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Filters: Keyword is Genetic Predisposition to Disease  [Clear All Filters]
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.
F. Légaré, Robitaille, H., Gane, C., Hébert, J., Labrecque, M., and Rousseau, F., Improving Decision Making about Genetic Testing in the Clinic: An Overview of Effective Knowledge Translation Interventions., PLoS One, vol. 11, no. 3, p. e0150123, 2016.
T. Paccalet, Gilbert, E., Berthelot, N., Marquet, P., Jomphe, V., Lussier, D., Bouchard, R. - H., Cliche, D., Gingras, N., and Maziade, M., Liability indicators aggregate many years before transition to illness in offspring descending from kindreds affected by schizophrenia or bipolar disorder., Schizophr Res, vol. 175, no. 1-3, pp. 186-192, 2016.
K. Habbout, Poulin, H., Rivier, F., Giuliano, S., Sternberg, D., Fontaine, B., Eymard, B., Morales, R. Juntas, Echenne, B., King, L., Hanna, M. G., Männikkö, R., Chahine, M., Nicole, S., and Bendahhou, S., A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis., Neurology, vol. 86, no. 2, pp. 161-9, 2016.

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