Analysis of reelin as a candidate gene for autism (Q34265761)

1 August 2017

Analysis of reelin as a candidate gene for autism (English)

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1 August 2017

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12

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1 August 2017

E Bonora

1

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author name string

K S Beyer

2

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1 August 2017

J A Lamb

3

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1 August 2017

J R Parr

4

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1 August 2017

S M Klauck

5

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1 August 2017

A Benner

6

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1 August 2017

M Paolucci

7

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1 August 2017

A Abbott

8

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1 August 2017

I Ragoussis

9

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1 August 2017

A Poustka

10

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1 August 2017

A J Bailey

11

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1 August 2017

International Molecular Genetic Study of Autism (IMGSAC)

13

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1 August 2017

language of work or name

English

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publication date

1 October 2003

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1 August 2017

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1 August 2017

8

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1 August 2017

10

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1 August 2017

885-892

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4001310

1 August 2017

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cites work

Pervasive Developmental Disorders in Preschool Children

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The epidemiology of autism: a review.

21 January 2018

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Infantile autism: a genetic study of 21 twin pairs

21 January 2018

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A case-control family history study of autism

21 January 2018

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

21 January 2018

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Autism: in search of susceptibility genes

21 January 2018

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

21 January 2018

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Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

Role of the reelin signaling pathway in central nervous system development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

Gender effect on Purkinje cell loss in the cerebellum of the heterozygous reeler mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

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

21 January 2018

1 reference

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A clinicopathological study of autism.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

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.4001310

The role of Reelin in pathology of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

Reelin is a serine protease of the extracellular matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

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.4001310

Are rare variants responsible for susceptibility to complex diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

The phenotypic characteristics of heterozygous reeler mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

Dysregulation of Reelin and Bcl-2 proteins in autistic cerebellum

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

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.4001310

GOLD--graphical overview of linkage disequilibrium

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

7 January 2021

inferred from DOI database lookup

2-year-old boy who has been diagnosed with autism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

7 January 2021

inferred from DOI database lookup

A likelihood ratio test for detecting patterns of disease-marker association

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001310

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/SJ.MP.4001310

1 reference

release_chp6eypvjvhrrc6b7g45qqcjzu

1 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/chp6eypvjvhrrc6b7g45qqcjzu

24 November 2022

mapped directly with Wikidata item

1 reference