Publications
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, “Detection of phenotype modifier genes using two-locus linkage analysis in complex disorders such as major psychosis.”, Hum Hered, vol. 73, no. 4, pp. 195-207, 2012.
, “Genome-wide epigenetic regulation by early-life trauma.”, Arch Gen Psychiatry, vol. 69, no. 7, pp. 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, pp. 1182-8, 2012.
, “Global gene expression profiling of the polyamine system in suicide completers.”, Int J Neuropsychopharmacol, vol. 14, no. 5, pp. 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, pp. 182-9, 2011.
, “Polychlorinated biphenyls and organochlorine pesticides in plasma of older Canadians.”, Environ Res, vol. 111, no. 8, pp. 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, pp. 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, pp. 831-43, 2010.
, “High-density polymorphisms analysis of 23 candidate genes for association with bone mineral density.”, Bone, vol. 47, no. 5, pp. 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, pp. 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, pp. 1343-50, 2009.
, “A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity.”, Hum Hered, vol. 68, no. 4, pp. 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, pp. 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, pp. 281-90, 2008.
, “Estimating interaction between genetic and environmental risk factors: efficiency of sampling designs within a cohort.”, Epidemiology, vol. 19, no. 1, pp. 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, pp. 737-44, 2008.
, “Using disease symptoms to improve detection of linkage under genetic heterogeneity.”, Genet Epidemiol, vol. 32, no. 5, pp. 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, pp. 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, pp. 477-83, 2005.
, “Identifying SNPs predictive of phenotype using random forests.”, Genet Epidemiol, vol. 28, no. 2, pp. 171-82, 2005.
