Publications
Export 25 results:
Filtres: Keyword is Genetic Predisposition to Disease [Enlever les filtres]
Improving Decision Making about Genetic Testing in the Clinic: An Overview of Effective Knowledge Translation Interventions. PLoS ONE. 2016;11(3):e0150123.
Common Genetic Polymorphisms Influence Blood Biomarker Measurements in COPD. PLoS Genet. 2016;12(8):e1006011.
Liability indicators aggregate many years before transition to illness in offspring descending from kindreds affected by schizophrenia or bipolar disorder. Schizophr Res. 2016;175(1-3):186-192.
A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis. Neurology. 2016;86(2):161-9.
On the validity of within-nuclear-family genetic association analysis in samples of extended families. Stat Appl Genet Mol Biol. 2015;14(6):533-49.
Glycogen synthase kinase-3 overexpression replicates electroretinogram anomalies of offspring at high genetic risk for schizophrenia and bipolar disorder. Biol Psychiatry. 2014;76(2):93-100.
Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. Bioinformatics. 2014;30(15):2189-96.
A protective-compensatory model may reconcile the genetic and the developmental findings in schizophrenia. Schizophr Res. 2013;144(1-3):9-15.
Association with replication between estrogen-related receptor gamma (ESRRgamma) polymorphisms and bone phenotypes in women of European ancestry. J Bone Miner Res. 2010;25(4):901-11.
Association of polyaminergic loci with anxiety, mood disorders, and attempted suicide. PLoS ONE. 2010;5(11):e15146.
Shared neurocognitive dysfunctions in young offspring at extreme risk for schizophrenia or bipolar disorder in eastern quebec multigenerational families. Schizophr Bull. 2009;35(5):919-30.
Chromosome 13q13-q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype. Eur J Hum Genet. 2009;17(8):1034-42.
Using disease symptoms to improve detection of linkage under genetic heterogeneity. Genet Epidemiol. 2008;32(5):476-86.
Estimating interaction between genetic and environmental risk factors: efficiency of sampling designs within a cohort. Epidemiology. 2008;19(1):83-93.
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.
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.
Informative phenotypes for genetic studies of psychiatric disorders. Am J Med Genet B Neuropsychiatr Genet. 2007;144B(5):581-8.
New movements in neurofilament transport, turnover and disease. Exp Cell Res. 2007;313(10):2110-20.
Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification. Am J Hum Genet. 2005;77(3):477-83.
Identifying SNPs predictive of phenotype using random forests. Genet Epidemiol. 2005;28(2):171-82.
Up-regulation of peripherin is associated with alterations in synaptic plasticity in CA1 and CA3 regions of hippocampus. Neurobiol Dis. 2005;18(2):409-20.
Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome. Can J Cardiol. 2004;20(4):425-30.
[Genetics of schizophrenia and bipolar disorder: recent success of linkage studies with evidence of specific and shared susceptibility loci]. Med Sci (Paris). 2003;19(10):960-6.
