9 Result(s)
within
C. LAURENT
Behavioral Sciences
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Article
A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia
We performed a meta-analysis of over 30 case-control studies of association between schizophrenia and a bi-allelic, BalI polymorphism in exon 1 of the dopamine D3 receptor gene. We observed a significant excess o...
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Article
Erratum: A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia
We performed a meta-analysis of over 30 case-control studies of association between schizophrenia and a bi-allelic, BalI polymorphism in exon 1 of the dopamine D3 receptor gene. We observed a significant exces...
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Article
Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder
Manic-depressive (bipolar) illness is a serious psychiatric disorder with a strong genetic predisposition. The disorder is likely to be multifactorial and etiologically complex, and the causes of genetic susce...
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Article
Multicenter linkage study of schizophrenia loci on chromosome 22q
The hypothesis of the existence of one or more schizophrenia susceptibility loci on chromosome 22q is supported by reports of genetic linkage and association, meta-analyses of linkage, and the observation of e...
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Article
Meta-analysis of 32 genome-wide linkage studies of schizophrenia
A genome scan meta-a nalysis (GSMA) was carried out on 32 independent genome-wide linkage scan analyses that included 3255 pedigrees with 7413 genotyped cases affected with schizophrenia (SCZ) or related disor...
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Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms
A genomewide linkage scan was carried out in eight clinical samples of informative schizophrenia families. After all quality control checks, the analysis of 707 European-ancestry families included 1615 affecte...
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Article
Open AccessAnalysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE
The striking excess of affected males in autism spectrum disorders (ASD) suggests that genes located on chromosome X contribute to the etiology of these disorders. To identify new X-linked genes associated wit...
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Erratum: A2A adenosine receptor deletion is protective in a mouse model of Tauopathy
Correction to: Molecular Psychiatry advance online publication, 2 December 2014; doi:10.1038/mp.2014.151 Following publication of this paper, the authors noticed that the eighth author’s name was misspelled. T...
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Open AccessA2A adenosine receptor deletion is protective in a mouse model of Tauopathy
Consumption of caffeine, a non-selective adenosine A2A receptor (A2AR) antagonist, reduces the risk of develo** Alzheimer’s disease (AD) in humans and mitigates both amyloid and Tau burden in transgenic mouse m...
