scholarly article | Q13442814 |
P356 | DOI | 10.1038/EJHG.2017.55 |
P2888 | exact match | https://scigraph.springernature.com/pub.10.1038/ejhg.2017.55 |
P932 | PMC publication ID | 5520067 |
P698 | PubMed publication ID | 28422133 |
P50 | author | Arija G Jansen | Q92190837 |
Danielle Posthuma | Q21257977 | ||
Tinca Polderman | Q42634768 | ||
Matthijs Verhage | Q56905118 | ||
P2093 | author name string | August B Smit | |
Frank C Verhulst | |||
Gwen C Dieleman | |||
P2860 | cites work | DSM-5 | Q3064664 |
Biological insights from 108 schizophrenia-associated genetic loci | Q24561833 | ||
Functional impact of global rare copy number variation in autism spectrum disorders | Q24596191 | ||
Common genetic variants on 5p14.1 associate with autism spectrum disorders | Q24603204 | ||
Rare structural variation of synapse and neurotransmission genes in autism | Q24608775 | ||
Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis | Q24630557 | ||
FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism | Q24631425 | ||
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1 | Q24634148 | ||
PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
Fragile X spectrum disorders | Q26824376 | ||
The role of glutamate and its receptors in autism and the use of glutamate receptor antagonists in treatment | Q26998975 | ||
The FMRP regulon: from targets to disease convergence | Q27014002 | ||
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? | Q27326701 | ||
FMRP targets distinct mRNA sequence elements to regulate protein expression | Q28117931 | ||
Synaptic, transcriptional and chromatin genes disrupted in autism | Q28250800 | ||
The contribution of de novo coding mutations to autism spectrum disorder | Q28250812 | ||
Meta-analysis of the heritability of human traits based on fifty years of twin studies | Q28262090 | ||
Patterns and rates of exonic de novo mutations in autism spectrum disorders | Q28264242 | ||
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome | Q28273791 | ||
Individual common variants exert weak effects on the risk for autism spectrum disorders | Q28943296 | ||
A genome-wide scan for common alleles affecting risk for autism | Q28943508 | ||
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations | Q29030218 | ||
De Novo Gene Disruptions in Children on the Autistic Spectrum | Q29394534 | ||
De novo mutations revealed by whole-exome sequencing are strongly associated with autism | Q29547269 | ||
MAGMA: generalized gene-set analysis of GWAS data | Q30935493 | ||
A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale | Q33161703 | ||
A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples | Q33556118 | ||
Functional gene group analysis reveals a role of synaptic heterotrimeric G proteins in cognitive ability | Q33645949 | ||
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders | Q33794546 | ||
Genetic architectures of psychiatric disorders: the emerging picture and its implications | Q33949729 | ||
A polygenic burden of rare disruptive mutations in schizophrenia | Q34060200 | ||
Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages | Q34211584 | ||
INRICH: interval-based enrichment analysis for genome-wide association studies | Q34269233 | ||
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci | Q34495555 | ||
De novo mutations in schizophrenia implicate synaptic networks | Q34540372 | ||
A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism | Q34557745 | ||
Copy number variation in schizophrenia in Sweden | Q34742638 | ||
Pathway analyses implicate glial cells in schizophrenia | Q35107323 | ||
Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders | Q35196556 | ||
Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. | Q36253911 | ||
Myelination-related genes are associated with decreased white matter integrity in schizophrenia | Q36591201 | ||
Pathway analysis of seven common diseases assessed by genome-wide association | Q37014849 | ||
Impaired activity-dependent neural circuit assembly and refinement in autism spectrum disorder genetic models | Q37564195 | ||
Impaired mitochondrial function in psychiatric disorders | Q38003304 | ||
The glial perspective of autism spectrum disorders | Q38168409 | ||
The role of de novo mutations in the genetics of autism spectrum disorders | Q38178892 | ||
Recent advances in the genetics of autism spectrum disorder | Q38462559 | ||
Gene set analysis: A step-by-step guide | Q38522741 | ||
The statistical properties of gene-set analysis | Q38806240 | ||
Comorbid Symptomology in Adults with Autism Spectrum Disorder and Intellectual Disability. | Q41501872 | ||
Up-Regulation of Oligodendrocyte Lineage Markers in the Cerebellum of Autistic Patients: Evidence from Network Analysis of Gene Expression. | Q50309596 | ||
P433 | issue | 7 | |
P921 | main subject | autism | Q38404 |
autism spectrum disorder | Q1436063 | ||
P304 | page(s) | 863-868 | |
P577 | publication date | 2017-04-19 | |
P1433 | published in | European Journal of Human Genetics | Q2155433 |
P1476 | title | Gene-set analysis shows association between FMRP targets and autism spectrum disorder | |
P478 | volume | 25 |
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