Genetic association studies

REVIEW-ARTICLE Intermediate alleles of Huntington's disease HTT gene in different populations worldwide: a systematic review.

T. A. Apolinário, Paiva, C. L. A., and Agostinho, L. A., “REVIEW-ARTICLE Intermediate alleles of Huntington's disease HTT gene in different populations worldwide: a systematic review.”, Genet Mol Res, vol. 16, no. 2, 2017.

Polymorphism E23K (rs5219) in the KCNJ11 gene in Euro-Brazilian subjects with type 1 and 2 diabetes.

S. W. Souza, Alcazar, L. P., Arakaki, P. A., Santos-Weiss, I. C. R., Alberton, D., Picheth, G., and Rego, F. G. M., “Polymorphism E23K (rs5219) in the KCNJ11 gene in Euro-Brazilian subjects with type 1 and 2 diabetes.”, Genet Mol Res, vol. 16, no. 2, 2017.

Association between interleukin-4 polymorphisms and risk of pre-eclampsia in a population of Chinese pregnant women.

J. Chen, Zhong, M., and Yu, Y. H., “Association between interleukin-4 polymorphisms and risk of pre-eclampsia in a population of Chinese pregnant women.”, Genet Mol Res, vol. 16, no. 2, 2017.

Multicollinearity in canonical correlation analysis in maize.

B. M. Alves, A Filho, C., and Burin, C., “Multicollinearity in canonical correlation analysis in maize.”, Genet Mol Res, vol. 16, no. 1, 2017.

Leptin (rs7799039) and solute carrier family 30 zinc transporter (rs13266634) polymorphisms in Euro-Brazilian pregnant women with gestational diabetes.

A. Teleginski, Welter, M., Frigeri, H. R., Réa, R. R., Souza, E. M., Alberton, D., Rego, F. G. M., and Picheth, G., “Leptin (rs7799039) and solute carrier family 30 zinc transporter (rs13266634) polymorphisms in Euro-Brazilian pregnant women with gestational diabetes.”, Genet Mol Res, vol. 16, no. 1, 2017.

Association between interleukin-17 gene polymorphisms and the risk of laryngeal cancer in a Chinese population.

F. Z. Si, Feng, Y. Q., and Han, M., “Association between interleukin-17 gene polymorphisms and the risk of laryngeal cancer in a Chinese population.”, Genet Mol Res, vol. 16, no. 1, 2017.

GSTM1 polymorphism in patients with clinical manifestations of atherosclerosis.

D. A. Rodrigues, Martins, J. V. M., Silva, K. S. F. E., Costa, I. R., Lagares, M. H., Campedelli, F. L., Barbosa, A. M., de Morais, M. P., and Moura, K. K. V. O., “GSTM1 polymorphism in patients with clinical manifestations of atherosclerosis.”, Genet Mol Res, vol. 16, no. 1, 2017.

Association of RUNX2 and TNFSF11 genes with production traits in a paternal broiler line.

N. V. Grupioni, Stafuzza, N. B., Carvajal, A. B., Ibelli, A. M. G., Peixoto, J. O., Ledur, M. C., and Munari, D. P., “Association of RUNX2 and TNFSF11 genes with production traits in a paternal broiler line.”, Genet Mol Res, vol. 16, no. 1, 2017.

Lack of association between CARD10/CARMA3 tag SNPs and psoriasis vulgaris in the southern Chinese population.

G. Shi, Zhang, M. F., Liao, P. Y., Wang, T. T., Li, S. J., Fan, Y. M., and Zhu, K. J., “Lack of association between CARD10/CARMA3 tag SNPs and psoriasis vulgaris in the southern Chinese population.”, Genet Mol Res, vol. 16, no. 1, 2017.

IL-8 -251A/T polymorphism contributes to coronary artery disease susceptibility in a Chinese population.

R. J. Zhang, Li, X. D., Zhang, S. W., Li, X. H., and Wu, L., “IL-8 -251A/T polymorphism contributes to coronary artery disease susceptibility in a Chinese population.”, Genet Mol Res, vol. 16, no. 1, 2017.

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