Analysis of the RELN gene as a genetic risk factor for autism (Q28294614)

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Y Shao

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J E Stenger

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J Jaworski

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E R Martin

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G R DeLong

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J H Moore

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J L McCauley

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J S Sutcliffe

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A E Ashley-Koch

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M L Cuccaro

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S E Folstein

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J R Gilbert

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M A Pericak-Vance

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

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language of work or name

English

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publication date

June 2005

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published in

Molecular Psychiatry

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volume

10

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page(s)

563-71

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issue

6

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cites work

1 reference

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Synergistic contributions of cyclin-dependant kinase 5/p35 and Reelin/Dab1 to the positioning of cortical neurons in the developing mouse brain

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A decrease of reelin expression as a putative vulnerability factor in schizophrenia

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

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Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

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Epidemiological trends in rates of autism.

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Prevalence of autism in a US metropolitan area

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Genetics of autism: overview and new directions

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

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Autism and genetics. A decade of research

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

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Patterns of cell and fiber distribution in the neocortex of the reeler mutant mouse

21 January 2018

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

21 January 2018

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Disruption of hippocampal development in vivo by CR-50 mAb against reelin

21 January 2018

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Reelin binds alpha3beta1 integrin and inhibits neuronal migration.

21 January 2018

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Reelin controls position of autonomic neurons in the spinal cord

21 January 2018

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Rescue of ataxia and preplate splitting by ectopic expression of Reelin in reeler mice

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Decrease in reelin and glutamic acid decarboxylase67 (GAD67) expression in schizophrenia and bipolar disorder: a postmortem brain study

21 January 2018

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

21 January 2018

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Defining the autism minimum candidate gene region on chromosome 7.

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Genomic screen and follow-up analysis for autistic disorder.

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A genomewide screen for autism susceptibility loci

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Incorporating language phenotypes strengthens evidence of linkage to autism.

21 January 2018

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

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Reelin gene alleles and susceptibility to autism spectrum disorders

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

21 January 2018

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Analysis of reelin as a candidate gene for autism

21 January 2018

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

21 January 2018

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Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 January 2018

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Diagnosing autism: analyses of data from the Autism Diagnostic Interview.

21 January 2018

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Fluorescence-based oligonucleotide ligation assay for analysis of cystic fibrosis transmembrane conductance regulator gene mutations

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Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease

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

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Exact tests for association between alleles at arbitrary numbers of loci

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

21 January 2018

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Correcting for a potential bias in the pedigree disequilibrium test

21 January 2018

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Genotype‐based association test for general pedigrees: The genotype‐PDT

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A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

21 January 2018

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Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics

21 January 2018

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The neurobiology and genetics of infantile autism

21 January 2018

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7 January 2021

Regulation of Purkinje cell alignment by reelin as revealed with CR-50 antibody.

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7 January 2021

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

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7 January 2021

Allelic discrimination using fluorogenic probes and the 5' nuclease assay

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001614

7 January 2021

GOLD--graphical overview of linkage disequilibrium

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001614

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001614

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1602696

1020958482

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1602696

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference