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20142023

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  • 2017

    Rheumatoid Arthritis and Coronary Artery Disease: Genetic Analyses Do Not Support a Causal Relationship

    Jansen, H., Willenborg, C., Lieb, W., Zeng, L., Ferrario, P. G., Loley, C., König, I. R., Erdmann, J., Samani, N. J., Schunkert, H. & Consortium, C. ARDIRAM., 01.01.2017, In: Journal of Rheumatology. 44, 1, p. 4-10 7 p.

    Research output: Journal ArticlesJournal articlesResearchpeer-review

  • Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease

    Wellcome Trust Case Control Consortium, Webb, T. R., Erdmann, J., Stirrups, K. E., Stitziel, N. O., Masca, N. G. D., Jansen, H., Kanoni, S., Nelson, C. P., Ferrario, P. G., König, I. R., Eicher, J. D., Johnson, A. D., Hamby, S. E., Betsholtz, C., Ruusalepp, A., Franzén, O., Schadt, E. E., Björkegren, J. L. M., Weeke, P. E., & 31 othersAuer, P. L., Schick, U. M., Lu, Y., Zhang, H., Dube, M-P., Goel, A., Farrall, M., Peloso, G. M., Won, H-H., Do, R., van Iperen, E., Kruppa, J., Mahajan, A., Scott, R. A., Willenborg, C., Braund, P. S., van Capelleveen, J. C., Doney, A. S. F., Donnelly, L. A., Asselta, R., Merlini, P. A., Duga, S., Marziliano, N., Denny, J. C., Shaffer, C., El-Mokhtari, N. E., Franke, A., Kessler, T., Vogt, T. F., Lieb, W. & Schunkert, H., 21.02.2017, In: Journal of the American College of Cardiology. 69, 7, p. 823-836 14 p.

    Research output: Journal ArticlesJournal articlesResearchpeer-review

  • 2016

    Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease

    Stitziel, N. O., Stirrups, K. E., Masca, N. G. D., Erdmann, J., Ferrario, P. G., König, I. R., Weeke, P. E., Webb, T. R., Auer, P. L., Schick, U. M., Lu, Y., Zhang, H., Dube, M. P., Goel, A., Farrall, M., Peloso, G. M., Won, H. H., Do, R., Van Iperen, E., Kanoni, S., & 109 othersKruppa, J., Mahajan, A., Scott, R. A., Willenborg, C., Braund, P. S., Van Capelleveen, J. C., Doney, A. S. F., Donnelly, L. A., Asselta, R., Merlini, P. A., Duga, S., Marziliano, N., Denny, J. C., Shaffer, C. M., El-Mokhtari, N. E., Franke, A., Gottesman, O., Heilmann, S., Hengstenberg, C., Hoffmann, P., Holmen, O. L., Hveem, K., Jansson, J. H., Jöckel, K. H., Kessler, T., Kriebel, J., Laugwitz, K. L., Marouli, E., Martinelli, N., McCarthy, M. I., Van Zuydam, N. R., Meisinger, C., Esko, T., Mihailov, E., Escher, S. A., Alver, M., Moebus, S., Morris, A. D., Müller-Nurasyid, M., Nikpay, M., Olivieri, O., Perreault, L. P. L., AlQarawi, A., Robertson, N. R., Akinsanya, K. O., Reilly, D. F., Vogt, T. F., Yin, W., Asselbergs, F. W., Kooperberg, C., Jackson, R. D., Stahl, E., Strauch, K., Varga, T. V., Waldenberger, M., Zeng, L., Kraja, A. T., Liu, C., Ehret, G. B., Newton-Cheh, C., Chasman, D. I., Chowdhury, R., Ferrario, M., Ford, I., Jukema, J. W., Kee, F., Kuulasmaa, K., Nordestgaard, B. G., Perola, M., Saleheen, D., Sattar, N., Surendran, P., Tregouet, D., Young, R., Howson, J. M. M., Butterworth, A. S., Danesh, J., Ardissino, D., Bottinger, E. P., Erbel, R., Franks, P. W., Girelli, D., Hall, A. S., Hovingh, G. K., Kastrati, A., Lieb, W., Meitinger, T., Kraus, W. E., Shah, S. H., McPherson, R., Orho-Melander, M., Melander, O., Metspalu, A., Palmer, C. N. A., Peters, A., Rader, D. J., Reilly, M. P., Loos, R. J. F., Reiner, A. P., Roden, D. M., Tardif, J. C., Thompson, J. R., Wareham, N. J., Watkins, H., Willer, C. J., Kathiresan, S., Deloukas, P., Samani, N. J. & Schunkert, H., 24.03.2016, In: New England Journal of Medicine. 374, 12, p. 1134-1144 11 p.

    Research output: Journal ArticlesJournal articlesResearchpeer-review

    97 Citations (Scopus)
  • 2015

    Genetic variants associated with celiac disease and the risk for coronary artery disease

    Jansen, H., Willenborg, C., Schlesinger, S., Ferrario, P. G., König, I. R., Erdmann, J., Samani, N. J., Lieb, W. & Schunkert, H., 23.10.2015, In: Molecular Genetics and Genomics. 290, 5, p. 1911-1917 7 p.

    Research output: Journal ArticlesJournal articlesResearchpeer-review

    5 Citations (Scopus)
  • 2014

    Inactivating mutations in NPC1L1 and protection from coronary heart disease

    The Myocardial Infarction Genetics Consortium Investigators, Stitziel, N. O., Won, H. H., Morrison, A. C., Peloso, G. M., Do, R., Lange, L. A., Fontanillas, P., Gupta, N., Duga, S., Goel, A., Farrall, M., Saleheen, D., Ferrario, P., König, I., Asselta, R., Merlini, P. A., Marziliano, N., Notarangelo, M. F., Schick, U., & 31 othersAuer, P., Assimes, T. L., Reilly, M., Wilensky, R., Rader, D. J., Kees Hovingh, G., Meitinger, T., Kessler, T., Kastrati, A., Laugwitz, K. L., Siscovick, D., Rotter, J. I., Hazen, S. L., Tracy, R., Cresci, S., Spertus, J., Jackson, R., Schwartz, S. M., Natarajan, P., Crosby, J., Muzny, D., Ballantyne, C., Rich, S. S., O'Donnell, C. J., Abecasis, G., Sunyaev, S., Nickerson, D. A., Buring, J. E., Ridker, P. M., Erdmann, J. & Schunkert, H., 27.11.2014, In: New England Journal of Medicine. 371, 22, p. 2072-2082 11 p.

    Research output: Journal ArticlesJournal articlesResearchpeer-review

    185 Citations (Scopus)