(Q22251430)

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Discovery of allelic variants ofHOXA1 andHOXB1: Genetic susceptibility to autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Evidence supporting WNT2 as an autism susceptibility gene.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Autism spectrum disorder in fragile X syndrome: communication, social interaction, and specific behaviors.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Astrocyte-specific TSC1 conditional knockout mice exhibit abnormal neuronal organization and seizures.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Olfactory structures of the forebrain in the reeler mutant mouse.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

The morphology of the hippocampus and dentate gyrus in normal and reeler mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Thalamocortical projections in the reeler mutant mouse

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Rho GTPases, dendritic structure, and mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Embryological origin for autism: developmental anomalies of the cranial nerve motor nuclei

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Animal Models of Autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

The embryonic development of the cerebellum in normal and reeler mutant mice.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Kinetics of 3H-serotonin uptake by platelets in infantile autism and developmental language disorder (including five pairs of twins).

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Platelet serotonin, a possible marker for familial autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Polymorphic GGC repeat differentially regulates human reelin gene expression levels

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Neurocognitive dysfunction in children with neurofibromatosis type 1.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Events governing organization of postmigratory neurons: studies on brain development in normal and reeler mice.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Reelin signaling is impaired in autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

The Arg473Cys-neuroligin-1 mutation modulates NMDA mediated synaptic transmission and receptor distribution in hippocampal neurons

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Neuropeptides and the social brain: potential rodent models of autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

The complexity of PDZ domain-mediated interactions at glutamatergic synapses: a case study on neuroligin

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Postnatal shifts of interneuron position in the neocortex of normal and reeler mice: evidence for inward radial migration

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Regulation of neocortical interneuron development and the implications for neurodevelopmental disorders.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Association of Reelin gene polymorphisms with autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Plasma oxytocin levels in autistic children.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Behavioral consequences of congenital rubella.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Bornavirus tropism and targeted pathogenesis: virus-host interactions in a neurodevelopmental model

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Reduced blood levels of reelin as a vulnerability factor in pathophysiology of autistic disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Possible association between congenital cytomegalovirus infection and autistic disorder.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Levels of Bcl-2 and P53 are altered in superior frontal and cerebellar cortices of autistic subjects.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

The amygdala and autism: implications from non‐human primate studies

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

A neurofibromatosis-1-regulated pathway is required for learning in Drosophila.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Monogenic causes of X-linked mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Genetics of austim: complex aetiology for a heterogeneous disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

A role for Cajal-Retzius cells and reelin in the development of hippocampal connections.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Mechanism for the learning deficits in a mouse model of neurofibromatosis type 1

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

A mouse model for the learning and memory deficits associated with neurofibromatosis type I

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Abnormal cortical voice processing in autism.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Regulation of neuronal morphology and function by the tumor suppressors Tsc1 and Tsc2

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Linkage and association of the glutamate receptor 6 gene with autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Absence of association between a polymorphic GGC repeat in the 5' untranslated region of the reelin gene and autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Reelin gene alleles and susceptibility to autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Analysis of reelin as a candidate gene for autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Autism as a disorder of neural information processing: directions for research and targets for therapy

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Examination of AVPR1a as an autism susceptibility gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Molecular genetics of autism spectrum disorder.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Analysis of the RELN gene as a genetic risk factor for autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

ProSAP/Shank proteins - a family of higher order organizing molecules of the postsynaptic density with an emerging role in human neurological disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Interaction of "readthrough" acetylcholinesterase with RACK1 and PKCbeta II correlates with intensified fear-induced conflict behavior.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Pervasive social deficits, but normal parturition, in oxytocin receptor-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Neuroligin 1 is a postsynaptic cell-adhesion molecule of excitatory synapses

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Reelin is a serine protease of the extracellular matrix

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Neuroligin 2 is exclusively localized to inhibitory synapses

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Incidence of autism spectrum disorders: Changes over time and their meaning*

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

A clinicopathological study of autism.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Disorder-associated mutations lead to functional inactivation of neuroligins

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Regional brain enlargement in autism: a magnetic resonance imaging study.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

The neuropathology of autism: a review

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Aberrant trajectory of thalamocortical axons associated with abnormal localization of neurocan immunoreactivity in the cerebral neocortex of reeler mutant mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Autism in thalidomide embryopathy: a population study.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Fetal valproate syndrome: clinical and neuro-developmental features in two sibling pairs.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Control of excitatory and inhibitory synapse formation by neuroligins

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Activity-dependent regulation of MEF2 transcription factors suppresses excitatory synapse number

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

A calcium-regulated MEF2 sumoylation switch controls postsynaptic differentiation

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Association study with two markers of a human homeogene in infantile autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Dysregulated innate immune responses in young children with autism spectrum disorders: their relationship to gastrointestinal symptoms and dietary intervention

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Neuroanatomic variation in monozygotic twin pairs discordant for the narrow phenotype for autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Methodological factors influencing measurement and processing of plasma reelin in humans

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Unusual brain growth patterns in early life in patients with autistic disorder: an MRI study.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Minicolumnar pathology in autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Reelin is a positional signal for the lamination of dentate granule cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Reelin signaling is necessary for a specific step in the migration of hindbrain efferent neurons

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Grasping the intentions of others with one's own mirror neuron system

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Abnormal development of dendritic spines in FMR1 knock-out mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

Cyclin-dependent kinase 5/p35 contributes synergistically with Reelin/Dab1 to the positioning of facial branchiomotor and inferior olive neurons in the developing mouse hindbrain.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021

No evidence for a new variant of measles-mumps-rubella-induced autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2006.05.010

7 January 2021