Genetics of Thoracic Aortic Aneurysm: At the Crossroad of Transforming Growth Factor-β Signaling and Vascular Smooth Muscle Cell Contractility von Gillis, Elisabeth, Van Laer, Lut, Loeys, Bart L

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Marfan Syndrome and Related Disorders: 25 Years of Gene Discovery von Verstraeten, Aline, Alaerts, Maaike, Van Laer, Lut, Loeys, Bart

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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 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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Arterial Tortuosity: Novel Implications for an Old Phenotype von Ciurică, Simina, Lopez-Sublet, Marilucy, Loeys, Bart L, Radhouani, Ibtissem, Natarajan, Nalin, Vikkula, Miikka, Maas, Angela H.E.M, Adlam, David, Persu, Alexandre

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Angiotensin receptor blockers: a panacea for Marfan syndrome and related disorders? von Loeys, Bart L.

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Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia von Bolar, Nikhita Ajit, Golzio, Christelle, Živná, Martina, Hayot, Gaëlle, Van Hemelrijk, Christine, Schepers, Dorien, Vandeweyer, Geert, Hoischen, Alexander, Huyghe, Jeroen R., Raes, Ann, Matthys, Erve, Sys, Emiel, Azou, Myriam, Gubler, Marie-Claire, Praet, Marleen, Van Camp, Guy, McFadden, Kelsey, Pediaditakis, Igor, Přistoupilová, Anna, Hodaňová, Kateřina, Vyleťal, Petr, Hartmannová, Hana, Stránecký, Viktor, Hůlková, Helena, Barešová, Veronika, Jedličková, Ivana, Sovová, Jana, Hnízda, Aleš, Kidd, Kendrah, Bleyer, Anthony J., Spong, Richard S., Vande Walle, Johan, Mortier, Geert, Brunner, Han, Van Laer, Lut, Kmoch, Stanislav, Katsanis, Nicholas, Loeys, Bart L.

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Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome von Meester, Josephina A. N., Verstraeten, Aline, Schepers, Dorien, Alaerts, Maaike, Van Laer, Lut, Loeys, Bart L.

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The revised Ghent nosology for the Marfan syndrome von Loeys, Bart L, Dietz, Harry C, Braverman, Alan C, Callewaert, Bert L, De Backer, Julie, Devereux, Richard B, Hilhorst-Hofstee, Yvonne, Jondeau, Guillaume, Faivre, Laurence, Milewicz, Dianna M, Pyeritz, Reed E, Sponseller, Paul D, Wordsworth, Paul, De Paepe, Anne M

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The genetic architecture of non-syndromic thoracic aortic aneurysm von Luyckx, Ilse, Loeys, Bart L

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iPSC-Cardiomyocyte Models of Brugada Syndrome-Achievements, Challenges and Future Perspectives von Nijak, Aleksandra, Saenen, Johan, Labro, Alain J., Schepers, Dorien, Loeys, Bart L., Alaerts, Maaike

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The fibrillinopathies: New insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2 von Peeters, Silke, De Kinderen, Pauline, Meester, Josephina A. N., Verstraeten, Aline, Loeys, Bart L.

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Genetic association analysis of 77,539 genomes reveals rare disease etiologies von Greene, Daniel, Pirri, Daniela, Frudd, Karen, Sackey, Ege, Al-Owain, Mohammed, Giese, Arnaud P. J., Ramzan, Khushnooda, Riaz, Sehar, Yamanaka, Itaru, Boeckx, Nele, Thys, Chantal, Gelb, Bruce D., Brennan, Paul, Hartill, Verity, Harvengt, Julie, Kosho, Tomoki, Mansour, Sahar, Masuno, Mitsuo, Ohata, Takako, Stewart, Helen, Taibah, Khalid, Turner, Claire L. S., Imtiaz, Faiqa, Riazuddin, Saima, Morisaki, Takayuki, Ostergaard, Pia, Loeys, Bart L., Morisaki, Hiroko, Ahmed, Zubair M., Birdsey, Graeme M., Freson, Kathleen, Mumford, Andrew, Turro, Ernest

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The role of biglycan in the healthy and thoracic aneurysmal aorta von Meester, Josephina A N, De Kinderen, Pauline, Verstraeten, Aline, Loeys, Bart L

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Performant Mutation Identification Using Targeted Next-Generation Sequencing of 14 Thoracic Aortic Aneurysm Genes von Proost, Dorien, Vandeweyer, Geert, Meester, Josephina A.N., Salemink, Simone, Kempers, Marlies, Ingram, Christie, Peeters, Nils, Saenen, Johan, Vrints, Christiaan, Lacro, Ronald V., Roden, Dan, Wuyts, Wim, Dietz, Harry C., Mortier, Geert, Loeys, Bart L., Van Laer, Lut

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Generation of an induced pluripotent stem cell (iPSC) line of a Marfan syndrome patient with a pathogenic FBN1 c.5372G > A (p.Cys1791Tyr) variant von Peeters, Silke, Fedoryshchenko, Ivanna, Rabaut, Laura, Verstraeten, Aline, Loeys, Bart L.

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Losartan, an AT1 Antagonist, Prevents Aortic Aneurysm in a Mouse Model of Marfan Syndrome von Habashi, Jennifer P, Judge, Daniel P, Holm, Tammy M, Cohn, Ronald D, Loeys, Bart L, Cooper, Timothy K, Myers, Loretha, Klein, Erin C, Liu, Guosheng, Calvi, Carla, Podowski, Megan, Neptune, Enid R, Halushka, Marc K, Bedja, Djahida, Gabrielson, Kathleen, Rifkin, Daniel B, Carta, Luca, Ramirez, Francesco, Huso, David L, Dietz, Harry C

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A Decade of Discovery in the Genetic Understanding of Thoracic Aortic Disease von Andelfinger, Gregor, MD, Loeys, Bart, MD, PhD, Dietz, Hal, MD, PhD

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Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics von Arbustini, Eloisa, Behr, Elijah R, Carrier, Lucie, van Duijn, Cornelia, Evans, Paul, Favalli, Valentina, van der Harst, Pim, Haugaa, Kristina Hermann, Jondeau, Guillaume, Kääb, Stefan, Kaski, Juan Pablo, Kavousi, Maryam, Loeys, Bart, Pantazis, Antonis, Pinto, Yigal, Schunkert, Heribert, Di Toro, Alessandro, Thum, Thomas, Urtis, Mario, Waltenberger, Johannes, Elliott, Perry

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Biglycan in the Skeleton von Kram, Vardit, Shainer, Reut, Jani, Priyam, Meester, Josephina A.N., Loeys, Bart, Young, Marian F.

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Loss-of-function mutations in the X-linked biglycan gene cause a severe syndromic form of thoracic aortic aneurysms and dissections von Meester, Josephina A.N., Vandeweyer, Geert, Pintelon, Isabel, Lammens, Martin, Van Hoorick, Lana, De Belder, Simon, Waitzman, Kathryn, Young, Luciana, Markham, Larry W., Vogt, Julie, Richer, Julie, Beauchesne, Luc M., Unger, Sheila, Superti-Furga, Andrea, Prsa, Milan, Dhillon, Rami, Reyniers, Edwin, Dietz, Harry C., Wuyts, Wim, Mortier, Geert, Verstraeten, Aline, Van Laer, Lut, Loeys, Bart L.

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