Export 56 results:
Filtres: Author is Chantal Mérette [Enlever les filtres]
How prevalent are anxiety disorders in schizophrenia? A meta-analysis and critical review on a significant association. Schizophr Bull. 2011;37(4):811-21.
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.
Prevalence of insomnia and its treatment in Canada. Can J Psychiatry. 2011;56(9):540-8.
Verbal and visual memory impairments among young offspring and healthy adult relatives of patients with schizophrenia and bipolar disorder: selective generational patterns indicate different developmental trajectories. Schizophr Bull. 2011;37(6):1218-28.
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.
Retinal response to light in young nonaffected offspring at high genetic risk of neuropsychiatric brain disorders. Biol Psychiatry. 2010;67(3):270-4.
Chromosome 13q13-q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype. Eur J Hum Genet. 2009;17(8):1034-42.
Cognitive behavioral therapy, singly and combined with medication, for persistent insomnia: a randomized controlled trial. JAMA. 2009;301(19):2005-15.
Incidence and risk factors of insomnia in a population-based sample. Sleep. 2009;32(8):1027-37.
The natural history of insomnia: a population-based 3-year longitudinal study. Arch Intern Med. 2009;169(5):447-53.
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.
Decomposing the autism phenotype into familial dimensions. Am J Med Genet B Neuropsychiatr Genet. 2008;147B(1):3-9.
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.
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.
Family history of insomnia in a population-based sample. Sleep. 2007;30(12):1739-45.
Informative phenotypes for genetic studies of psychiatric disorders. Am J Med Genet B Neuropsychiatr Genet. 2007;144B(5):581-8.
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.
Psychological and health-related quality of life factors associated with insomnia in a population-based sample. J Psychosom Res. 2007;63(2):157-66.
A factor analysis of the Strauss and Carpenter revised outcome criteria scale: a validation of the French translation. J Nerv Ment Dis. 2004;192(12):864-7.
Fine motor dexterity is correlated to social functioning in schizophrenia. Schizophr Res. 2003;62(3):269-73.