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Filtres: Author is Chagnon, Yvon C [Enlever les filtres]
A multimodal attempt to follow-up linkage regions using RNA expression, SNPs and CpG methylation in schizophrenia and bipolar disorder kindreds. Eur J Hum Genet. 2020;28(4):499-507.
The interaction of GSK3B and FXR1 genotypes may influence the mania and depression dimensions in mood disorders. J Affect Disord. 2017;213:172-177.
BDNF Val66Met Polymorphism Influences Visuomotor Associative Learning and the Sensitivity to Action Observation. Sci Rep. 2016;6:34907.
BDNF Val66Met Polymorphism Is Associated with Self-Reported Empathy. PLoS ONE. 2016;11(2):e0149911.
DNA methylation and single nucleotide variants in the brain-derived neurotrophic factor (BDNF) and oxytocin receptor (OXTR) genes are associated with anxiety/depression in older women. Front Genet. 2015;6:230.
Measuring how genetic and epigenetic variants can filter emotion perception. Psychiatr Genet. 2015;25(5):216-22.
Extension of the generalized disequilibrium test to polytomous phenotypes and two-locus models. Front Genet. 2014;5:258.
Follow-up of a major psychosis linkage site in 13q13-q14 reveals significant association in both case-control and family samples. Biol Psychiatry. 2013;74(6):444-50.
Relationship between cortisol level and prevalent/incident cognitive impairment and its moderating factors in older adults. Int Psychogeriatr. 2013;25(2):252-62.
Detection of phenotype modifier genes using two-locus linkage analysis in complex disorders such as major psychosis. Hum Hered. 2012;73(4):195-207.
Chromosome 13q13-q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype. Eur J Hum Genet. 2009;17(8):1034-42.
A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity. Hum Hered. 2009;68(4):231-42.
Replication of linkage with bipolar disorder on chromosome 16p in the Eastern Quebec population. Am J Med Genet B Neuropsychiatr Genet. 2008;147B(6):737-44.
[Genetics of schizophrenia and bipolar disorder: recent success of linkage studies with evidence of specific and shared susceptibility loci]. Med Sci (Paris). 2003;19(10):960-6.