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Global gene expression profiling of the polyamine system in suicide completers. Int J Neuropsychopharmacol. 2011;14(5):595-605.
Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies. Genet Epidemiol. 2011;35(3):182-9.
Polychlorinated biphenyls and organochlorine pesticides in plasma of older Canadians. Environ Res. 2011;111(8):1313-20.
Association of polyaminergic loci with anxiety, mood disorders, and attempted suicide. PLoS ONE. 2010;5(11):e15146.
Association with replication between estrogen-related receptor gamma (ESRRgamma) polymorphisms and bone phenotypes in women of European ancestry. J Bone Miner Res. 2010;25(4):901-11.
Differences and similarities in the serotonergic diathesis for suicide attempts and mood disorders: a 22-year longitudinal gene-environment study. Mol Psychiatry. 2010;15(8):831-43.
High-density polymorphisms analysis of 23 candidate genes for association with bone mineral density. Bone. 2010;47(5):975-81.
Chromosome 13q13-q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype. Eur J Hum Genet. 2009;17(8):1034-42.
Considerations for the development of a reference method for sequencing of haploid DNA--an opinion paper on behalf of the IFCC Committee on Molecular Diagnostics, International Federation of Clinical Chemistry and Laboratory Medicine. Clin Chem Lab Med. 2009;47(11):1343-50.
A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity. Hum Hered. 2009;68(4):231-42.
Profiling brain expression of the spermidine/spermine N1-acetyltransferase 1 (SAT1) gene in suicide. Am J Med Genet B Neuropsychiatr Genet. 2009;150B(7):934-43.
Application of microarray outlier detection methodology to psychiatric research. BMC Psychiatry. 2008;8:29.
Differential RNA expression between schizophrenic patients and controls of the dystrobrevin binding protein 1 and neuregulin 1 genes in immortalized lymphocytes. Schizophr Res. 2008;100(1-3):281-90.
Estimating interaction between genetic and environmental risk factors: efficiency of sampling designs within a cohort. Epidemiology. 2008;19(1):83-93.
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.
Using disease symptoms to improve detection of linkage under genetic heterogeneity. Genet Epidemiol. 2008;32(5):476-86.
Possible association of the pro-melanin-concentrating hormone gene with a greater body mass index as a side effect of the antipsychotic olanzapine. Am J Med Genet B Neuropsychiatr Genet. 2007;144B(8):1063-9.
Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification. Am J Hum Genet. 2005;77(3):477-83.
Identifying SNPs predictive of phenotype using random forests. Genet Epidemiol. 2005;28(2):171-82.