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Filtres: Keyword is Genetic Predisposition to Disease and Author is Alexandre Bureau [Enlever les filtres]
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.
Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. Bioinformatics. 2014;30(15):2189-96.
Association of polyaminergic loci with anxiety, mood disorders, and attempted suicide. PLoS ONE. 2010;5(11):e15146.
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.
Chromosome 13q13-q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype. Eur J Hum Genet. 2009;17(8):1034-42.
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.
Using disease symptoms to improve detection of linkage under genetic heterogeneity. Genet Epidemiol. 2008;32(5):476-86.
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.
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.