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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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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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Graff, M., Scott, R. A., Justice, A. E., Young, K. L., Feitosa, M. F., Barata, L., et al. (2017). Genome-wide physical activity interactions in adiposity – A meta-analysis of 200,452 adults (Vol. 13).
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Helgadottir, A., Thorleifsson, G., Gretarsdottir, S., Stefansson, O. A., Tragante, V., Thorolfsdottir, R. B., et al. (2018). Genome-wide analysis yields new loci associating with aortic valve stenosis. Nat Commun, 9(1), 987.
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Holmen, O. L., Zhang, H., Fan, Y., Hovelson, D. H., Schmidt, E. M., Zhou, W., et al. (2014). Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk. Nat Genet, 46(4), 345–351.
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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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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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Lu, X., Peloso, G. M., Liu, D. J., Wu, Y., Zhang, H., Zhou, W., et al. (2017). Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease (Vol. 49).
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Marquez, M., Huyvaert, M., Perry, J. R. B., Pearson, R. D., Falchi, M., Morris, A. P., et al. (2012). Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk. Diabetes, 61(2), 524–530.
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Nielsen, J. B., Fritsche, L. G., Zhou, W., Teslovich, T. M., Holmen, O. L., Gustafsson, S., et al. (2018). Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development. Am J Hum Genet, 102(1), 103–115.
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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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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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Thomsen, L. C. V., McCarthy, N. S., Melton, P. E., Cadby, G., Austgulen, R., Nygard, O. K., et al. (2017). The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia. J Hypertens, 35(1), 132–139.
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Webb, T. R., Erdmann, J., Stirrups, K. E., Stitziel, N. O., Masca, N. G. D., Jansen, H., et al. (2017). Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease. J Am Coll Cardiol, 69(7), 823–836.
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Winsvold, B. S., Palta, P., Eising, E., Page, C. M., van den Maagdenberg, A. M., Palotie, A., et al. (2018). Epigenetic DNA methylation changes associated with headache chronification: A retrospective case-control study. Cephalalgia, 38(2), 312–322.
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Wood, A. R., Esko, T., Yang, J., Vedantam, S., Pers, T. H., Gustafsson, S., et al. (2014). Defining the role of common variation in the genomic and biological architecture of adult human height (Vol. 46).
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