miRVaS: a tool to predict the impact of genetic variants on miRNAs
Cammaerts, Sophia, Strazisar, Mojca, Dierckx, Jenne, Del Favero, Jurgen, De Rijk, Peter
Published in Nucleic acids research (18.02.2016)
Published in Nucleic acids research (18.02.2016)
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miRNA genes and the brain: implications for psychiatric disordersa
Forero, Diego A, van der Ven, Karlijn, Callaerts, Patrick, Del‐Favero, Jurgen
Published in Human mutation (01.11.2010)
Published in Human mutation (01.11.2010)
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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
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
Published in Oncotarget (06.12.2016)
Published in Oncotarget (06.12.2016)
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Journal Article
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population
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
Published in Human mutation (01.07.2009)
Published in Human mutation (01.07.2009)
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Journal Article
Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing
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
Published in Human mutation (01.03.2009)
Published in Human mutation (01.03.2009)
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Journal Article
Identification of rare copy number variants in high burden schizophrenia families
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
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.04.2013)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.04.2013)
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Journal Article
Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders
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
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.06.2012)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.06.2012)
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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 Expression Patterns
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
Published in European urology (01.08.2017)
Published in European urology (01.08.2017)
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Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies
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
Published in Kidney international (01.04.2018)
Published in Kidney international (01.04.2018)
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Journal Article
Thrombomodulin Mutations in Atypical Hemolytic–Uremic Syndrome
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
Published in The New England journal of medicine (23.07.2009)
Published in The New England journal of medicine (23.07.2009)
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Journal Article
Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing
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
Published in Nature biotechnology (01.01.2012)
Published in Nature biotechnology (01.01.2012)
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Journal Article
No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity
Izzi, Benedetta, de Zegher, Francis, Francois, Inge, del Favero, Jurgen, Goossens, Dirk, Wittevrongel, Christine, Thys, Chantal, Van Geet, Chris, Freson, Kathleen
Published in Journal of human genetics (01.04.2012)
Published in Journal of human genetics (01.04.2012)
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Journal Article
PCM1 and schizophrenia: A replication study in the Northern Swedish population
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
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.09.2010)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.09.2010)
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Journal Article
BioGraph: unsupervised biomedical knowledge discovery via automated hypothesis generation
Liekens, Anthony M L, De Knijf, Jeroen, Daelemans, Walter, Goethals, Bart, De Rijk, Peter, Del-Favero, Jurgen
Published in Genome biology (22.06.2011)
Published in Genome biology (22.06.2011)
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novoSNP, a novel computational tool for sequence variation discovery
Weckx, Stefan, Del-Favero, Jurgen, Rademakers, Rosa, Claes, Lieve, Cruts, Marc, De Jonghe, Peter, Van Broeckhoven, Christine, De Rijk, Peter
Published in Genome research (01.03.2005)
Published in Genome research (01.03.2005)
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Journal Article
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis
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
Published in Nature genetics (01.12.2008)
Published in Nature genetics (01.12.2008)
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Gene-based SNP genetic association study of the corticotropin-releasing hormone receptor-2 (CRHR2) in major depression
Villafuerte, Sandra M, Del-Favero, Jurgen, Adolfsson, Rolf, Souery, Daniel, Massat, Isabelle, Mendlewicz, Julien, Van Broeckhoven, Christine, Claes, Stephan
Published in American journal of medical genetics (08.03.2002)
Published in American journal of medical genetics (08.03.2002)
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Journal Article
Schizophrenia-Associated MIR204 Regulates Noncoding RNAs and Affects Neurotransmitter and Ion Channel Gene Sets
Cammaerts, Sophia, Strazisar, Mojca, Smets, Bart, Weckhuysen, Sarah, Nordin, Annelie, De Jonghe, Peter, Adolfsson, Rolf, De Rijk, Peter, Del Favero, Jurgen
Published in PloS one (29.12.2015)
Published in PloS one (29.12.2015)
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