(Q28250796)

1

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R Benayed

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V Mancuso

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L M Brzustowicz

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J H Millonig

Infantile autism: a genetic study of 21 twin pairs

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language of work or name

English

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publication date

May 2004

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published in

Molecular Psychiatry

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volume

9

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page(s)

474-84

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issue

5

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

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

21 January 2018

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A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

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Genetics of austim: complex aetiology for a heterogeneous disorder

21 January 2018

1 reference

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Autism: recent molecular genetic advances

21 January 2018

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Histoanatomic observations of the brain in early infantile autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Lower Purkinje cell counts in the cerebella of four autistic subjects: initial findings of the UCLA-NSAC Autopsy Research Report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Brainstem, cerebellar and limbic neuroanatomical abnormalities in autism

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

A clinicopathological study of autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Midsagittal magnetic resonance imaging of autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Hypoplasia of Cerebellar Vermal Lobules VI and VII in Autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Reduced cerebellar hemisphere size and its relationship to vermal hypoplasia in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

The brain in infantile autism: are posterior fossa structures abnormal?

21 January 2018

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Development of the brainstem and cerebellum in autistic patients.

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Evidence of brain overgrowth in the first year of life in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Attentional activation of the cerebellum independent of motor involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Differential effects of developmental cerebellar abnormality on cognitive and motor functions in the cerebellum: an fMRI study of autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Prediction and preparation, fundamental functions of the cerebellum

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

A procedure for identifying regions preferentially activated by attention to semantic and phonological relations using functional magnetic resonance imaging

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Activation of a cerebellar output nucleus during cognitive processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Mechanisms of neural patterning and specification in the developing cerebellum

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Genes involved in cerebellar cell specification and differentiation

21 January 2018

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The Engrailed-2 homeobox gene and patterning of spinocerebellar mossy fiber afferents.

21 January 2018

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A genomewide screen for autism susceptibility loci

21 January 2018

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Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

21 January 2018

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The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

An efficient procedure for genotyping single nucleotide polymorphisms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

A sequencing method based on real-time pyrophosphate

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Polygenic disease: methods for mapping complex disease traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

A test for linkage and association in general pedigrees: the pedigree disequilibrium test

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

An extended transmission/disequilibrium test (TDT) for multi-allele marker loci.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Analysis of transmission of novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene in patients with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

No association between single nucleotide polymorphisms in DLX6 and piccolo genes at 7q21‐q22 and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Reelin gene alleles and susceptibility to autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Investigation of two variants in the DOPA decarboxylase gene in patients with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Linkage and association of the glutamate receptor 6 gene with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Serotonin transporter (5-HTT) gene variants associated with autism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Evidence of linkage between the serotonin transporter and autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

A genomewide screen of 345 families for autism-susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

No association between the EN2 gene and autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

How introns influence and enhance eukaryotic gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Introns in gene evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Impaired feedback regulation of XBP1 as a genetic risk factor for bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

Impairment in shifting attention in autistic and cerebellar patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

7 January 2021

Cerebellum implicated in sensory acquisition and discrimination rather than motor control

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

7 January 2021

Attention coordination and anticipatory control

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

7 January 2021

Pattern deformities and cell loss in Engrailed-2 mutant mice suggest two separate patterning events during cerebellar development.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

7 January 2021

Ectopic overexpression of engrailed-2 in cerebellar Purkinje cells causes restricted cell loss and retarded external germinal layer development at lobule junctions.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

7 January 2021

Selective disruption of "late onset" sagittal banding patterns by ectopic expression of engrailed-2 in cerebellar Purkinje cells.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

7 January 2021

Single-nucleotide polymorphism analysis by pyrosequencing

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

7 January 2021

Linkage disequilibrium in finite populations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001498

7 January 2021