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Anttila, V., Winsvold, B. S., Gormley, P., Kurth, T., Bettella, F., McMahon, G., et al. (2013). Genome-wide meta-analysis identifies new susceptibility loci for migraine (Vol. 45).
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Berndt, S. I., Gustafsson, S., Magi, R., Ganna, A., Wheeler, E., Feitosa, M. F., et al. (2013). Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet, 45(5), 501–512.
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Bjorngaard, J. H., Gunnell, D., Elvestad, M. B., Davey Smith, G., Skorpen, F., Krokan, H., et al. (2013). The causal role of smoking in anxiety and depression: a Mendelian randomization analysis of the HUNT study. Psychol Med, 43(4), 711–719.
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Chen, C. H., Peng, Q., Schork, A. J., Lo, M. T., Fan, C. C., Wang, Y., et al. (2015). Large-scale genomics unveil polygenic architecture of human cortical surface area. Nature communications, 6, 7549.
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Dastani, Z., Hivert, M. - F., Timpson, N., Perry, J. R. B., Yuan, X., Scott, R. A., et al. (2012). Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet, 8(3), e1002607.
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Demirkan, A., van Duijn, C. M., Ugocsai, P., Isaacs, A., Pramstaller, P. P., Liebisch, G., et al. (2012). Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. PLoS Genet, 8(2), e1002490.
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Ferreira, M. A., Vonk, J. M., Baurecht, H., Marenholz, I., Tian, C., Hoffman, J. D., et al. (2017). Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology (Vol. 49).
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Gaulton, K. J., Ferreira, T., Lee, Y., Raimondo, A., Magi, R., Reschen, M. E., et al. (2015). Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. Nature genetics, 47(12), 1415–1425.
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Hung, R. J., McKay, J. D., Gaborieau, V., Boffetta, P., Hashibe, M., Zaridze, D., et al. (2008). A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. Nature, 452(7187), 633–637.
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Johnson, M. P., Brennecke, S. P., East, C. E., Dyer, T. D., Roten, L. T., Proffitt, J. M., et al. (2013). Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease. Mol Hum Reprod, 19(7), 423–437.
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Johnson, M. P., Brennecke, S. P., East, C. E., Goring, H. H. H., Kent, J. W. J., Dyer, T. D., et al. (2012). Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. PLoS One, 7(3), e33666.
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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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Liu, J. Z., Hov, J. R., Folseraas, T., Ellinghaus, E., Rushbrook, S. M., Doncheva, N. T., et al. (2013). Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Nat Genet, 45(6), 670–675.
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Palmer, N. D., McDonough, C. W., Hicks, P. J., Roh, B. H., Wing, M. R., An, S. S., et al. (2012). A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One, 7(1), e29202.
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Purdue, M. P., Johansson, M., Zelenika, D., Toro, J. R., Scelo, G., Moore, L. E., et al. (2011). Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3. Nat Genet, 43(1), 60–65.
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Rawal, R., Teumer, A., Volzke, H., Wallaschofski, H., Ittermann, T., Asvold, B. O., et al. (2012). Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function. Hum Mol Genet, 21(14), 3275–3282.
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Shungin, D., Winkler, T. W., Croteau-Chonka, D. C., Ferreira, T., Locke, A. E., Magi, R., et al. (2015). New genetic loci link adipose and insulin biology to body fat distribution. Nature, 518(7538), 187–196.
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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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Sorgjerd, E. P., Skorpen, F., Kvaloy, K., Midthjell, K., & Grill, V. (2013). Prevalence of ZnT8 antibody in relation to phenotype and SLC30A8 polymorphism in adult autoimmune diabetes: results from the HUNT study, Norway. Autoimmunity, 46(1), 74–79.
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Tanskanen, T., van den Berg, L., Valimaki, N., Aavikko, M., Ness-Jensen, E., Hveem, K., et al. (2018). Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci (Vol. 142).
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Tanskanen, T., van den Berg, L., Valimaki, N., Aavikko, M., Ness-Jensen, E., Hveem, K., et al. (2018). Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci. Int J Cancer, 142(3), 540–546.
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