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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.
Post-immunisation fever and the antibody response to measles-containing vaccines. Epidemiol Infect. 2018:1-9.
Referential Choices in a Collaborative Storytelling Task: Discourse Stages and Referential Complexity Matter. Front Psychol. 2018;9:176.
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.
Whole exome association of rare deletions in multiplex oral cleft families. Genet Epidemiol. 2017;41(1):61-69.
Association between expression of inflammatory markers in normal breast tissue and mammographic density among premenopausal and postmenopausal women. Menopause. 2017;24(5):524-535.
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.
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.
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.
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.
A genome-wide copy number variant study of suicidal behavior. PLoS ONE. 2015;10(5):e0128369.
A genome-wide association study of suicidal behavior. Am J Med Genet B Neuropsychiatr Genet. 2015;168(7):557-63.
Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. Bioinformatics. 2014;30(15):2189-96.
Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts. Genetics. 2014;197(3):1039-44.
Plasma polychlorinated biphenyl and organochlorine pesticide concentrations in dementia: the Canadian Study of Health and Aging. Environ Int. 2014;69:141-7.
Extension of the generalized disequilibrium test to polytomous phenotypes and two-locus models. Front Genet. 2014;5:258.
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.
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.
Detection of phenotype modifier genes using two-locus linkage analysis in complex disorders such as major psychosis. Hum Hered. 2012;73(4):195-207.