Submissions from 2022
Ex Vivo Thrombus Magnetic Resonance Imaging Features and Patient Clinical Data Enable Prediction of Acute Ischemic Stroke Cause, Spencer D. Christiansen, Junmin Liu, Maria Bres Bullrich, Manas Sharma, Sachin K. Pandey, Melfort Boulton, Sebastian Fridman, Luciano A. Sposato, and Maria Drangova
Submissions from 2021
Supplementary material for: Ex Vivo Thrombus MR Imaging Features and Patient Clinical Data Enable Prediction of Acute Ischemic Stroke Cause, Spencer D. Christiansen
Submissions from 2012
Utility of Cardiovascular Magnetic Resonance in Identifying Substrate for Malignant Ventricular Arrhythmias, James A. White, Nowell M. Fine, Lorne Gula, Raymond Yee, Allan Skanes, George Klein, Peter Leong-Sit, Heather Warren, Terry Thompson, Maria Drangova, and Andrew Krahn
Submissions from 2011
Mechanical Tension Increases CCN2/CTGF Expression and Proliferation in Gingival Fibroblasts via a TGFβ-Dependent Mechanism, Fen Guo, David E. Carter, and Andrew Leask
Genetic Determinants of Plasma Triglycerides, Christopher T. Johansen, Sekar Kathiresan, and Robert A. Hegele
HNF1A G319S Variant, Active Cigarette Smoking and Incident Type 2 Diabetes in Aboriginal Canadians: A Population-based Epidemiological Study, Sylvia H. Ley, Robert A. Hegele, Stewart B. Harris, Mary Mamakeesick, Henian Cao, Philip W. Connelly, Joel Gittelsohn, Ravi Retnakaran, Bernard Zinman, and Anthony J. Hanley
High-risk Asymptomatic Carotid Stenosis: Ulceration on 3D Ultrasound vs TCD Microemboli, A. Madani, V. Beletsky, A. Tamayo, C. Munoz, and J. D. Spence
Understanding the Complexity of Homocysteine Lowering with Vitamins: The Potential Role of Subgroup Analyses, J. David Spence and Meir J. Stampfer
Submissions from 2010
Polyploidy Impairs Human Aortic Endothelial Cell Function and Is Prevented by Nicotinamide Phosphoribosyltransferase, Nica M. Borradaile and J. Geoffrey Pickering
Genome-Wide Association Studies of Plasma Lipids: Have We Reached the Limit?, Robert A. Hegele
Advances in Stroke 2009: Update on the Genetics of Stroke and Cerebrovascular Disease 2009, Robert A. Hegele and Martin Dichgans
Increased Blood Pressure and Hyperdynamic Cardiovascular Responses in Carriers of a Common Hyperfunctional Variant of Adenylyl Cyclase 6, Gary J. Hodges, Robert Gros, Robert A. Hegele, Stan Van Uum, J. Kevin Shoemaker, and Ross D. Feldman
Rare ATGL Haplotypes Are Associated with Increased Plasma Triglyceride Concentrations in the Greenland Inuit, Christopher T. Johansen, Zane R. Gallinger, Jian Wang, Matthew R. Ban, T. Kue Young, Peter Bjerregaard, and Robert A. Hegele
Translating Genomic Analyses into Improved Management of Coronary Artery Disease, Christopher T. Johansen, Matthew B. Lanktree, and Robert A. Hegele
Excess of Rare Variants in Genes Identified by Genome-wide Association Study of Hypertriglyceridemia, Christopher T. Johansen, Jian Wang, Matthew B. Lanktree, Henian Cao, Adam D. McIntyre, Matthew R. Ban, Rebecca A. Martins, Brooke A. Kennedy, Reina G. Hassell, Maartje E. Visser, Stephen M. Schwartz, Benjamin F. Voight, Roberto Elosua, Veikko Salomaa, Christopher J. O'Donnell, Geesje M. Dallinga-Thie, Sonia S. Anand, Salim Yusuf, Murray W. Huff, Sekar Kathiresan, and Robert A. Hegele
APOC1 T45S Polymorphism Is Associated with Reduced Obesity Indices and Lower Plasma Concentrations of Leptin and Apolipoprotein C-I in Aboriginal Canadians, Piya Lahiry, Henian Cao, Matthew R. Ban, Rebecca L. Pollex, Mary Mamakeesick, Bernard Zinman, Stewart B. Harris, Anthony J. G. Hanley, Murray W. Huff, Philip W. Connelly, and Robert A. Hegele
Kinase Mutations in Human Disease: Interpreting Genotype-phenotype Relationships, Piya Lahiry, Ali Torkamani, Nicholas J. Schork, and Robert A. Hegele
Comprehensive Analysis of Genomic Variation in the LPA Locus and Its Relationship to Plasma Lipoprotein(a) in South Asians, Chinese, and European Caucasians, Matthew B. Lanktree, Sonia S. Anand, Salim Yusuf, Robert A. Hegele, and SHARE Investigators
Advances in Genomic Analysis of Stroke: What Have We Learned and Where Are We Headed?, Matthew B. Lanktree, Martin Dichgans, and Robert A. Hegele
Phenomics: Expanding the Role of Clinical Evaluation in Genomic Studies, Matthew B. Lanktree, Reina G. Hassell, Piya Lahiry, and Robert A. Hegele
Extremes of Unexplained Variation as a Phenotype: An Efficient Approach for Genome-Wide Association Studies of Cardiovascular Disease, Matthew B. Lanktree, Robert A. Hegele, Nicholas J. Schork, and J. David Spence
A Translational View of the Genetics of Lipodystrophy and Ectopic Fat Deposition, Matthew B. Lanktree, Christopher T. Johansen, Tisha R. Joy, and Robert A. Hegele
Association of Apolipoprotein B with Incident Type 2 Diabetes in an Aboriginal Canadian Population, Sylvia H. Ley, Stewart B. Harris, Philip W. Connelly, Mary Mamakeesick, Joel Gittelsohn, Thomas M. Wolever, Robert A. Hegele, Bernard Zinman, and Anthony J. Hanley
Assessing the Association of the HNF1A G319S Variant with C-reactive Protein in Aboriginal Canadians: A Population-based Epidemiological Study, Sylvia H. Ley, Robert A. Hegele, Philip W. Connelly, Stewart B. Harris, Mary Mamakeesick, Henian Cao, Joel Gittelsohn, Ravi Retnakaran, Bernard Zinman, and Anthony J. Hanley
Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling, Yun Li, Kathrin Laue, Samia Temtamy, Mona Aglan, L. Damla Kotan, Gökhan Yigit, Husniye Canan, Barbara Pawlik, Gudrun Nürnberg, Emma L. Wakeling, Oliver W. Quarrell, Ingelore Baessmann, Matthew B. Lanktree, Mustafa Yilmaz, Robert A. Hegele, Khalda Amr, Klaus W. May, Peter Nürnberg, A. Kemal Topaloglu, Matthias Hammerschmidt, and Bernd Wollnik