Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection von Renard, Marjolijn, Francis, Catherine, Ghosh, Rajarshi, Scott, Alan F., Witmer, P. Dane, Adès, Lesley C., Andelfinger, Gregor U., Arnaud, Pauline, Boileau, Catherine, Callewaert, Bert L., Guo, Dongchuan, Hanna, Nadine, Lindsay, Mark E., Morisaki, Hiroko, Morisaki, Takayuki, Pachter, Nicholas, Robert, Leema, Van Laer, Lut, Dietz, Harry C., Loeys, Bart L., Milewicz, Dianna M., De Backer, Julie

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Human Genetics of Ebstein Anomaly von Sedaghat-Hamedani, Farbod, Andelfinger, Gregor U., Meder, Benjamin

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Molecular Pathways and Animal Models of Ebstein’s Anomaly von Jensen, Bjarke, Andelfinger, Gregor U., Postma, Alex V.

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eNOS controls angiogenic sprouting and retinal neovascularization through the regulation of endothelial cell polarity von Smith, Tracy L., Oubaha, Malika, Cagnone, Gael, Boscher, Cécile, Kim, Jin Sung, El Bakkouri, Yassine, Zhang, Ying, Chidiac, Rony, Corriveau, Jeanne, Delisle, Chantal, Andelfinger, Gregor U., Sapieha, Przemyslaw, Joyal, Jean-Sébastien, Gratton, Jean-Philippe

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The PETALE study: Late adverse effects and biomarkers in childhood acute lymphoblastic leukemia survivors von Marcoux, Sophie, Drouin, Simon, Laverdière, Caroline, Alos, Nathalie, Andelfinger, Gregor U., Bertout, Laurence, Curnier, Daniel, Friedrich, Matthias G., Kritikou, Ekaterini A., Lefebvre, Geneviève, Levy, Emile, Lippé, Sarah, Marcil, Valérie, Raboisson, Marie‐Josée, Rauch, Frank, Robaey, Philippe, Samoilenko, Mariia, Séguin, Chantal, Sultan, Serge, Krajinovic, Maja, Sinnett, Daniel

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Risk of congenital heart defects is influenced by genetic variation in folate metabolism von Christensen, Karen E., Zada, Yassamin Feroz, Rohlicek, Charles V., Andelfinger, Gregor U., Michaud, Jacques L., Bigras, Jean-Luc, Richter, Andrea, Dubé, Marie-Pierre, Rozen, Rima

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Partitioning of copy-number genotypes in pedigrees von Perreault, Louis-Philippe Lemieux, Andelfinger, Gregor U, Asselin, Géraldine, Dubé, Marie-Pierre

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Genetic factors in treatment-related cardiovascular complications in survivors of childhood acute lymphoblastic leukemia von Petrykey, Kateryna, Rezgui, Aziz M, Guern, Mathilde Le, Beaulieu, Patrick, St-Onge, Pascal, Drouin, Simon, Bertout, Laurence, Wang, Fan, Baedke, Jessica L, Yasui, Yutaka, Hudson, Melissa M, Raboisson, Marie-Josée, Laverdière, Caroline, Sinnett, Daniel, Andelfinger, Gregor U, Krajinovic, Maja

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MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects von Christensen, Karen E, Rohlicek, Charles V, Andelfinger, Gregor U, Michaud, Jacques, Bigras, Jean-Luc, Richter, Andrea, MacKenzie, Robert E, Rozen, Rima

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379. Molecular Pathways Underpinning Cannabis-Related Variations in Cortical Thickness During Adolescence von Navarri, Xavier, Robertson, Derek N., Charfi, Iness, Wünnemann, Florian, Fernandes do Nascimento, Antônia Sâmia, Leclerc, Sévérine, Andelfinger, Gregor U., Di Cristo, Graziella, Piñeyro, Graciela, Paus, Tomáš

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Genetic analyses in two extended families with deletion 22q11 syndrome: Importance of extracardiac manifestations von Shooner, Kerry A., Rope, Alan F., Hopkin, Robert J., Andelfinger, Gregor U., Benson, D. Woodrow

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Clinical validity of genes for heritable thoracic aortic aneurysm and dissection von Renard, Marjolijn, Francis, Catherine, Ghosh, Rajarshi, Scott, Alan F, Witmer, P Dane, Adès, Lesley C, Andelfinger, Gregor U, Arnaud, Pauline, Boileau, Catherine, Callewaert, Bert, Guo, Dongchuan, Hanna, Nadine, Lindsay, Mark E, Morisaki, Hiroko, Morisaki, Takayuki, Pachter, Nicholas, Robert, Leema, Van Laer, Lut, Dietz, Harry C, Loeys, Bart L, Milewicz, Dianna M, De Backer, Julie

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Functional Consequences of a Novel Cardiac Troponin T Mutation Linked to Infantile Restrictive Cardiomyopathy von Parvatiyar, Michelle S., Yang, Shi Wei, Pinto, José R., Jones, Michelle A., Liang, Jingsheng, Andelfinger, Gregor U., Potter, James D.

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Genetic factors in anthracycline-induced cardiotoxicity in patients treated for pediatric cancer von Petrykey, Kateryna, Andelfinger, Gregor U., Laverdière, Caroline, Sinnett, Daniel, Krajinovic, Maja

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Partitioning of copy-number genotypes in pedigrees von Perreault, Louis-Philippe Lemieux, Andelfinger, Gregor U, Asselin, Géraldine, Dubé, Marie-Pierre

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Polymorphic ventricular tachycardia and KCNJ2 mutations von Chun, Terrence U.H., Epstein, Michael R., Dick, Macdonald, Andelfinger, Gregor, Ballester, Leomar, Vanoye, Carlos G., George, Alfred L., Benson, D.Woodrow

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