(Q28294614)

15

object named as

M A Pericak-Vance

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author name string

D A Skaar

1

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Y Shao

2

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J E Stenger

4

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J Jaworski

5

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E R Martin

6

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G R DeLong

7

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J H Moore

8

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J L McCauley

9

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J S Sutcliffe

10

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A E Ashley-Koch

11

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M L Cuccaro

12

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S E Folstein

13

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J R Gilbert

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

14

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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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issue

6

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page(s)

563-71

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cites work

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001614

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001614

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001614

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001614

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

21 April 2017

2 references

https://api.crossref.org/works/10.1038/SJ.MP.4001614

21 April 2017

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

21 January 2018

1 reference

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

Epidemiological trends in rates of autism.

21 April 2017

1 reference

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

Prevalence of autism in a US metropolitan area

21 January 2018

1 reference

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

Genetics of autism: overview and new directions

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Autism and genetics. A decade of research

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Reelin binds alpha3beta1 integrin and inhibits neuronal migration.

21 January 2018

1 reference

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

Reelin controls position of autonomic neurons in the spinal cord

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Defining the autism minimum candidate gene region on chromosome 7.

21 January 2018

1 reference

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

Genomic screen and follow-up analysis for autistic disorder

21 January 2018

1 reference

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

A genomewide screen for autism susceptibility loci

21 January 2018

1 reference

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

Incorporating language phenotypes strengthens evidence of linkage to autism

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Reelin gene alleles and susceptibility to autism spectrum disorders

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Analysis of reelin as a candidate gene for autism

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Exact tests for association between alleles at arbitrary numbers of loci

21 January 2018

1 reference

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

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.4001614

Correcting for a potential bias in the pedigree disequilibrium test

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

The neurobiology and genetics of infantile autism

21 January 2018

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Allelic discrimination using fluorogenic probes and the 5' nuclease assay

1 reference

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

7 January 2021

GOLD--graphical overview of linkage disequilibrium

1 reference

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

7 January 2021