Centre for Genetic Origins of Health and Diseases


Dive into the research topics where Centre for Genetic Origins of Health and Diseases is active. These topic labels come from the works of this organisation's members. Together they form a unique fingerprint.


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  • Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

    China Kadoorie Biobank Collaborative Group, Qatar Genome Program Research (QGPR) Consortium, Shrine, N., Izquierdo, A. G., Chen, J., Packer, R., Hall, R. J., Guyatt, A. L., Batini, C., Thompson, R. J., Pavuluri, C., Malik, V., Hobbs, B. D., Moll, M., Kim, W., Tal-Singer, R., Bakke, P., Fawcett, K. A., John, C., Coley, K., & 130 othersPiga, N. N., Pozarickij, A., Lin, K., Millwood, I. Y., Chen, Z., Li, L., Wijnant, S. R. A., Lahousse, L., Brusselle, G., Uitterlinden, A. G., Manichaikul, A., Oelsner, E. C., Rich, S. S., Barr, R. G., Kerr, S. M., Vitart, V., Brown, M. R., Wielscher, M., Imboden, M., Jeong, A., Bartz, T. M., Gharib, S. A., Flexeder, C., Karrasch, S., Gieger, C., Peters, A., Stubbe, B., Hu, X., Ortega, V. E., Meyers, D. A., Bleecker, E. R., Gabriel, S. B., Gupta, N., Smith, A. V., Luan, J., Zhao, J. H., Hansen, A. F., Langhammer, A., Willer, C., Bhatta, L., Porteous, D., Smith, B. H., Campbell, A., Sofer, T., Lee, J., Daviglus, M. L., Yu, B., Lim, E., Xu, H., O'Connor, G. T., Thareja, G., Albagha, O. M. E., Suhre, K., Granell, R., Faquih, T. O., Hiemstra, P. S., Slats, A. M., Mullin, B. H., Hui, J., James, A., Beilby, J., Patasova, K., Hysi, P., Koskela, J. T., Wyss, A. B., Jin, J., Sikdar, S., Lee, M., May-Wilson, S., Pirastu, N., Kentistou, K. A., Joshi, P. K., Timmers, P. R. H. J., Williams, A. T., Free, R. C., Wang, X., Morrison, J. L., Gilliland, F. D., Chen, Z., Wang, C. A., Foong, R. E., Harris, S. E., Taylor, A., Redmond, P., Cook, J. P., Mahajan, A., Lind, L., Palviainen, T., Lehtimäki, T., Raitakari, O. T., Kaprio, J., Rantanen, T., Pietiläinen, K. H., Cox, S. R., Pennell, C. E., Hall, G. L., Gauderman, W. J., Brightling, C., Wilson, J. F., Vasankari, T., Laitinen, T., Salomaa, V., Mook-Kanamori, D. O., Timpson, N. J., Zeggini, E., Dupuis, J., Hayward, C., Brumpton, B., Langenberg, C., Weiss, S., Homuth, G., Schmidt, C. O., Probst-Hensch, N., Jarvelin, M. R., Morrison, A. C., Polasek, O., Rudan, I., Lee, J. H., Sayers, I., Rawlins, E. L., Dudbridge, F., Silverman, E. K., Strachan, D. P., Walters, R. G., Morris, A. P., London, S. J., Cho, M. H., Wain, L. V., Hall, I. P. & Tobin, M. D., Mar 2023, In: Nature Genetics. 55, 3, p. 410-422 13 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    2 Citations (Scopus)
  • Open Access
  • Common genetic variants do not predict recurrent events in coronary heart disease patients

    Thompson, P. L., Hui, J., Beilby, J., Palmer, L. J., Watts, G. F., West, M. J., Kirby, A., Marschner, S., Simes, R. J., Sullivan, D. R., White, H. D., Stewart, R. & Tonkin, A. M., Dec 2022, In: BMC Cardiovascular Disorders. 22, 1, 96.

    Research output: Contribution to journalArticlepeer-review

    Open Access