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Findings and concepts from children at genetic risk that may transform prevention research and practice in schizophrenia and mood disorders. In: From research to practice in child and adolescent mental health. Lanham, Maryland: Rowman & Littlefield; 2014.
Hippocampus and amygdala volumes in children and young adults at high-risk of schizophrenia: research synthesis. Schizophr Res. 2014;156(1):76-86.
Follow-up of a major psychosis linkage site in 13q13-q14 reveals significant association in both case-control and family samples. Biol Psychiatry. 2013;74(6):444-50.
A protective-compensatory model may reconcile the genetic and the developmental findings in schizophrenia. Schizophr Res. 2013;144(1-3):9-15.
Detection of phenotype modifier genes using two-locus linkage analysis in complex disorders such as major psychosis. Hum Hered. 2012;73(4):195-207.
Principal components of heritability for high dimension quantitative traits and general pedigrees. Stat Appl Genet Mol Biol. 2012;11(2).
Symptom dimensions as alternative phenotypes to address genetic heterogeneity in schizophrenia and bipolar disorder. Eur J Hum Genet. 2012;20(11):1182-8.
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.
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.
An examination of the relative contribution of saturation and selective attention to memory deficits in patients with recent-onset schizophrenia and their unaffected parents. J Abnorm Psychol. 2010;119(1):60-70.
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.