Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach

Jorie Versmissen, Daniella M. Oosterveer, Mojgan Yazdanpanah, Abbas Dehghan, Hilma Holm, Jeanette Erdman, Yurii S. Aulchenko, Gudmar Thorleifsson, Heribert Schunkert, Roeland Huijgen, Ranitha Vongpromek, Andre G. Uitterlinden, Joep C. Defesche, Cornelia M. van Duijn, Monique Mulder, Tony Dadd, Hrobjartur D. Karlsson, Jose Ordovas, Iris Kindt, Amelia JarmanAlbert Hofman, Leonie van Vark-van der Zee, Adriana C. Blommesteijn-Touw, Jaap Kwekkeboom, Anho H. Liem, Frans J. van der Ouderaa, Sebastiano Calandra, Stefano Bertolini, Maurizio Averna, Gisle Langslet, Leiv Ose, Emilio Ros, Fatima Almagro, Peter W. de Leeuw, Fernando Civeira, Luis Masana, Xavier Pinto, Maarten L. Simoons, Arend F. L. Schinkel, Martin R. Green, Aeilko H. Zwinderman, Keith J. Johnson, Arne Schaefer, Andrew Neil, Jacqueline C. M. Witteman, Steve E. Humphries, John J. P. Kastelein, Eric J. G. Sijbrands*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Biochemistry, Genetics and Molecular Biology