Publications
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Filtres: Author is Alexandre Bureau [Enlever les filtres]
, « Detection of phenotype modifier genes using two-locus linkage analysis in complex disorders such as major psychosis. », Hum Hered, vol. 73, nᵒ 4, p. 195-207, 2012.
, « Genome-wide epigenetic regulation by early-life trauma. », Arch Gen Psychiatry, vol. 69, nᵒ 7, p. 722-31, 2012.
, « Symptom dimensions as alternative phenotypes to address genetic heterogeneity in schizophrenia and bipolar disorder. », Eur J Hum Genet, vol. 20, nᵒ 11, p. 1182-8, 2012.
, « Global gene expression profiling of the polyamine system in suicide completers. », Int J Neuropsychopharmacol, vol. 14, nᵒ 5, p. 595-605, 2011.
, « Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies. », Genet Epidemiol, vol. 35, nᵒ 3, p. 182-9, 2011.
, « Polychlorinated biphenyls and organochlorine pesticides in plasma of older Canadians. », Environ Res, vol. 111, nᵒ 8, p. 1313-20, 2011.
, « Association of polyaminergic loci with anxiety, mood disorders, and attempted suicide. », PLoS One, vol. 5, nᵒ 11, p. e15146, 2010.
, « Association with replication between estrogen-related receptor gamma (ESRRgamma) polymorphisms and bone phenotypes in women of European ancestry. », J Bone Miner Res, vol. 25, nᵒ 4, p. 901-11, 2010.
, « Differences and similarities in the serotonergic diathesis for suicide attempts and mood disorders: a 22-year longitudinal gene-environment study. », Mol Psychiatry, vol. 15, nᵒ 8, p. 831-43, 2010.
, « High-density polymorphisms analysis of 23 candidate genes for association with bone mineral density. », Bone, vol. 47, nᵒ 5, p. 975-81, 2010.
, « Chromosome 13q13-q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype. », Eur J Hum Genet, vol. 17, nᵒ 8, p. 1034-42, 2009.
, « 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, vol. 47, nᵒ 11, p. 1343-50, 2009.
, « A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity. », Hum Hered, vol. 68, nᵒ 4, p. 231-42, 2009.
, « Profiling brain expression of the spermidine/spermine N1-acetyltransferase 1 (SAT1) gene in suicide. », Am J Med Genet B Neuropsychiatr Genet, vol. 150B, nᵒ 7, p. 934-43, 2009.
, « Application of microarray outlier detection methodology to psychiatric research. », BMC Psychiatry, vol. 8, p. 29, 2008.
, « Differential RNA expression between schizophrenic patients and controls of the dystrobrevin binding protein 1 and neuregulin 1 genes in immortalized lymphocytes. », Schizophr Res, vol. 100, nᵒ 1-3, p. 281-90, 2008.
, « Estimating interaction between genetic and environmental risk factors: efficiency of sampling designs within a cohort. », Epidemiology, vol. 19, nᵒ 1, p. 83-93, 2008.
, « Replication of linkage with bipolar disorder on chromosome 16p in the Eastern Quebec population. », Am J Med Genet B Neuropsychiatr Genet, vol. 147B, nᵒ 6, p. 737-44, 2008.
, « Using disease symptoms to improve detection of linkage under genetic heterogeneity. », Genet Epidemiol, vol. 32, nᵒ 5, p. 476-86, 2008.
, « 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, vol. 144B, nᵒ 8, p. 1063-9, 2007.
, « Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification. », Am J Hum Genet, vol. 77, nᵒ 3, p. 477-83, 2005.
, « Identifying SNPs predictive of phenotype using random forests. », Genet Epidemiol, vol. 28, nᵒ 2, p. 171-82, 2005.
