Publications | Cervo Brain Research Centre

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2016

W. Sun, Kechris, K., Jacobson, S., M Drummond, B., Hawkins, G. A., Yang, J., Chen, T. - H., Quibrera, P. Miguel, Anderson, W., R Barr, G., Basta, P. V., Bleecker, E. R., Beaty, T., Casaburi, R., Castaldi, P., Cho, M. H., Comellas, A., Crapo, J. D., Criner, G., Demeo, D., Christenson, S. A., Couper, D. J., Curtis, J. L., Doerschuk, C. M., Freeman, C. M., Gouskova, N. A., Han, M. L. K., Hanania, N. A., Hansel, N. N., Hersh, C. P., Hoffman, E. A., Kaner, R. J., Kanner, R. E., Kleerup, E. C., Lutz, S., Martinez, F. J., Meyers, D. A., Peters, S. P., Regan, E. A., Rennard, S. I., Scholand, M. Beth, Silverman, E. K., Woodruff, P. G., O'Neal, W. K., and Bowler, R. P., “Common Genetic Polymorphisms Influence Blood Biomarker Measurements in COPD.”, PLoS Genet, vol. 12, no. 8, p. e1006011, 2016.

2015

H. Galfalvy, Haghighi, F., Hodgkinson, C., Goldman, D., Oquendo, M. A., Burke, A., Huang, Y. - Y., Giegling, I., Rujescu, D., Bureau, A., Turecki, G., and J Mann, J., “A genome-wide association study of suicidal behavior.”, Am J Med Genet B Neuropsychiatr Genet, vol. 168, no. 7, pp. 557-63, 2015.

V. Riva, Battaglia, M., Nobile, M., Cattaneo, F., Lazazzera, C., Mascheretti, S., Giorda, R., Mérette, C., Emond, C., Maziade, M., and Marino, C., “GRIN2B predicts attention problems among disadvantaged children.”, Eur Child Adolesc Psychiatry, vol. 24, no. 7, pp. 827-36, 2015.

2014

F. A. Wright, Sullivan, P. F., Brooks, A. I., Zou, F., Sun, W., Xia, K., Madar, V., Jansen, R., Chung, W., Zhou, Y. - H., Abdellaoui, A., Batista, S., Butler, C., Chen, G., Chen, T. - H., D'Ambrosio, D., Gallins, P., Ha, M. Jin, Hottenga, J. Jan, Huang, S., Kattenberg, M., Kochar, J., Middeldorp, C. M., Qu, A., Shabalin, A., Tischfield, J., Todd, L., Tzeng, J. - Y., van Grootheest, G., Vink, J. M., Wang, Q., Wang, W., Wang, W., Willemsen, G., Smit, J. H., de Geus, E. J., Yin, Z., Penninx, B. W. J. H., and Boomsma, D. I., “Heritability and genomics of gene expression in peripheral blood.”, Nat Genet, vol. 46, no. 5, pp. 430-7, 2014.

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.

L. Elfassihi, Giroux, S., Bureau, A., Laflamme, N., Cole, D. Ec, and Rousseau, F., “Association with replication between estrogen-related receptor gamma (ESRRgamma) polymorphisms and bone phenotypes in women of European ancestry.”, J Bone Miner Res, vol. 25, no. 4, pp. 901-11, 2010.

J. Brezo, Bureau, A., Mérette, C., Jomphe, V., Barker, E. D., Vitaro, F., Hébert, M., Carbonneau, R., Tremblay, R. E., and Turecki, G., “Differences and similarities in the serotonergic diathesis for suicide attempts and mood disorders: a 22-year longitudinal gene-environment study.”, Mol Psychiatry, vol. 15, no. 8, pp. 831-43, 2010.

S. Giroux, Elfassihi, L., Clément, V., Bussières, J., Bureau, A., Cole, D. E. C., and Rousseau, F., “High-density polymorphisms analysis of 23 candidate genes for association with bone mineral density.”, Bone, vol. 47, no. 5, pp. 975-81, 2010.

2009

E. Canu, Boccardi, M., Ghidoni, R., Benussi, L., Duchesne, S., Testa, C., Binetti, G., and Frisoni, G. B., “HOXA1 A218G polymorphism is associated with smaller cerebellar volume in healthy humans.”, J Neuroimaging, vol. 19, no. 4, pp. 353-8, 2009.

2007

Y. C. Chagnon, Bureau, A., Gendron, D., Bouchard, R. H., Mérette, C., M-A Roy, and Maziade, M., “Possible association of the pro-melanin-concentrating hormone gene with a greater body mass index as a side effect of the antipsychotic olanzapine.”, Am J Med Genet B Neuropsychiatr Genet, vol. 144B, no. 8, pp. 1063-9, 2007.

2005

A. Bureau, Dupuis, J., Falls, K., Lunetta, K. L., Hayward, B., Keith, T. P., and Van Eerdewegh, P., “Identifying SNPs predictive of phenotype using random forests.”, Genet Epidemiol, vol. 28, no. 2, pp. 171-82, 2005.

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