Autism Knowledgebase

Names

More detailed information about this field from each metasource. ×

Autism Knowledgebase

metasource: Fairsharing.org
version: FAIRsharing.org: Autism KB; Autism Knowledgebase; DOI: https://doi.org/10.25504/FAIRsharing.990a1b; Last edited: April 26, 2021, 8:19 a.m.; Last accessed: Jan 03 2022 7:05 p.m.

---

Autism KB

metasource: Fairsharing.org
version: FAIRsharing.org: Autism KB; Autism Knowledgebase; DOI: https://doi.org/10.25504/FAIRsharing.990a1b; Last edited: April 26, 2021, 8:19 a.m.; Last accessed: Jan 03 2022 7:05 p.m.

---

AutismKB

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:10.061603

---

autismkb

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:10.061603

Close

Other names: Autism KB, AutismKB, autismkb

Autism genetics KnowledgeBase, an evidence-based knowledgebase of autism genetics.

Webpage:

Publications:

Publications

More detailed information about this field from each metasource. ×

AutismKB: an evidence-based knowledgebase of autism genetics
PMID: 22139918

metasource: Fairsharing.org
version: FAIRsharing.org: Autism KB; Autism Knowledgebase; DOI: https://doi.org/10.25504/FAIRsharing.990a1b; Last edited: April 26, 2021, 8:19 a.m.; Last accessed: Jan 03 2022 7:05 p.m.

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:10.061603

---

http://dx.doi.org/10.1093/nar/GKR1145

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

Close

• AutismKB: an evidence-based knowledgebase of autism genetics PubMed citations: 90.

  90 articles citing: AutismKB: an evidence-based knowledgebase of autism genetics

  ×

  Systematic identification and characterization of long noncoding RNAs (lncRNAs) during Aedes albopictus development. PMID:35417446

  ---

  Slc6a20a Heterozygous and Homozygous Mutant Mice Display Differential Behavioral and Transcriptomic Changes. PMID:35321029

  ---

  Early Chronic Memantine Treatment-Induced Transcriptomic Changes in Wild-Type and Shank2-Mutant Mice. PMID:34594187

  ---

  Comparative analysis of the autism‑related variants between different autistic children in a family pedigree. PMID:34368859

  ---

  Drug repositioning based on network-specific core genes identifies potential drugs for the treatment of autism spectrum disorder in children. PMID:34306572

  ---

  Predicting the Risk Genes of Autism Spectrum Disorders. PMID:34194469

  ---

  Gene Dosage- and Age-Dependent Differential Transcriptomic Changes in the Prefrontal Cortex of Shank2-Mutant Mice. PMID:34177464

  ---

  Autism-associated miR-873 regulates ARID1B, SHANK3 and NRXN2 involved in neurodevelopment. PMID:33262327

  ---

  Integrated Systems Analysis Explores Dysfunctional Molecular Modules and Regulatory Factors in Children with Autism Spectrum Disorder. PMID:32653993

  ---

  Low-Dose Exposure of Silica Nanoparticles Induces Neurotoxicity via Neuroactive Ligand-Receptor Interaction Signaling Pathway in Zebrafish Embryos. PMID:32606685

  ---

  Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons. PMID:32503625

  ---

  Transcriptome analysis of neural progenitor cells derived from Lowe syndrome induced pluripotent stem cells: identification of candidate genes for the neurodevelopmental and eye manifestations. PMID:32393163

  ---

  Epigenetic activation of O-linked β-N-acetylglucosamine transferase overrides the differentiation blockage in acute leukemia. PMID:32272438

  ---

  Genome-wide, integrative analysis of circular RNA dysregulation and the corresponding circular RNA-microRNA-mRNA regulatory axes in autism. PMID:32127416

  ---

  Genome-Wide DNA Methylation Analysis Reveals Epigenetic Pattern of SH2B1 in Chinese Monozygotic Twins Discordant for Autism Spectrum Disorder. PMID:31379474

  ---

  Placental DNA methylation levels at CYP2E1 and IRS2 are associated with child outcome in a prospective autism study. PMID:31009952

  ---

  Phenotypic subgrouping and multi-omics analyses reveal reduced diazepam-binding inhibitor (DBI) protein levels in autism spectrum disorder with severe language impairment. PMID:30921354

  ---

  Deletion of the KH1 Domain of Fmr1 Leads to Transcriptional Alterations and Attentional Deficits in Rats. PMID:30877790

  ---

  Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability. PMID:30827496

  ---

  Brief Report: A Gene Enrichment Approach Applied to Sleep and Autism. PMID:30790196

  ---

  Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. PMID:30763456

  ---

  Identifying Genomic Variations in Monozygotic Twins Discordant for Autism Spectrum Disorder Using Whole-Genome Sequencing. PMID:30623854

  ---

  Co-expression of long non-coding RNAs and autism risk genes in the developing human brain. PMID:30547845

  ---

  Temporal proteomic profiling of postnatal human cortical development. PMID:30518843

  ---

  AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder. PMID:30339214

  ---

  The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on. PMID:30218584

  ---

  Regulatory genes and pathways disrupted in autism spectrum disorders. PMID:30165121

  ---

  Rare gene deletions in genetic generalized and Rolandic epilepsies. PMID:30148849

  ---

  Oxytocin as a Modulator of Synaptic Plasticity: Implications for Neurodevelopmental Disorders. PMID:29970997

  ---

  Placental H3K27me3 establishes female resilience to prenatal insults. PMID:29967448

  ---

  Clinical Application of Chromosome Microarray Analysis in Han Chinese Children with Neurodevelopmental Disorders. PMID:29948840

  ---

  Whole-Exome Sequencing Identifies One De Novo Variant in the FGD6 Gene in a Thai Family with Autism Spectrum Disorder. PMID:29888248

  ---

  Salivary biomarkers for the diagnosis and monitoring of neurological diseases. PMID:29866603

  ---

  A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies. PMID:29754769

  ---

  Enriched expression of genes associated with autism spectrum disorders in human inhibitory neurons. PMID:29317598

  ---

  Focus on the Social Aspect of Autism. PMID:29188587

  ---

  Cell Type-Specific mRNA Dysregulation in Hippocampal CA1 Pyramidal Neurons of the Fragile X Syndrome Mouse Model. PMID:29104533

  ---

  Autism-like behavior caused by deletion of vaccinia-related kinase 3 is improved by TrkB stimulation. PMID:28899869

  ---

  Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families. PMID:28720891

  ---

  Comprehensive investigation of temporal and autism-associated cell type composition-dependent and independent gene expression changes in human brains. PMID:28646201

  ---

  Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations. PMID:28503910

  ---

  Developmental activities of the complement pathway in migrating neurons. PMID:28462915

  ---

  Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing. PMID:28386848

  ---

  CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in cerebral organoids derived from iPS cells. PMID:28321286

  ---

  Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders. PMID:28289279

  ---

  Lysine Acetylation and Deacetylation in Brain Development and Neuropathies. PMID:28161493

  ---

  A systematic variant annotation approach for ranking genes associated with autism spectrum disorders. PMID:27790361

  ---

  Neonicotinoid Insecticides Alter the Gene Expression Profile of Neuron-Enriched Cultures from Neonatal Rat Cerebellum. PMID:27782041

  ---

  Disruption of an Evolutionarily Novel Synaptic Expression Pattern in Autism. PMID:27685936

  ---

  Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders. PMID:27483382

  ---

  Functional Genomic Analyses Identify Pathways Dysregulated in Animal Model of Autism. PMID:27321591

  ---

  Salivary miRNA profiles identify children with autism spectrum disorder, correlate with adaptive behavior, and implicate ASD candidate genes involved in neurodevelopment. PMID:27105825

  ---

  Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression. PMID:26985359

  ---

  Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders. PMID:26942287

  ---

  Mutation of the CH1 Domain in the Histone Acetyltransferase CREBBP Results in Autism-Relevant Behaviors in Mice. PMID:26730956

  ---

  NERI: network-medicine based integrative approach for disease gene prioritization by relative importance. PMID:26696568

  ---

  PCOSKB: A KnowledgeBase on genes, diseases, ontology terms and biochemical pathways associated with PolyCystic Ovary Syndrome. PMID:26578565

  ---

  CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment. PMID:26491539

  ---

  Shared Pathways Among Autism Candidate Genes Determined by Co-expression Network Analysis of the Developing Human Brain Transcriptome. PMID:26399424

  ---

  Investigation of sex differences in the expression of RORA and its transcriptional targets in the brain as a potential contributor to the sex bias in autism. PMID:26056561

  ---

  Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders. PMID:25969726

  ---

  Network-based Phenome-Genome Association Prediction by Bi-Random Walk. PMID:25933025

  ---

  A case of autism spectrum disorder arising from a de novo missense mutation in POGZ. PMID:25694107

  ---

  Genome-wide analysis identifies a role for common copy number variants in specific language impairment. PMID:25585696

  ---

  Genetics studies indicate that neural induction and early neuronal maturation are disturbed in autism. PMID:25477785

  ---

  Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons. PMID:25385366

  ---

  EpilepsyGene: a genetic resource for genes and mutations related to epilepsy. PMID:25324312

  ---

  CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors. PMID:25294932

  ---

  Enteric bacterial metabolites propionic and butyric acid modulate gene expression, including CREB-dependent catecholaminergic neurotransmission, in PC12 cells--possible relevance to autism spectrum disorders. PMID:25170769

  ---

  Duplication of the NPHP1 gene in patients with autism spectrum disorder and normal intellectual ability: a case series. PMID:25126106

  ---

  An inside job: how endosomal Na(+)/H(+) exchangers link to autism and neurological disease. PMID:25002837

  ---

  Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families. PMID:24906019

  ---

  Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese Han population. PMID:24599690

  ---

  Protein signatures of oxidative stress response in a patient specific cell line model for autism. PMID:24512814

  ---

  A direct molecular link between the autism candidate gene RORa and the schizophrenia candidate MIR137. PMID:24500708

  ---

  Glutamatergic candidate genes in autism spectrum disorder: an overview. PMID:24493018

  ---

  Development of a versatile enrichment analysis tool reveals associations between the maternal brain and mental health disorders, including autism. PMID:24245670

  ---

  SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs). PMID:24090431

  ---

  In-Silico Algorithms for the Screening of Possible microRNA Binding Sites and Their Interactions. PMID:24082822

  ---

  IQdb: an intelligence quotient score-associated gene resource for human intelligence. PMID:24030781

  ---

  The dynamics of autism spectrum disorders: how neurotoxic compounds and neurotransmitters interact. PMID:23924882

  ---

  Genome-wide identification of transcriptional targets of RORA reveals direct regulation of multiple genes associated with autism spectrum disorder. PMID:23697635

  ---

  Sex-biased gene expression in the developing brain: implications for autism spectrum disorders. PMID:23651621

  ---

  Prenatal expression of MET receptor tyrosine kinase in the fetal mouse dorsal raphe nuclei and the visceral motor/sensory brainstem. PMID:23548689

  ---

  Autworks: a cross-disease network biology application for Autism and related disorders. PMID:23190929

  ---

  Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders. PMID:23032108

  ---

  Systems biology of complex symptom profiles: capturing interactivity across behavior, brain and immune regulation. PMID:23022717

  ---

  Brain transcriptional and epigenetic associations with autism. PMID:22984548

  ---

  Autism-associated promoter variant in MET impacts functional and structural brain networks. PMID:22958829

  ---

  A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections. PMID:22909152
• http://dx.doi.org/10.1093/nar/GKR1145

Tags:

Tags

More detailed information about this field from each metasource. ×

autistic disorder

metasource: Fairsharing.org
version: FAIRsharing.org: Autism KB; Autism Knowledgebase; DOI: https://doi.org/10.25504/FAIRsharing.990a1b; Last edited: April 26, 2021, 8:19 a.m.; Last accessed: Jan 03 2022 7:05 p.m.

---

copy number variation

metasource: Fairsharing.org
version: FAIRsharing.org: Autism KB; Autism Knowledgebase; DOI: https://doi.org/10.25504/FAIRsharing.990a1b; Last edited: April 26, 2021, 8:19 a.m.; Last accessed: Jan 03 2022 7:05 p.m.

---

disease

metasource: Fairsharing.org
version: FAIRsharing.org: Autism KB; Autism Knowledgebase; DOI: https://doi.org/10.25504/FAIRsharing.990a1b; Last edited: April 26, 2021, 8:19 a.m.; Last accessed: Jan 03 2022 7:05 p.m.

---

gene

metasource: Fairsharing.org
version: FAIRsharing.org: Autism KB; Autism Knowledgebase; DOI: https://doi.org/10.25504/FAIRsharing.990a1b; Last edited: April 26, 2021, 8:19 a.m.; Last accessed: Jan 03 2022 7:05 p.m.

---

genetic polymorphism

metasource: Fairsharing.org
version: FAIRsharing.org: Autism KB; Autism Knowledgebase; DOI: https://doi.org/10.25504/FAIRsharing.990a1b; Last edited: April 26, 2021, 8:19 a.m.; Last accessed: Jan 03 2022 7:05 p.m.

---

human genes and diseases

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

---

gene-, system- or disease-specific databases

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

---

mapping

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:10.061603

---

genetics

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:10.061603

---

molecular interactions, pathways and networks

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:10.061603

---

dna polymorphism

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:10.061603

---

pharmacogenomics

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:10.061603

Close

autistic disorder copy number variation disease gene polymorphism human genes and diseases gene-, system- or disease-specific mapping genetics molecular interactions, pathways and networks dna polymorphism pharmacogenomics