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

https://doi.org/10.1101/127712
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What this work says

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

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The Epidemiology of Obsessive-Compulsive Disorder in Five US Communities
inferredcites →https://doi.org/10.1001/archpsyc.56.2.121openalex-snapshot
A 40-Year Follow-up of Patients With Obsessive-compulsive Disorder
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The Structure of Genetic and Environmental Risk Factors for Dimensional Representations ofDSM-5Obsessive-Compulsive Spectrum Disorders
inferredcites →https://doi.org/10.1001/jamapsychiatry.2015.3105openalex-snapshot
Mortality Among Persons With Obsessive-Compulsive Disorder in Denmark
inferredcites →https://doi.org/10.1002/0471142905.hg0725s87openalex-snapshot
Interpreting de novo Variation in Human Disease Using denovolyzeR
inferredcites →https://doi.org/10.1006/geno.2000.6370openalex-snapshot
Cloning, Mapping, and Expression Analysis of a Gene Encoding a Novel Mammalian EGF-Related Protein (SCUBE1)
inferredcites →https://doi.org/10.1007/s00787-014-0543-xopenalex-snapshot
The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methods
inferredcites →https://doi.org/10.1016/j.biopsych.2004.12.004openalex-snapshot
Increased serum levels of interleukin-12 and tumor necrosis factor-alpha in Tourette’s syndrome
inferredcites →https://doi.org/10.1016/j.cardiores.2006.04.010openalex-snapshot
Localization and characterization of a novel secreted protein SCUBE1 in human platelets
inferredcites →https://doi.org/10.1016/j.cell.2007.05.009openalex-snapshot
High-Resolution Profiling of Histone Methylations in the Human Genome
inferredcites →https://doi.org/10.1016/j.cell.2013.06.049openalex-snapshot
Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network
inferredcites →https://doi.org/10.1016/j.cell.2013.10.020openalex-snapshot
Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
inferredcites →https://doi.org/10.1016/j.cell.2014.06.017openalex-snapshot
Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development
inferredcites →https://doi.org/10.1016/j.celrep.2014.08.068openalex-snapshot
De Novo Insertions and Deletions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder
inferredcites →https://doi.org/10.1016/j.celrep.2017.02.007openalex-snapshot
Varying Intolerance of Gene Pathways to Mutational Classes Explain Genetic Convergence across Neuropsychiatric Disorders
inferredcites →https://doi.org/10.1016/j.comppsych.2014.05.020openalex-snapshot
Comorbidity in obsessive–compulsive disorder (OCD): A report from the International College of Obsessive–Compulsive Spectrum Disorders (ICOCS)
inferredcites →https://doi.org/10.1016/j.cpr.2011.09.008openalex-snapshot
Etiology of obsessions and compulsions: A meta-analysis and narrative review of twin studies
inferredcites →https://doi.org/10.1016/j.jaac.2013.11.013openalex-snapshot
Inflammation in Children and Adolescents With Neuropsychiatric Disorders: A Systematic Review
inferredcites →https://doi.org/10.1016/j.jpsychires.2014.06.010openalex-snapshot
Phenomenology of OCD: Lessons from a large multicenter study and implications for ICD-11
inferredcites →https://doi.org/10.1016/j.neuron.2010.10.006openalex-snapshot
The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors
inferredcites →https://doi.org/10.1016/j.neuron.2012.04.009openalex-snapshot
De Novo Gene Disruptions in Children on the Autistic Spectrum
inferredcites →https://doi.org/10.1016/j.neuron.2015.09.016openalex-snapshot
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
inferredcites →https://doi.org/10.1016/j.neuron.2017.04.024openalex-snapshot
De Novo Coding Variants Are Strongly Associated with Tourette Disorder
inferredcites →https://doi.org/10.1016/j.pnpbp.2005.11.001openalex-snapshot
The descriptive epidemiology of obsessive–compulsive disorder
inferredcites →https://doi.org/10.1016/j.pnpbp.2009.05.001openalex-snapshot
A cytokine study in children and adolescents with Tourette's disorder
inferredcites →https://doi.org/10.1016/s0140-6736(12)61480-9openalex-snapshot
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
inferredcites →https://doi.org/10.1016/s0924-9338(01)00571-5openalex-snapshot
Quality of life and disability in patients with obsessive-compulsive disorder
inferredcites →https://doi.org/10.1038/mp.2008.94openalex-snapshot
The epidemiology of obsessive-compulsive disorder in the National Comorbidity Survey Replication
inferredcites →https://doi.org/10.1038/mp.2012.85openalex-snapshot
Genome-wide association study of obsessive-compulsive disorder
inferredcites →https://doi.org/10.1038/mp.2014.29openalex-snapshot
De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability
inferredcites →https://doi.org/10.1038/mp.2014.43openalex-snapshot
Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS
inferredcites →https://doi.org/10.1038/nature06104openalex-snapshot
Cortico-striatal synaptic defects and OCD-like behaviours in Sapap3-mutant mice
inferredcites →https://doi.org/10.1038/nature10945openalex-snapshot
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
inferredcites →https://doi.org/10.1038/nature10989openalex-snapshot
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
inferredcites →https://doi.org/10.1038/nature11011openalex-snapshot
Patterns and rates of exonic de novo mutations in autism spectrum disorders
inferredcites →https://doi.org/10.1038/nature12439openalex-snapshot
De novo mutations in epileptic encephalopathies
inferredcites →https://doi.org/10.1038/nature12929openalex-snapshot
De novo mutations in schizophrenia implicate synaptic networks
inferredcites →https://doi.org/10.1038/nature13394openalex-snapshot
Genome sequencing identifies major causes of severe intellectual disability
inferredcites →https://doi.org/10.1038/nature13772openalex-snapshot
Synaptic, transcriptional and chromatin genes disrupted in autism
inferredcites →https://doi.org/10.1038/nature13908openalex-snapshot
The contribution of de novo coding mutations to autism spectrum disorder
inferredcites →https://doi.org/10.1038/nature14135openalex-snapshot
Large-scale discovery of novel genetic causes of developmental disorders
inferredcites →https://doi.org/10.1038/nature19057openalex-snapshot
Analysis of protein-coding genetic variation in 60,706 humans
inferredcites →https://doi.org/10.1038/nature21062openalex-snapshot
Prevalence and architecture of de novo mutations in developmental disorders
inferredcites →https://doi.org/10.1038/nbt1295openalex-snapshot
A human phenome-interactome network of protein complexes implicated in genetic disorders
inferredcites →https://doi.org/10.1038/ncomms7404openalex-snapshot
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
inferredcites →https://doi.org/10.1038/ng.886openalex-snapshot
Increased exonic de novo mutation rate in individuals with schizophrenia
inferredcites →https://doi.org/10.1038/ng.902openalex-snapshot
Exome sequencing supports a de novo mutational paradigm for schizophrenia
inferredcites →https://doi.org/10.1038/tp.2016.30openalex-snapshot
Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways
inferredcites →https://doi.org/10.1038/tp.2016.34openalex-snapshot
Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia
inferredcites →https://doi.org/10.1056/nejmoa1206524openalex-snapshot
Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
inferredcites →https://doi.org/10.1074/jbc.m207410200openalex-snapshot
Identification of a Novel Family of Cell-surface Proteins Expressed in Human Vascular Endothelium
inferredcites →https://doi.org/10.1093/acrefore/9780199975839.013.104openalex-snapshot
Diagnostic and Statistical Manual of Mental Disorders
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btp698openalex-snapshot
Fast and accurate long-read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btq559openalex-snapshot
Robust relationship inference in genome-wide association studies
inferredcites →https://doi.org/10.1093/bioinformatics/btr330openalex-snapshot
The variant call format and VCFtools
inferredcites →https://doi.org/10.1093/nar/gkq603openalex-snapshot
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
inferredcites →https://doi.org/10.1093/nar/gks1055openalex-snapshot
The ConsensusPathDB interaction database: 2013 update
inferredcites →https://doi.org/10.1101/gr.107524.110openalex-snapshot
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
inferredcites →https://doi.org/10.1126/science.1227764openalex-snapshot
Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
inferredcites →https://doi.org/10.1126/science.aac9396openalex-snapshot
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies
inferredcites →https://doi.org/10.1128/mcb.00322-08openalex-snapshot
CHD8 Is an ATP-Dependent Chromatin Remodeling Factor That Regulates β-Catenin Target Genes
inferredcites →https://doi.org/10.1128/mcb.00846-07openalex-snapshot
CHD8 Associates with Human Staf and Contributes to Efficient U6 RNA Polymerase III Transcription
inferredcites →https://doi.org/10.1136/bmj.g2183openalex-snapshot
Obsessive-compulsive disorder
inferredcites →https://doi.org/10.1146/annurev-pharmtox-011613-135943openalex-snapshot
The Druggable Genome: Evaluation of Drug Targets in Clinical Trials Suggests Major Shifts in Molecular Class and Indication
inferredcites →https://doi.org/10.1161/atvbaha.114.303779openalex-snapshot
Inhibition of the Plasma SCUBE1, a Novel Platelet Adhesive Protein, Protects Mice Against Thrombosis
inferredcites →https://doi.org/10.1176/ajp.152.1.76openalex-snapshot
A family study of obsessive-compulsive disorder
inferredcites →https://doi.org/10.1176/ajp.2006.163.11.1978openalex-snapshot
Obsessive-Compulsive Disorder: Prevalence, Comorbidity, Impact, and Help-Seeking in the British National Psychiatric Morbidity Survey of 2000
inferredcites →https://doi.org/10.1176/appi.books.9780890425596openalex-snapshot
Diagnostic and Statistical Manual of Mental Disorders
inferredcites →https://doi.org/10.1186/s11689-016-9170-9openalex-snapshot
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation
inferredcites →https://doi.org/10.1371/journal.pgen.1003671openalex-snapshot
Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes
inferredcites →https://doi.org/10.1371/journal.pgen.1004772openalex-snapshot
De Novo Mutations in Moderate or Severe Intellectual Disability
inferredcites →https://doi.org/10.1375/183242705774310060openalex-snapshot
Twin Studies on Obsessive–Compulsive Disorder: A Review
inferredcites →https://doi.org/10.4049/jimmunol.159.6.2994openalex-snapshot
Cerebrospinal fluid cytokines in pediatric neuropsychiatric disease
inferredcites →https://doi.org/10.4088/jcp.12m07657openalex-snapshot
Five-Year Course of Obsessive-Compulsive Disorder
inferredcites →https://doi.org/10.4088/jcp.v61n0213openalex-snapshot
Sensory Phenomena in Obsessive-Compulsive Disorder and Tourette's Disorder

What points at this work

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

inferred← citeshttps://doi.org/10.1007/978-981-10-4358-1_11openalex-snapshot
Treatment Resistance in Obsessive-Compulsive Disorder
inferred← citeshttps://doi.org/10.1016/j.cell.2018.06.016openalex-snapshot
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.08.082openalex-snapshot
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis
inferred← citeshttps://doi.org/10.1038/s41386-021-01130-2openalex-snapshot
The prefrontal cortex and OCD
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/10.1101/730952openalex-snapshot
Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify candidate risk genes and biological pathways
inferred← citeshttps://doi.org/10.1186/s13073-017-0497-yopenalex-snapshot
Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders
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