Methylation analysis of Gasdermin E shows great promise as a biomarker for colorectal cancer

por Ibrahim, Joe, Op de Beeck, Ken, Fransen, Erik, Croes, Lieselot, Beyens, Matthias, Suls, Arvid, Vanden Berghe, Wim, Peeters, Marc, Van Camp, Guy
Publicado 2019

Large-scale analysis of DFNA5 methylation reveals its potential as biomarker for breast cancer

por Croes, Lieselot, Beyens, Matthias, Fransen, Erik, Ibrahim, Joe, Vanden Berghe, Wim, Suls, Arvid, Peeters, Marc, Pauwels, Patrick, Van Camp, Guy, Op de Beeck, Ken
Publicado 2018

Large-scale copy number analysis reveals variations in genes not previously associated with malignant pleural mesothelioma

por Hylebos, Marieke, Van Camp, Guy, Vandeweyer, Geert, Fransen, Erik, Beyens, Matthias, Cornelissen, Robin, Suls, Arvid, Pauwels, Patrick, van Meerbeeck, Jan P., Op de Beeck, Ken
Publicado 2017

Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy

por Dejanovic, Borislav, Djémié, Tania, Grünewald, Nora, Suls, Arvid, Kress, Vanessa, Hetsch, Florian, Craiu, Dana, Zemel, Matthew, Gormley, Padhraig, Lal, Dennis, Myers, Candace T, Mefford, Heather C, Palotie, Aarno, Helbig, Ingo, Meier, Jochen C, De Jonghe, Peter, Weckhuysen, Sarah, Schwarz, Guenter
Publicado 2015

Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy

por Dejanovic, Borislav, Djémié, Tania, Grünewald, Nora, Suls, Arvid, Kress, Vanessa, Hetsch, Florian, Craiu, Dana, Zemel, Matthew, Gormley, Padhraig, Lal, Dennis, Myers, Candace T, Mefford, Heather C, Palotie, Aarno, Helbig, Ingo, Meier, Jochen C, De Jonghe, Peter, Weckhuysen, Sarah, Schwarz, Guenter
Publicado 2017

GRIN2B Mutations in West Syndrome and Intellectual Disability with Focal Epilepsy

por Lemke, Johannes R, Hendrickx, Rik, Geider, Kirsten, Laube, Bodo, Schwake, Michael, Harvey, Robert J, James, Victoria M, Pepler, Alex, Steiner, Isabelle, Hörtnagel, Konstanze, Neidhardt, John, Ruf, Susanne, Wolff, Markus, Bartholdi, Deborah, Caraballo, Roberto, Platzer, Konrad, Suls, Arvid, De Jonghe, Peter, Biskup, Saskia, Weckhuysen, Sarah
Publicado 2014

Preexisting memory CD4 T cells in naïve individuals confer robust immunity upon hepatitis B vaccination

por Elias, George, Meysman, Pieter, Bartholomeus, Esther, De Neuter, Nicolas, Keersmaekers, Nina, Suls, Arvid, Jansens, Hilde, Souquette, Aisha, De Reu, Hans, Emonds, Marie-Paule, Smits, Evelien, Lion, Eva, Thomas, Paul G, Mortier, Geert, Van Damme, Pierre, Beutels, Philippe, Laukens, Kris, Van Tendeloo, Viggo, Ogunjimi, Benson
Publicado 2022

Loss of synaptic Zn(2+) transporter function increases risk of febrile seizures

por Hildebrand, Michael S., Phillips, A. Marie, Mullen, Saul A., Adlard, Paul A., Hardies, Katia, Damiano, John A., Wimmer, Verena, Bellows, Susannah T., McMahon, Jacinta M., Burgess, Rosemary, Hendrickx, Rik, Weckhuysen, Sarah, Suls, Arvid, De Jonghe, Peter, Scheffer, Ingrid E., Petrou, Steven, Berkovic, Samuel F., Reid, Christopher A.
Publicado 2015

Diagnosing enterovirus meningitis via blood transcriptomics: an alternative for lumbar puncture?

por Bartholomeus, Esther, De Neuter, Nicolas, Lemay, Annelies, Pattyn, Luc, Tuerlinckx, David, Weynants, David, Van Lede, Koen, van Berlaer, Gerlant, Bulckaert, Dominique, Boiy, Tine, Vander Auwera, Ann, Raes, Marc, Van der Linden, Dimitri, Verhelst, Helene, Van Steijn, Susanne, Jonckheer, Tijl, Dehoorne, Joke, Joos, Rik, Jansens, Hilde, Suls, Arvid, Van Damme, Pierre, Laukens, Kris, Mortier, Geert, Meysman, Pieter, Ogunjimi, Benson
Publicado 2019

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1

por Suls, Arvid, Dedeken, Peter, Goffin, Karolien, Van Esch, Hilde, Dupont, Patrick, Cassiman, David, Kempfle, Judith, Wuttke, Thomas V., Weber, Yvonne, Lerche, Holger, Afawi, Zaid, Vandenberghe, Wim, Korczyn, Amos D., Berkovic, Samuel F., Ekstein, Dana, Kivity, Sara, Ryvlin, Philippe, Claes, Lieve R. F., Deprez, Liesbet, Maljevic, Snezana, Vargas, Alberto, Van Dyck, Tine, Goossens, Dirk, Del-Favero, Jurgen, Van Laere, Koen, De Jonghe, Peter, Van Paesschen, Wim
Publicado 2008

Burden Analysis of Rare Microdeletions Suggests a Strong Impact of Neurodevelopmental Genes in Genetic Generalised Epilepsies

por Lal, Dennis, Ruppert, Ann-Kathrin, Trucks, Holger, Schulz, Herbert, de Kovel, Carolien G., Kasteleijn-Nolst Trenité, Dorothée, Sonsma, Anja C. M., Koeleman, Bobby P., Lindhout, Dick, Weber, Yvonne G., Lerche, Holger, Kapser, Claudia, Schankin, Christoph J., Kunz, Wolfram S., Surges, Rainer, Elger, Christian E., Gaus, Verena, Schmitz, Bettina, Helbig, Ingo, Muhle, Hiltrud, Stephani, Ulrich, Klein, Karl M., Rosenow, Felix, Neubauer, Bernd A., Reinthaler, Eva M., Zimprich, Fritz, Feucht, Martha, Møller, Rikke S., Hjalgrim, Helle, De Jonghe, Peter, Suls, Arvid, Lieb, Wolfgang, Franke, Andre, Strauch, Konstantin, Gieger, Christian, Schurmann, Claudia, Schminke, Ulf, Nürnberg, Peter, Sander, Thomas
Publicado 2015

Blood transcriptomics to facilitate diagnosis and stratification in pediatric rheumatic diseases – a proof of concept study

por Ha, My Kieu, Bartholomeus, Esther, Van Os, Luc, Dandelooy, Julie, Leysen, Julie, Aerts, Olivier, Siozopoulou, Vasiliki, De Smet, Eline, Gielen, Jan, Guerti, Khadija, De Maeseneer, Michel, Herregods, Nele, Lechkar, Bouchra, Wittoek, Ruth, Geens, Elke, Claes, Laura, Zaqout, Mahmoud, Dewals, Wendy, Lemay, Annelies, Tuerlinckx, David, Weynants, David, Vanlede, Koen, van Berlaer, Gerlant, Raes, Marc, Verhelst, Helene, Boiy, Tine, Van Damme, Pierre, Jansen, Anna C., Meuwissen, Marije, Sabato, Vito, Van Camp, Guy, Suls, Arvid, Werff ten Bosch, Jutte Van der, Dehoorne, Joke, Joos, Rik, Laukens, Kris, Meysman, Pieter, Ogunjimi, Benson
Publicado 2022

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

por Syrbe, Steffen, Hedrich, Ulrike B.S., Riesch, Erik, Djémié, Tania, Müller, Stephan, Møller, Rikke S., Maher, Bridget, Hernandez-Hernandez, Laura, Synofzik, Matthis, Caglayan, Hande S., Arslan, Mutluay, Serratosa, José M., Nothnagel, Michael, May, Patrick, Krause, Roland, Löffler, Heidrun, Detert, Katja, Dorn, Thomas, Vogt, Heinrich, Krämer, Günter, Schöls, Ludger, Mullis, Primus E., Linnankivi, Tarja, Lehesjoki, Anna-Elina, Sterbova, Katalin, Craiu, Dana C., Hoffman-Zacharska, Dorota, Korff, Christian M., Weber, Yvonne G., Steinlin, Maja, Gallati, Sabina, Bertsche, Astrid, Bernhard, Matthias K., Merkenschlager, Andreas, Kiess, Wieland, Gonzalez, Michael, Züchner, Stephan, Palotie, Aarno, Suls, Arvid, De Jonghe, Peter, Helbig, Ingo, Biskup, Saskia, Wolff, Markus, Maljevic, Snezana, Schüle, Rebecca, Sisodiya, Sanjay M., Weckhuysen, Sarah, Lerche, Holger, Lemke, Johannes R.
Publicado 2015

Pitfalls in genetic testing: the story of missed SCN1A mutations

por Djémié, Tania, Weckhuysen, Sarah, von Spiczak, Sarah, Carvill, Gemma L., Jaehn, Johanna, Anttonen, Anna‐Kaisa, Brilstra, Eva, Caglayan, Hande S., de Kovel, Carolien G., Depienne, Christel, Gaily, Eija, Gennaro, Elena, Giraldez, Beatriz G., Gormley, Padhraig, Guerrero‐López, Rosa, Guerrini, Renzo, Hämäläinen, Eija, Hartmann, Corinna, Hernandez‐Hernandez, Laura, Hjalgrim, Helle, Koeleman, Bobby P. C., Leguern, Eric, Lehesjoki, Anna‐Elina, Lemke, Johannes R., Leu, Costin, Marini, Carla, McMahon, Jacinta M., Mei, Davide, Møller, Rikke S., Muhle, Hiltrud, Myers, Candace T., Nava, Caroline, Serratosa, Jose M., Sisodiya, Sanjay M., Stephani, Ulrich, Striano, Pasquale, van Kempen, Marjan J. A., Verbeek, Nienke E., Usluer, Sunay, Zara, Federico, Palotie, Aarno, Mefford, Heather C., Scheffer, Ingrid E., De Jonghe, Peter, Helbig, Ingo, Suls, Arvid
Publicado 2016

Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients

por de Kovel, Carolien G.F., Brilstra, Eva H., van Kempen, Marjan J.A., van‘t Slot, Ruben, Nijman, Isaac J., Afawi, Zaid, De Jonghe, Peter, Djémié, Tania, Guerrini, Renzo, Hardies, Katia, Helbig, Ingo, Hendrickx, Rik, Kanaan, Moine, Kramer, Uri, Lehesjoki, Anna‐Elina E., Lemke, Johannes R., Marini, Carla, Mei, Davide, Møller, Rikke S., Pendziwiat, Manuela, Stamberger, Hannah, Suls, Arvid, Weckhuysen, Sarah, Koeleman, Bobby P.C., R, Balling, N, Barisic, S, Baulac, HS, Caglayan, DC, Craiu, C, Depienne, P, Gormley, H, Hjalgrim, D, Hoffman‐Zacharska, J, Jähn, KM, Klein, V, Komarek, E, LeGuern, H, Lerche, P, May, H, Muhle, D, Pal, A, Palotie, F, Rosenow, K, Selmer, JM, Serratosa, SM, Sisodiya, U, Stephani, K, Sterbova, P, Striano, T, Talvik, M, van Haelst, N, Verbeek, S, von Spiczak, YG, Weber
Publicado 2016