Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder (Q33943718)

30 July 2017

title

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

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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

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Kalle Reichelt

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K L Reichelt

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30 July 2017

A M Persico

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L D'Agruma

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N Maiorano

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A Totaro

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R Militerni

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C Bravaccio

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T H Wassink

7

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C Schneider

8

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R Melmed

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S Trillo

10

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F Montecchi

11

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M Palermo

12

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S Puglisi-Allegra

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M Conciatori

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R Marino

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C C Quattrocchi

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L Zelante

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P Gasparini

21

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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

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

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

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

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

21 January 2018

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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

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

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Autism diagnostic interview: a standardized investigator-based instrument

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Microcephaly and macrocephaly in autism

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

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

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Genomic organization of the mouse reelin gene.

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Serotonin and amino acid content in platelets of autistic children

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Platelet serotonin, a possible marker for familial autism

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

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Power and sample size calculations. A review and computer program

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Alzheimer's disease: neurodevelopment converges with neurodegeneration

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Detection of the reelin breakpoint in reeler mice.

21 January 2018

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

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

21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

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

21 January 2018

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7 January 2021

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

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7 January 2021

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

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

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

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7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4000850

1 reference

30 July 2017

1 reference