Chondrodysplasias and Aneurysmal Thoracic Aortopathy: An Emerging Tale of Molecular Intersection by Verstraeten, Aline, Meester, Josephina, Peeters, Silke, Mortier, Geert, Loeys, Bart

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Differentiation of Induced Pluripotent Stem Cells Into Chondrocytes: Methods and Applications for Disease Modeling and Drug Discovery by De Kinderen, Pauline, Meester, Josephina, Loeys, Bart, Peeters, Silke, Gouze, Elvire, Woods, Steven, Mortier, Geert, Verstraeten, Aline

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Intermittent Brugada syndrome in an anorexic adolescent girl by Docx, Martine K.F., MD, Loeys, Bart, MD, PhD, Simons, Annik, MD, Gewillig, Marc, MD, PhD, Proost, Dorien, PhD student, Van Laer, Lut, PhD, Mertens, Luc, MD, PhD

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Neutrophilic dermatoses and aneurysms: An overlooked association? by Stappers, Sofie, Swinnen, Inge, Siozopoulou, Vasiliki, Bastin, Julie, De Smet, Anthony, Dubois, Marc, Loeys, Bart, Aerts, Olivier

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The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): Report... by Chitayat, David, Sroka, Hana, Keating, Sarah, Colby, Randall S., Ryan, Greg, Toi, Ants, Blaser, Susan, Viero, Sandra, Devisme, Louise, Boute-Bénéjean, Odile, Manouvrier-Hanu, Sylvie, Mortier, Geert, Loeys, Bart, Rauch, Anita, Bitoun, Pierre

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Integration of genetic testing into diagnostic pathways for cardiomyopathies: a clinical consensus statement by the ESC Council on Cardiovascular Genomics by Elliott, Perry, Schunkert, Heribert, Bondue, Antoine, Behr, Elijah, Carrier, Lucie, Van Duijn, Cornelia, García-Pavía, Pablo, van der Harst, Pim, Kavousi, Maryam, Loeys, Bart, Rocha Lopes, Luis, Pinto, Yigal, Di Toro, Alessandro, Thum, Thomas, Kääb, Stefan, Urtis, Mario, Arbustini, Eloisa

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pBRIT: gene prioritization by correlating functional and phenotypic annotations through integrative data fusion by Kumar, Ajay Anand, Van Laer, Lut, Alaerts, Maaike, Ardeshirdavani, Amin, Moreau, Yves, Laukens, Kris, Loeys, Bart, Vandeweyer, Geert

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Extracellular Matrix in Vascular Disease, Part 2/4 by Barallobre-Barreiro, Javier, Loeys, Bart, Mayr, Manuel, Rienks, Marieke, Verstraeten, Aline, Kovacic, Jason C.

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Genetic counselling and testing in adults with congenital heart disease: A consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group o... by De Backer, Julie, Bondue, Antoine, Budts, Werner, Evangelista, Arturo, Gallego, Pastora, Jondeau, Guillaume, Loeys, Bart, Peña, Maria L, Teixido-Tura, Gisela, van de Laar, Ingrid, Verstraeten, Aline, Roos Hesselink, Jolien

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Mesenchymal state of intimal cells may explain higher propensity to ascending aortic aneurysm in bicuspid aortic valves by Maleki, Shohreh, Kjellqvist, Sanela, Paloschi, Valentina, Magné, Joelle, Branca, Rui Miguel Mamede, Du, Lei, Hultenby, Kjell, Petrini, Johan, Fuxe, Jonas, Dietz, Harry C., Loeys, Bart, Van Laer, Lut, McCallion, Andrew S., Mertens, Luc, Mital, Seema, Mohamed, Salah A., Andelfinger, Gregor, Lehtiö, Janne, Franco-Cereceda, Anders, Eriksson, Per, Björck, Hanna M.

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Altered DNA methylation indicates an oscillatory flow mediated epithelial-to-mesenchymal transition signature in ascending aorta of patients with bicuspid aortic valve by Björck, Hanna M., Du, Lei, Pulignani, Silvia, Paloschi, Valentina, Lundströmer, Karin, Kostina, Alexandra S., Österholm, Cecilia, Malashicheva, Anna, Kostareva, Anna, Evangelista, Arturo, Teixidó-Tura, Gisela, Maleki, Shohreh, Franco-Cereceda, Anders, Eriksson, Per

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The diagnostic value of the facial features of Marfan syndrome by Ting, Beverlie L., Mathur, Deepti, Loeys, Bart L., Dietz, Harry C., Sponseller, Paul D.

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Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling by Snijders Blok, Lot, Madsen, Erik, Juusola, Jane, Gilissen, Christian, Baralle, Diana, Reijnders, Margot R.F., Venselaar, Hanka, Helsmoortel, Céline, Cho, Megan T., Hoischen, Alexander, Vissers, Lisenka E.L.M., Koemans, Tom S., Wissink-Lindhout, Willemijn, Eichler, Evan E., Romano, Corrado, Van Esch, Hilde, Stumpel, Connie, Vreeburg, Maaike, Smeets, Eric, Oberndorff, Karin, van Bon, Bregje W.M., Shaw, Marie, Gecz, Jozef, Haan, Eric, Bienek, Melanie, Jensen, Corinna, Loeys, Bart L., Van Dijck, Anke, Innes, A. Micheil, Racher, Hilary, Vermeer, Sascha, Di Donato, Nataliya, Rump, Andreas, Tatton-Brown, Katrina, Parker, Michael J., Henderson, Alex, Lynch, Sally A., Fryer, Alan, Ross, Alison, Vasudevan, Pradeep, Kini, Usha, Newbury-Ecob, Ruth, Chandler, Kate, Male, Alison, Dijkstra, Sybe, Schieving, Jolanda, Giltay, Jacques, van Gassen, Koen L.I., Schuurs-Hoeijmakers, Janneke, Tan, Perciliz L., Pediaditakis, Igor, Haas, Stefan A., Retterer, Kyle, Reed, Patrick, Monaghan, Kristin G., Haverfield, Eden, Natowicz, Marvin, Myers, Angela, Kruer, Michael C., Stein, Quinn, Strauss, Kevin A., Brigatti, Karlla W., Keating, Katherine, Burton, Barbara K., Kim, Katherine H., Charrow, Joel, Norman, Jennifer, Foster-Barber, Audrey, Kline, Antonie D., Kimball, Amy, Zackai, Elaine, Harr, Margaret, Fox, Joyce, McLaughlin, Julie, Lindstrom, Kristin, Haude, Katrina M., van Roozendaal, Kees, Brunner, Han, Chung, Wendy K., Kooy, R. Frank, Pfundt, Rolph, Kalscheuer, Vera, Mehta, Sarju G., Katsanis, Nicholas, Kleefstra, Tjitske

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Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections by Bertoli-Avella, Aida M., MD, PhD, Gillis, Elisabeth, MSc, Morisaki, Hiroko, MD, PhD, Verhagen, Judith M.A., MD, de Graaf, Bianca M., BSc, van de Beek, Gerarda, BSc, Gallo, Elena, PhD, Kruithof, Boudewijn P.T., PhD, Venselaar, Hanka, PhD, Myers, Loretha A., BSc, Laga, Steven, MD, Doyle, Alexander J., MD, PhD, Oswald, Gretchen, MS, CGC, van Cappellen, Gert W.A., PhD, Yamanaka, Itaru, PhD, van der Helm, Robert M., BSc, Beverloo, Berna, PhD, de Klein, Annelies, PhD, Pardo, Luba, MD, PhD, Lammens, Martin, MD, PhD, Evers, Christina, MD, Devriendt, Koenraad, MD, PhD, Dumoulein, Michiel, MD, Timmermans, Janneke, MD, Bruggenwirth, Hennie T., PhD, Verheijen, Frans, PhD, Rodrigus, Inez, MD, Baynam, Gareth, MD, Kempers, Marlies, MD, PhD, Saenen, Johan, MD, PhD, Van Craenenbroeck, Emeline M., MD, PhD, Minatoya, Kenji, MD, PhD, Matsukawa, Ritsu, MD, PhD, Tsukube, Takuro, MD, PhD, Kubo, Noriaki, MD, PhD, Hofstra, Robert, PhD, Goumans, Marie Jose, PhD, Bekkers, Jos A., MD, PhD, Roos-Hesselink, Jolien W., MD, PhD, van de Laar, Ingrid M.B.H., MD, PhD, Dietz, Harry C., MD, Van Laer, Lut, PhD, Morisaki, Takayuki, MD, PhD, Wessels, Marja W., MD, PhD, Loeys, Bart L., MD, PhD

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Phenotype of COL3A1/COL5A2 deletion patients by Kempers, Marlies JE, Wessels, Marja, Van Berendoncks, An, van de Laar, Ingrid MBH, de Leeuw, Nicole, Loeys, Bart

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varAmpliCNV: analyzing variance of amplicons to detect CNVs in targeted NGS data by Kumar, Ajay Anand, Loeys, Bart, Van De Beek, Gerarda, Peeters, Nils, Wuyts, Wim, Van Laer, Lut, Vandeweyer, Geert, Alaerts, Maaike

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Altered TGFbeta signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency by Renard, Marjolijn, Holm, Tammy, Veith, Regan, Callewaert, Bert L, Adès, Lesley C, Baspinar, Osman, Pickart, Angela, Dasouki, Majed, Hoyer, Juliane, Rauch, Anita, Trapane, Pamela, Earing, Michael G, Coucke, Paul J, Sakai, Lynn Y, Dietz, Harry C, De Paepe, Anne M, Loeys, Bart L

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Spontaneous Coronary Artery Dissection in a Man With a Novel Missense Mutation in SMAD2 Treated by Optical Coherence Tomography–Guided Percutaneous Coronary Intervention by Vandeloo, Bert, Azzano, Alessia, Schoors, Danny, Verstraeten, Aline, Van Laer, Lut, Loeys, Bart, Vermeersch, Paul

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Circulating Transforming Growth Factor-β in Marfan Syndrome by MATT, Peter, SCHOENHOFF, Florian, LOEYS, Bart, HUSO, David L, MCDONNELL, Nazli B, VAN EYK, Jennifer E, DIETZ, Harry C, HABASHI, Jennifer, HOLM, Tammy, VAN ERP, Christel, LOCH, David, CARLSON, Olga D, GRISWOLD, Benjamin F, QIN FU, DE BACKER, Julie

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