Novel variants of major drug-metabolising enzyme genes in diverse African populations and their predicted functional effects

Por Matimba, Alice, Del-Favero, Jurgen, Van Broeckhoven, Christine, Masimirembwa, Collen
Publicado em 2009

Genetic variants in microRNA genes: impact on microRNA expression, function, and disease

Por Cammaerts, Sophia, Strazisar, Mojca, De Rijk, Peter, Del Favero, Jurgen
Publicado no Front Genet (2015)

SNPbox: web-based high-throughput primer design from gene to genome

Por Weckx, Stefan, De Rijk, Peter, Van Broeckhoven, Christine, Del-Favero, Jurgen
Publicado em 2004

miRVaS: a tool to predict the impact of genetic variants on miRNAs

Por Cammaerts, Sophia, Strazisar, Mojca, Dierckx, Jenne, Del Favero, Jurgen, De Rijk, Peter
Publicado no Nucleic Acids Res (2016)

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

Por Claes, Lieve, Del-Favero, Jurgen, Ceulemans, Berten, Lagae, Lieven, Van Broeckhoven, Christine, De Jonghe, Peter
Publicado em 2001

The Relationship between the Val158Met Catechol-o-Methyltransferase (COMT) Polymorphism and Irritable Bowel Syndrome

Por Karling, Pontus, Danielsson, Åke, Wikgren, Mikael, Söderström, Ingegerd, Del-Favero, Jurgen, Adolfsson, Rolf, Norrback, Karl-Fredrik
Publicado em 2011

BioGraph: unsupervised biomedical knowledge discovery via automated hypothesis generation

Por Liekens, Anthony ML, De Knijf, Jeroen, Daelemans, Walter, Goethals, Bart, De Rijk, Peter, Del-Favero, Jurgen
Publicado em 2011

novoSNP, a novel computational tool for sequence variation discovery

Por Weckx, Stefan, Del-Favero, Jurgen, Rademakers, Rosa, Claes, Lieve, Cruts, Marc, De Jonghe, Peter, Van Broeckhoven, Christine, De Rijk, Peter
Publicado em 2005

Genomewide Scan for Affective Disorder Susceptibility Loci in Families of a Northern Swedish Isolated Population

Por Venken, Tine, Claes, Stephan, Sluijs, Samuël, Paterson, Andrew D., van Duijn, Cornelia, Adolfsson, Rolf, Del-Favero, Jurgen, Van Broeckhoven, Christine
Publicado em 2005

Multiplex Amplicon Quantification (MAQ), a fast and efficient method for the simultaneous detection of copy number alterations in neuroblastoma

Por Kumps, Candy, Van Roy, Nadine, Heyrman, Lien, Goossens, Dirk, Del-Favero, Jurgen, Noguera, Rosa, Vandesompele, Jo, Speleman, Frank, De Preter, Katleen
Publicado em 2010

NR4A2: Effects of an “Orphan” Receptor on Sustained Attention in a Schizophrenic Population

Por Ancín, Inés, Cabranes, José A., Vázquez-Álvarez, Blanca, Santos, José Luis, Sánchez-Morla, Eva, Alaerts, Maaike, Del-Favero, Jurgen, Barabash, Ana
Publicado em 2013

Schizophrenia-Associated MIR204 Regulates Noncoding RNAs and Affects Neurotransmitter and Ion Channel Gene Sets

Por Cammaerts, Sophia, Strazisar, Mojca, Smets, Bart, Weckhuysen, Sarah, Nordin, Annelie, De Jonghe, Peter, Adolfsson, Rolf, De Rijk, Peter, Del Favero, Jurgen
Publicado no PLoS One (2015)

A genome-wide search for linkage to allergic rhinitis in Danish sib-pair families

Por Kruse, Lisbeth Venø, Nyegaard, Mette, Christensen, Ulla, Møller-Larsen, Steffen, Haagerup, Annette, Deleuran, Mette, Hansen, Lars Gudmund, Venø, Stine Krogh, Goossens, Dirk, Del-Favero, Jurgen, Børglum, Anders Dupont
Publicado em 2012

A qPCR Assay to Detect and Quantify Shiga Toxin-Producing E. coli (STEC) in Cattle and on Farms: A Potential Predictive Tool for STEC Culture-Positive Farms

Por Verstraete, Karen, Van Coillie, Els, Werbrouck, Hadewig, Van Weyenberg, Stephanie, Herman, Lieve, Del-Favero, Jurgen, De Rijk, Peter, De Zutter, Lieven, Joris, Maria-Adelheid, Heyndrickx, Marc, De Reu, Koen
Publicado em 2014

Thrombomodulin Mutations in Atypical Hemolytic–Uremic Syndrome

Por 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.
Publicado em 2009

Camelid Ig V genes reveal significant human homology not seen in therapeutic target genes, providing for a powerful therapeutic antibody platform

Por Klarenbeek, Alex, Mazouari, Khalil El, Desmyter, Aline, Blanchetot, Christophe, Hultberg, Anna, de Jonge, Natalie, Roovers, Rob C, Cambillau, Christian, Spinelli, Sylvia, Del-Favero, Jurgen, Verrips, Theo, de Haard, Hans J, Achour, Ikbel
Publicado no MAbs (2015)

A High-Resolution Physical Map of Human Chromosome 21p Using Yeast Artificial Chromosomes

Por Wang, Sheng-Yue, Cruts, Marc, Del-Favero, Jurgen, Zhang, Yi, Tissir, Fadel, Potier, Marie-Claude, Patterson, David, Nizetic, Dean, Bosch, Assumpció, Chen, Haiming, Bennett, Lynda, Estivill, Xavier, Kessling, Anna, Antonarakis, Stylianos E., van Broeckhoven, Christine
Publicado em 1999

Linkage and Association Studies Identify a Novel Locus for Alzheimer Disease at 7q36 in a Dutch Population-Based Sample

Por Rademakers, Rosa, Cruts, Marc, Sleegers, Kristel, Dermaut, Bart, Theuns, Jessie, Aulchenko, Yurii, Weckx, Stefan, De Pooter, Tim, Van den Broeck, Marleen, Corsmit, Ellen, De Rijk, Peter, Del-Favero, Jurgen, van Swieten, John, van Duijn, Cornelia M., Van Broeckhoven, Christine
Publicado em 2005

Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population

Por Moens, Lotte N., De Rijk, Peter, Reumers, Joke, Van Den Bossche, Maarten J. A., Glassee, Wim, De Zutter, Sonia, Lenaerts, An-Sofie, Nordin, Annelie, Nilsson, Lars-Göran, Medina Castello, Ignacio, Norrback, Karl-Fredrik, Goossens, Dirk, Van Steen, Kristel, Adolfsson, Rolf, Del-Favero, Jurgen
Publicado em 2011

Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness

Por Johnstone, Mandy, MacLean, Alan, Heyrman, Lien, Lenaerts, An-Sofie, Nordin, Annelie, Nilsson, Lars-Göran, De Rijk, Peter, Goossens, Dirk, Adolfsson, Rolf, Clair, David M. St., Hall, Jeremy, Lawrie, Stephen M., McIntosh, Andrew M., Del-Favero, Jurgen, Blackwood, Douglas H.R., Pickard, Benjamin S.
Publicado no Mol Neuropsychiatry (2015)