miRVaS: a tool to predict the impact of genetic variants on miRNAs von Cammaerts, Sophia, Strazisar, Mojca, Dierckx, Jenne, Del Favero, Jurgen, De Rijk, Peter

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Searching genetic risk factors for schizophrenia and bipolar disorder: learn from the past and back to the future von Alaerts, Maaike, Del-Favero, Jurgen

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miRNA genes and the brain: implications for psychiatric disordersa von Forero, Diego A, van der Ven, Karlijn, Callaerts, Patrick, Del‐Favero, Jurgen

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Performance of multiplicom's BRCA MASTR Dx kit on the detection of BRCA1 and BRCA2 mutations in fresh frozen ovarian and breast tumor samples von Badoer, Cindy, Garrec, Céline, Goossens, Dirk, Ellison, Gillian, Mills, John, Dzial, Mélina, El Housni, Hakim, Berwouts, Sarah, Concolino, Paola, Guibert-Le Guevellou, Virginie, Delnatte, Capucine, Del Favero, Jurgen, Capoluongo, Ettore, Bézieau, Stéphane

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Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population von Nuytemans, Karen, Meeus, Bram, Crosiers, David, Brouwers, Nathalie, Goossens, Dirk, Engelborghs, Sebastiaan, Pals, Philippe, Pickut, Barbara, Van den Broeck, Marleen, Corsmit, Ellen, Cras, Patrick, De Deyn, Peter P, Del-Favero, Jurgen, Van Broeckhoven, Christine, Theuns, Jessie

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Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing von Goossens, Dirk, Moens, Lotte N, Nelis, Eva, Lenaerts, An-Sofie, Glassee, Wim, Kalbe, Andreas, Frey, Bruno, Kopal, Guido, Jonghe, Peter De, Rijk, Peter De, Del-Favero, Jurgen

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Identification of rare copy number variants in high burden schizophrenia families von Van Den Bossche, Maarten J., Strazisar, Mojca, Cammaerts, Sophia, Liekens, Anthony M., Vandeweyer, Geert, Depreeuw, Veerle, Mattheijssens, Maria, Lenaerts, An-Sofie, De Zutter, Sonia, De Rijk, Peter, Sabbe, Bernard, Del-Favero, Jurgen

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Comprehensive Profiling of the Androgen Receptor in Liquid Biopsies from Castration-resistant Prostate Cancer Reveals Novel Intra-AR Structural Variation and Splice Variant Express... von De Laere, Bram, van Dam, Pieter-Jan, Whitington, Tom, Mayrhofer, Markus, Diaz, Emanuela Henao, Van den Eynden, Gert, Vandebroek, Jean, Del-Favero, Jurgen, Van Laere, Steven, Dirix, Luc, Grönberg, Henrik, Lindberg, Johan

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Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies von Ashton, Emma J., Legrand, Anne, Benoit, Valerie, Roncelin, Isabelle, Venisse, Annabelle, Zennaro, Maria-Christina, Jeunemaitre, Xavier, Iancu, Daniela, van’t Hoff, William G., Walsh, Stephen B., Godefroid, Nathalie, Rotthier, Annelies, Del Favero, Jurgen, Devuyst, Olivier, Schaefer, Franz, Jenkins, Lucy A., Kleta, Robert, Dahan, Karin, Vargas-Poussou, Rosa, Bockenhauer, Detlef

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Thrombomodulin Mutations in Atypical Hemolytic–Uremic Syndrome von Delvaeye, Mieke, Noris, Marina, De Vriese, Astrid, Esmon, Charles T, Esmon, Naomi L, Ferrell, Gary, Del-Favero, Jurgen, Plaisance, Stephane, Claes, Bart, Lambrechts, Diether, Zoja, Carla, Remuzzi, Giuseppe, Conway, Edward M

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Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders von Van Den Bossche, Maarten J., Strazisar, Mojca, De Bruyne, Stephan, Bervoets, Chris, Lenaerts, An-Sofie, De Zutter, Sonia, Nordin, Annelie, Norrback, Karl-Fredrik, Goossens, Dirk, De Rijk, Peter, Green, Elaine K., Grozeva, Detelina, Mendlewicz, Julien, Craddock, Nick, Sabbe, Bernard G., Adolfsson, Rolf, Souery, Daniel, Del-Favero, Jurgen

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Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing von Reumers, Joke, De Rijk, Peter, Zhao, Hui, Liekens, Anthony, Smeets, Dominiek, Cleary, John, Van Loo, Peter, Van Den Bossche, Maarten, Catthoor, Kirsten, Sabbe, Bernard, Despierre, Evelyn, Vergote, Ignace, Hilbush, Brian, Lambrechts, Diether, Del-Favero, Jurgen

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BioGraph: unsupervised biomedical knowledge discovery via automated hypothesis generation von Liekens, Anthony M L, De Knijf, Jeroen, Daelemans, Walter, Goethals, Bart, De Rijk, Peter, Del-Favero, Jurgen

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De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy von Claes, Lieve, Del-Favero, Jurgen, Ceulemans, Berten, Lagae, Lieven, Van Broeckhoven, Christine, De Jonghe, Peter

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novoSNP, a novel computational tool for sequence variation discovery von Weckx, Stefan, Del-Favero, Jurgen, Rademakers, Rosa, Claes, Lieve, Cruts, Marc, De Jonghe, Peter, Van Broeckhoven, Christine, De Rijk, Peter

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No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity von Izzi, Benedetta, de Zegher, Francis, Francois, Inge, del Favero, Jurgen, Goossens, Dirk, Wittevrongel, Christine, Thys, Chantal, Van Geet, Chris, Freson, Kathleen

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PCM1 and schizophrenia: A replication study in the Northern Swedish population von Moens, Lotte N., Ceulemans, Shana, Alaerts, Maaike, Van Den Bossche, Maarten J.A., Lenaerts, An-Sofie, De Zutter, Sonia, Norrback, Karl-Fredrik, Adolfsson, Rolf, Del-Favero, Jurgen

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Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis von Van Broeckhoven, Christine, Dessa Sadovnick, A, Del-Favero, Jurgen, Greiner, Eva, van Duijn, Cornelia M, Oostra, Ben A, Goossens, Dirk, Hintzen, Rogier Q, Link, Jenny, Hoppenbrouwers, Ilse A, Broer, Linda, Ramagopalan, Sreeram V, Aulchenko, Yurii S, Hillert, Jan, Lundström, Wangko, Jafari, Naghmeh, Ebers, George C

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The kynurenine pathway in major depression: Haplotype analysis of three related functional candidate genes von Claes, Stephan, Myint, Aye-Mu, Domschke, Katharina, Del-Favero, Jurgen, Entrich, Kathrin, Engelborghs, Sebastiaan, De Deyn, Peter, Mueller, Norbert, Baune, Bernhard, Rothermundt, Matthias

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Schizophrenia-Associated MIR204 Regulates Noncoding RNAs and Affects Neurotransmitter and Ion Channel Gene Sets von Cammaerts, Sophia, Strazisar, Mojca, Smets, Bart, Weckhuysen, Sarah, Nordin, Annelie, De Jonghe, Peter, Adolfsson, Rolf, De Rijk, Peter, Del Favero, Jurgen

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