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Filtres: Author is Alexandre Bureau [Enlever les filtres]
Detection of rare disease variants in extended pedigrees using RVS. Bioinformatics. 2018.
Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants. Genet Epidemiol. 2018.
Polygenic risk scores distinguish patients from non-affected adult relatives and from normal controls in schizophrenia and bipolar disorder multi-affected kindreds. Am J Med Genet B Neuropsychiatr Genet. 2018;177(3):329-336.
Post-immunisation fever and the antibody response to measles-containing vaccines. Epidemiol Infect. 2018:1-9.
Association between expression of inflammatory markers in normal breast tissue and mammographic density among premenopausal and postmenopausal women. Menopause. 2017;24(5):524-535.
Association between local inflammation and breast tissue age-related lobular involution among premenopausal and postmenopausal breast cancer patients. PLoS ONE. 2017;12(8):e0183579.
The interaction of GSK3B and FXR1 genotypes may influence the mania and depression dimensions in mood disorders. J Affect Disord. 2017;213:172-177.
Reduced antibody response to infant measles vaccination: effects based on type and timing of the first vaccine dose persist after the second dose. Clin Infect Dis. 2017.
Whole exome association of rare deletions in multiplex oral cleft families. Genet Epidemiol. 2017;41(1):61-69.
Development of a molecular test of Paget's disease of bone. Bone. 2016;84:213-21.
Disinfection by-products exposure and intra-uterine growth restriction: Do genetic polymorphisms of CYP2E1or deletion of GSTM1 or GSTT1 modify the association? Environ Int. 2016;92-93:220-31.
Estimating genetic effect sizes under joint disease-endophenotype models in presence of gene-environment interactions. Front Genet. 2015;6:248.
A genome-wide association study of suicidal behavior. Am J Med Genet B Neuropsychiatr Genet. 2015;168(7):557-63.
A genome-wide copy number variant study of suicidal behavior. PLoS ONE. 2015;10(5):e0128369.
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.
Extension of the generalized disequilibrium test to polytomous phenotypes and two-locus models. Front Genet. 2014;5:258.
Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. Bioinformatics. 2014;30(15):2189-96.
Plasma polychlorinated biphenyl and organochlorine pesticide concentrations in dementia: the Canadian Study of Health and Aging. Environ Int. 2014;69:141-7.
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.
Detection of phenotype modifier genes using two-locus linkage analysis in complex disorders such as major psychosis. Hum Hered. 2012;73(4):195-207.
Genome-wide epigenetic regulation by early-life trauma. Arch Gen Psychiatry. 2012;69(7):722-31.
Symptom dimensions as alternative phenotypes to address genetic heterogeneity in schizophrenia and bipolar disorder. Eur J Hum Genet. 2012;20(11):1182-8.