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From rare Copy Number Variations to biological processes in ADHD
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ajmg.b.32169openalex-snapshot
Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: Genome‐wide association study of both common and rare variants
inferredcites →https://doi.org/10.1002/ajmg.b.32446openalex-snapshot
Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach
inferredcites →https://doi.org/10.1007/s00439-009-0663-4openalex-snapshot
Genome-wide association studies in ADHD
inferredcites →https://doi.org/10.1007/s00439-009-0694-xopenalex-snapshot
Candidate gene studies of ADHD: a meta-analytic review
inferredcites →https://doi.org/10.1016/j.ajhg.2015.11.024openalex-snapshot
Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules
inferredcites →https://doi.org/10.1016/j.bbrc.2005.09.197openalex-snapshot
Bruce/apollon promotes hippocampal neuron survival and is downregulated by kainic acid
inferredcites →https://doi.org/10.1016/j.biopsych.2004.11.006openalex-snapshot
Imaging the Effects of Methylphenidate on Brain Dopamine: New Model on Its Therapeutic Actions for Attention-Deficit/Hyperactivity Disorder
inferredcites →https://doi.org/10.1016/j.euroneuro.2017.11.012openalex-snapshot
RBFOX1, encoding a splicing regulator, is a candidate gene for aggressive behavior
inferredcites →https://doi.org/10.1016/j.jaac.2014.03.004openalex-snapshot
Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants
inferredcites →https://doi.org/10.1016/j.jpsychires.2013.10.022openalex-snapshot
Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorder
inferredcites →https://doi.org/10.1016/j.neubiorev.2017.01.013openalex-snapshot
Brain imaging genetics in ADHD and beyond – Mapping pathways from gene to disorder at different levels of complexity
inferredcites →https://doi.org/10.1016/s0021-9258(18)42619-1openalex-snapshot
rab15, a novel low molecular weight GTP-binding protein specifically expressed in rat brain.
inferredcites →https://doi.org/10.1016/s0140-6736(10)61109-9openalex-snapshot
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
inferredcites →https://doi.org/10.1017/s1461145708009127openalex-snapshot
Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism
inferredcites →https://doi.org/10.1038/emboj.2008.39openalex-snapshot
cdc2–cyclin B regulates eEF2 kinase activity in a cell cycle‐ and amino acid‐dependent manner
inferredcites →https://doi.org/10.1038/mp.2009.57openalex-snapshot
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
inferredcites →https://doi.org/10.1038/mp.2010.29openalex-snapshot
Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree
inferredcites →https://doi.org/10.1038/mp.2010.7openalex-snapshot
Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility
inferredcites →https://doi.org/10.1038/mp.2011.138openalex-snapshot
The genetics of attention deficit/hyperactivity disorder in adults, a review
inferredcites →https://doi.org/10.1038/mp.2012.161openalex-snapshot
Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder
inferredcites →https://doi.org/10.1038/mp.2015.163openalex-snapshot
Psychiatric gene discoveries shape evidence on ADHD’s biology
inferredcites →https://doi.org/10.1038/mp.2016.117openalex-snapshot
Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study
inferredcites →https://doi.org/10.1038/nature10130openalex-snapshot
NMDA receptor blockade at rest triggers rapid behavioural antidepressant responses
inferredcites →https://doi.org/10.1038/nature11405openalex-snapshot
An anatomically comprehensive atlas of the adult human brain transcriptome
inferredcites →https://doi.org/10.1038/ng.1013openalex-snapshot
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
inferredcites →https://doi.org/10.1038/ng.2555openalex-snapshot
Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease
inferredcites →https://doi.org/10.1038/ng.841openalex-snapshot
The splicing regulator Rbfox1 (A2BP1) controls neuronal excitation in the mammalian brain
inferredcites →https://doi.org/10.1038/nn.3922openalex-snapshot
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
inferredcites →https://doi.org/10.1038/nprot.2007.324openalex-snapshot
Integration of biological networks and gene expression data using Cytoscape
inferredcites →https://doi.org/10.1038/nrdp.2015.20openalex-snapshot
Attention-deficit/hyperactivity disorder
inferredcites →https://doi.org/10.1038/nrm2728openalex-snapshot
Rab GTPases as coordinators of vesicle traffic
inferredcites →https://doi.org/10.1038/s41588-018-0269-7openalex-snapshot
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
inferredcites →https://doi.org/10.1038/srep30805openalex-snapshot
Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development
inferredcites →https://doi.org/10.1042/bj20041090openalex-snapshot
The septin Sept5/CDCrel-1 competes with α-SNAP for binding to the SNARE complex
inferredcites →https://doi.org/10.1073/pnas.0802741106openalex-snapshot
PKCη regulates occludin phosphorylation and epithelial tight junction integrity
inferredcites →https://doi.org/10.1074/jbc.m113.544312openalex-snapshot
Dopamine D2 Receptor Relies upon PPM/PP2C Protein Phosphatases to Dephosphorylate Huntingtin Protein
inferredcites →https://doi.org/10.1074/jbc.m400656200openalex-snapshot
Regulation of the Multifunctional Ca2+/Calmodulin-dependent Protein Kinase II by the PP2C Phosphatase PPM1F in Fibroblasts
inferredcites →https://doi.org/10.1080/21688370.2015.1138017openalex-snapshot
Tight junction modulation of the blood brain barrier: CNS delivery of small molecules
inferredcites →https://doi.org/10.1093/brain/awn323openalex-snapshot
Gene expression profiling of substantia nigra dopamine neurons: further insights into Parkinson's disease pathology
inferredcites →https://doi.org/10.1093/brain/awt338openalex-snapshot
The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation
inferredcites →https://doi.org/10.1093/hmg/ddp086openalex-snapshot
Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice
inferredcites →https://doi.org/10.1093/hmg/dds180openalex-snapshot
Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain
inferredcites →https://doi.org/10.1093/hmg/ddv259openalex-snapshot
Non-coding genetic variants in human disease: Figure 1.
inferredcites →https://doi.org/10.1093/nar/gkw1128openalex-snapshot
The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species
inferredcites →https://doi.org/10.1101/528117openalex-snapshot
Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
inferredcites →https://doi.org/10.1101/gr.178855.114openalex-snapshot
The discovery of integrated gene networks for autism and related disorders
inferredcites →https://doi.org/10.1111/gbb.12096openalex-snapshot
Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia
inferredcites →https://doi.org/10.1126/science.aad6469openalex-snapshot
Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap
inferredcites →https://doi.org/10.1126/scitranslmed.3002464openalex-snapshot
Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD
inferredcites →https://doi.org/10.1176/ajp.2007.164.6.942openalex-snapshot
The Worldwide Prevalence of ADHD: A Systematic Review and Metaregression Analysis
inferredcites →https://doi.org/10.1176/appi.ajp.2011.11040551openalex-snapshot
Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD
inferredcites →https://doi.org/10.1176/appi.ajp.2011.11060822openalex-snapshot
Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3
inferredcites →https://doi.org/10.1186/s13052-017-0380-xopenalex-snapshot
Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series
inferredcites →https://doi.org/10.1186/s13229-015-0049-5openalex-snapshot
Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex
inferredcites →https://doi.org/10.1186/s40303-016-0017-9openalex-snapshot
αT-catenin in restricted brain cell types and its potential connection to autism
inferredcites →https://doi.org/10.1242/dmm.010322openalex-snapshot
Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish
inferredcites →https://doi.org/10.1242/jcs.013557openalex-snapshot
Functional interactions between phosphatase POPX2 and mDia modulate RhoA pathways
inferredcites →https://doi.org/10.12688/f1000research.2-30.v2openalex-snapshot
Construction and accessibility of a cross-species phenotype ontology along with gene annotations for biomedical research
inferredcites →https://doi.org/10.1371/journal.pcbi.1004219openalex-snapshot
MAGMA: Generalized Gene-Set Analysis of GWAS Data
inferredcites →https://doi.org/10.1371/journal.pcbi.1004584openalex-snapshot
Computing the Local Field Potential (LFP) from Integrate-and-Fire Network Models
inferredcites →https://doi.org/10.1371/journal.pgen.1001273openalex-snapshot
Proteins Encoded in Genomic Regions Associated with Immune-Mediated Disease Physically Interact and Suggest Underlying Biology
inferredcites →https://doi.org/10.1371/journal.pone.0055837openalex-snapshot
BIRC6 Protein, an Inhibitor of Apoptosis: Role in Survival of Human Prostate Cancer Cells
inferredcites →https://doi.org/10.1371/journal.pone.0131080openalex-snapshot
Biodiversity on the Rocks: Macrofauna Inhabiting Authigenic Carbonate at Costa Rica Methane Seeps
inferredcites →https://doi.org/10.1371/journal.pone.0141568openalex-snapshot
Learning-Induced Gene Expression in the Hippocampus Reveals a Role of Neuron -Astrocyte Metabolic Coupling in Long Term Memory
inferredcites →https://doi.org/10.3389/fnins.2015.00313openalex-snapshot
Characterizing autism spectrum disorders by key biochemical pathways
inferredcites →https://doi.org/10.3390/toxics2030464openalex-snapshot
Zebrafish as a Model for Developmental Neurotoxicity Assessment: The Application of the Zebrafish in Defining the Effects of Arsenic, Methylmercury, or Lead on Early Neurodevelopment
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1111/jcpp.13161openalex-snapshot
From man to fly – convergent evidence links FBXO25 to ADHD and comorbid psychiatric phenotypes
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