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International Journal of Cardiology|March 7, 2017
Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillationKrystien V Lieve, Arie O Verkerk, Svitlana Podliesna, et al.
Bone|October 17, 2017
The effect of raloxifene on bone marrow adipose tissue and bone turnover in postmenopausal women with osteoporosisKerensa M Beekman, Annegreet G Veldhuis-Vlug, Martin den Heijer, et al.
Plos One|August 28, 2009
Both paraoxonase-1 genotype and activity do not predict the risk of future coronary artery disease; the EPIC-Norfolk Prospective Population StudyRakesh S Birjmohun, Menno Vergeer, Erik S G Stroes, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 1, 2010
Chemokine ligand 2 genetic variants, serum monocyte chemoattractant protein-1 levels, and the risk of coronary artery diseaseDiederik F van Wijk, Sander I van Leuven, Manjinder S Sandhu, et al.
European Heart Journal|September 11, 2019
Predicting cardiac electrical response to sodium-channel blockade and Brugada syndrome using polygenic risk scoresRafik Tadros, Hanno L Tan, , et al.
Critical Care Medicine|September 29, 2007
Systemic and local high mobility group box 1 concentrations during severe infectionMarieke A D van Zoelen, Pierre-François Laterre, Suzanne Q van Veen, et al.
American Journal of Respiratory and Critical Care Medicine|September 19, 2009
Expression and role of myeloid-related protein-14 in clinical and experimental sepsisMarieke A D van Zoelen, Thomas Vogl, Dirk Foell, et al.
Journal of Neuroinflammation|December 30, 2019
Complement factor H contributes to mortality in humans and mice with bacterial meningitisE Soemirien Kasanmoentalib, Mercedes Valls Serón, Joo Yeon Engelen-Lee, et al.
Heart Rhythm|March 3, 2009
Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathiesPaola G Meregalli, Hanno L Tan, Vincent Probst, et al.
European Journal of Human Genetics : EJHG|November 14, 2013
Common genetic variants do not associate with CAD in familial hypercholesterolemiaErik P A van Iperen, Suthesh Sivapalaratnam, S Matthijs Boekholdt, et al.
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