Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways.
- Authors
- Nishimura, Yuhei; Martin, Christa L; Vazquez-Lopez, Araceli; Spence, Sarah J; Alvarez-Retuerto, Ana Isabel; Sigman, Marian; Steindler, Corinna; Pellegrini, Sandra; Schanen, N Carolyn; Warren, Stephen T; Geschwind, Daniel H
- Year
- 2007
- Journal
- Human molecular genetics
- PMID
- 17519220
- DOI
- 10.1093/hmg/ddm116
Autism is a heterogeneous condition that is likely to result from the combined effects of multiple genetic factors interacting with environmental factors. Given its complexity, the study of autism associated with Mendelian single gene disorders or known chromosomal etiologies provides an important perspective. We used microarray analysis to compare the mRNA expression profile in lymphoblastoid cells from males with autism due to a fragile X mutation (FMR1-FM), or a 15q11-q13 duplication (dup(15q)), and non-autistic controls. Gene expression profiles clearly distinguished autism from controls and separated individuals with autism based on their genetic etiology. We identified 68 genes that were dysregulated in common between autism with FMR1-FM and dup(15q). We also identified a potential molecular link between FMR1-FM and dup(15q), the cytoplasmic FMR1 interacting protein 1 (CYFIP1), which was up-regulated in dup(15q) patients. We were able to confirm this link in vitro by showing common regulation of two other dysregulated genes, JAKMIP1 and GPR155, downstream of FMR1 or CYFIP1. We also confirmed the reduction of the Jakmip1 protein in Fmr1 knock-out mice, demonstrating in vivo relevance. Finally, we showed independent confirmation of roles for JAKMIP1 and GPR155 in autism spectrum disorders (ASDs) by showing their differential expression in male sib pairs discordant for idiopathic ASD. These results provide evidence that blood derived lymphoblastoid cells gene expression is likely to be useful for identifying etiological subsets of autism and exploring its pathophysiology.
No figures extracted from this document.
No chunks β full text not yet ingested.
No entities extracted from this document yet.
No uploaded files.
No citations found.
In this knowledge base
| Title | Year | PMID |
|---|---|---|
| Ethanol treatment of lymphoblastoid cell lines from alcoholics and non-alcoholics causes many subtle changes in gene expression. | 2014 | 25129674 |
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| Divergence in expression of a singing-related neuroplasticity gene in the brains of 2 Ficedula flycatchers and their hybrids. | Wheatcroft D et al. | β | 2025 | β |
| DNA methylationΒ biomarkersΒ of intellectual/developmental disability across the lifespan. | LaSalle JM | β | 2025 | β |
| Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism. | Kim SW et al. | β | 2025 | β |
| Impaired macroautophagy confers substantial risk for intellectual disability in children with autism spectrum disorders. | Ham A et al. | β | 2025 | β |
| Prenatal stress alters mouse offspring dorsal striatal development and placental function in sex-specific ways. | Maurer SV et al. | β | 2025 | β |
| The WAVE complex in developmental and adulthood brain disorders. | Kim HG et al. | β | 2025 | β |
| A critical assessment of sparse PCA (research): why (one should acknowledge that) weights are not loadings. | Park S et al. | β | 2024 | β |
| Autism spectrum disorder: pathogenesis, biomarker, and intervention therapy. | Zhuang H et al. | β | 2024 | β |
| Cell-type-specific effects of autism-associated 15q duplication syndrome in the human brain. | Dias C et al. | β | 2024 | β |
| Epigenetic disruptions in the offspring hypothalamus in response to maternal infection. | Alsegehy S et al. | β | 2024 | β |
| Is developmental plasticity triggered by DNA methylation changes in the invasive cane toad (<i>Rhinella marina</i>)? | Yagound B et al. | β | 2024 | β |
| NARP-related alterations in the excitatory and inhibitory circuitry of socially isolated mice: developmental insights and implications for autism spectrum disorder. | Yamaguchi Y et al. | β | 2024 | β |
| Neuregulin 2 Is a Candidate Gene for Autism Spectrum Disorder. | Chien WH et al. | β | 2024 | β |
| Overexpression of TIAM2S, a Critical Regulator for the Hippocampal-Medial Prefrontal Cortex Network, Progresses Age-Related Spatial Memory Impairment. | Chu CH et al. | β | 2024 | β |
| Neuroanatomical Alterations in the CNTNAP2 Mouse Model of Autism Spectrum Disorder. | Gandhi T et al. | β | 2023 | β |
| Simultaneous clustering and variable selection: A novel algorithm and model selection procedure. | Yuan S et al. | β | 2023 | β |
| TIAM2S-positive microglia enhance inflammation and neurotoxicity through soluble ICAM-1-mediated immune priming. | Chu CH et al. | β | 2023 | β |
| A Double Jeopardy: Loss of FMRP Results in DSB and Down-regulated DNA Repair. | Chakraborty A et al. | β | 2022 | β |
| CYFIP1 Dosages Exhibit Divergent Behavioral Impact via Diametric Regulation of NMDA Receptor Complex Translation in Mouse Models of Psychiatric Disorders. | Kim NS et al. | β | 2022 | β |
| Evolution of the Membrane Transport Protein Domain. | Dabravolski SA et al. | β | 2022 | β |
| Genetic Characteristics Associated With Drug Resistance in Lung Cancer and Colorectal Cancer Using Whole Exome Sequencing of Cell-Free DNA. | Lee JW et al. | β | 2022 | β |
| Integrated microRNA-mRNA Expression Profiling Identifies Novel Targets and Networks Associated with Autism. | Gill PS et al. | β | 2022 | β |
| Pirenperone relieves the symptoms of fragile X syndrome in Fmr1 knockout mice | Kim Y et al. | β | 2022 | β |
| Translational relevance of forward genetic screens in animal models for the study of psychiatric disease. | Sheardown E et al. | β | 2022 | β |
| A Guide for Sparse PCA: Model Comparison and Applications. | Guerra-Urzola R et al. | β | 2021 | β |
| Anchor maintains gut homeostasis by restricting the JNK and Notch pathways in Drosophila. | Wang J et al. | β | 2021 | β |
| Autism-like social deficit generated by Dock4 deficiency is rescued by restoration of Rac1 activity and NMDA receptor function. | Guo D et al. | β | 2021 | β |
| Biological implications of genetic variations in autism spectrum disorders from genomics studies. | Zhang Y et al. | β | 2021 | β |
| Genetic contributions to autism spectrum disorder. | Havdahl A et al. | β | 2021 | β |
| Prenatal lead exposure and cord blood DNA methylation in the Korean Exposome Study. | Park J et al. | β | 2021 | β |
| Wnt/Ξ²-Catenin-Dependent Transcription in Autism Spectrum Disorders. | Caracci MO et al. | β | 2021 | β |
| Biomarkers in autism spectrum disorders: Current progress. | Shen L et al. | β | 2020 | β |
| Elevated blood urea nitrogen alters the transcriptome of equine embryos. | Boakari YL et al. | β | 2020 | β |
| On the Nature of Monozygotic Twin Concordance and Discordance for Autistic Trait Severity: A Quantitative Analysis. | Castelbaum L et al. | β | 2020 | β |
| Phenotypic Subtyping and Re-analyses of Existing Transcriptomic Data from Autistic Probands in Simplex Families Reveal Differentially Expressed and ASD Trait-Associated Genes. | Hu VW et al. | β | 2020 | β |
| Replication Stress Induces Global Chromosome Breakage in the Fragile X Genome. | Chakraborty A et al. | β | 2020 | β |
| Transcriptome signatures from discordant sibling pairs reveal changes in peripheral blood immune cell composition in Autism Spectrum Disorder. | Filosi M et al. | β | 2020 | β |
| Advances in Biomarker Studies in Autism Spectrum Disorders. | Shen L et al. | β | 2019 | β |
| A perturbed gene network containing PI3K-AKT, RAS-ERK and WNT-Ξ²-catenin pathways in leukocytes is linked to ASD genetics and symptom severity. | Gazestani VH et al. | β | 2019 | β |
| Autism and Schizophrenia-Associated CYFIP1 Regulates the Balance of Synaptic Excitation and Inhibition. | Davenport EC et al. | β | 2019 | β |
| CYFIP1 overexpression increases fear response in mice but does not affect social or repetitive behavioral phenotypes. | Fricano-Kugler C et al. | β | 2019 | β |
| Deletion of Semaphorin 3F in Interneurons Is Associated with Decreased GABAergic Neurons, Autism-like Behavior, and Increased Oxidative Stress Cascades. | Li Z et al. | β | 2019 | β |
| Genetics and epigenetics of autism spectrum disorder-current evidence in the field. | WiΕniowiecka-Kowalnik B et al. | β | 2019 | β |
| Pathobiology of Christianson syndrome: Linking disrupted endosomal-lysosomal function with intellectual disability and sensory impairments. | Kerner-Rossi M et al. | β | 2019 | β |
| Protein Biomarkers in Major Depressive Disorder: An Update. | Woods AG et al. | β | 2019 | β |
| Proteomics Study of Peripheral Blood Mononuclear Cells (PBMCs) in Autistic Children. | Shen L et al. | β | 2019 | β |
| Rhythms of life: circadian disruption and brain disorders across the lifespan. | Logan RW et al. | β | 2019 | β |
| Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autism. | van Eyk CL et al. | β | 2018 | β |
| Control of CNS functions by RNA-binding proteins in neurological diseases. | Zhou Y et al. | β | 2018 | β |
| Cytoplasmic FMRP interacting protein 1/2 (CYFIP1/2) expression analysis in autism. | Noroozi R et al. | β | 2018 | β |
| Dendritic spine actin cytoskeleton in autism spectrum disorder. | Joensuu M et al. | β | 2018 | β |
| Exon Array Biomarkers for the Differential Diagnosis of Schizophrenia and Bipolar Disorder. | Vawter MP et al. | β | 2018 | β |
| iTRAQ-Based Proteomic Analysis Reveals Protein Profile in Plasma from Children with Autism. | Shen L et al. | β | 2018 | β |
| Microarray analysis of gene expression in the cyclooxygenase knockout mice - a connection to autism spectrum disorder. | Rai-Bhogal R et al. | β | 2018 | β |
| Significant transcriptional changes in 15q duplication but not Angelman syndrome deletion stem cell-derived neurons. | Urraca N et al. | β | 2018 | β |
| The role of reduced expression of fragile X mental retardation protein in neurons and increased expression in astrocytes in idiopathic and syndromic autism (duplications 15q11.2-q13). | Wegiel J et al. | β | 2018 | β |
| UBE3A and Its Link With Autism. | Vatsa N et al. | β | 2018 | β |
| A Scaled Framework for CRISPR Editing of Human Pluripotent Stem Cells to Study Psychiatric Disease. | Hazelbaker DZ et al. | β | 2017 | β |
| Dysfunctional mTORC1 Signaling: A Convergent Mechanism between Syndromic and Nonsyndromic Forms of Autism Spectrum Disorder? | Magdalon J et al. | β | 2017 | β |
| Emerging Synaptic Molecules as Candidates in the Etiology of Neurological Disorders. | Torres VI et al. | β | 2017 | β |
| Identification of Novel Signal Transduction, Immune Function, and Oxidative Stress Genes and Pathways by Topiramate for Treatment of Methamphetamine Dependence Based on Secondary Outcomes. | Niu T et al. | β | 2017 | β |
| RNA sequencing of transformed lymphoblastoid cells from siblings discordant for autism spectrum disorders reveals transcriptomic and functional alterations: Evidence for sex-specific effects. | Tylee DS et al. | β | 2017 | β |
| Selection signature analysis reveals genes associated with tail type in Chinese indigenous sheep. | Yuan Z et al. | β | 2017 | β |
| Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families. | Al-Mubarak B et al. | β | 2017 | β |
| A common molecular signature in ASD gene expression: following Root 66 to autism. | Diaz-Beltran L et al. | β | 2016 | β |
| Advancing the understanding of autism disease mechanisms through genetics. | de la Torre-Ubieta L et al. | β | 2016 | β |
| Comparative Transcriptome Analysis Identifies CCDC80 as a Novel Gene Associated with Pulmonary Arterial Hypertension. | Sasagawa S et al. | β | 2016 | β |
| EP300 Protects from Light-Induced Retinopathy in Zebrafish. | Kawase R et al. | β | 2016 | β |
| Human iPSC-derived neurons and lymphoblastoid cells for personalized medicine research in neuropsychiatric disorders. | Gurwitz D | β | 2016 | β |
| If genetic variation could talk: What genomic data may teach us about the importance of gene expression regulation in the genetics of autism. | Yeh E et al. | β | 2016 | β |
| Perturbed proteostasis in autism spectrum disorders. | Louros SR et al. | β | 2016 | β |
| Selection of Suitable Reference Genes for Analysis of Salivary Transcriptome in Non-Syndromic Autistic Male Children. | Panahi Y et al. | β | 2016 | β |
| Variation in Gene Expression in Autism Spectrum Disorders: An Extensive Review of Transcriptomic Studies. | Ansel A et al. | β | 2016 | β |
| Autism Spectrum Disorder - A Complex Genetic Disorder. | Ivanov HY et al. | β | 2015 | β |
| Comparative two-dimensional polyacrylamide gel electrophoresis of the salivary proteome of children with autism spectrum disorder. | Ngounou Wetie AG et al. | β | 2015 | β |
| Comparison of microarray expression profiles between follicular variant of papillary thyroid carcinomas and follicular adenomas of the thyroid. | Schulten HJ et al. | β | 2015 | β |
| Increased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTOR. | Oguro-Ando A et al. | β | 2015 | β |
| Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems. | Kumar R et al. | β | 2015 | β |
| JAKMIP1, a Novel Regulator of Neuronal Translation, Modulates Synaptic Function and Autistic-like Behaviors in Mouse. | Berg JM et al. | β | 2015 | β |
| JAKMIP1: Translating the Message for Social Behavior. | Penney J et al. | β | 2015 | β |
| Meta-Analysis of Gene Expression in Autism Spectrum Disorder. | Ch'ng C et al. | β | 2015 | β |
| Pharmacological profiling of zebrafish behavior using chemical and genetic classification of sleep-wake modifiers. | Nishimura Y et al. | β | 2015 | β |
| Quantitative profiling of brain lipid raft proteome in a mouse model of fragile X syndrome. | Kalinowska M et al. | β | 2015 | β |
| Role of long purine stretches in controlling the expression of genes associated with neurological disorders. | Singh HN et al. | β | 2015 | β |
| The Anti-Inflammatory Effects of the Small Molecule Pifithrin-Β΅ on BV2 Microglia. | Fleiss B et al. | β | 2015 | β |
| The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles. | Kusenda M et al. | β | 2015 | β |
| The Role of Epigenetic Change in Autism Spectrum Disorders. | Loke YJ et al. | β | 2015 | β |
| THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability. | Kumar R et al. | β | 2015 | β |
| Transcriptome Profiling of Peripheral Blood in 22q11.2 Deletion Syndrome Reveals Functional Pathways Related to Psychosis and Autism Spectrum Disorder. | Jalbrzikowski M et al. | β | 2015 | β |
| Aberrant Rho GTPases signaling and cognitive dysfunction: in vivo evidence for a compelling molecular relationship. | De Filippis B et al. | β | 2014 | β |
| Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs. | Prandini P et al. | β | 2014 | β |
| Assessing the impact of copy number variants on miRNA genes in autism by Monte Carlo simulation. | Marrale M et al. | β | 2014 | β |
| Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders. | Waltes R et al. | β | 2014 | β |
| Epigenetic epidemiology: promises for public health research. | Bakulski KM et al. | β | 2014 | β |
| Ethanol treatment of lymphoblastoid cell lines from alcoholics and non-alcoholics causes many subtle changes in gene expression. | McClintick JN et al. | β | 2014 | β |
| Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1. | Germain ND et al. | β | 2014 | β |
| Glutamatergic candidate genes in autism spectrum disorder: an overview. | Chiocchetti AG et al. | β | 2014 | β |
| iPSC-derived neurons as a higher-throughput readout for autism: promises and pitfalls. | Prilutsky D et al. | β | 2014 | β |
| miR-338-3p is over-expressed in blood, CFS, serum and spinal cord from sporadic amyotrophic lateral sclerosis patients. | De Felice B et al. | β | 2014 | β |
| Modeling a genetic risk for schizophrenia in iPSCs and mice reveals neural stem cell deficits associated with adherens junctions and polarity. | Yoon KJ et al. | β | 2014 | β |
| Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder. | Berko ER et al. | β | 2014 | β |
| Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2. | Fogel BL et al. | β | 2014 | β |
| Performing DISCO-SCA to search for distinctive and common information in linked data. | Schouteden M et al. | β | 2014 | β |
| Protein interaction networks reveal novel autism risk genes within GWAS statistical noise. | Correia C et al. | β | 2014 | β |
| The autism and schizophrenia associated gene CYFIP1 is critical for the maintenance of dendritic complexity and the stabilization of mature spines. | Pathania M et al. | β | 2014 | β |
| Transcriptome analysis reveals dysregulation of innate immune response genes and neuronal activity-dependent genes in autism. | Gupta S et al. | β | 2014 | β |
| Translational regulation of NeuroD1 expression by FMRP: involvement in glutamatergic neuronal differentiation of cultured rat primary neural progenitor cells. | Jeon SJ et al. | β | 2014 | β |
| An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk. | Cheng Y et al. | β | 2013 | β |
| Comparative DNA methylation among females with neurodevelopmental disorders and seizures identifies TAC1 as a MeCP2 target gene. | Aldinger KA et al. | β | 2013 | β |
| CYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic spine formation. | De Rubeis S et al. | β | 2013 | β |
| DNA repair/replication transcripts are down regulated in patients with Fragile X Syndrome. | Xu H et al. | β | 2013 | β |
| Expression quantitative trait loci: present and future. | Nica AC et al. | β | 2013 | β |
| From genes to environment: using integrative genomics to build a "systems-level" understanding of autism spectrum disorders. | Hu VW | β | 2013 | β |
| Gene expression profile of SOD1-G93A mouse spinal cord, blood and muscle. | Saris CG et al. | β | 2013 | β |
| Immune dysregulation in autism spectrum disorder. | Hsiao EY | β | 2013 | β |
| Increased gene expression of FOXP1 in patients with autism spectrum disorders. | Chien WH et al. | β | 2013 | β |
| Overexpression of JAKMIP1 associates with Wnt/Ξ²-catenin pathway activation and promotes cancer cell proliferation in vitro. | Okai I et al. | β | 2013 | β |
| Pathway-based outlier method reveals heterogeneous genomic structure of autism in blood transcriptome. | Campbell MG et al. | β | 2013 | β |
| Peripheral blood gene expression signature differentiates children with autism from unaffected siblings. | Kong SW et al. | β | 2013 | β |
| RIM3Ξ³ and RIM4Ξ³ are key regulators of neuronal arborization. | Alvarez-Baron E et al. | β | 2013 | β |
| Role of conserved cis-regulatory elements in the post-transcriptional regulation of the human MECP2 gene involved in autism. | Bagga JS et al. | β | 2013 | β |
| Stem cells as a good tool to investigate dysregulated biological systems in autism spectrum disorders. | Griesi-Oliveira K et al. | β | 2013 | β |
| The 5' untranslated region of the serotonin receptor 2C pre-mRNA generates miRNAs and is expressed in non-neuronal cells. | Zhang Z et al. | β | 2013 | β |
| The orthographic sensitivity to written Chinese in the occipital-temporal cortex. | Liu H et al. | β | 2013 | β |
| 15q11.2 microdeletion and FMR1 premutation in a family with intellectual disabilities and autism. | Madrigal I et al. | β | 2012 | β |
| 15q11.2 proximal imbalances associated with a diverse array of neuropsychiatric disorders and mild dysmorphic features. | Abdelmoity AT et al. | β | 2012 | β |
| Altered mTOR signaling and enhanced CYFIP2 expression levels in subjects with fragile X syndrome. | Hoeffer CA et al. | β | 2012 | β |
| A miRNA signature in leukocytes from sporadic amyotrophic lateral sclerosis. | De Felice B et al. | β | 2012 | β |
| A novel X-linked disorder with developmental delay and autistic features. | Kaya N et al. | β | 2012 | β |
| Blood-based gene expression signatures of infants and toddlers with autism. | Glatt SJ et al. | β | 2012 | β |
| Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders. | Kong SW et al. | β | 2012 | β |
| Characterization of DNA methylation and its association with other biological systems in lymphoblastoid cell lines. | Zhang Z et al. | β | 2012 | β |
| Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci. | Hedges DJ et al. | β | 2012 | β |
| Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics. | Bagni C et al. | β | 2012 | β |
| Gene expression studies in autism: moving from the genome to the transcriptome and beyond. | Voineagu I | β | 2012 | β |
| Genome-wide expression studies in autism spectrum disorder, Rett syndrome, and Down syndrome. | Lintas C et al. | β | 2012 | β |
| Genome-wide gene expression profiling of human narcolepsy. | Bernardini C et al. | β | 2012 | β |
| Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders. | Luo R et al. | β | 2012 | β |
| Genome-wide transcriptomic variations of human lymphoblastoid cell lines: insights from pairwise gene-expression correlations. | Vincent M et al. | β | 2012 | β |
| HERVs expression in Autism Spectrum Disorders. | Balestrieri E et al. | β | 2012 | β |
| Longitudinal follow-up of autism spectrum features and sensory behaviors in Angelman syndrome by deletion class. | Peters SU et al. | β | 2012 | β |
| Molecular signatures of cardiac defects in Down syndrome lymphoblastoid cell lines suggest altered ciliome and Hedgehog pathways. | Ripoll C et al. | β | 2012 | β |
| Psychoactive pharmaceuticals induce fish gene expression profiles associated with human idiopathic autism. | Thomas MA et al. | β | 2012 | β |
| RNA interference of Marlin-1/Jakmip1 results in abnormal morphogenesis and migration of cortical pyramidal neurons. | Vidal RL et al. | β | 2012 | β |
| The contributions of oxytocin and vasopressin pathway genes to human behavior. | Ebstein RP et al. | β | 2012 | β |
| Vignettes: models in absentia. | Denman RB | β | 2012 | β |
| Abnormal cell properties and down-regulated FAK-Src complex signaling in B lymphoblasts of autistic subjects. | Wei H et al. | β | 2011 | β |
| Are retinoids potential therapeutic agents in disorders of social cognition including autism? | Ebstein RP et al. | β | 2011 | β |
| Autism-associated gene expression in peripheral leucocytes commonly observed between subjects with autism and healthy women having autistic children. | Kuwano Y et al. | β | 2011 | β |
| FMR1 premutation and full mutation molecular mechanisms related to autism. | Hagerman R et al. | β | 2011 | β |
| Fragile x syndrome. | McLennan Y et al. | β | 2011 | β |
| Functional genomics of the brain: uncovering networks in the CNS using a systems approach. | Konopka G | β | 2011 | β |
| Gene and miRNA expression profiles in autism spectrum disorders. | Ghahramani Seno MM et al. | β | 2011 | β |
| Gene expression analysis in lymphoblasts derived from patients with autism spectrum disorder. | Yasuda Y et al. | β | 2011 | β |
| Gene expression biomarkers of response to citalopram treatment in major depressive disorder. | Mamdani F et al. | β | 2011 | β |
| Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders. | Anney RJ et al. | β | 2011 | β |
| Hydration-sensitive gene expression in brain. | Tang C et al. | β | 2011 | β |
| Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples. | Scoles HA et al. | β | 2011 | β |
| Increased gene dosage of Ube3a results in autism traits and decreased glutamate synaptic transmission in mice. | Smith SE et al. | β | 2011 | β |
| Multiple autism-like behaviors in a novel transgenic mouse model. | Hamilton SM et al. | β | 2011 | β |
| Prader-Willi syndrome and autism spectrum disorders: an evolving story. | Dykens EM et al. | β | 2011 | β |
| The neurobiology of mouse models syntenic to human chromosome 15q. | Takumi T | β | 2011 | β |
| The plausibility of a role for mercury in the etiology of autism: a cellular perspective. | Garrecht M et al. | β | 2011 | β |
| What can we learn about autism from studying fragile X syndrome? | Budimirovic DB et al. | β | 2011 | β |
| A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder. | van der Zwaag B et al. | β | 2010 | β |
| A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism. | Kumar RA et al. | β | 2010 | β |
| A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C. | Jensen LR et al. | β | 2010 | β |
| Autism in children and adolescents with cancer. | Blatt J et al. | β | 2010 | β |
| Autism spectrum disorders and epigenetics. | Grafodatskaya D et al. | β | 2010 | β |
| Blood mononuclear cell gene expression signature of postpartum depression. | Segman RH et al. | β | 2010 | β |
| EBV transformation and cell culturing destabilizes DNA methylation in human lymphoblastoid cell lines. | Grafodatskaya D et al. | β | 2010 | β |
| Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia. | Crespi B et al. | β | 2010 | β |
| Fragile X and autism: Intertwined at the molecular level leading to targeted treatments. | Hagerman R et al. | β | 2010 | β |
| Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. | Anttila V et al. | β | 2010 | β |
| Global methylation profiling of lymphoblastoid cell lines reveals epigenetic contributions to autism spectrum disorders and a novel autism candidate gene, RORA, whose protein product is reduced in autistic brain. | Nguyen A et al. | β | 2010 | β |
| GPR155: Gene organization, multiple mRNA splice variants and expression in mouse central nervous system. | Trifonov S et al. | β | 2010 | β |
| Hif1Ξ± down-regulation is associated with transposition of great arteries in mice treated with a retinoic acid antagonist. | Amati F et al. | β | 2010 | β |
| Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex. | Gao MC et al. | β | 2010 | β |
| The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13. | Hogart A et al. | β | 2010 | β |
| Transcriptional profiling of fibroblasts from patients with mutations in MCT8 and comparative analysis with the human brain transcriptome. | Visser WE et al. | β | 2010 | β |
| Transcriptome profile in Williams-Beuren syndrome lymphoblast cells reveals gene pathways implicated in glucose intolerance and visuospatial construction deficits. | Antonell A et al. | β | 2010 | β |
| Advances in autism. | Geschwind DH | β | 2009 | β |
| Advances in the treatment of fragile X syndrome. | Hagerman RJ et al. | β | 2009 | β |
| A functional network module for Smith-Magenis syndrome. | Girirajan S et al. | β | 2009 | β |
| Cellular and subcellular localization of Marlin-1 in the brain. | Vidal RL et al. | β | 2009 | β |
| Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number. | Hogart A et al. | β | 2009 | β |
| Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism. | Hu VW et al. | β | 2009 | β |
| Gene expression profiling of lymphoblasts from autistic and nonaffected sib pairs: altered pathways in neuronal development and steroid biosynthesis. | Hu VW et al. | β | 2009 | β |
| Genetic advances in autism: heterogeneity and convergence on shared pathways. | Bill BR et al. | β | 2009 | β |
| Genetic and environmental pathways to complex diseases. | Gohlke JM et al. | β | 2009 | β |
| Genetic variation of regulatory systems. | Dimas AS et al. | β | 2009 | β |
| Genomic landscape of a three-generation pedigree segregating affective disorder. | Yang S et al. | β | 2009 | β |
| Medical conditions in autism spectrum disorders. | Bolton PF | β | 2009 | β |
| Network analysis of differential expression for the identification of disease-causing genes. | Nitsch D et al. | β | 2009 | β |
| Neuroscience in the era of functional genomics and systems biology. | Geschwind DH et al. | β | 2009 | β |
| Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders. | Sebat J et al. | β | 2009 | β |
| Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders. | Depienne C et al. | β | 2009 | β |
| Testing the hypothesis of tissue selectivity: the intersection-union test and a Bayesian approach. | Van Deun K et al. | β | 2009 | β |
| The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders. | Levitt P et al. | β | 2009 | β |
| The genetic landscape of intellectual disability arising from chromosome X. | GΓ©cz J et al. | β | 2009 | β |
| The role of DNA copy number variation in schizophrenia. | Tam GW et al. | β | 2009 | β |
| Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients. | Saris CG et al. | β | 2009 | β |
| Whole-genome approach implicates CD44 in cellular resistance to carboplatin. | Shukla SJ et al. | β | 2009 | β |
| Advances in autism genetics: on the threshold of a new neurobiology. | Abrahams BS et al. | β | 2008 | β |
| Advances in behavioral genetics: mouse models of autism. | Moy SS et al. | β | 2008 | β |
| An association study of ADSS gene polymorphisms with schizophrenia. | Zhang F et al. | β | 2008 | β |
| Association analyses of the interaction between the ADSS and ATM genes with schizophrenia in a Chinese population. | Zhang F et al. | β | 2008 | β |
| Autism genetics: strategies, challenges, and opportunities. | O'Roak BJ et al. | β | 2008 | β |
| Behavior in Prader-Willi syndrome: relationship to genetic subtypes and age. | Dykens EM et al. | β | 2008 | β |
| Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism. | Maussion G et al. | β | 2008 | β |
| Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism. | Talebizadeh Z et al. | β | 2008 | β |
| Gene expression study on peripheral blood identifies progranulin mutations. | Coppola G et al. | β | 2008 | β |
| Genetic and expression analyses reveal elevated expression of syntaxin 1A ( STX1A) in high functioning autism. | Nakamura K et al. | β | 2008 | β |
| Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region. | Jiang YH et al. | β | 2008 | β |
| GRSDB2 and GRS_UTRdb: databases of quadruplex forming G-rich sequences in pre-mRNAs and mRNAs. | Kikin O et al. | β | 2008 | β |
| Immune transcriptome alterations in the temporal cortex of subjects with autism. | Garbett K et al. | β | 2008 | β |
| The DISC locus in psychiatric illness. | Chubb JE et al. | β | 2008 | β |
| The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP. | Napoli I et al. | β | 2008 | β |
| The potential role for emergence in autism. | Anderson GM | β | 2008 | β |
| Autism: the quest for the genes. | Sykes NH et al. | β | 2007 | β |
| The neurobiology of autism. | Pardo CA et al. | β | 2007 | β |