Publications
Export 28 results:
Filtres: Keyword is Genetic Predisposition to Disease [Enlever les filtres]
, « Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis. », JAMA Neurol, vol. 79, nᵒ 2, p. 185-193, 2022.
, « Genetic associations of protein-coding variants in human disease. », Nature, vol. 603, nᵒ 7899, p. 95-102, 2022.
, « Understanding Gene-Lifestyle Interaction in Obesity: The Role of Mediation versus Moderation. », Lifestyle Genom, vol. 15, nᵒ 2, p. 67-76, 2022.
, « 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, p. 186-192, 2016.
, « A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis. », Neurology, vol. 86, nᵒ 2, p. 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, p. 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, p. 93-100, 2014.
, « Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. », Bioinformatics, vol. 30, nᵒ 15, p. 2189-96, 2014.
, « A protective-compensatory model may reconcile the genetic and the developmental findings in schizophrenia. », Schizophr Res, vol. 144, nᵒ 1-3, p. 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, p. 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, p. 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, p. 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, p. 919-30, 2009.
, « Estimating interaction between genetic and environmental risk factors: efficiency of sampling designs within a cohort. », Epidemiology, vol. 19, nᵒ 1, p. 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, p. 737-44, 2008.
, « Using disease symptoms to improve detection of linkage under genetic heterogeneity. », Genet Epidemiol, vol. 32, nᵒ 5, p. 476-86, 2008.
, « Informative phenotypes for genetic studies of psychiatric disorders. », Am J Med Genet B Neuropsychiatr Genet, vol. 144B, nᵒ 5, p. 581-8, 2007.
, « New movements in neurofilament transport, turnover and disease. », Exp Cell Res, vol. 313, nᵒ 10, p. 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, p. 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, p. 477-83, 2005.
, « Identifying SNPs predictive of phenotype using random forests. », Genet Epidemiol, vol. 28, nᵒ 2, p. 171-82, 2005.
