Items where Author is "Bouchard, G."

Article

Hamet, P., Seda, O., Merlo, E., Tremblay, J., Broeckel, U., Gaudet, D., Bouchard, G., Gagnon, F., Antoniol, G., Wan, R., Pausova, Z., Gossard, F., Kotchen, T. A., Pintos, J., & Cowley, A. W. (2005). Partitioning of Extra/Intracellular Body Water Plays a Role in Specific Subsets of Hypertension Featuring Metabolic Syndrome and Premature Death. Journal of Hypertension, 23, S264-S264. Unavailable

Hamet, P., Merlo, E., Šeda, O., Broeckel, U., Tremblay, J., Kaldunski, M., Gaudet, D., Bouchard, G., Deslauriers, B., Gagnon, F., Antoniol, G., Pausová, Z., Labuda, M., Jomphe, M., Gossard, F., Tremblay, G., Kirova, R., Tonellato, P., Orlov, S. N., ... Cowley, A. W. (2005). Quantitative founder effect analysis of French-Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension. American Journal on Human Genetics, 76(5), 815-832. External link

Hamet, P., Seda, O., Merlo, E., Gaudet, D., Broeckel, U., Gagnon, F., Antoniol, G., Bouchard, G., Kotchen, T. A., & Cowley, A. W. (2004). Resolution of Complex Trait of Hypertension by Linkage, Systematic Allelic Contribution Analysis and Ancestral Data in French-Canadian Families. Journal of Hypertension, 22, S5-S5. External link

Merlo, E., Seda, O., Antoniol, G., Gaudet, D., Deslauriers, B., Tremblay, J., Cowley, A. W., Bouchard, G., & Hamet, P. (2003). Differential Genetic Contribution Density of Separable Layered Founders in Saguenay (Québec) Population. Journal of Hypertension, 21, S305-S305. Unavailable

Abstract

Seda, O., Merlo, E., Tremblay, J., Broeckel, U., Kaldunski, M., Gaudet, D., Bouchard, G., Gagnon, F., Antoniol, G., Brunelle, P. L., Gurau, A., Gossard, F., Kotchen, T. A., Pausova, Z., Orlov, S. N., Wan, R., Jomphe, M., Pintos, J., Cowley, A. W., & Hamet, P. (2005, May). Hypertension with and without metabolic syndrome presents as distinct clinical and genetic entities in French-Canadians [Abstract]. European Human Genetics Conference, Prague, Czech Republic. Published in European Journal of Human Genetics, 13(S1). External link