| P50 | author | Jacob Gratten | Q47502535 |
| | Peter M. Visscher | Q30530678 |
| P2093 | author name string | Paul A Dawson | |
| | Soohyun Lee | |
| | Stephen Rudd | |
| | Johannes B Prins | |
| P2860 | cites work | Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin | Q22010466 |
| | Importance of Shank3 protein in regulating metabotropic glutamate receptor 5 (mGluR5) expression and signaling at synapses | Q24317227 |
| | Biological insights from 108 schizophrenia-associated genetic loci | Q24561833 |
| | Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation | Q24629491 |
| | XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing | Q24632796 |
| | RIM genes differentially contribute to organizing presynaptic release sites | Q26269874 |
| | Essential roles in synaptic plasticity for synaptogyrin I and synaptophysin I | Q28140166 |
| | Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study | Q28275978 |
| | Neurexin-neuroligin adhesions capture surface-diffusing AMPA receptors through PSD-95 scaffolds | Q28505247 |
| | Ephrin-A5 and EphA5 Interaction Induces Synaptogenesis during Early Hippocampal Development | Q28574096 |
| | A framework for the interpretation of de novo mutation in human disease | Q29031873 |
| | Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability | Q29144196 |
| | A human phenome-interactome network of protein complexes implicated in genetic disorders | Q29614448 |
| | Spatio-temporal transcriptome of the human brain | Q29614572 |
| | Loss of predominant Shank3 isoforms results in hippocampus-dependent impairments in behavior and synaptic transmission | Q30438299 |
| | ENU-mutagenesis mice with a non-synonymous mutation in Grin1 exhibit abnormal anxiety-like behaviors, impaired fear memory, and decreased acoustic startle response | Q30453712 |
| | Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice | Q30461096 |
| | Regulation of AMPA receptor extrasynaptic insertion by 4.1N, phosphorylation and palmitoylation | Q30488873 |
| | Association of the 120-bp duplication in the dopamine D4 receptor gene and schizophrenia in a sample of Danish subjects | Q45164659 |
| | A Systematic Approach to Subgroup Classification in Intellectual Disability | Q47561304 |
| | Deep sequencing reveals 50 novel genes for recessive cognitive disorders | Q48884202 |
| | The impact of caring for an adult with intellectual disability and psychiatric comorbidity on carer stress and psychological distress | Q50305337 |
| | De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy | Q50307422 |
| | Costs of caring for children with an intellectual developmental disorder. | Q50553049 |
| | How much does intellectual disability really cost? First estimates for Australia. | Q50768851 |
| | Prevalence of epilepsy and associated health service utilization and mortality among patients with intellectual disability. | Q53652412 |
| | Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis. | Q54765282 |
| | New mutations and sporadic intellectual disability | Q57733922 |
| | Phenotype-genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature | Q57757783 |
| | Genetic polymorphisms in the dopamine-2 receptor (DRD2), dopamine-3 receptor (DRD3), and dopamine transporter (SLC6A3) genes in schizophrenia: Data from an association study | Q33505008 |
| | Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology | Q33797864 |
| | Ephrin-B3 is a myelin-based inhibitor of neurite outgrowth | Q33897550 |
| | X-linked intellectual disability: unique vulnerability of the male genome | Q34088379 |
| | The genetic basis of non-syndromic intellectual disability: a review | Q34283901 |
| | Molecular-clinical spectrum of the ATR-X syndrome | Q34306141 |
| | Identification of the gene FMR2, associated with FRAXE mental retardation | Q34385889 |
| | Dual diagnosis in offenders with intellectual disability: setting research priorities: a review of research findings concerning psychiatric disorder (excluding personality disorder) among offenders with intellectual disability | Q34657407 |
| | Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways | Q35230796 |
| | Identification of a novel in-frame de novo mutation in SPTAN1 in intellectual disability and pontocerebellar atrophy | Q36035682 |
| | Psychopathology in young people with intellectual disability | Q36710278 |
| | Assembly and forward trafficking of NMDA receptors (Review). | Q37150922 |
| | Quantitative analysis of locomotor defects in neonatal mice lacking proprioceptive feedback | Q37259635 |
| | Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant? | Q37687569 |
| | Prevalence of intellectual disability: a meta-analysis of population-based studies | Q37828783 |
| | Synaptic dysfunction and intellectual disability | Q37986669 |
| | Calcium-dependent networks in dopamine-glutamate interaction: the role of postsynaptic scaffolding proteins. | Q38024032 |
| | Genetics and the investigation of developmental delay/intellectual disability | Q38171795 |
| | An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia and behavioral abnormalities | Q38197420 |
| | An overview of the neurobiology of suicidal behaviors as one meta-system. | Q38245264 |
| | A systematic review of neuropsychiatric comorbidities in patients with both epilepsy and intellectual disability | Q38840044 |
| | X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome. | Q40156896 |
| | Cranial sensory ganglia neurons require intrinsic N-cadherin function for guidance of afferent fibers to their final targets | Q43147116 |
| | De novo mutations in SYNGAP1 associated with non-syndromic mental retardation | Q43148088 |
| | Mental ill-health in adults with intellectual disabilities: prevalence and associated factors | Q43628280 |
| P921 | main subject | non-syndromic intellectual disability | Q18553537 |
| P304 | page(s) | 1-9 | |
| P577 | publication date | 2017-12-04 | |
| P1433 | published in | Journal of Neurogenetics | Q6295646 |
| P1476 | title | Gene networks associated with non-syndromic intellectual disability | |