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Items: 1 to 50 of 70

2.

Passion for Exercise: Passion's Relationship to General Fitness Indicators and Exercise Addiction.

Bureau AT, Blom LC, Bolin J, Nagelkirk P.

Int J Exerc Sci. 2019 Jan 1;12(5):122-135. eCollection 2019.

3.

Detection of rare disease variants in extended pedigrees using RVS.

Sherman T, Fu J, Scharpf RB, Bureau A, Ruczinski I.

Bioinformatics. 2018 Nov 30. doi: 10.1093/bioinformatics/bty976. [Epub ahead of print]

PMID:
30500888
4.

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.

Genet Epidemiol. 2019 Feb;43(1):37-49. doi: 10.1002/gepi.22155. Epub 2018 Sep 24.

PMID:
30246882
5.

Post-immunisation fever and the antibody response to measles-containing vaccines.

Carazo Perez S, Bureau A, De Serres G.

Epidemiol Infect. 2018 Sep;146(12):1584-1592. doi: 10.1017/S0950268818001474. Epub 2018 Jun 11.

PMID:
29886856
6.

Referential Choices in a Collaborative Storytelling Task: Discourse Stages and Referential Complexity Matter.

Fossard M, Achim AM, Rousier-Vercruyssen L, Gonzalez S, Bureau A, Champagne-Lavau M.

Front Psychol. 2018 Feb 20;9:176. doi: 10.3389/fpsyg.2018.00176. eCollection 2018.

7.

Polygenic risk scores distinguish patients from non-affected adult relatives and from normal controls in schizophrenia and bipolar disorder multi-affected kindreds.

Boies S, Mérette C, Paccalet T, Maziade M, Bureau A.

Am J Med Genet B Neuropsychiatr Genet. 2018 Apr;177(3):329-336. doi: 10.1002/ajmg.b.32614. Epub 2017 Nov 28.

PMID:
29193655
8.

Association between local inflammation and breast tissue age-related lobular involution among premenopausal and postmenopausal breast cancer patients.

Hanna M, Dumas I, Orain M, Jacob S, Têtu B, Sanschagrin F, Bureau A, Poirier B, Diorio C.

PLoS One. 2017 Aug 28;12(8):e0183579. doi: 10.1371/journal.pone.0183579. eCollection 2017.

9.

Prenatal exposure to drinking-water chlorination by-products, cytochrome P450 gene polymorphisms and small-for-gestational-age neonates.

Bonou SG, Levallois P, Giguère Y, Rodriguez M, Bureau A.

Reprod Toxicol. 2017 Oct;73:75-86. doi: 10.1016/j.reprotox.2017.07.019. Epub 2017 Jul 31.

10.

Reduced Antibody Response to Infant Measles Vaccination: Effects Based on Type and Timing of the First Vaccine Dose Persist After the Second Dose.

Carazo Perez S, De Serres G, Bureau A, Skowronski DM.

Clin Infect Dis. 2017 Oct 1;65(7):1094-1102. doi: 10.1093/cid/cix510.

PMID:
28595358
11.

Passion for Academics and Problematic Health Behaviors.

Bureau AT, Razon S, Saville BK, Tokac U, Judge LW.

Int J Exerc Sci. 2017 May 1;10(3):417-433. eCollection 2017.

12.

The interaction of GSK3B and FXR1 genotypes may influence the mania and depression dimensions in mood disorders.

Bureau A, Beaulieu JM, Paccalet T, Chagnon YC, Maziade M.

J Affect Disord. 2017 Apr 15;213:172-177. doi: 10.1016/j.jad.2017.02.023. Epub 2017 Feb 16.

PMID:
28242499
13.

Polyunphased: an extension to polytomous outcomes of the Unphased package for family-based genetic association analysis.

Bureau A, Croteau J.

Stat Appl Genet Mol Biol. 2017 Mar 1;16(1):75-81. doi: 10.1515/sagmb-2016-0035.

14.

Association between expression of inflammatory markers in normal breast tissue and mammographic density among premenopausal and postmenopausal women.

Hanna M, Dumas I, Orain M, Jacob S, Têtu B, Sanschagrin F, Bureau A, Poirier B, Diorio C.

Menopause. 2017 May;24(5):524-535. doi: 10.1097/GME.0000000000000794.

PMID:
28002200
15.

Whole exome association of rare deletions in multiplex oral cleft families.

Fu J, Beaty TH, Scott AF, Hetmanski J, Parker MM, Wilson JE, Marazita ML, Mangold E, Albacha-Hejazi H, Murray JC, Bureau A, Carey J, Cristiano S, Ruczinski I, Scharpf RB.

Genet Epidemiol. 2017 Jan;41(1):61-69. doi: 10.1002/gepi.22010. Epub 2016 Dec 1.

17.

Disinfection by-products exposure and intra-uterine growth restriction: Do genetic polymorphisms of CYP2E1or deletion of GSTM1 or GSTT1 modify the association?

Levallois P, Giguère Y, Nguile-Makao M, Rodriguez M, Campagna C, Tardif R, Bureau A.

Environ Int. 2016 Jul-Aug;92-93:220-31. doi: 10.1016/j.envint.2016.03.033. Epub 2016 Apr 22.

18.

Development of a molecular test of Paget's disease of bone.

Guay-Bélanger S, Simonyan D, Bureau A, Gagnon E, Albert C, Morissette J, Siris ES, Orcel P, Brown JP, Michou L.

Bone. 2016 Mar;84:213-221. doi: 10.1016/j.bone.2016.01.007. Epub 2016 Jan 6.

19.

On the validity of within-nuclear-family genetic association analysis in samples of extended families.

Bureau A, Duchesne T.

Stat Appl Genet Mol Biol. 2015 Dec;14(6):533-49. doi: 10.1515/sagmb-2015-0056.

20.

Estimating genetic effect sizes under joint disease-endophenotype models in presence of gene-environment interactions.

Bureau A, Croteau J, Couture C, Vohl MC, Bouchard C, Pérusse L.

Front Genet. 2015 Jul 28;6:248. doi: 10.3389/fgene.2015.00248. eCollection 2015.

21.

A genome-wide association study of suicidal behavior.

Galfalvy H, Haghighi F, Hodgkinson C, Goldman D, Oquendo MA, Burke A, Huang YY, Giegling I, Rujescu D, Bureau A, Turecki G, Mann JJ.

Am J Med Genet B Neuropsychiatr Genet. 2015 Oct;168(7):557-63. doi: 10.1002/ajmg.b.32330. Epub 2015 Jun 16.

PMID:
26079190
22.

A genome-wide copy number variant study of suicidal behavior.

Gross JA, Bureau A, Croteau J, Galfalvy H, Oquendo MA, Haghighi F, Mérette C, Giegling I, Hodgkinson C, Goldman D, Rujescu D, Mann JJ, Turecki G.

PLoS One. 2015 May 26;10(5):e0128369. doi: 10.1371/journal.pone.0128369. eCollection 2015.

23.

An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia.

Mascheretti S, Bureau A, Trezzi V, Giorda R, Marino C.

Hum Genet. 2015 Jul;134(7):749-60. doi: 10.1007/s00439-015-1555-4. Epub 2015 Apr 28.

PMID:
25916574
24.

Extension of the generalized disequilibrium test to polytomous phenotypes and two-locus models.

Bureau A, Croteau J, Chagnon YC, Roy MA, Maziade M.

Front Genet. 2014 Aug 8;5:258. doi: 10.3389/fgene.2014.00258. eCollection 2014.

25.

Plasma polychlorinated biphenyl and organochlorine pesticide concentrations in dementia: the Canadian Study of Health and Aging.

Medehouenou TC, Ayotte P, Carmichael PH, Kröger E, Verreault R, Lindsay J, Dewailly É, Tyas SL, Bureau A, Laurin D.

Environ Int. 2014 Aug;69:141-7. doi: 10.1016/j.envint.2014.04.016. Epub 2014 May 20.

PMID:
24846810
26.

Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.

Bureau A, Parker MM, Ruczinski I, Taub MA, Marazita ML, Murray JC, Mangold E, Noethen MM, Ludwig KU, Hetmanski JB, Bailey-Wilson JE, Cropp CD, Li Q, Szymczak S, Albacha-Hejazi H, Alqosayer K, Field LL, Wu-Chou YH, Doheny KF, Ling H, Scott AF, Beaty TH.

Genetics. 2014 Jul;197(3):1039-44. doi: 10.1534/genetics.114.165225. Epub 2014 May 2.

27.

Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.

Bureau A, Younkin SG, Parker MM, Bailey-Wilson JE, Marazita ML, Murray JC, Mangold E, Albacha-Hejazi H, Beaty TH, Ruczinski I.

Bioinformatics. 2014 Aug 1;30(15):2189-96. doi: 10.1093/bioinformatics/btu198. Epub 2014 Apr 16.

28.

Follow-up of a major psychosis linkage site in 13q13-q14 reveals significant association in both case-control and family samples.

Bureau A, Chagnon YC, Croteau J, Fournier A, Roy MA, Paccalet T, Mérette C, Maziade M.

Biol Psychiatry. 2013 Sep 15;74(6):444-50. doi: 10.1016/j.biopsych.2013.03.004. Epub 2013 Apr 18.

29.

An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes.

Mascheretti S, Bureau A, Battaglia M, Simone D, Quadrelli E, Croteau J, Cellino MR, Giorda R, Beri S, Maziade M, Marino C.

Genes Brain Behav. 2013 Feb;12(1):47-55. doi: 10.1111/gbb.12000. Epub 2012 Nov 24.

30.

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.

Hum Hered. 2012;73(4):195-207. doi: 10.1159/000341392. Epub 2012 Aug 15.

31.

Genome-wide epigenetic regulation by early-life trauma.

Labonté B, Suderman M, Maussion G, Navaro L, Yerko V, Mahar I, Bureau A, Mechawar N, Szyf M, Meaney MJ, Turecki G.

Arch Gen Psychiatry. 2012 Jul;69(7):722-31. doi: 10.1001/archgenpsychiatry.2011.2287.

32.

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.

Eur J Hum Genet. 2012 Nov;20(11):1182-8. doi: 10.1038/ejhg.2012.67. Epub 2012 Apr 25.

33.

Polychlorinated biphenyls and organochlorine pesticides in plasma of older Canadians.

Medehouenou TC, Ayotte P, Carmichael PH, Kröger E, Verreault R, Lindsay J, Dewailly É, Tyas SL, Bureau A, Laurin D.

Environ Res. 2011 Nov;111(8):1313-20. doi: 10.1016/j.envres.2011.09.017. Epub 2011 Oct 14.

PMID:
22001220
34.

Autologous transplantation in CLL patients with B and C Binet stages: final results of the prospective randomized GOELAMS LLC 98 trial.

Brion A, Mahé B, Kolb B, Audhuy B, Colombat P, Maisonneuve H, Foussard C, Bureau A, Ferrand C, Lesesve JF, Béné MC, Feugier P; Groupe Ouest Est d’Etude des Leucémies et autres Maladies du Sang.

Bone Marrow Transplant. 2012 Apr;47(4):542-8. doi: 10.1038/bmt.2011.117. Epub 2011 Jul 4.

PMID:
21725374
35.

UGT2B17 gene deletion associated with an increase in bone mineral density similar to the effect of hormone replacement in postmenopausal women.

Giroux S, Bussières J, Bureau A, Rousseau F.

Osteoporos Int. 2012 Mar;23(3):1163-70. doi: 10.1007/s00198-011-1662-6. Epub 2011 May 26.

PMID:
21614655
36.

Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies.

Bureau A, Croteau J, Tayeb A, Mérette C, Labbe A.

Genet Epidemiol. 2011 Apr;35(3):182-9. doi: 10.1002/gepi.20566. Epub 2011 Feb 9.

37.

Safety in the preparation of cytotoxic drugs: How to integrate gravimetric control in the quality assurance policy?

Lecordier J, Heluin Y, Plivard C, Bureau A, Mouawad C, Chaillot B, Lahet JJ.

Biomed Pharmacother. 2011 Feb;65(1):17-21. doi: 10.1016/j.biopha.2010.12.014. Epub 2011 Jan 5.

PMID:
21276695
38.

Global gene expression profiling of the polyamine system in suicide completers.

Fiori LM, Bureau A, Labbe A, Croteau J, Noël S, Mérette C, Turecki G.

Int J Neuropsychopharmacol. 2011 Jun;14(5):595-605. doi: 10.1017/S1461145710001574. Epub 2011 Jan 6.

PMID:
21208503
39.

Association of polyaminergic loci with anxiety, mood disorders, and attempted suicide.

Fiori LM, Wanner B, Jomphe V, Croteau J, Vitaro F, Tremblay RE, Bureau A, Turecki G.

PLoS One. 2010 Nov 30;5(11):e15146. doi: 10.1371/journal.pone.0015146.

40.

High-density polymorphisms analysis of 23 candidate genes for association with bone mineral density.

Giroux S, Elfassihi L, Clément V, Bussières J, Bureau A, Cole DE, Rousseau F.

Bone. 2010 Nov;47(5):975-81. doi: 10.1016/j.bone.2010.06.030. Epub 2010 Jul 30.

PMID:
20654748
41.

Association with replication between estrogen-related receptor gamma (ESRRgamma) polymorphisms and bone phenotypes in women of European ancestry.

Elfassihi L, Giroux S, Bureau A, Laflamme N, Cole DE, Rousseau F.

J Bone Miner Res. 2010 Apr;25(4):901-11. doi: 10.1359/jbmr.091014.

42.

Considerations for the development of a reference method for sequencing of haploid DNA--an opinion paper on behalf of the IFCC Committee on Molecular Diagnostics, International Federation of Clinical Chemistry and Laboratory Medicine.

Rousseau F, Gancberg D, Schimmel H, Neumaier M, Bureau A, Mamotte C, van Schaik R, Payne D, Pazzagli M, Young I.

Clin Chem Lab Med. 2009;47(11):1343-50. doi: 10.1515/CCLM.2009.319.

PMID:
19817648
43.

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.

Hum Hered. 2009;68(4):231-42. doi: 10.1159/000228921. Epub 2009 Jul 22.

44.

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.

Mol Psychiatry. 2010 Aug;15(8):831-43. doi: 10.1038/mp.2009.19. Epub 2009 Apr 21.

PMID:
19381154
45.

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.

Eur J Hum Genet. 2009 Aug;17(8):1034-42. doi: 10.1038/ejhg.2008.268. Epub 2009 Jan 28.

46.

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.

Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):934-43. doi: 10.1002/ajmg.b.30920.

PMID:
19152344
47.

Protective effect of candesartan in experimental ischemic stroke in the rat mediated by AT2 and AT4 receptors.

Faure S, Bureau A, Oudart N, Javellaud J, Fournier A, Achard JM.

J Hypertens. 2008 Oct;26(10):2008-15. doi: 10.1097/HJH.0b013e32830dd5ee.

PMID:
18806625
48.

Application of microarray outlier detection methodology to psychiatric research.

Ernst C, Bureau A, Turecki G.

BMC Psychiatry. 2008 Apr 23;8:29. doi: 10.1186/1471-244X-8-29.

49.

Effects of various osmolarity on human red blood cells in terms of potassium efflux and hemolysis induced by free radicals.

Lahet JJ, Lenfant F, Lecordier J, Bureau A, Duvillard L, Chaillot B, Freysz M.

Biomed Pharmacother. 2008 Dec;62(10):697-700. doi: 10.1016/j.biopha.2008.03.001. Epub 2008 Mar 26.

PMID:
18411008
50.

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

Bureau A, Labbe A, Croteau J, Mérette C.

Genet Epidemiol. 2008 Jul;32(5):476-86. doi: 10.1002/gepi.20320.

PMID:
18330904

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