(Q33943718)

30 July 2017

title

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

1 reference

30 July 2017

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T Pascucci

13

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Flavio Keller

object named as

F Keller

22

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Alfonso Baldi

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A Baldi

19

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Kalle Reichelt

15

object named as

K L Reichelt

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30 July 2017

A M Persico

1

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30 July 2017

L D'Agruma

2

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30 July 2017

N Maiorano

3

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30 July 2017

A Totaro

4

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30 July 2017

R Militerni

5

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30 July 2017

C Bravaccio

6

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30 July 2017

T H Wassink

7

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30 July 2017

C Schneider

8

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30 July 2017

R Melmed

9

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30 July 2017

S Trillo

10

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30 July 2017

F Montecchi

11

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30 July 2017

M Palermo

12

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30 July 2017

S Puglisi-Allegra

14

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30 July 2017

M Conciatori

16

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30 July 2017

R Marino

17

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30 July 2017

C C Quattrocchi

18

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30 July 2017

L Zelante

20

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30 July 2017

P Gasparini

21

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30 July 2017

Collaborative Linkage Study of Autism

23

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30 July 2017

language of work or name

English

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publication date

1 March 2001

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30 July 2017

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30 July 2017

volume

6

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30 July 2017

issue

2

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30 July 2017

page(s)

150-159

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The Neurobiology of Infantile Autism

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

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The autistic spectrum

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

21 January 2018

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Genetic studies of autistic disorder and chromosome 7

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A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

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A clinicopathological study of autism

21 January 2018

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Brainstem, cerebellar and limbic neuroanatomical abnormalities in autism

21 January 2018

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

21 January 2018

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Movement analysis in infancy may be useful for early diagnosis of autism

21 January 2018

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Cerebellar phenotype of two alleles of the 'reeler' mutation on similar backgrounds

21 January 2018

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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

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

Distribution of a reeler gene-related antigen in the developing cerebellum: an immunohistochemical study with an allogeneic antibody CR-50 on normal and reeler mice

21 January 2018

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Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

21 January 2018

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Behavior checklist for identifying severely handicapped individuals with high levels of autistic behavior

21 January 2018

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https://api.crossref.org/works/10.1038/SJ.MP.4000850

Autism diagnostic interview: a standardized investigator-based instrument

21 January 2018

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Microcephaly and macrocephaly in autism

21 January 2018

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A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies

21 January 2018

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The human reelin gene: isolation, sequencing, and mapping on chromosome 7.

21 January 2018

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Genomic organization of the mouse reelin gene.

21 January 2018

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Computer methods to locate signals in nucleic acid sequences

21 January 2018

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Serotonin and amino acid content in platelets of autistic children

21 January 2018

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Platelet serotonin, a possible marker for familial autism

21 January 2018

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

21 January 2018

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A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.

21 January 2018

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https://api.crossref.org/works/10.1038/SJ.MP.4000850

The transmission/disequilibrium test and parental-genotype reconstruction: the reconstruction-combined transmission/ disequilibrium test

21 January 2018

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Power and sample size calculations. A review and computer program

21 January 2018

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Alzheimer's disease: neurodevelopment converges with neurodegeneration

21 January 2018

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Calcium signalling in the guidance of nerve growth by netrin-1.

21 January 2018

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Detection of the reelin breakpoint in reeler mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

The reeler gene encodes a protein with an EGF–like motif expressed by pioneer neurons

21 January 2018

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Regional brain enlargement in autism: a magnetic resonance imaging study

21 January 2018

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Oculomotor evidence for neocortical systems but not cerebellar dysfunction in autism

21 January 2018

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Defective corticogenesis and reduction in Reelin immunoreactivity in cortex and hippocampus of prenatally infected neonatal mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

Expression ofreelin, the gene responsible for the reeler mutation, in embryonic development and adulthood in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

Autism: recent molecular genetic advances

21 January 2018

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

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

21 January 2018

1 reference

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7 January 2021

The mouse mutation reeler causes increased adhesion within a subpopulation of early postmitotic cortical neurons

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

7 January 2021

Adenosine deaminase alleles and autistic disorder: Case-control and family-based association studies

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

7 January 2021

Development of RNA-SSCP protocols for the identification and screening of CFTR mutations: identification of two new mutations

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

7 January 2021

Monte Carlo tests for associations between disease and alleles at highly polymorphic loci

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

7 January 2021

Embryonic and early fetal development of the human neocortex

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4000850

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4000850

1 reference

30 July 2017

1 reference