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Kelly, M. A., Rees, S. D., Hydrie, M. Z. I., Shera, A. S., Bellary, S., O'Hare, J. P., et al. (2012). Circadian gene variants and susceptibility to type 2 diabetes: a pilot study. PLoS One, 7(4), e32670.
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Kvaloy, K., Holmen, J., Hveem, K., & Holmen, T. L. (2015). Genetic Effects on Longitudinal Changes from Healthy to Adverse Weight and Metabolic Status – The HUNT Study. PloS one, 10(10), e0139632.
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Kvehaugen, A. S., Melien, O., Holmen, O. L., Laivuori, H., Dechend, R., & Staff, A. C. (2014). Hypertension after preeclampsia and relation to the C1114G polymorphism (rs4606) in RGS2: data from the Norwegian HUNT2 study. BMC Med Genet, 15, 28.
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Kvehaugen, A. S., Melien, O., Holmen, O. L., Laivuori, H., Oian, P., Andersgaard, A. B., et al. (2013). Single nucleotide polymorphisms in G protein signaling pathway genes in preeclampsia. Hypertension, 61(3), 655–661.
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Lange, L. A., Hu, Y., Zhang, H., Xue, C., Schmidt, E. M., Tang, Z. - Z., et al. (2014). Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. Am J Hum Genet, 94(2), 233–245.
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Skarpengland, T., Laugsand, L. E., Janszky, I., Luna, L., Halvorsen, B., Platou, C. G., et al. (2015). Genetic variants in the DNA repair gene NEIL3 and the risk of myocardial infarction in a nested case-control study. The HUNT Study. DNA repair, 28, 21–27.
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