(Q39366490)

11 September 2017

A noncoding RNA antisense to moesin at 5p14.1 in autism (English)

1 reference

11 September 2017

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Gerhard A Coetzee

5

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author name string

Tara Kerin

1

1 reference

11 September 2017

Anita Ramanathan

2

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11 September 2017

Kasey Rivas

3

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11 September 2017

Nicole Grepo

4

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11 September 2017

Daniel B Campbell

6

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11 September 2017

language of work or name

English

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publication date

1 April 2012

1 reference

Science Translational Medicine

11 September 2017

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11 September 2017

4

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11 September 2017

128ra40

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11 September 2017

128

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Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

11 September 2017

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Residential proximity to freeways and autism in the CHARGE study

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Differential monocyte responses to TLR ligands in children with autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Genetic influences and infantile autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Concordance for the syndrome of autism in 40 pairs of afflicted twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Autism as a strongly genetic disorder: evidence from a British twin study

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Genetic influences on the broad spectrum of autism: study of proband-ascertained twins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Characteristics and concordance of autism spectrum disorders among 277 twin pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Recent advances in the genetics of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Autism spectrum disorders: developmental disconnection syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Genetic advances in autism: heterogeneity and convergence on shared pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Risk factors for autism: translating genomic discoveries into diagnostics

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Genome-wide association studies (GWAS): impact on elucidating the aetiology of diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Replication of signals from recent studies of Crohn's disease identifies previously unknown disease loci for ulcerative colitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

A common genetic risk factor for colorectal and prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Multiple regions within 8q24 independently affect risk for prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Functional enhancers at the gene-poor 8q24 cancer-linked locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Common genetic variants on 5p14.1 associate with autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

A genome-wide linkage and association scan reveals novel loci for autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

A genome-wide scan for common alleles affecting risk for autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

A systematic approach to understand the functional consequences of non-protein coding risk regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Immune transcriptome alterations in the temporal cortex of subjects with autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Suppression of radixin and moesin alters growth cone morphology, motility, and process formation in primary cultured neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

ERMs colocalize transiently with L1 during neocortical axon outgrowth

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Rapid signaling of estrogen to WAVE1 and moesin controls neuronal spine formation via the actin cytoskeleton.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Normal development of mice and unimpaired cell adhesion/cell motility/actin-based cytoskeleton without compensatory up-regulation of ezrin or radixin in moesin gene knockout

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Why the frontal cortex in autism might be talking only to itself: local over-connectivity but long-distance disconnection

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Corpus callosum volume in children with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

A meta-analysis of the corpus callosum in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Diffusion tensor imaging findings in school-aged autistic children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Abnormalities of intrinsic functional connectivity in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

The nature of brain dysfunction in autism: functional brain imaging studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Brain growth across the life span in autism: age-specific changes in anatomical pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Manifold reduction of moesin in fetal Down syndrome brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

A coding-independent function of gene and pseudogene mRNAs regulates tumour biology

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

Functional impact of global rare copy number variation in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3003479

10.1126/SCITRANSLMED.3003479

21 January 2018

Identifiers

DOI

1 reference

11 September 2017

1 reference