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Filters: Author is Croteau, Jordie  [Clear All Filters]
2020
C. Hudon, Escudier, F., De Roy, J., Croteau, J., Cross, N., Dang-Vu, T. Thanh, Zomahoun, H. Tchala Vig, Grenier, S., Gagnon, J. - F., Parent, A., Bruneau, M. - A., and Belleville, S., “Behavioral and Psychological Symptoms that Predict Cognitive Decline or Impairment in Cognitively Normal Middle-Aged or Older Adults: a Meta-Analysis.”, Neuropsychol Rev, 2020.
Y. C. Chagnon, Maziade, M., Paccalet, T., Croteau, J., Fournier, A., M-A Roy, and Bureau, A., “A multimodal attempt to follow-up linkage regions using RNA expression, SNPs and CpG methylation in schizophrenia and bipolar disorder kindreds.”, Eur J Hum Genet, vol. 28, no. 4, pp. 499-507, 2020.
2017
S. Belleville, Fouquet, C., Hudon, C., Zomahoun, H. Tchala Vig, and Croteau, J., “Neuropsychological Measures that Predict Progression from Mild Cognitive Impairment to Alzheimer's type dementia in Older Adults: a Systematic Review and Meta-Analysis.”, Neuropsychol Rev, vol. 27, no. 4, pp. 328-353, 2017.
2016
A. Bureau and Croteau, J., “When Is an Endophenotype Useful to Detect Association to a Disease? Exploring the Relationships between Disease Status, Endophenotype and Genetic Polymorphisms.”, Hum Hered, vol. 81, no. 1, pp. 11-25, 2016.
2015
A. Bureau, Croteau, J., Couture, C., Vohl, M. - C., Bouchard, C., and Pérusse, L., “Estimating genetic effect sizes under joint disease-endophenotype models in presence of gene-environment interactions.”, Front Genet, vol. 6, p. 248, 2015.
J. A. Gross, Bureau, A., Croteau, J., Galfalvy, H., Oquendo, M. A., Haghighi, F., Mérette, C., Giegling, I., Hodgkinson, C., Goldman, D., Rujescu, D., J Mann, J., and Turecki, G., “A genome-wide copy number variant study of suicidal behavior.”, PLoS One, vol. 10, no. 5, p. e0128369, 2015.
2014
A. Bureau, Croteau, J., Chagnon, Y. C., M-A Roy, and Maziade, M., “Extension of the generalized disequilibrium test to polytomous phenotypes and two-locus models.”, Front Genet, vol. 5, p. 258, 2014.
2013
A. Bureau, Chagnon, Y. C., Croteau, J., Fournier, A., M-A Roy, Paccalet, T., Mérette, C., and Maziade, M., “Follow-up of a major psychosis linkage site in 13q13-q14 reveals significant association in both case-control and family samples.”, Biol Psychiatry, vol. 74, no. 6, pp. 444-50, 2013.
2012
A. Bureau, Croteau, J., Mérette, C., Fournier, A., Chagnon, Y. C., M-A Roy, and Maziade, M., “Detection of phenotype modifier genes using two-locus linkage analysis in complex disorders such as major psychosis.”, Hum Hered, vol. 73, no. 4, pp. 195-207, 2012.
2011
L. M. Fiori, Bureau, A., Labbe, A., Croteau, J., Noël, S., Mérette, C., and Turecki, G., “Global gene expression profiling of the polyamine system in suicide completers.”, Int J Neuropsychopharmacol, vol. 14, no. 5, pp. 595-605, 2011.
A. Bureau, Croteau, J., Tayeb, A., Mérette, C., and Labbe, A., “Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies.”, Genet Epidemiol, vol. 35, no. 3, pp. 182-9, 2011.
2010
L. M. Fiori, Wanner, B., Jomphe, V., Croteau, J., Vitaro, F., Tremblay, R. E., Bureau, A., and Turecki, G., “Association of polyaminergic loci with anxiety, mood disorders, and attempted suicide.”, PLoS One, vol. 5, no. 11, p. e15146, 2010.
2009
A. Bureau, Mérette, C., Croteau, J., Fournier, A., Chagnon, Y. C., M-A Roy, and Maziade, M., “A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity.”, Hum Hered, vol. 68, no. 4, pp. 231-42, 2009.
2008
A. Bureau, Labbe, A., Croteau, J., and Mérette, C., “Using disease symptoms to improve detection of linkage under genetic heterogeneity.”, Genet Epidemiol, vol. 32, no. 5, pp. 476-86, 2008.

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