Genetic Variation in <i>LRP1</i> Associates with Stanford Type B Aortic Dissection Risk and Clinical Outcome by Philipp Erhart, Daniel Körfer, Caspar Grond-Ginsbach, Jia-Lu Qiao, Moritz S. Bischoff, Maja Hempel, Christian P. Schaaf, Armin Grau, Dittmar Böckler

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Unexpected excessive apixaban exposure: case report of a patient with polymorphisms of multiple apixaban elimination pathways by Andrea Huppertz, Caspar Grond-Ginsbach, Chris Dumschat, Kathrin I. Foerster, Jürgen Burhenne, Johanna Weiss, David Czock, Jan C. Purrucker, Timolaos Rizos, Walter E. Haefeli

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A novel scatterplot-based method to detect copy number variation (CNV) by Jia-Lu Qiao, Rebecca T. Levinson, Rebecca T. Levinson, Bowang Chen, Stefan T. Engelter, Philipp Erhart, Brady J. Gaynor, Patrick F. McArdle, Kristina Schlicht, Michael Krawczak, Martin Stenman, Martin Stenman, Arne G. Lindgren, John W. Cole, John W. Cole, Caspar Grond-Ginsbach

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The copy number variation and stroke (CaNVAS) risk and outcome study. by John W Cole, Taiwo Adigun, Rufus Akinyemi, Onoja Matthew Akpa, Steven Bell, Bowang Chen, Jordi Jimenez Conde, Uxue Lazcano Dobao, Israel Fernandez, Myriam Fornage, Cristina Gallego-Fabrega, Christina Jern, Michael Krawczak, Arne Lindgren, Hugh S Markus, Olle Melander, Mayowa Owolabi, Kristina Schlicht, Martin Söderholm, Vinodh Srinivasasainagendra, Carolina Soriano Tárraga, Martin Stenman, Hemant Tiwari, Margaret Corasaniti, Natalie Fecteau, Beth Guizzardi, Haley Lopez, Kevin Nguyen, Brady Gaynor, Timothy O'Connor, O Colin Stine, Steven J Kittner, Patrick McArdle, Braxton D Mitchell, Huichun Xu, Caspar Grond-Ginsbach

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