Publications
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Filters: Keyword is Genetic Predisposition to Disease [Clear All Filters]
, “Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer.”, J Natl Cancer Inst, vol. 109, no. 11, 2017.
, “Common Genetic Polymorphisms Influence Blood Biomarker Measurements in COPD.”, PLoS Genet, vol. 12, no. 8, p. e1006011, 2016.
, “Improving Decision Making about Genetic Testing in the Clinic: An Overview of Effective Knowledge Translation Interventions.”, PLoS One, vol. 11, no. 3, p. e0150123, 2016.
, “Liability indicators aggregate many years before transition to illness in offspring descending from kindreds affected by schizophrenia or bipolar disorder.”, Schizophr Res, vol. 175, no. 1-3, pp. 186-192, 2016.
, “A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis.”, Neurology, vol. 86, no. 2, pp. 161-9, 2016.
, “On the validity of within-nuclear-family genetic association analysis in samples of extended families.”, Stat Appl Genet Mol Biol, vol. 14, no. 6, pp. 533-49, 2015.
, “Glycogen synthase kinase-3 overexpression replicates electroretinogram anomalies of offspring at high genetic risk for schizophrenia and bipolar disorder.”, Biol Psychiatry, vol. 76, no. 2, pp. 93-100, 2014.
, “Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.”, Bioinformatics, vol. 30, no. 15, pp. 2189-96, 2014.
, “A protective-compensatory model may reconcile the genetic and the developmental findings in schizophrenia.”, Schizophr Res, vol. 144, no. 1-3, pp. 9-15, 2013.
, “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.
, “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.
, “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.
, “Shared neurocognitive dysfunctions in young offspring at extreme risk for schizophrenia or bipolar disorder in eastern quebec multigenerational families.”, Schizophr Bull, vol. 35, no. 5, pp. 919-30, 2009.
, “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.
, “Informative phenotypes for genetic studies of psychiatric disorders.”, Am J Med Genet B Neuropsychiatr Genet, vol. 144B, no. 5, pp. 581-8, 2007.
, “New movements in neurofilament transport, turnover and disease.”, Exp Cell Res, vol. 313, no. 10, pp. 2110-20, 2007.
, “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.
, “Up-regulation of peripherin is associated with alterations in synaptic plasticity in CA1 and CA3 regions of hippocampus.”, Neurobiol Dis, vol. 18, no. 2, pp. 409-20, 2005.
, “Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome.”, Can J Cardiol, vol. 20, no. 4, pp. 425-30, 2004.
, “[Genetics of schizophrenia and bipolar disorder: recent success of linkage studies with evidence of specific and shared susceptibility loci].”, Med Sci (Paris), vol. 19, no. 10, pp. 960-6, 2003.
