Bureau A - Search Results

1

Applications of continuous time hidden Markov models to the study of misclassified disease outcomes.

Bureau A, Shiboski S, Hughes JP. Bureau A, et al. Stat Med. 2003 Feb 15;22(3):441-62. doi: 10.1002/sim.1270. Stat Med. 2003. PMID: 12529874

2

Symptom dimensions as alternative phenotypes to address genetic heterogeneity in schizophrenia and bipolar disorder.

Labbe A, Bureau A, Moreau I, Roy MA, Chagnon Y, Maziade M, Merette C. Labbe A, et al. Among authors: bureau a. Eur J Hum Genet. 2012 Nov;20(11):1182-8. doi: 10.1038/ejhg.2012.67. Epub 2012 Apr 25. Eur J Hum Genet. 2012. PMID: 22535187 Free PMC article.

3

Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants.

Bureau A, Begum F, Taub MA, Hetmanski JB, Parker MM, Albacha-Hejazi H, Scott AF, Murray JC, Marazita ML, Bailey-Wilson JE, Beaty TH, Ruczinski I. Bureau A, et al. Genet Epidemiol. 2019 Feb;43(1):37-49. doi: 10.1002/gepi.22155. Epub 2018 Sep 24. Genet Epidemiol. 2019. PMID: 30246882 Free PMC article.

4

Time trends in social contacts before and during the COVID-19 pandemic: the CONNECT study.

Drolet M, Godbout A, Mondor M, Béraud G, Drolet-Roy L, Lemieux-Mellouki P, Bureau A, Demers É, Boily MC, Sauvageau C, De Serres G, Hens N, Beutels P, Dervaux B, Brisson M. Drolet M, et al. Among authors: bureau a. BMC Public Health. 2022 May 23;22(1):1032. doi: 10.1186/s12889-022-13402-7. BMC Public Health. 2022. PMID: 35606703 Free PMC article.

5

Chromosome 13q13-q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype.

Maziade M, Chagnon YC, Roy MA, Bureau A, Fournier A, Mérette C. Maziade M, et al. Among authors: bureau a. Eur J Hum Genet. 2009 Aug;17(8):1034-42. doi: 10.1038/ejhg.2008.268. Epub 2009 Jan 28. Eur J Hum Genet. 2009. PMID: 19172987 Free PMC article.

6

A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity.

Bureau A, Mérette C, Croteau J, Fournier A, Chagnon YC, Roy MA, Maziade M. Bureau A, et al. Hum Hered. 2009;68(4):231-42. doi: 10.1159/000228921. Epub 2009 Jul 22. Hum Hered. 2009. PMID: 19622890 Free article.

7

Detection of phenotype modifier genes using two-locus linkage analysis in complex disorders such as major psychosis.

Bureau A, Croteau J, Mérette C, Fournier A, Chagnon YC, Roy MA, Maziade M. Bureau A, et al. Hum Hered. 2012;73(4):195-207. doi: 10.1159/000341392. Epub 2012 Aug 15. Hum Hered. 2012. PMID: 22907187 Free article.

8

A multimodal attempt to follow-up linkage regions using RNA expression, SNPs and CpG methylation in schizophrenia and bipolar disorder kindreds.

Chagnon YC, Maziade M, Paccalet T, Croteau J, Fournier A, Roy MA, Bureau A. Chagnon YC, et al. Among authors: bureau a. Eur J Hum Genet. 2020 Apr;28(4):499-507. doi: 10.1038/s41431-019-0526-y. Epub 2019 Nov 6. Eur J Hum Genet. 2020. PMID: 31695175 Free PMC article.

9

Detection of rare disease variants in extended pedigrees using RVS.

Sherman T, Fu J, Scharpf RB, Bureau A, Ruczinski I. Sherman T, et al. Among authors: bureau a. Bioinformatics. 2019 Jul 15;35(14):2509-2511. doi: 10.1093/bioinformatics/bty976. Bioinformatics. 2019. PMID: 30500888 Free PMC article.

10

Replication of linkage with bipolar disorder on chromosome 16p in the Eastern Quebec population.

Mérette C, Roy MA, Bureau A, Fournier A, Emond C, Cliche D, Jomphe V, Chagnon YC, Maziade M. Mérette C, et al. Among authors: bureau a. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):737-44. doi: 10.1002/ajmg.b.30673. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18165973

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