Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder
暂无分享,去创建一个
J. Sunyer | M. Soler Artigas | B. Cormand | C. Sánchez-Mora | J. Ramos-Quiroga | M. Casas | M. Ribasés | M. Bustamante | M. Corrales | V. Richarte | I. Garcia-Martínez | M. Pagerols | P. Rovira | E. Calvo-Sánchez | María Soler Artigas | Eva Calvo-Sánchez
[1] R. Reid,et al. ADHD Rating Scale-IV: School Checklist , 2018 .
[2] G. Salmon,et al. Attention deficit hyperactivity disorder. , 2018, British journal of hospital medicine.
[3] I. Kohane,et al. Integrative analysis of genetic data sets reveals a shared innate immune component in autism spectrum disorder and its co-morbidities , 2016, Genome Biology.
[4] J. Qian,et al. Correlative study of peripheral ATP1A1 gene expression level to anxiety severity score on major depressive disorder patients , 2016, Journal of basic and clinical physiology and pharmacology.
[5] Ebru Fındıklı,et al. Serum levels of G protein-coupled estrogen receptor 1 (GPER1) in drug-naive patients with generalized anxiety disorder , 2016, Psychiatry Research.
[6] Wim E Crusio,et al. Transcriptome analysis of genes and gene networks involved in aggressive behavior in mouse and zebrafish , 2016, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[7] Benjamin A. Logsdon,et al. Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia , 2016, Nature Neuroscience.
[8] Jingyu Liu,et al. Correspondence of DNA Methylation Between Blood and Brain Tissue and Its Application to Schizophrenia Research. , 2016, Schizophrenia bulletin.
[9] G. Hardiman,et al. Acute stress enhances the expression of neuroprotection- and neurogenesis-associated genes in the hippocampus of a mouse restraint model , 2016, Oncotarget.
[10] C. Cardozo,et al. The Ubiquitin-Proteasome System: Potential Therapeutic Targets for Alzheimer’s Disease and Spinal Cord Injury , 2016, Front. Mol. Neurosci..
[11] Timothy C. Bates,et al. Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences☆ , 2016, Intelligence.
[12] Á. Carracedo,et al. Female patient with autistic disorder, intellectual disability, and co‐morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13.2–q13.31 microdeletion , 2015, American journal of medical genetics. Part A.
[13] B. Franke,et al. Transcriptomic and genetic studies identify NFAT5 as a candidate gene for cocaine dependence , 2015, Translational Psychiatry.
[14] Gabor T. Marth,et al. A global reference for human genetic variation , 2015, Nature.
[15] D. Horn,et al. A Novel Oculo-Skeletal syndrome with intellectual disability caused by a particular MAB21L2 mutation. , 2015, European journal of medical genetics.
[16] M. Vinberg,et al. A composite peripheral blood gene expression measure as a potential diagnostic biomarker in bipolar disorder , 2015, Translational Psychiatry.
[17] P. Falkai,et al. Proteomics of the corpus callosum unravel pivotal players in the dysfunction of cell signaling, structure, and myelination in schizophrenia brains , 2015, European Archives of Psychiatry and Clinical Neuroscience.
[18] P. Sullivan,et al. Genome-Wide Meta-Analysis of Longitudinal Alcohol Consumption Across Youth and Early Adulthood , 2015, Twin Research and Human Genetics.
[19] Young Jae Woo,et al. Reciprocal Relationship between Head Size, an Autism Endophenotype, and Gene Dosage at 19p13.12 Points to AKAP8 and AKAP8L , 2015, PloS one.
[20] L. Sun,et al. Gene expression profiling in peripheral blood mononuclear cells of early-onset schizophrenia , 2015, Genomics data.
[21] Joana S. Ferreira,et al. GluN2B-Containing NMDA Receptors Regulate AMPA Receptor Traffic through Anchoring of the Synaptic Proteasome , 2015, The Journal of Neuroscience.
[22] B. Gener,et al. Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders , 2015, Molecular Autism.
[23] W. Kao,et al. Relative performance of gene- and pathway-level methods as secondary analyses for genome-wide association studies , 2015, BMC Genetics.
[24] Joris M. Mooij,et al. MAGMA: Generalized Gene-Set Analysis of GWAS Data , 2015, PLoS Comput. Biol..
[25] Stephan J Sanders,et al. The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment , 2015, Nature Communications.
[26] L. Kiemeney,et al. Case–Control Genome-Wide Association Study of Persistent Attention-Deficit Hyperactivity Disorder Identifies FBXO33 as a Novel Susceptibility Gene for the Disorder , 2015, Neuropsychopharmacology.
[27] Gustavo Glusman,et al. Rare variants in neuronal excitability genes influence risk for bipolar disorder , 2015, Proceedings of the National Academy of Sciences.
[28] B. Crespo-Facorro,et al. Schizophrenia Gene Expression Profile Reverted to Normal Levels by Antipsychotics , 2015, The international journal of neuropsychopharmacology.
[29] T. Cummins,et al. The molecular genetic architecture of attention deficit hyperactivity disorder , 2015, Molecular Psychiatry.
[30] Matthew E. Ritchie,et al. limma powers differential expression analyses for RNA-sequencing and microarray studies , 2015, Nucleic acids research.
[31] Laura J. Scott,et al. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways , 2015, Nature Neuroscience.
[32] S. Scherer,et al. Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes , 2015, Human Genetics.
[33] Suhua Chang,et al. Molecular genetic studies of ADHD and its candidate genes: A review , 2014, Psychiatry Research.
[34] J. García-Sevilla,et al. FADD adaptor and PEA-15/ERK1/2 partners in major depression and schizophrenia postmortem brains: Basal contents and effects of psychotropic treatments , 2014, Neuroscience.
[35] A. Pillai,et al. Ubiquitin-proteasome dependent degradation of GABAAα1 in autism spectrum disorder , 2014, Molecular Autism.
[36] C. Schwarzer,et al. GPER1 (GPR30) knockout mice display reduced anxiety and altered stress response in a sex and paradigm dependent manner , 2014, Hormones and Behavior.
[37] S. Scherer,et al. Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants , 2014, Journal of the American Academy of Child and Adolescent Psychiatry.
[38] M C O'Donovan,et al. Copy number variation in schizophrenia in Sweden , 2014, Molecular Psychiatry.
[39] John J. Foxe,et al. Mosaic Epigenetic Dysregulation of Ectodermal Cells in Autism Spectrum Disorder , 2014, bioRxiv.
[40] Christopher D. Brown,et al. Genomic View of Bipolar Disorder Revealed by Whole Genome Sequencing in a Genetic Isolate , 2014, PLoS genetics.
[41] Simon C. Potter,et al. A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation , 2014, Biological Psychiatry.
[42] M. Pirinen,et al. A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation , 2014, Biological Psychiatry.
[43] A. Pillai,et al. Glucocorticoid Regulates Parkin Expression in Mouse Frontal Cortex: Implications in Schizophrenia , 2014, Current neuropharmacology.
[44] Joseph T. Glessner,et al. Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population , 2014, Molecular Autism.
[45] Eliona Tsefou,et al. Conditional inactivation of nicastrin restricts amyloid deposition in an Alzheimer's disease mouse model , 2013, Aging cell.
[46] John P. Rice,et al. A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53 , 2013, Molecular Psychiatry.
[47] Jianxin Shi,et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs , 2013, Nature Genetics.
[48] B. Franke,et al. AKAPs integrate genetic findings for autism spectrum disorders , 2013, Translational Psychiatry.
[49] P. Wong,et al. Multiple variants aggregate in the neuregulin signaling pathway in a subset of schizophrenia patients , 2013, Translational Psychiatry.
[50] M. Daly,et al. Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis , 2013, The Lancet.
[51] V. Haroutunian,et al. Dysfunction of the Ubiquitin Proteasome and Ubiquitin-Like Systems in Schizophrenia , 2013, Neuropsychopharmacology.
[52] N. Wray,et al. A mega-analysis of genome-wide association studies for major depressive disorder , 2013, Molecular Psychiatry.
[53] K. Zito,et al. Breaking It Down: The Ubiquitin Proteasome System in Neuronal Morphogenesis , 2013, Neural plasticity.
[54] Stephan Ripke,et al. Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies. , 2013, The American journal of psychiatry.
[55] S Cichon,et al. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder , 2012, Molecular Psychiatry.
[56] J. Schweitzer,et al. Correlations of gene expression with ratings of inattention and hyperactivity/impulsivity in tourette syndrome: a pilot study , 2012, BMC Medical Genomics.
[57] J. Ramos-Quiroga,et al. Validez de criterio y concurrente de la versión española de la Conners Adult ADHD Diagnostic Interview for DSM-IV , 2012 .
[58] R. Handsaker,et al. Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder , 2012, Molecular Psychiatry.
[59] J. Marchini,et al. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing , 2012, Nature Genetics.
[60] Zhen Yan,et al. Repeated Stress Causes Cognitive Impairment by Suppressing Glutamate Receptor Expression and Function in Prefrontal Cortex , 2012, Neuron.
[61] Nicholas J. Schork,et al. Age-Dependent Brain Gene Expression and Copy Number Anomalies in Autism Suggest Distinct Pathological Processes at Young Versus Mature Ages , 2012, PLoS genetics.
[62] Bradley P. Coe,et al. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations , 2012, Nature.
[63] R. Schekman,et al. Ubiquitin-dependent regulation of COPII coat size and function , 2012, Nature.
[64] B. Franke,et al. The genetics of attention deficit/hyperactivity disorder in adults, a review , 2011, Molecular Psychiatry.
[65] J. Leek,et al. Temporal dynamics and genetic control of transcription in the human prefrontal cortex , 2011, Nature.
[66] Wei Chen,et al. Deep sequencing reveals 50 novel genes for recessive cognitive disorders , 2011, Nature.
[67] Peilin Jia,et al. Gene set analysis of genome-wide association studies: methodological issues and perspectives. , 2011, Genomics.
[68] K. Iwamoto,et al. Survey of the effect of genetic variations on gene expression in human prefrontal cortex and its application to genetics of psychiatric disorders , 2011, Neuroscience Research.
[69] Chia-Hsiang Chen,et al. Clinical and molecular characterization of a transmitted reciprocal translocation t(1;12)(p32.1;q21.3) in a family co-segregating with mental retardation, language delay, and microcephaly , 2011, BMC Medical Genetics.
[70] N. Datson,et al. Hippocampal CA1 region shows differential regulation of gene expression in mice displaying extremes in behavioral sensitization to amphetamine: relevance for psychosis susceptibility? , 2011, Psychopharmacology.
[71] John H. Byrne,et al. Protein degradation and memory formation , 2011, Brain Research Bulletin.
[72] Yang Wang,et al. Common SNPs in CSF2RB are associated with major depression and schizophrenia in the Chinese Han population , 2011, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.
[73] B. Franke,et al. Integrated genome-wide association study findings: identification of a neurodevelopmental network for attention deficit hyperactivity disorder. , 2011, The American journal of psychiatry.
[74] T. Shaikh,et al. Rare structural variation of synapse and neurotransmission genes in autism , 2011, Molecular Psychiatry.
[75] G. Churchill,et al. Gene expression patterns in the hippocampus and amygdala of endogenous depression and chronic stress models , 2010, Molecular Psychiatry.
[76] K. Strimbu,et al. What are biomarkers? , 2010, Current opinion in HIV and AIDS.
[77] H. Stefánsson,et al. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis , 2010, BDJ.
[78] Rafael A. Irizarry,et al. A framework for oligonucleotide microarray preprocessing , 2010, Bioinform..
[79] Susanne Walitza,et al. Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. , 2010, Journal of the American Academy of Child and Adolescent Psychiatry.
[80] Margaret A. Pericak-Vance,et al. A genome-wide scan for common alleles affecting risk for autism , 2010, Human molecular genetics.
[81] P. Visscher,et al. A versatile gene-based test for genome-wide association studies. , 2010, American journal of human genetics.
[82] A. Hegde. The ubiquitin-proteasome pathway and synaptic plasticity. , 2010, Learning & memory.
[83] Zhi-Yong Peng,et al. RNF122: A novel ubiquitin ligase associated with calcium-modulating cyclophilin ligand , 2010, BMC Cell Biology.
[84] Stephen J Glatt,et al. Preliminary evidence of ubiquitin proteasome system dysregulation in schizophrenia and bipolar disorder: Convergent pathway analysis findings from two independent samples , 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[85] A. Hoischen,et al. Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of LRFN5 Expression , 2010, Molecular Syndromology.
[86] W. Brown,et al. Increased activities of Na+/K+-ATPase and Ca2+/Mg2+-ATPase in the frontal cortex and cerebellum of autistic individuals. , 2009, Life sciences.
[87] John P. Rice,et al. Genome-wide association study of bipolar disorder in European American and African American individuals , 2009, Molecular Psychiatry.
[88] I. Waldman,et al. Candidate gene studies of ADHD: a meta-analytic review , 2009, Human Genetics.
[89] P. Donnelly,et al. A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies , 2009, PLoS genetics.
[90] R. Ebstein,et al. Association Between Sodium- and Potassium-Activated Adenosine Triphosphatase α Isoforms and Bipolar Disorders , 2009, Biological Psychiatry.
[91] Robert T. Schultz,et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes , 2009, Nature.
[92] Robert T. Schultz,et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders , 2009, Nature.
[93] Jack A. Taylor,et al. SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies , 2009, Nucleic Acids Res..
[94] N. Craddock,et al. Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk , 2009, Molecular Psychiatry.
[95] Hwan‐Ching Tai,et al. Ubiquitin, the proteasome and protein degradation in neuronal function and dysfunction , 2008, Nature Reviews Neuroscience.
[96] A. Fanous,et al. Association study of CSF2RB with schizophrenia in Irish family and case – control samples , 2008, Molecular Psychiatry.
[97] D. Stephan,et al. A survey of genetic human cortical gene expression , 2007, Nature Genetics.
[98] D. M. Lyons,et al. Stress-induced changes in primate prefrontal profiles of gene expression , 2007, Molecular Psychiatry.
[99] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.
[100] M. Ehlers,et al. Emerging Roles for Ubiquitin and Protein Degradation in Neuronal Function , 2007, Pharmacological Reviews.
[101] D. Rubinsztein,et al. The roles of intracellular protein-degradation pathways in neurodegeneration , 2006, Nature.
[102] D. James,et al. Molecular Dissection of the Munc18c/Syntaxin4 Interaction: Implications for Regulation of Membrane Trafficking , 2006, Traffic.
[103] Michael Q. Zhang,et al. An increased specificity score matrix for the prediction of SF2/ASF-specific exonic splicing enhancers. , 2006, Human molecular genetics.
[104] M. Webster,et al. Gene expression analysis of bipolar disorder reveals downregulation of the ubiquitin cycle and alterations in synaptic genes , 2006, Molecular Psychiatry.
[105] Danielle N. Pappas. ADHD Rating Scale-IV: Checklists, Norms, and Clinical Interpretation , 2006 .
[106] Charles M Perou,et al. Evaluating the comparability of gene expression in blood and brain , 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[107] D. Nyholt. A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. , 2004, American journal of human genetics.
[108] B. Dubois,et al. Subtle cognitive impairment but no dementia in patients with spastin mutations. , 2003, Archives of neurology.
[109] Jinhua Wang,et al. ESEfinder: a web resource to identify exonic splicing enhancers , 2003, Nucleic Acids Res..
[110] Molecular genetic delineation of a deletion of chromosome 13q12→q13 in a patient with autism and auditory processing deficits , 2003, Cytogenetic and Genome Research.
[111] K. Broadie,et al. The Ubiquitin Proteasome System Acutely Regulates Presynaptic Protein Turnover and Synaptic Efficacy , 2003, Current Biology.
[112] Thomas D. Schmittgen,et al. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.
[113] Nobutaka Hattori,et al. Ubiquitination of a New Form of α-Synuclein by Parkin from Human Brain: Implications for Parkinson's Disease , 2001, Science.
[114] C. Pickart,et al. Inhibition of the ubiquitin-proteasome system in Alzheimer's disease. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[115] P. Wender,et al. The Wender Utah Rating Scale: an aid in the retrospective diagnosis of childhood attention deficit hyperactivity disorder. , 1993, The American journal of psychiatry.
[116] D. Sheehan,et al. The Anxiety Disease , 1984 .
[117] P. Guest,et al. Peripheral profiling analysis for bipolar disorder reveals markers associated with reduced cell survival , 2011, Proteomics.
[118] M. Biasi,et al. The Ubiquitin–Proteasome System Regulates the Stability of Neuronal Nicotinic Acetylcholine Receptors , 2009, Journal of Molecular Neuroscience.
[119] X. Estivill,et al. Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB , 2009, Molecular Psychiatry.
[120] Y. Benjamini,et al. Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .
[121] Conners Ck. The computerized continuous performance test. , 1985 .
[122] C. Conners. The computerized continuous performance test. , 1985, Psychopharmacology bulletin.
[123] R. Amann,et al. Predictive Identification of Exonic Splicing Enhancers in Human Genes , 2022 .
[124] J. Qian,et al. Central European Journal of Biology , 2022 .