Cell-free DNA methylation-based preeclampsia prediction: A journey to improve maternal health von Aerden, Mio, De Borre, Marie, Thienpont, Bernard

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Cell-free DNA methylation-based preeclampsia prediction: A journey to improve maternal health von Mio, Aerden, Marie, De Borre, Bernard, Thienpont

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Cell-free DNA methylome analysis for early preeclampsia prediction von De Borre, Marie, Che, Huiwen, Yu, Qian, Lannoo, Lore, De Ridder, Kobe, Vancoillie, Leen, Dreesen, Pauline, Van Den Ackerveken, Mika, Aerden, Mio, Galle, Eva, Breckpot, Jeroen, Van Keirsbilck, Joachim, Gyselaers, Wilfried, Devriendt, Koen, Vermeesch, Joris Robert, Van Calsteren, Kristel, Thienpont, Bernard

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Cell-free DNA methylome analysis for early preeclampsia prediction von De Borre, Marie, Che, Huiwen, Yu, Qian, Lannoo, Lore, De Ridder, Kobe, Vancoillie, Leen, Dreesen, Pauline, Van Den Ackerveken, Mika, Aerden, Mio, Galle, Eva, Breckpot, Jeroen, Van Keirsbilck, Joachim, Gyselaers, Wilfried, Devriendt, Koen, Vermeesch, Joris Robert, Van Calsteren, Kristel, Thienpont, Bernard

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Differential alternative splicing analysis links variation in ZRSR2 to a novel type of oral-facial-digital syndrome von Hannes, Laurens, Atzori, Marta, Goldenberg, Alice, Argente, Jesus, Attie-Bitach, Tania, Amiel, Jeanne, Attanasio, Catia, Braslavsky, Debora G, Bruel, Ange-Line, Castanet, Mireille, Dubourg, Christèle, Jacobs, An, Lyonnet, Stanislas, Martinez Mayer, Juliàn, Pérez Millan, Maria Inés, Pezzella, Nunziana, Pelgrims, Elise, Aerden, Mio, Bauters, Marijke, Rochtus, Anne, Scaglia, Paula, Swillen, Ann, Sifrim, Alejandro, Tammaro, Roberta, Tran Mau-Them, Frederic, Odent, Sylvie, Thauvin-Robinet, Christel, Franco, Brunella, Breckpot, Jeroen

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Genotype-phenotype correlations of UBA2 mutations in patients with ectrodactyly von Aerden, Mio, Bauters, Marijke, Van Den Bogaert, Kris, Vermeesch, Joris R., Holvoet, Maureen, Plasschaert, Frank, Devriendt, Koenraad

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Homozygous missense STRADA mutation in a patient with polyhydramnios, megalencephaly and symptomatic epilepsy syndrome von Aerden, Mio, Vallaeys, Lore, Holvoet, Maureen, De Waele, Liesbeth, Van den Bogaert, Kris, Devriendt, Koen

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Differential alternative splicing analysis links variation in ZRSR2 to a novel type of oral-facial-digital syndrome von Hannes, Laurens, Atzori, Marta, Goldenberg, Alice, Argente, Jesús, Attie-Bitach, Tania, Amiel, Jeanne, Attanasio, Catia, Braslavsky, Débora G., Bruel, Ange-Line, Castanet, Mireille, Dubourg, Christèle, Jacobs, An, Lyonnet, Stanislas, Martinez-Mayer, Julian, Pérez Millán, María Inés, Pezzella, Nunziana, Pelgrims, Elise, Aerden, Mio, Bauters, Marijke, Rochtus, Anne, Scaglia, Paula, Swillen, Ann, Sifrim, Alejandro, Tammaro, Roberta, Mau-Them, Frederic Tran, Odent, Sylvie, Thauvin-Robinet, Christel, Franco, Brunella, Breckpot, Jeroen

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The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant von Aerden, Mio, Denommé-Pichon, Anne-Sophie, Bonneau, Dominique, Bruel, Ange-Line, Delanne, Julian, Gérard, Bénédicte, Mazel, Benoît, Philippe, Christophe, Pinson, Lucile, Prouteau, Clément, Putoux, Audrey, Tran Mau-Them, Frédéric, Viora-Dupont, Éléonore, Vitobello, Antonio, Ziegler, Alban, Piton, Amélie, Isidor, Bertrand, Francannet, Christine, Maillard, Pierre-Yves, Julia, Sophie, Philippe, Anais, Schaefer, Elise, Koene, Saskia, Ruivenkamp, Claudia, Hoffer, Mariette, Legius, Eric, Theunis, Miel, Keren, Boris, Buratti, Julien, Charles, Perrine, Courtin, Thomas, Misra-Isrie, Mala, van Haelst, Mieke, Waisfisz, Quinten, Wieczorek, Dagmar, Schmetz, Ariane, Herget, Theresia, Kortüm, Fanny, Lisfeld, Jasmin, Debray, François-Guillaume, Bramswig, Nuria C, Atallah, Isis, Fodstad, Heidi, Jouret, Guillaume, Almoguera, Berta, Tahsin-Swafiri, Saoud, Santos-Simarro, Fernando, Palomares-Bralo, Maria, López-González, Vanesa, Kibaek, Maria, Tørring, Pernille M, Renieri, Alessandra, Bruno, Lucia Pia, Õunap, Katrin, Wojcik, Monica, Hsieh, Tzung-Chien, Krawitz, Peter, Van Esch, Hilde

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Genotype-phenotype correlations of UBA2 mutations in patients with ectrodactyly von Aerden, Mio, Bauters, Marijke, Van Den Bogaert, Kris, Vermeesch, Joris R, Holvoet, Maureen, Plasschaert, Frank, Devriendt, Koenraad

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Episignature Mapping of TRIP12 Provides Functional Insight into Clark-Baraitser Syndrome von van der Laan, Liselot, Rooney, Kathleen, Alders, Mariëlle, Relator, Raissa, McConkey, Haley, Kerkhof, Jennifer, Levy, Michael A, Lauffer, Peter, Aerden, Mio, Theunis, Miel, Legius, Eric, Tedder, Matthew L, Vissers, Lisenka E L M, Koene, Saskia, Ruivenkamp, Claudia, Hoffer, Mariette J V, Wieczorek, Dagmar, Bramswig, Nuria C, Herget, Theresia, González, Vanesa López, Santos-Simarro, Fernando, Tørring, Pernille M, Denomme-Pichon, Anne-Sophie, Isidor, Bertrand, Keren, Boris, Julia, Sophie, Schaefer, Elise, Francannet, Christine, Maillard, Pierre-Yves, Misra-Isrie, Mala, Van Esch, Hilde, Mannens, Marcel M A M, Sadikovic, Bekim, van Haelst, Mieke M, Henneman, Peter

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The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant von Aerden, Mio, Denomme-Pichon, Anne-Sophie, Bonneau, Dominique, Bruel, Ange-Line, Delanne, Julian, Gerard, Benedicte, Mazel, Benoit, Philippe, Christophe, Pinson, Lucile, Prouteau, Clement, Putoux, Audrey, Tran Mau-Them, Frederic, Viora-Dupont, Eleonore, Vitobello, Antonio, Ziegler, Alban, Piton, Amelie, Isidor, Bertrand, Francannet, Christine, Maillard, Pierre-Yves, Julia, Sophie, Philippe, Anais, Schaefer, Elise, Koene, Saskia, Ruivenkamp, Claudia, Hoffer, Mariette, Legius, Eric, Theunis, Miel, Keren, Boris, Buratti, Julien, Charles, Perrine, Courtin, Thomas, Misra-Isrie, Mala, van Haelst, Mieke, Waisfisz, Quinten, Wieczorek, Dagmar, Schmetz, Ariane, Herget, Theresia, Kortuem, Fanny, Lisfeld, Jasmin, Debray, Francois-Guillaume, Bramswig, Nuria C, Atallah, Isis, Fodstad, Heidi, Jouret, Guillaume, Almoguera, Berta, Tahsin-Swafiri, Saoud, Santos-Simarro, Fernando, Palomares-Bralo, Maria, Lopez-Gonzalez, Vanesa, Kibaek, Maria, Torring, Pernille M, Renieri, Alessandra, Bruno, Lucia Pia, Ounap, Katrin, Wojcik, Monica, Hsieh, Tzung-Chien, Krawitz, Peter, Van Esch, Hilde

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Episignature Mapping of TRIP12 Provides Functional Insight into Clark-Baraitser Syndrome von van der Laan, Liselot, Rooney, Kathleen, Alders, Marielle, Relator, Raissa, McConkey, Haley, Kerkhof, Jennifer, Levy, Michael A, Lauffer, Peter, Aerden, Mio, Theunis, Miel, Legius, Eric, Tedder, Matthew L, Vissers, Lisenka E.L.M, Koene, Saskia, Ruivenkamp, Claudia, Hoffer, Mariette J, Wieczorek, Dagmar, Bramswig, Nuria C, Herget, Theresia, Lopez Gonzalez, Vanesa, Santos-Simarro, Fernando, Torring, Pernille M, Denomme-Pichon, Anne-Sophie, Isidor, Bertrand, Keren, Boris, Julia, Sophie, Schaefer, Elise, Francannet, Christine, Maillard, Pierre-Yves, Misra-Isrie, Mala, Van Esch, Hilde, Mannens, Marcel M.A.M, Sadikovic, Bekim, van Haelst, Mieke M, Henneman, Peter

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