Disentangling the heterogeneity of autism spectrum disorder through genetic findings
about
The Broad Autism (Endo)Phenotype: Neurostructural and Neurofunctional Correlates in Parents of Individuals with Autism Spectrum DisordersSelf-Reported Empathy in Adult Women with Autism Spectrum Disorders - A Systematic Mini ReviewSynaptic Wnt/GSK3β Signaling Hub in AutismCortico-Cerebellar Connectivity in Autism Spectrum Disorder: What Do We Know So Far?Genetics of Autism Spectrum Disorder: Current Status and Possible Clinical ApplicationsImaging Brain Development: Benefiting from Individual VariabilityGenetics and genomics of psychiatric diseaseBehavioral phenotypes of genetic mouse models of autism.The role of cerebellar circuitry alterations in the pathophysiology of autism spectrum disordersThe promise of multi-omics and clinical data integration to identify and target personalized healthcare approaches in autism spectrum disordersBehavioral and Neuroanatomical Phenotypes in Mouse Models of AutismNeonatal inflammatory pain and systemic inflammatory responses as possible environmental factors in the development of autism spectrum disorder of juvenile rats.Somatosensory cortex functional connectivity abnormalities in autism show opposite trends, depending on direction and spatial scale.A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?PX-RICS-deficient mice mimic autism spectrum disorder in Jacobsen syndrome through impaired GABAA receptor traffickingHyperactive mTOR signals in the proopiomelanocortin-expressing hippocampal neurons cause age-dependent epilepsy and premature death in miceGain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy.A common molecular signature in ASD gene expression: following Root 66 to autismModeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit developmentThe contribution of de novo coding mutations to autism spectrum disorderLow load for disruptive mutations in autism genes and their biased transmissionGenetic Evidence for Elevated Pathogenicity of Mitochondrial DNA Heteroplasmy in Autism Spectrum DisorderLanguage Impairments in ASD Resulting from a Failed Domestication of the Human BrainApproaching motor and language deficits in autism from below: a biolinguistic perspectiveSocial communication in mice--are there optimal cage conditions?A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseasesCNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersRisk Factors Associated With Language in Autism Spectrum Disorder: Clues to Underlying Mechanisms.Trans-synaptic zinc mobilization improves social interaction in two mouse models of autism through NMDAR activationAutism diagnosis differentiates neurophysiological responses to faces in adults with tuberous sclerosis complexDevelopment of large-scale functional networks from birth to adulthood: A guide to the neuroimaging literature.Novel metrics to measure coverage in whole exome sequencing datasets reveal local and global non-uniformity.The EU-AIMS Longitudinal European Autism Project (LEAP): clinical characterisation.PUNCH: Population Characterization of Heterogeneity.Future directions for research in autism spectrum disorders.Cytokine profiles by peripheral blood monocytes are associated with changes in behavioral symptoms following immune insults in a subset of ASD subjects: an inflammatory subtype?The Autism Spectrum Disorders Stem Cell Resource at Children's Hospital of Orange County: Implications for Disease Modeling and Drug DiscoveryThe autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopmentCardiac autonomic regulation in autism and Fragile X syndrome: a review.Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder.
P2860
Q26738652-A7F1FC26-A8A3-4DA0-AAD8-F1EC3B011F47Q26753065-B2583EA1-D6FD-4186-8BDB-D13ADBD990BCQ26765504-051E3FE5-A6FB-4C7E-A7C5-0D2044178949Q26768576-ADBA979C-1E40-491F-9B7B-1061249E1FAFQ26771770-981023F6-2B55-4DB8-B489-C3B8747B2B3EQ26773197-8E059881-9D97-46F7-AAFF-4E474C8D625FQ26781213-7F62DCDD-B539-4BD9-8553-10969BD3730AQ26781456-29A4A9D8-2972-493B-950A-6FF1D66E63FAQ26783008-15DEFE97-41F8-454E-84D3-9BCAA4BF678BQ27005952-DBE28F96-75C8-46D5-BA97-302B38F8B8A0Q27025227-B07D0238-B395-48A4-89A6-67F288F3F90DQ27303121-1AE15DDC-ABA0-4D0F-877A-A18E96BD94B3Q27303812-13BF7B2B-A4A6-4B22-B868-ABF39AFC4F42Q27326701-90353EFD-C636-481F-AC34-8CE47CCB3621Q27326861-7780258E-F4F6-44C6-84DB-6490BE73D316Q27332424-19033842-84A6-49D5-A503-2725DD5EF068Q27340721-AF4AC452-406D-4E99-AD5B-0A49BD9E10F8Q28077428-15233C2D-756C-4487-A25F-7DB0C409EA98Q28081179-BDA8B988-052A-49DE-8883-B2A0F65F668EQ28250812-F92CFD4B-BFCE-45A2-A34A-9A27059D7A42Q28267714-9FBE6758-60F7-487C-B6EF-44F68EA199A0Q28553061-1302E0AD-F411-4A80-B211-27B2AB676913Q28596914-F51C9CE3-C4C7-4481-A208-CD6457ED9F21Q28651108-FBD2EF23-B9D6-45D9-B9DE-38D3569AD47CQ28651572-94C8955E-2221-407D-B1DD-7250AEB25A89Q30276804-FC613DDC-2025-4098-9A21-12DBD61E6DE2Q30358026-739BFFB7-3AB8-4589-AA81-DA6F88BBF97BQ30377846-4B9C7CAD-7D65-4499-A666-CA5747C44EB4Q30655543-3B71F840-B00C-4D69-9250-FE556DDC93A6Q30667213-E16EA067-98D6-429A-AC24-3D990C389A40Q31159591-041E1C05-BA58-428E-9DFA-C7D5366C57ACQ33678448-DDCCEF7D-86F5-41B8-98A1-2C56D67AF6F2Q33827667-EB51FE36-55F0-4411-9719-584EF6B6725CQ33905377-41724E91-6BCA-4DB5-8CC5-293C8D63507AQ34180429-974C26CC-E531-415E-A182-85A591FD1D7FQ34422875-20C7A752-19B2-4763-925E-91E98E3C67E4Q34428986-78D1281F-B7C5-47BF-A81F-0219D1134344Q34466281-18FCE843-022E-471C-B6A4-9651A43561A1Q34943193-3A7E8C56-5A51-401C-8F87-3446FB312908Q35043876-C78DFA86-7A2B-4E95-A74E-FCFC63B6576F
P2860
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
@ast
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
@en
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
@nl
type
label
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
@ast
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
@en
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
@nl
prefLabel
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
@ast
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
@en
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
@nl
P2860
P1476
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
@en
P2093
Shafali S Jeste
P2860
P2888
P356
10.1038/NRNEUROL.2013.278
P407
P577
2014-01-28T00:00:00Z
P5875
P6179
1003198951