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Filtres: Keyword is Humans and Author is Maziade, Michel [Enlever les filtres]
Uptrend in distress and psychiatric symptomatology in pregnant women during the coronavirus disease 2019 pandemic. Acta Obstet Gynecol Scand. 2020;99(7):848-855.
Childhood abuse and neglect may induce deficits in cognitive precursors of psychosis in high-risk children. J Psychiatry Neurosci. 2015;40(5):336-43.
GRIN2B predicts attention problems among disadvantaged children. Eur Child Adolesc Psychiatry. 2015;24(7):827-36.
The brain through the retina: the flash electroretinogram as a tool to investigate psychiatric disorders. Prog Neuropsychopharmacol Biol Psychiatry. 2014;48:129-34.
Common childhood determinants of psychiatric and cardiovascular disorders call for common prevention and clinical research. JAMA Pediatr. 2014;168(1):3-4.
Hippocampus and amygdala volumes in children and young adults at high-risk of schizophrenia: research synthesis. Schizophr Res. 2014;156(1):76-86.
A protective-compensatory model may reconcile the genetic and the developmental findings in schizophrenia. Schizophr Res. 2013;144(1-3):9-15.
Animal models of human anxiety disorders: reappraisal from a developmental psychopathology vantage point. Pediatr Res. 2011;69(5 Pt 2):77R-84R.
How prevalent are anxiety disorders in schizophrenia? A meta-analysis and critical review on a significant association. Schizophr Bull. 2011;37(4):811-21.
Familiarity and recollection processes in patients with recent-onset schizophrenia and their unaffected parents. Psychiatry Res. 2010;175(1-2):15-21.
Retinal response to light in young nonaffected offspring at high genetic risk of neuropsychiatric brain disorders. Biol Psychiatry. 2010;67(3):270-4.
Atomoxetine and neuropsychological function in children with attention-deficit/hyperactivity disorder: results of a pilot study. J Child Adolesc Psychopharmacol. 2009;19(6):709-18.
Chromosome 13q13-q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype. Eur J Hum Genet. 2009;17(8):1034-42.
Effects of phonological and semantic cuing on encoding and retrieval processes in adolescent psychosis. J Clin Exp Neuropsychol. 2009;31(5):533-44.
A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity. Hum Hered. 2009;68(4):231-42.
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.
Gene-environment interaction and behavioral disorders: a developmental perspective based on endophenotypes. Novartis Found Symp. 2008;293:31-41; discussion 41-7, 68-70.
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.
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.
A pilot feasibility study of an extension of the acquaintanceship recruitment procedure in recent-onset psychosis. J Nerv Ment Dis. 2005;193(8):560-3.
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.