doi.org/10.1038/s41386-018-0307-2openalex-snapshot

Impaired instrumental reversal learning is associated with increased medial prefrontal cortex activity in Sapap3 knockout mouse model of compulsive behavior

inferred← citeshttps://doi.org/10.1038/s41386-019-0344-5openalex-snapshot

Kainate receptor auxiliary subunit NETO2 is required for normal fear expression and extinction

inferred← citeshttps://doi.org/10.1038/s41386-021-01130-2openalex-snapshot

The prefrontal cortex and OCD

inferred← citeshttps://doi.org/10.1038/s41398-019-0410-0openalex-snapshot

Do polygenic risk and stressful life events predict pharmacological treatment response in obsessive compulsive disorder? A gene–environment interaction approach

inferred← citeshttps://doi.org/10.1038/s41398-019-0558-7openalex-snapshot

Btbd3 expression regulates compulsive-like and exploratory behaviors in mice

inferred← citeshttps://doi.org/10.1038/s41398-019-0559-6openalex-snapshot

Converging evidence points towards a role of insulin signaling in regulating compulsive behavior

inferred← citeshttps://doi.org/10.1038/s41398-020-00966-4openalex-snapshot

Integration of postmortem amygdala expression profiling, GWAS, and functional cell culture assays: neuroticism-associated synaptic vesicle glycoprotein 2A (SV2A) gene is regulated by miR-133a and miR-218

inferred← citeshttps://doi.org/10.1038/s41398-020-01121-9openalex-snapshot

Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder

inferred← citeshttps://doi.org/10.1038/s41398-020-0793-yopenalex-snapshot

Shared genetic etiology between obsessive-compulsive disorder, obsessive-compulsive symptoms in the population, and insulin signaling

inferred← citeshttps://doi.org/10.1038/s41398-021-01290-1openalex-snapshot

Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1038/s41398-021-01519-zopenalex-snapshot

A dimensional perspective on the genetics of obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1038/s41467-017-00831-xopenalex-snapshot

Integrating evolutionary and regulatory information with a multispecies approach implicates genes and pathways in obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1038/s41467-019-13544-0openalex-snapshot

Genetic correlations of psychiatric traits with body composition and glycemic traits are sex- and age-dependent

inferred← citeshttps://doi.org/10.1038/s41467-023-41026-xopenalex-snapshot

Unraveling the mechanisms of deep-brain stimulation of the internal capsule in a mouse model

inferred← citeshttps://doi.org/10.1038/s41467-025-59685-3openalex-snapshot

Alternatively spliced mini-exon B in PTPδ regulates excitatory synapses through cell-type-specific trans-synaptic PTPδ-IL1RAP interaction

inferred← citeshttps://doi.org/10.1038/s41467-025-62190-2openalex-snapshot

Mechanisms and interventions promoting healthy frontostriatal dynamics in obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1038/s41588-025-02189-zopenalex-snapshot

Genome-wide analyses identify 30 loci associated with obsessive–compulsive disorder

inferred← citeshttps://doi.org/10.1038/s41593-021-00876-8openalex-snapshot

Exome sequencing in obsessive–compulsive disorder reveals a burden of rare damaging coding variants

inferred← citeshttps://doi.org/10.1038/s41598-019-38965-1openalex-snapshot

Initial findings of striatum tripartite model in OCD brain samples based on transcriptome analysis

inferred← citeshttps://doi.org/10.1038/s41598-022-05480-9openalex-snapshot

Changes in the stool and oropharyngeal microbiome in obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1038/s42003-019-0558-4openalex-snapshot

Social and non-social autism symptoms and trait domains are genetically dissociable

inferred← citeshttps://doi.org/10.1038/tp.2015.223openalex-snapshot

Obsessive–compulsive symptoms in a large population-based twin-family sample are predicted by clinically based polygenic scores and by genome-wide SNPs

inferred← citeshttps://doi.org/10.1038/tp.2016.30openalex-snapshot

Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways

inferred← citeshttps://doi.org/10.1038/tp.2016.34openalex-snapshot

Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia

inferred← citeshttps://doi.org/10.1080/15257770.2024.2336213openalex-snapshot

Association of rs11081062 polymorphism of DLGAP1 gene and levels of SLC1A1 protein with obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1080/15622975.2016.1181783openalex-snapshot

Biological markers for anxiety disorders, OCD and PTSD – a consensus statement. Part I: Neuroimaging and genetics

inferred← citeshttps://doi.org/10.1080/15622975.2017.1327669openalex-snapshot

Human-leukocyte antigen class II genes in early-onset obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1080/17460441.2024.2387127openalex-snapshot

New horizons for obsessive-compulsive disorder drug discovery: is targeting glutamate receptors the answer?

inferred← citeshttps://doi.org/10.1089/cap.2018.0073openalex-snapshot

Genetic Associations of Serotoninergic and GABAergic Genes in an Extended Collection of Early-Onset Obsessive-Compulsive Disorder Trios

inferred← citeshttps://doi.org/10.1089/cap.2018.0140openalex-snapshot

Immune-Related Comorbidities in Childhood-Onset Obsessive Compulsive Disorder: Lifetime Prevalence in the Obsessive Compulsive Disorder Collaborative Genetics Association Study

inferred← citeshttps://doi.org/10.1093/cercor/bhad058openalex-snapshot

Functional connectivity between pre-supplementary motor area and inferior parietal lobule associated with impaired motor response inhibition in first-degree relatives of patients with obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1093/cercor/bhad170openalex-snapshot

Gyrification of the medial and lateral orbitofrontal cortex in first-degree relatives of patients with obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1093/eep/dvz023openalex-snapshot

Epigenome-wide association of father’s smoking with offspring DNA methylation: a hypothesis-generating study

inferred← citeshttps://doi.org/10.1093/hmg/ddw083openalex-snapshot

Genome wide association study identifies two loci associated with cadmium in erythrocytes among never-smokers

inferred← citeshttps://doi.org/10.1093/med/9780190681425.003.0033openalex-snapshot

Genetics of Anxiety Disorders

inferred← citeshttps://doi.org/10.1093/med/9780190681425.003.0065openalex-snapshot

The Neurobiology of Tic Disorders and Obsessive-Compulsive Disorder

inferred← citeshttps://doi.org/10.1093/med/9780198713005.003.0096openalex-snapshot

Genetics of obsessive–compulsive disorder

inferred← citeshttps://doi.org/10.1093/oso/9780198793014.003.0025openalex-snapshot

Genetics of obsessive–compulsive disorder and Tourette’s syndrome

inferred← citeshttps://doi.org/10.1093/oxfordhb/9780190068752.013.6openalex-snapshot

Genetic Understanding of Obsessive-Compulsive Disorder and Related Disorders

inferred← citeshttps://doi.org/10.1093/schbul/sbu169openalex-snapshot

Obsessive-Compulsive Disorder, Psychosis, and Bipolarity: A Longitudinal Cohort and Multigenerational Family Study

inferred← citeshttps://doi.org/10.1097/hrp.0000000000000330openalex-snapshot

Ketamine in the Treatment of Obsessive-Compulsive Disorder: A Systematic Review

inferred← citeshttps://doi.org/10.1097/ypg.0000000000000230openalex-snapshot

New insights and perspectives on the genetics of obsessive-compulsive disorder

inferred← citeshttps://doi.org/10.1097/ypg.0000000000000241openalex-snapshot

Endophenotypes of executive functions in obsessive compulsive disorder? A meta-analysis in unaffected relatives

inferred← citeshttps://doi.org/10.1101/107193openalex-snapshot

Evolutionary and functional data power search for obsessive-compulsive disorder genes

inferred← citeshttps://doi.org/10.1101/127712openalex-snapshot

De novo damaging coding mutations are strongly associated with obsessive-compulsive disorder and overlap with autism

inferred← citeshttps://doi.org/10.1101/2021.01.21.426000openalex-snapshot

Single-cell deconvolution of 3,000 post-mortem brain samples for eQTL and GWAS dissection in mental disorders

inferred← citeshttps://doi.org/10.1101/2021.10.10.21264819openalex-snapshot

Structural Variants Are a Major Component of the Missing Heritability of Autism Spectrum Disorder

inferred← citeshttps://doi.org/10.1101/2021.10.13.21261078openalex-snapshot

Genome-wide association study identifies new locus associated with OCD

inferred← citeshttps://doi.org/10.1101/2022.10.28.514214openalex-snapshot

Mice lacking Ptprd exhibit deficits in goal-directed behavior and female-specific impairments in sensorimotor gating

inferred← citeshttps://doi.org/10.1101/2024.03.06.24303776openalex-snapshot

Genome-wide association study identifies new loci associated with OCD

inferred← citeshttps://doi.org/10.1101/2025.02.08.25321933openalex-snapshot

Sex and gender differences in OCD: A scoping review and a two subtypes hypothesis

inferred← citeshttps://doi.org/10.1101/2025.08.05.25332874openalex-snapshot

Development and validation of electronic health record-based ascertainment of obsessive-compulsive disorder cases and controls

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