(Q21261437)

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Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis

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Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis (English)

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Pierre Lindenbaum

7

object named as

Pierre Lindenbaum

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Pierre

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Lindenbaum

1 reference

17 August 2022

Frédéric Tores

2

object named as

Frédéric Tores

author given names

Frédéric

author last names

Tores

1 reference

17 August 2022

Jérome Carayol

object named as

Jérome Carayol

3

author given names

Jérome

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Carayol

1 reference

17 August 2022

object named as

Anne Philippi

1

author given names

Anne

author last names

Philippi

1 reference

17 August 2022

author name string

Francis Rousseau

4

author given names

Francis

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Rousseau

1 reference

17 August 2022

Mélanie Letexier

5

author given names

Mélanie

author last names

Letexier

1 reference

17 August 2022

Elke Roschmann

6

author given names

Elke

author last names

Roschmann

1 reference

17 August 2022

Abdel Benajjou

8

author given names

Abdel

author last names

Benajjou

1 reference

17 August 2022

Karine Fontaine

9

author given names

Karine

author last names

Fontaine

1 reference

17 August 2022

Céline Vazart

10

author given names

Céline

author last names

Vazart

1 reference

17 August 2022

Philippe Gesnouin

11

author given names

Philippe

author last names

Gesnouin

1 reference

17 August 2022

Peter Brooks

12

author given names

Peter

author last names

Brooks

1 reference

17 August 2022

Jörg Hager

13

author given names

Jörg

author last names

Hager

1 reference

17 August 2022

language of work or name

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publication date

2007

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BMC Medical Genetics

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8

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1

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74

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https://scigraph.springernature.com/pub.10.1186/1471-2350-8-74

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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

1 reference

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19 March 2017

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism

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19 March 2017

A note on exact tests of Hardy-Weinberg equilibrium

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19 March 2017

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

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19 March 2017

A genomic screen of autism: evidence for a multilocus etiology

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19 March 2017

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

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19 March 2017

Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31

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19 March 2017

Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism

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19 March 2017

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

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19 March 2017

The genetics of autism

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19 March 2017

Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2222245

19 March 2017

Pituitary homeobox factor 1, a novel transcription factor in the adrenal regulating steroid 11beta-hydroxylase

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2222245

19 March 2017

An autosomal genomic screen for autism. Collaborative linkage study of autism

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19 March 2017

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

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19 March 2017

https://api.crossref.org/works/10.1186/1471-2350-8-74

22 April 2017

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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19 March 2017

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

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2222245

19 March 2017

https://api.crossref.org/works/10.1186/1471-2350-8-74

22 April 2017

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2222245

19 March 2017

Ptx1, a bicoid-related homeo box transcription factor involved in transcription of the pro-opiomelanocortin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2222245

19 March 2017

Pervasive Developmental Disorders in Preschool Children

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22 April 2017

Controlling the false discovery rate in behavior genetics research

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7 April 2017

Estimating haplotype relative risks in complex disease from unphased SNPs data in families using a likelihood adjusted for ascertainment.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2222245

12 September 2017

Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.

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12 September 2017

A genomewide scan for loci involved in attention-deficit/hyperactivity disorder

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2222245

12 September 2017

Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder

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12 September 2017

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

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12 September 2017

A genomewide screen for autism susceptibility loci

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12 September 2017

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

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12 September 2017

Histone macroH2A1.2 relocates to the inactive X chromosome after initiation and propagation of X-inactivation.

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12 September 2017

Neurogenin1 and neurogenin2 control two distinct waves of neurogenesis in developing dorsal root ganglia

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12 September 2017

Plasma beta-endorphin, adrenocorticotropin hormone, and cortisol in autism

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12 September 2017

A novel biochemical model linking dysfunctions in brain melatonin, proopiomelanocortin peptides, and serotonin in autism

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12 September 2017

Complex segregation analysis of autism

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12 September 2017

Bioinformatic analysis of autism positional candidate genes using biological databases and computational gene network prediction

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https://api.crossref.org/works/10.1186%2F1471-2350-8-74

21 January 2018

High blood monocyte counts and neopterin levels in children with autistic disorder

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https://api.crossref.org/works/10.1186%2F1471-2350-8-74

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Difference between plasma N- and C-terminally directed beta-endorphin immunoreactivity in infantile autism.

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21 January 2018

Lower cortisol and higher ACTH levels in individuals with autism

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

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Disregulation of proopiomelanocortin and contagious maladaptive behavior

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A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs

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21 January 2018

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10.1186/1471-2350-8-74

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