Bureau A - Search Results

1

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.

2

Molecular test of Paget's disease of bone in families not linked to SQSTM1 gene mutations.

You Y, Simonyan D, Bureau A, Gagnon E, Albert C, Guertin JR, Tarride JE, Brown JP, Michou L. You Y, et al. Among authors: bureau a. Bone Rep. 2023 Feb 28;18:101670. doi: 10.1016/j.bonr.2023.101670. eCollection 2023 Jun. Bone Rep. 2023. PMID: 36915391 Free PMC article.

3

Statistics to prioritize rare variants in family-based sequencing studies with disease subtypes.

Nieuwoudt C, Farooq FB, Brooks-Wilson A, Bureau A, Graham J. Nieuwoudt C, et al. Among authors: bureau a. Genet Epidemiol. 2024 Oct;48(7):324-343. doi: 10.1002/gepi.22579. Epub 2024 Jun 28. Genet Epidemiol. 2024. PMID: 38940260

4

Possible association of the pro-melanin-concentrating hormone gene with a greater body mass index as a side effect of the antipsychotic olanzapine.

Chagnon YC, Bureau A, Gendron D, Bouchard RH, Mérette C, Roy MA, Maziade M. Chagnon YC, et al. Among authors: bureau a. Am J Med Genet B Neuropsychiatr Genet. 2007 Dec 5;144B(8):1063-9. doi: 10.1002/ajmg.b.30554. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17541984

5

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

6

Differential RNA expression between schizophrenic patients and controls of the dystrobrevin binding protein 1 and neuregulin 1 genes in immortalized lymphocytes.

Chagnon YC, Roy MA, Bureau A, Mérette C, Maziade M. Chagnon YC, et al. Among authors: bureau a. Schizophr Res. 2008 Mar;100(1-3):281-90. doi: 10.1016/j.schres.2007.12.471. Epub 2008 Jan 30. Schizophr Res. 2008. PMID: 18234478

7

Using disease symptoms to improve detection of linkage under genetic heterogeneity.

Bureau A, Labbe A, Croteau J, Mérette C. Bureau A, et al. Genet Epidemiol. 2008 Jul;32(5):476-86. doi: 10.1002/gepi.20320. Genet Epidemiol. 2008. PMID: 18330904

8

Profiling brain expression of the spermidine/spermine N1-acetyltransferase 1 (SAT1) gene in suicide.

Klempan TA, Rujescu D, Mérette C, Himmelman C, Sequeira A, Canetti L, Fiori LM, Schneider B, Bureau A, Turecki G. Klempan TA, et al. Among authors: bureau a. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):934-43. doi: 10.1002/ajmg.b.30920. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19152344

9

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.

10

Differences and similarities in the serotonergic diathesis for suicide attempts and mood disorders: a 22-year longitudinal gene-environment study.

Brezo J, Bureau A, Mérette C, Jomphe V, Barker ED, Vitaro F, Hébert M, Carbonneau R, Tremblay RE, Turecki G. Brezo J, et al. Among authors: bureau a. Mol Psychiatry. 2010 Aug;15(8):831-43. doi: 10.1038/mp.2009.19. Epub 2009 Apr 21. Mol Psychiatry. 2010. PMID: 19381154

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