DIDA: A curated and annotated digenic diseases database von Gazzo, Andrea M, Daneels, Dorien, Cilia, Elisa, Bonduelle, Maryse, Abramowicz, Marc, Van Dooren, Sonia, Smits, Guillaume, Lenaerts, Tom

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Prolonged Right Ventricular Ejection Delay in Brugada Syndrome Depends on the Type of SCN5A Variant　― Electromechanical Coupling Through Tissue Velocity Imaging as a Bridge Between... von Malderen, Sophie C.H. Van, Daneels, Dorien, Kerkhove, Dirk, Peeters, Uschi, Theuns, Dominic A.M.J., Droogmans, Steven, Camp, Guy Van, Weytjens, Caroline, Biervliet, Martine, Bonduelle, Maryse, Dooren, Sonia Van, Brugada, Pedro

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Predicting disease-causing variant combinations von Papadimitriou, Sofia, Gazzo, Andrea, Versbraegen, Nassim, Nachtegael, Charlotte, Aerts, Jan, Moreau, Yves, Van Dooren, Sonia, Nowé, Ann, Smits, Guillaume, Lenaerts, Tom

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Understanding mutational effects in digenic diseases von Gazzo, Andrea, Raimondi, Daniele, Daneels, Dorien, Moreau, Yves, Smits, Guillaume, Van Dooren, Sonia, Lenaerts, Tom

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Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome von Peeters, Uschi, Scornik, Fabiana, Riuró, Helena, Pérez, Guillermo, Komurcu-Bayrak, Evrim, Malderen, Sophie Van, Pappaert, Gudrun, Tarradas, Anna, Pagans, Sara, Daneels, Dorien, Breckpot, Karine, Brugada, Pedro, Bonduelle, Maryse, Brugada, Ramon, Dooren, Sonia Van

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Identification of differentially methylated regions in rare diseases from a single-patient perspective von Grolaux, Robin, Hardy, Alexis, Olsen, Catharina, Van Dooren, Sonia, Smits, Guillaume, Defrance, Matthieu

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Human T-lymphotropic virus 1: recent knowledge about an ancient infection von Verdonck, Kristien, Dr, González, Elsa, MD, Van Dooren, Sonia, PhD, Vandamme, Anne-Mieke, Prof, Vanham, Guido, Prof, Gotuzzo, Eduardo, Prof

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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls von Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Glinge, Charlotte, Nannenberg, Eline A., Whiffin, Nicola, Mazzarotto, Francesco, Škorić-Milosavljević, Doris, Krijger, Christian, Arbelo, Elena, Breckpot, Jeroen, Campuzano, Oscar, Castelletti, Silvia, Clauss, Sebastian, Crotti, Lia, Dagradi, Federica, de Asmundis, Carlo, Denjoy, Isabelle, Ellinor, Patrick T., Giustetto, Carla, Gourraud, Jean-Baptiste, Hazeki, Daisuke, Horie, Minoru, Ishikawa, Taisuke, Itoh, Hideki, Kaneko, Yoshiaki, Kanters, Jørgen K., Kimoto, Hiroki, Kotta, Maria-Christina, Krapels, Ingrid P.C., Kurabayashi, Masahiko, Loeys, Bart L., Lundin, Catarina, Makiyama, Takeru, Mansourati, Jacques, Mazzanti, Andrea, Mörner, Stellan, Napolitano, Carlo, Ohkubo, Kimie, Papadakis, Michael, Rudic, Boris, Sahin, Hatice, Sarquella-Brugada, Georgia, Sharma, Sanjay, Sheppard, Mary N., Shoemaker, M.Benjamin, Stallmeyer, Birgit, Tanaka, Yuji, Tester, David J., van der Zwaag, Paul A., Van Dooren, Sonia, Van Laer, Lut, Winbo, Annika, Yamagata, Kenichiro, Zumhagen, Sven, Volders, Paul G.A., Lubitz, Steven A., Odening, Katja E., Roden, Dan M., Roberts, Jason D., Skinner, Jonathan R., Tfelt-Hansen, Jacob, van den Berg, Maarten P., Lambiase, Pier D., Borggrefe, Martin, Hayashi, Kenshi, Rydberg, Annika, Nakajima, Tadashi, Yoshinaga, Masao, Saenen, Johan B., Kääb, Stefan, Brugada, Pedro, Robyns, Tomas, Giachino, Daniela F., Brugada, Josep, Gimeno, Juan R., Hasdemir, Can, Guicheney, Pascale, Priori, Silvia G., Schulze-Bahr, Eric, Makita, Naomasa, Schwartz, Peter J., Shimizu, Wataru, Aiba, Takeshi, Schott, Jean-Jacques, Redon, Richard, Ohno, Seiko, Probst, Vincent, Arnaout, Alain Al, Amelot, Mathieu, Anselme, Frédéric, Billon, Olivier, Jesel, Laurence, Laurent, Gabriel, Maury, Philippe, Pasquie, Jean-Luc, Wiart, Francois, Behr, Elijah R., Barc, Julien, Bezzina, Connie R.

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Development and Validation of a Multiplex Real-Time PCR Assay for Simultaneous Genotyping and Human T-Lymphotropic Virus Type 1, 2, and 3 Proviral Load Determination von Moens, Britta, López, Giovanni, Adaui, Vanessa, González, Elsa, Kerremans, Lien, Clark, Daniel, Verdonck, Kristien, Gotuzzo, Eduardo, Vanham, Guido, Cassar, Olivier, Gessain, Antoine, Vandamme, Anne-Mieke, Van Dooren, Sonia

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Patient-reported outcome measures on mental health and psychosocial factors in patients with Brugada syndrome von Six, Stefaan, Theuns, Peter, Libin, Pieter, Nowé, Ann, Pannone, Luigi, Bogaerts, Bart, Jaxy, Simon, Olsen, Catharina, Pappaert, Gudrun, Grau, Isel, Sieira, Juan, Van Dooren, Sonia, Scheirlynck, Esther, Nekkebroeck, Julie, Mallefroy, Marina, de Asmundis, Carlo, Bilsen, Johan

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Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families von Shahi, Rajendra Bahadur, De Brakeleer, Sylvia, Caljon, Ben, Pauwels, Ingrid, Bonduelle, Maryse, Joris, Sofie, Fontaine, Christel, Vanhoeij, Marian, Van Dooren, Sonia, Teugels, Erik, De Grève, Jacques

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A milder form of NSRP1‐associated neurodevelopmental disorder, caused by a missense variant in the nuclear localization signal von Neuens, Sebastian, Kausar, Maiza, Kang, Sun‐Kyoung, Soblet, Julie, Van Dooren, Sonia, Olsen, Catharina, Janssen, Toon, Caljon, Ben, Jun, Chang‐Duk, Smits, Guillaume, Coppens, Sandra, Vilain, Catheline

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Ajmaline Testing and the Brugada Syndrome von Rizzo, Alessandro, Borio, Gianluca, Sieira, Juan, Van Dooren, Sonia, Overeinder, Ingrid, Bala, Gezim, Pappaert, Gudrun, Maj, Riccardo, Osório, Thiago Guimarães, Terasawa, Muryo, Galli, Alessio, Cecchini, Federico, Miraglia, Vincenzo, Ströker, Erwin, La Meir, Marc, Brugada, Pedro, Chierchia, Gian-Battista, de Asmundis, Carlo

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Intracerebral administration of CTLA-4 and PD-1 immune checkpoint blocking monoclonal antibodies in patients with recurrent glioblastoma: a phase I clinical trial von Duerinck, Johnny, Schwarze, Julia Katharina, Awada, Gil, Tijtgat, Jens, Vaeyens, Freya, Bertels, Cleo, Geens, Wietse, Klein, Samuel, Seynaeve, Laura, Cras, Louise, D’Haene, Nicky, Michotte, Alex, Caljon, Ben, Salmon, Isabelle, Bruneau, Michaël, Kockx, Mark, Van Dooren, Sonia, Vanbinst, Anne-Marie, Everaert, Hendrik, Forsyth, Ramses, Neyns, Bart

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Heart rate variability and microvolt T wave alternans changes during ajmaline test may predict prognosis in Brugada syndrome von Călburean, Paul-Adrian, Pannone, Luigi, Sorgente, Antonio, Gauthey, Anaïs, Monaco, Cinzia, Strazdas, Antanas, Almorad, Alexandre, Bisignani, Antonio, Bala, Gezim, Ramak, Robbert, Overeinder, Ingrid, Ströker, Erwin, Pappaert, Gudrun, Van Dooren, Sonia, de Ravel, Thomy, La Meir, Mark, Brugada, Pedro, Sieira, Juan, Chierchia, Gian-Battista, de Asmundis, Carlo

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Compound heterozygous null mutations of NOBOX in sisters with delayed puberty and primary amenorrhea von Sassi, Asma, Désir, Julie, Duerinckx, Sarah, Soblet, Julie, Van Dooren, Sonia, Bonduelle, Maryse, Abramowicz, Marc, Delbaere, Anne

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Novel inactivating follicle-stimulating hormone receptor mutations in a patient with premature ovarian insufficiency identified by next-generation sequencing gene panel analysis von Sassi, Asma, Désir, Julie, Janssens, Véronique, Marangoni, Martina, Daneels, Dorien, Gheldof, Alexander, Bonduelle, Maryse, Van Dooren, Sonia, Costagliola, Sabine, Delbaere, Anne

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Barriers and facilitators for the implementation of patient-centered care in cardiogenetics: a Delphi study among ERN GUARD-heart members von van Pottelberghe, Saar, Heine, Fenja, Van Dooren, Sonia, Hes, Frederik, Kupper, Nina

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Simian T-Cell Leukemia Virus (STLV) Infection in Wild Primate Populations in Cameroon: Evidence for Dual STLV Type 1 and Type 3 Infection in Agile Mangabeys (Cercocebus agilis) von COURGNAUD, Valerie, VAN DOOREN, Sonia, LIEGEOIS, Florian, POURRUT, Xavier, ABELA, Bernadette, LOUL, Severin, MPOUDI-NGOLE, Eitel, VANDAMME, Annemieke, DELAPORTE, Eric, PEETERS, Martine

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Searching for a sense of closure: parental experiences of recontacting after a terminated pregnancy for congenital malformations von Slegers, Ileen, Keymolen, Kathelijn, Van Berkel, Kim, Dimitrov, Boyan, Van Dooren, Sonia, Cooreman, Rani, Hes, Frederik, Fobelets, Maaike

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