(Q38612196)

4 September 2017

title

Regulation of neuronal migration, an emerging topic in autism spectrum disorders (English)

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4 September 2017

main subject

autism spectrum disorder

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1

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4 September 2017

Eyal Karzbrun

2

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author name string

Aditya Kshirsagar

series ordinal

3

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4 September 2017

Kozo Kaibuchi

series ordinal

4

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4 September 2017

language of work or name

English

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publication date

20 October 2015

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Journal of Neurochemistry

4 September 2017

published in

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4 September 2017

volume

136

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4 September 2017

issue

3

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4 September 2017

page(s)

440-456

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Advances in autism genetics: on the threshold of a new neurobiology

4 September 2017

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21 January 2018

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Progressive loss of PAX6, TBR2, NEUROD and TBR1 mRNA gradients correlates with translocation of EMX2 to the cortical plate during human cortical development

21 January 2018

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Autism: highly heritable but not inherited

21 January 2018

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Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex

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Autism susceptibility candidate 2 (Auts2) encodes a nuclear protein expressed in developing brain regions implicated in autism neuropathology

21 January 2018

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Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression.

21 January 2018

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Inherited and de novo SHANK2 variants associated with autism spectrum disorder impair neuronal morphogenesis and physiology

21 January 2018

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Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus

21 January 2018

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Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome.

21 January 2018

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Increased LIS1 expression affects human and mouse brain development

21 January 2018

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Genetic and epigenetic networks in intellectual disabilities.

21 January 2018

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Analysis of reelin as a candidate gene for autism

21 January 2018

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DISC1, PDE4B, and NDE1 at the centrosome and synapse

21 January 2018

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Clonal production and organization of inhibitory interneurons in the neocortex.

21 January 2018

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Elucidating the relationship between DISC1, NDEL1 and NDE1 and the risk for schizophrenia: evidence of epistasis and competitive binding

21 January 2018

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Whole exome sequencing in females with autism implicates novel and candidate genes

21 January 2018

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Reduced minicolumns in the frontal cortex of patients with autism

21 January 2018

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Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization

21 January 2018

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Radial glia: multi-purpose cells for vertebrate brain development

21 January 2018

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Autism as a sequence: from heterochronic germinal cell divisions to abnormalities of cell migration and cortical dysplasias

21 January 2018

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Minicolumnar pathology in autism

21 January 2018

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Genetic analysis of AUTS2 as a susceptibility gene of heroin dependence

21 January 2018

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The emerging picture of autism spectrum disorder: genetics and pathology

21 January 2018

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An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk

21 January 2018

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Possible association between suicide committed under influence of ethanol and a variant in the AUTS2 gene

21 January 2018

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T-Brain-1--A Potential Master Regulator in Autism Spectrum Disorders

21 January 2018

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p62/SQSTM1 and ALFY interact to facilitate the formation of p62 bodies/ALIS and their degradation by autophagy

21 January 2018

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Pathogenic SYNGAP1 mutations impair cognitive development by disrupting maturation of dendritic spine synapses

21 January 2018

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SYNGAP1 links the maturation rate of excitatory synapses to the duration of critical-period synaptic plasticity.

21 January 2018

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Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy

21 January 2018

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Arx is a direct target of Dlx2 and thereby contributes to the tangential migration of GABAergic interneurons

21 January 2018

1 reference

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

21 January 2018

1 reference

Distribution of language-related Cntnap2 protein in neural circuits critical for vocal learning

21 January 2018

1 reference

Genetic risk factors in two Utah pedigrees at high risk for suicide

21 January 2018

1 reference

LIS1, CLIP-170's key to the dynein/dynactin pathway

21 January 2018

1 reference

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

21 January 2018

1 reference

The evidence for the contribution of the autism susceptibility candidate 2 (AUTS2) gene in heroin dependence susceptibility.

21 January 2018

1 reference

21 January 2018

1 reference

Synaptic, transcriptional and chromatin genes disrupted in autism

21 January 2018

1 reference

De novo TBR1 mutations in sporadic autism disrupt protein functions

21 January 2018

1 reference

The developmental neurobiology of autism spectrum disorder.

21 January 2018

1 reference

Tbr1 conducts the orchestration of early cortical development.

21 January 2018

1 reference

21 January 2018

Genetics and alcoholism

1 reference

Astrotactin: a novel neuronal cell surface antigen that mediates neuron-astroglial interactions in cerebellar microcultures

21 January 2018

1 reference

21 January 2018

1 reference

CLIP-170 homologue and NUDE play overlapping roles in NUDF localization in Aspergillus nidulans

21 January 2018

1 reference

Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families.

21 January 2018

1 reference

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

21 January 2018

1 reference

Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex

21 January 2018

1 reference

Two new mutants, ‘trembler’ and ‘reeler’, with neurological actions in the house mouse (Mus musculus L.)

21 January 2018

1 reference

Reelin signaling is impaired in autism

21 January 2018

1 reference

Mitotic spindle regulation by Nde1 controls cerebral cortical size

21 January 2018

1 reference

LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome

21 January 2018

1 reference

Cortical progenitor expansion, self-renewal and neurogenesis-a polarized perspective

21 January 2018

1 reference

OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signaling

21 January 2018

1 reference

The selective macroautophagic degradation of aggregated proteins requires the PI3P-binding protein Alfy

21 January 2018

1 reference

The Simons Simplex Collection: a resource for identification of autism genetic risk factors

21 January 2018

1 reference

Making bigger brains-the evolution of neural-progenitor-cell division.

21 January 2018

1 reference

The involvement of Reelin in neurodevelopmental disorders

21 January 2018

1 reference

De novo mutations in schizophrenia implicate synaptic networks

21 January 2018

1 reference

Identification of Arx transcriptional targets in the developing basal forebrain

21 January 2018

1 reference

Rare structural variation of synapse and neurotransmission genes in autism

21 January 2018

1 reference

Molecular and morphological heterogeneity of neural precursors in the mouse neocortical proliferative zones.

21 January 2018

1 reference

An AUTS2-Polycomb complex activates gene expression in the CNS.

21 January 2018

1 reference

Generation of interneuron diversity in the mouse cerebral cortex.

21 January 2018

1 reference

The embryonic preoptic area is a novel source of cortical GABAergic interneurons.

21 January 2018

1 reference

Autism: many genes, common pathways?

21 January 2018

1 reference

Distinct cis-regulatory elements from the Dlx1/Dlx2 locus mark different progenitor cell populations in the ganglionic eminences and different subtypes of adult cortical interneurons

21 January 2018

1 reference

Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses

21 January 2018

1 reference

Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder

21 January 2018

1 reference

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

21 January 2018

1 reference

The cell biology of neurogenesis

21 January 2018

1 reference

Synaptopathies: diseases of the synaptome.

21 January 2018

1 reference

Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephaly

21 January 2018

1 reference

Reversal of neurological defects in a mouse model of Rett syndrome

21 January 2018

1 reference

Analysis of four DLX homeobox genes in autistic probands

21 January 2018

1 reference

Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept

21 January 2018

1 reference

TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract

21 January 2018

1 reference

Central nervous system neuronal migration

21 January 2018

1 reference

New directions in neuronal migration

21 January 2018

1 reference

Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: a major site of neurogenesis

21 January 2018

1 reference

Lis1 and Ndel1 influence the timing of nuclear envelope breakdown in neural stem cells

21 January 2018

1 reference

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes

21 January 2018

1 reference

From radial glia to pyramidal-projection neuron: transcription factor cascades in cerebral cortex development

21 January 2018

1 reference

Tbr1 regulates differentiation of the preplate and layer 6.

21 January 2018

1 reference

Cortical and thalamic axon pathfinding defects in Tbr1, Gbx2, and Pax6 mutant mice: evidence that cortical and thalamic axons interact and guide each other

21 January 2018

1 reference

Genetic mosaic dissection of Lis1 and Ndel1 in neuronal migration

21 January 2018

1 reference

The reeler gene encodes a protein with an EGF-like motif expressed by pioneer neurons

21 January 2018

1 reference

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality

21 January 2018

1 reference

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

21 January 2018

1 reference

Cytoskeletal regulation by AUTS2 in neuronal migration and neuritogenesis.

21 January 2018

1 reference

Development and applications of CRISPR-Cas9 for genome engineering

21 January 2018

1 reference

A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (AUTS2) gene in a patient with autism.

21 January 2018

1 reference

Tbr1 haploinsufficiency impairs amygdalar axonal projections and results in cognitive abnormality

21 January 2018

1 reference

Histological and magnetic resonance imaging assessment of cortical layering and thickness in autism spectrum disorders.

21 January 2018

1 reference

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

21 January 2018

1 reference

De Novo Gene Disruptions in Children on the Autistic Spectrum

21 January 2018

1 reference

The contribution of de novo coding mutations to autism spectrum disorder

21 January 2018

1 reference

Gene associated with seizures, autism, and hepatomegaly in an Amish girl

21 January 2018

1 reference

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

21 January 2018

1 reference

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

21 January 2018

1 reference

Disentangling the heterogeneity of autism spectrum disorder through genetic findings

21 January 2018

1 reference

Tangential migration in neocortical development.

21 January 2018

1 reference

Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation.

21 January 2018

1 reference

A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks

21 January 2018

1 reference

Regulators of the cytoplasmic dynein motor

21 January 2018

1 reference

Optimizing neuronal differentiation from induced pluripotent stem cells to model ASD

21 January 2018

1 reference

Direct association of LIS1, the lissencephaly gene product, with a mammalian homologue of a fungal nuclear distribution protein, rNUDE

21 January 2018

1 reference

Prevalence of parent-reported diagnosis of autism spectrum disorder among children in the US, 2007.

21 January 2018

1 reference

A unique subpopulation of Tbr1-expressing deep layer neurons in the developing cerebral cortex.

21 January 2018

1 reference

Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis.

21 January 2018

1 reference

Asymmetric distribution of the apical plasma membrane during neurogenic divisions of mammalian neuroepithelial cells

21 January 2018

1 reference

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

21 January 2018

1 reference

Patterns of neuronal migration in the embryonic cortex

21 January 2018

1 reference

Genome variation and complexity in the autism spectrum.

21 January 2018

1 reference

Functional interplay between LIS1, NDE1 and NDEL1 in dynein-dependent organelle positioning.

21 January 2018

1 reference

21 January 2018

1 reference

Cerebral organoids model human brain development and microcephaly

21 January 2018

1 reference

Spatially dependent dynamic MAPK modulation by the Nde1-Lis1-Brap complex patterns mammalian CNS.

21 January 2018

1 reference

Neurogenesis at the brain-cerebrospinal fluid interface

21 January 2018

1 reference

Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

21 January 2018

1 reference

Origin of GABAergic neurons in the human neocortex

21 January 2018

1 reference

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

21 January 2018

1 reference

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

21 January 2018

1 reference

The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

21 January 2018

1 reference

De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: a case report and a brief literature review.

21 January 2018

1 reference

Disrupted-in-schizophrenia (DISC1) functions presynaptically at glutamatergic synapses

21 January 2018

1 reference

Neuronal or glial progeny: regional differences in radial glia fate

21 January 2018

1 reference

Dcx reexpression reduces subcortical band heterotopia and seizure threshold in an animal model of neuronal migration disorder

21 January 2018

1 reference

A long, remarkable journey: tangential migration in the telencephalon.

21 January 2018

1 reference

Cell migration in the forebrain

21 January 2018

1 reference

Structural variation of chromosomes in autism spectrum disorder

21 January 2018

1 reference

Cellular and molecular basis of cerebellar development

21 January 2018

1 reference

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

21 January 2018

1 reference

The generation of neuronal diversity in the central nervous system

21 January 2018

1 reference

Tbr1 and Fezf2 regulate alternate corticofugal neuronal identities during neocortical development

21 January 2018

1 reference

LIS1 and NudE induce a persistent dynein force-producing state

21 January 2018

1 reference

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

21 January 2018

1 reference

The T-box brain 1 (Tbr1) transcription factor inhibits astrocyte formation in the olfactory bulb and regulates neural stem cell fate.

21 January 2018

1 reference

Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.

21 January 2018

1 reference

Autism spectrum disorders--a genetics review

21 January 2018

1 reference

Asymmetric inheritance of radial glial fibers by cortical neurons

21 January 2018

1 reference

Asymmetric production of surface-dividing and non-surface-dividing cortical progenitor cells

21 January 2018

1 reference

Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons

21 January 2018

1 reference

Subpallial origin of a population of projecting pioneer neurons during corticogenesis

21 January 2018

1 reference

The novel roles of glial cells revisited: the contribution of radial glia and astrocytes to neurogenesis

21 January 2018

1 reference

Recent developments in the genetics of autism spectrum disorders

21 January 2018

1 reference

Modes of neuronal migration in the developing cerebral cortex

21 January 2018

1 reference

Phenotypic manifestations of copy number variation in chromosome 16p13.11.

21 January 2018

1 reference

Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders

21 January 2018

1 reference

Patterns and rates of exonic de novo mutations in autism spectrum disorders

21 January 2018

1 reference

The caudal ganglionic eminence is a source of distinct cortical and subcortical cell populations.

21 January 2018

1 reference

NUDEL is a novel Cdk5 substrate that associates with LIS1 and cytoplasmic dynein

21 January 2018

1 reference

Neurons derived from radial glial cells establish radial units in neocortex

21 January 2018

1 reference

Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases

21 January 2018

1 reference

Distinct behaviors of neural stem and progenitor cells underlie cortical neurogenesis

21 January 2018

1 reference

The role of AUTS2 in neurodevelopment and human evolution

21 January 2018

1 reference

Function and regulation of AUTS2, a gene implicated in autism and human evolution

21 January 2018

1 reference

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

21 January 2018

1 reference

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

21 January 2018

1 reference

Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology

21 January 2018

1 reference

Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption.

21 January 2018

1 reference

Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies

21 January 2018

1 reference

Three-dimensional regulation of radial glial functions by Lis1-Nde1 and dystrophin glycoprotein complexes

21 January 2018

1 reference

Lis1-Nde1-dependent neuronal fate control determines cerebral cortical size and lamination

21 January 2018

1 reference

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits

21 January 2018

1 reference

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder

21 January 2018

1 reference

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

21 January 2018

1 reference

Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels

21 January 2018

1 reference

Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1

21 January 2018

1 reference

Novel embryonic neuronal migration and proliferation defects in Dcx mutant mice are exacerbated by Lis1 reduction

21 January 2018

1 reference

Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects

21 January 2018

1 reference

Mode of cell migration to the superficial layers of fetal monkey neocortex

21 January 2018

1 reference

16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders.

21 January 2018

1 reference

LIS1. let's interact sometimes... (part 1).

21 January 2018

1 reference

LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules.

21 January 2018

1 reference

LIS1 functions in normal development and disease

21 January 2018

1 reference

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

21 January 2018

1 reference

Asymmetric localization of Numb:EGFP in dividing neuroepithelial cells during neurulation in Danio rerio

21 January 2018

1 reference

The role of de novo mutations in the genetics of autism spectrum disorders

21 January 2018

1 reference

Behavioral phenotype of the reeler mutant mouse: effects of RELN gene dosage and social isolation

21 January 2018

1 reference

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

21 January 2018

1 reference

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

21 January 2018

1 reference

A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system

21 January 2018

1 reference

Solving the autism puzzle a few pieces at a time

21 January 2018

1 reference

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

21 January 2018

1 reference

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2

21 January 2018

1 reference

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

How does Reelin control neuronal migration and layer formation in the developing mammalian neocortex?

21 January 2018

1 reference

Control of asymmetric cell division of mammalian neural progenitors.

21 January 2018

1 reference

Oblique radial glial divisions in the developing mouse neocortex induce self-renewing progenitors outside the germinal zone that resemble primate outer subventricular zone progenitors.

21 January 2018

1 reference

Ndel1 palmitoylation: a new mean to regulate cytoplasmic dynein activity.

21 January 2018

1 reference

The exon junction complex component Magoh controls brain size by regulating neural stem cell division.

21 January 2018

1 reference

Alfy, a novel FYVE-domain-containing protein associated with protein granules and autophagic membranes

21 January 2018

1 reference

Unique morphological features of the proliferative zones and postmitotic compartments of the neural epithelium giving rise to striate and extrastriate cortex in the monkey

21 January 2018

1 reference

Synapse dysfunction in autism: a molecular medicine approach to drug discovery in neurodevelopmental disorders

21 January 2018

1 reference

A network of genetic repression and derepression specifies projection fates in the developing neocortex

21 January 2018

1 reference

Heterogeneity in ventricular zone neural precursors contributes to neuronal fate diversity in the postnatal neocortex.

21 January 2018

1 reference

Structural variation in the human genome and its role in disease

21 January 2018

1 reference

NudE and NudEL are required for mitotic progression and are involved in dynein recruitment to kinetochores

21 January 2018

1 reference

A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits

21 January 2018

1 reference

A genotype-first approach to defining the subtypes of a complex disease

21 January 2018

1 reference

Antibodies that recognize astrotactin block granule neuron binding to astroglia

21 January 2018

1 reference

Patches of disorganization in the neocortex of children with autism

21 January 2018

1 reference

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

21 January 2018

1 reference

Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX

21 January 2018

1 reference

Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins

21 January 2018

1 reference

Cytoarchitecture of mouse and human subventricular zone in developing cerebral neocortex

21 January 2018

1 reference

Compromised generation of GABAergic interneurons in the brains of Vax1-/- mice

21 January 2018

1 reference

Induction of pluripotent stem cells from adult human fibroblasts by defined factors

21 January 2018

1 reference

Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries.

21 January 2018

1 reference

Neocortical neurogenesis and neuronal migration

21 January 2018

1 reference

Separate progenitors for radial and tangential cell dispersion during development of the cerebral neocortex.

21 January 2018

1 reference

A resource of Cre driver lines for genetic targeting of GABAergic neurons in cerebral cortex.

21 January 2018

1 reference

The spatial and temporal origin of chandelier cells in mouse neocortex

21 January 2018

1 reference

Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2.

21 January 2018

1 reference

Key role for gene dosage and synaptic homeostasis in autism spectrum disorders

21 January 2018

1 reference

Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 Microdeletions

21 January 2018

1 reference

Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.

21 January 2018

1 reference

Nucleokinesis in neuronal migration

21 January 2018

1 reference

LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages

21 January 2018

1 reference

Dual subcellular roles for LIS1 and dynein in radial neuronal migration in live brain tissue

21 January 2018

1 reference

Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation

21 January 2018

1 reference

Loss of δ-catenin function in severe autism

21 January 2018

1 reference

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.

21 January 2018

1 reference

Neuropathology of the anterior midcingulate cortex in young children with autism.

21 January 2018

1 reference

Neuronal migration mechanisms in development and disease

21 January 2018

1 reference

Cenp-F links kinetochores to Ndel1/Nde1/Lis1/dynein microtubule motor complexes

21 January 2018

1 reference

A functional genetic link between distinct developmental language disorders

21 January 2018

1 reference

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

21 January 2018

1 reference

Transitin, a nestin-like intermediate filament protein, mediates cortical localization and the lateral transport of Numb in mitotic avian neuroepithelial cells

21 January 2018

1 reference

Autism and brain development

21 January 2018

1 reference

A new subtype of progenitor cell in the mouse embryonic neocortex

21 January 2018

1 reference

Polymorphisms within ASTN2 gene are associated with age at onset of Alzheimer's disease

21 January 2018

1 reference

Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis.

21 January 2018

1 reference

Coexistence of widespread clones and large radial clones in early embryonic ferret cortex

21 January 2018

1 reference

The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes

21 January 2018

1 reference

Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals.

21 January 2018

1 reference

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

21 January 2018

1 reference

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

21 January 2018

1 reference

Astn2, a novel member of the astrotactin gene family, regulates the trafficking of ASTN1 during glial-guided neuronal migration

21 January 2018

1 reference

Cortical interneurons and their origins

21 January 2018

1 reference

The origin and specification of cortical interneurons

21 January 2018

1 reference

Origins of cortical interneuron subtypes

21 January 2018

1 reference

Human Nudel and NudE as regulators of cytoplasmic dynein in poleward protein transport along the mitotic spindle

21 January 2018

1 reference

Neuroepithelial stem cell proliferation requires LIS1 for precise spindle orientation and symmetric division.

21 January 2018

1 reference

Neocortical excitation/inhibition balance in information processing and social dysfunction

21 January 2018

1 reference

A genomewide screen of 345 families for autism-susceptibility loci

21 January 2018

1 reference

Distinct dose-dependent cortical neuronal migration and neurite extension defects in Lis1 and Ndel1 mutant mice

21 January 2018

1 reference

The Caudal Migratory Stream: A Novel Migratory Stream of Interneurons Derived from the Caudal Ganglionic Eminence in the Developing Mouse Forebrain

21 January 2018

1 reference

Contributions of cortical subventricular zone to the development of the human cerebral cortex

21 January 2018

1 reference

Reelin gene alleles and susceptibility to autism spectrum disorders

21 January 2018

1 reference

Association study identifying a new susceptibility gene (AUTS2) for schizophrenia

21 January 2018

1 reference

A unified genetic theory for sporadic and inherited autism

21 January 2018

1 reference

CNS gene encoding astrotactin, which supports neuronal migration along glial fibers

21 January 2018

1 reference

Synaptic dysfunction in neurodevelopmental disorders associated with autism and intellectual disabilities

21 January 2018

1 reference

TBR1is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/JNC.13403

1 reference

4 September 2017

1 reference