(Q45942304)

18 December 2017

title

Heterogeneous dysregulation of microRNAs across the autism spectrum. (English)

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18 December 2017

main subject

autism spectrum disorder

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4

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18 December 2017

Daniel Geschwind

6

object named as

Daniel H Geschwind

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18 December 2017

Francesca S. Gazzaniga

3

object named as

Francesca S Gazzaniga

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18 December 2017

Kenneth S. Kosik

8

object named as

Kenneth S Kosik

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18 December 2017

author name string

Kawther Abu-Elneel

1

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18 December 2017

Tsunglin Liu

2

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18 December 2017

Dennis P Wall

5

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18 December 2017

Kaiqin Lao

7

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18 December 2017

language of work or name

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19 June 2008

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18 December 2017

published in

Neurogenetics

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18 December 2017

volume

9

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18 December 2017

issue

3

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18 December 2017

page(s)

153-161

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18 December 2017

The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing

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1 reference

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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

21 January 2018

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X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

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Contribution of SHANK3 mutations to autism spectrum disorder

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

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A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence

21 January 2018

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Structural variation of chromosomes in autism spectrum disorder

21 January 2018

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Strong association of de novo copy number mutations with autism

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Association of tuberous sclerosis of temporal lobes with autism and atypical autism

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Neuro-epileptic determinants of autism spectrum disorders in tuberous sclerosis complex

21 January 2018

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Genotype and psychological phenotype in tuberous sclerosis

21 January 2018

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Neuropsychological, psychiatric, and physical manifestations in 149 members from 18 fragile X families

21 January 2018

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Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients

21 January 2018

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21 January 2018

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21 January 2018

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Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism

21 January 2018

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The near universal presence of autism spectrum disorders in children with Smith-Lemli-Opitz syndrome

21 January 2018

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Behavior phenotype in the RSH/Smith-Lemli-Opitz syndrome

21 January 2018

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The genetics of autistic disorders and its clinical relevance: a review of the literature

21 January 2018

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Neuroanatomic observations of the brain in autism: a review and future directions

21 January 2018

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A clinicopathological study of autism

21 January 2018

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Purkinje cell vulnerability and autism: a possible etiological connection

21 January 2018

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The neuronal microRNA system

21 January 2018

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Brain development in autism: early overgrowth followed by premature arrest of growth

21 January 2018

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Brain overgrowth in autism during a critical time in development: implications for frontal pyramidal neuron and interneuron development and connectivity

21 January 2018

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Detection of a microRNA signal in an in vivo expression set of mRNAs

21 January 2018

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Evidence for multiple loci from a genome scan of autism kindreds.

21 January 2018

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microRNA expression in the prefrontal cortex of individuals with schizophrenia and schizoaffective disorder

21 January 2018

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21 January 2018

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21 January 2018

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Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

21 January 2018

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Global variation in copy number in the human genome

21 January 2018

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Multiplexing RT-PCR for the detection of multiple miRNA species in small samples.

21 January 2018

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Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder

21 January 2018

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A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands

21 January 2018

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Comprehensive human genetic maps: individual and sex-specific variation in recombination

21 January 2018

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Model-based analysis of oligonucleotide arrays: model validation, design issues and standard error application

21 January 2018

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12 December 2020

The neuropathology of the autism spectrum disorders: what have we learned?

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12 December 2020

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

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12 December 2020

Prevalence of autism spectrum disorders--autism and developmental disabilities monitoring network, 14 sites, United States, 2002.

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12 December 2020

Spatial attention deficits in patients with acquired or developmental cerebellar abnormality

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12 December 2020

Neuroanatomic imaging in autism

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12 December 2020

The contribution of neuropathologic studies to the understanding of autism

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12 December 2020

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

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12 December 2020

10.1007/S10048-008-0133-5

Identifiers

DOI

1 reference

18 December 2017

Dimensions Publication ID

1018575121

0 references

1 reference

18 December 2017