Publications | Centre de recherche CERVO

Export 13 results:

Filtres: Keyword is Polymorphism, Single Nucleotide [Enlever les filtres]

2022

L. Mangnier, Joly-Beauparlant, C., Droit, A., Bilodeau, S., et Bureau, A., « Cis-regulatory hubs: a new 3D model of complex disease genetics with an application to schizophrenia. », Life Sci Alliance, vol. 5, nᵒ 5, 2022.

B. B. Sun, Kurki, M. I., Foley, C. N., Mechakra, A., Chen, C. - Y., Marshall, E., Wilk, J. B., Chahine, M., Chevalier, P., Christé, G., Palotie, A., Daly, M. J., et Runz, H., « Genetic associations of protein-coding variants in human disease. », Nature, vol. 603, nᵒ 7899, p. 95-102, 2022.

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., et 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., et J Mann, J., « A genome-wide association study of suicidal behavior. », Am J Med Genet B Neuropsychiatr Genet, vol. 168, nᵒ 7, p. 557-63, 2015.

V. Riva, Battaglia, M., Nobile, M., Cattaneo, F., Lazazzera, C., Mascheretti, S., Giorda, R., Mérette, C., Emond, C., Maziade, M., et Marino, C., « GRIN2B predicts attention problems among disadvantaged children. », Eur Child Adolesc Psychiatry, vol. 24, nᵒ 7, p. 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., et Boomsma, D. I., « Heritability and genomics of gene expression in peripheral blood. », Nat Genet, vol. 46, nᵒ 5, p. 430-7, 2014.

2010

L. M. Fiori, Wanner, B., Jomphe, V., Croteau, J., Vitaro, F., Tremblay, R. E., Bureau, A., et 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, et 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, p. 901-11, 2010.

J. Brezo, Bureau, A., Mérette, C., Jomphe, V., Barker, E. D., Vitaro, F., Hébert, M., Carbonneau, R., Tremblay, R. E., et 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, p. 831-43, 2010.

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

2009

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

2007

Y. C. Chagnon, Bureau, A., Gendron, D., Bouchard, R. H., Mérette, C., M-A Roy, et 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, p. 1063-9, 2007.

2005

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

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