Modeling PNPLA3‐Associated NAFLD Using Human‐Induced Pluripotent Stem Cells von Tilson, Samantha G., Morell, Carola M., Lenaerts, An‐Sofie, Park, Seung Bum, Hu, Zongyi, Jenkins, Benjamin, Koulman, Albert, Liang, T. Jake, Vallier, Ludovic

Volltext

Simultaneous depletion of RB, RBL1 and RBL2 affects endoderm differentiation of human embryonic stem cells von Nakanoh, Shota, Kadiwala, Juned, Pinte, Laetitia, Morell, Carola Maria, Lenaerts, An-Sofie, Vallier, Ludovic

Volltext

The SMAD2/3 interactome reveals that TGFβ controls m 6 A mRNA methylation in pluripotency von Bertero, Alessandro, Brown, Stephanie, Madrigal, Pedro, Osnato, Anna, Ortmann, Daniel, Yiangou, Loukia, Kadiwala, Juned, Hubner, Nina C, de Los Mozos, Igor Ruiz, Sadée, Christoph, Lenaerts, An-Sofie, Nakanoh, Shota, Grandy, Rodrigo, Farnell, Edward, Ule, Jernej, Stunnenberg, Hendrik G, Mendjan, Sasha, Vallier, Ludovic

Volltext

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

Volltext

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

Volltext

Reticular adhesions are assembled at flat clathrin lattices and opposed by active integrin α5β1 von Hakanpää, Laura, Abouelezz, Amr, Lenaerts, An-Sofie, Culfa, Seyda, Algie, Michael, Bärlund, Jenny, Katajisto, Pekka, McMahon, Harvey, Almeida-Souza, Leonardo

Volltext

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

Volltext

Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not? von Van Den Bossche, Maarten J., Johnstone, Mandy, Strazisar, Mojca, Pickard, Benjamin S., Goossens, Dirk, Lenaerts, An-Sofie, De Zutter, Sonia, Nordin, Annelie, Norrback, Karl-Fredrik, Mendlewicz, Julien, Souery, Daniel, De Rijk, Peter, Sabbe, Bernard G., Adolfsson, Rolf, Blackwood, Douglas, Del-Favero, Jurgen

Volltext

Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population von 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

Volltext

Simultaneous depletion of RB, RBL1 and RBL2 affects endoderm differentiation of human embryonic stem cells von Shota Nakanoh, Juned Kadiwala, Laetitia Pinte, Carola Maria Morell, An-Sofie Lenaerts, Ludovic Vallier

Volltext

Detailed analysis of the serotonin transporter gene (SLC6A4) shows no association with bipolar disorder in the Northern Swedish population von Alaerts, Maaike, Ceulemans, Shana, Forero, Diego, Moens, Lotte N., De Zutter, Sonia, Heyrman, Lien, Lenaerts, An-Sofie, Norrback, Karl-Fredrik, Goossens, Dirk, De Rijk, Peter, Nilsson, Lars-Göran, Adolfsson, Rolf, Del-Favero, Jurgen

Volltext

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

Volltext

Platelet function is modified by common sequence variation in megakaryocyte super enhancers von Petersen, Romina, Lambourne, John J., Javierre, Biola M., Grassi, Luigi, Kreuzhuber, Roman, Ruklisa, Dace, Rosa, Isabel M., Tomé, Ana R., Elding, Heather, van Geffen, Johanna P., Jiang, Tao, Farrow, Samantha, Cairns, Jonathan, Al-Subaie, Abeer M., Ashford, Sofie, Attwood, Antony, Batista, Joana, Bouman, Heleen, Burden, Frances, Choudry, Fizzah A., Clarke, Laura, Flicek, Paul, Garner, Stephen F., Haimel, Matthias, Kempster, Carly, Ladopoulos, Vasileios, Lenaerts, An-Sofie, Materek, Paulina M., McKinney, Harriet, Meacham, Stuart, Mead, Daniel, Nagy, Magdolna, Penkett, Christopher J., Rendon, Augusto, Seyres, Denis, Sun, Benjamin, Tuna, Salih, van der Weide, Marie-Elise, Wingett, Steven W., Martens, Joost H., Stegle, Oliver, Richardson, Sylvia, Vallier, Ludovic, Roberts, David J., Freson, Kathleen, Wernisch, Lorenz, Stunnenberg, Hendrik G., Danesh, John, Fraser, Peter, Soranzo, Nicole, Butterworth, Adam S., Heemskerk, Johan W., Turro, Ernest, Spivakov, Mikhail, Ouwehand, Willem H., Astle, William J., Downes, Kate, Kostadima, Myrto, Frontini, Mattia

Volltext

Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorder von Pickard, Benjamin Simon, Van Den Bossche, Maarten J A, Malloy, Mary P, Johnstone, Mandy, Lenaerts, An-Sofie, Nordin, Annelie, Goossens, Dirk, St Clair, David, Muir, Walter J, Nilsson, Lars-Göran, Sabbe, Bernard, Adolfsson, Rolf, Blackwood, Douglas H R, Del-Favero, Jurgen

Volltext

Less Cognitive and Neurological Deficits in Schizophrenia Patients Carrying Risk Variant in ZNF804A von Van Den Bossche, Maarten J.A., Docx, Lise, Morrens, Manuel, Cammaerts, Sophia, Strazisar, Mojca, Bervoets, Chris, Smolders, Stefanie, Depreeuw, Veerle, Lenaerts, An-Sofie, De Rijk, Peter, Del-Favero, Jurgen, Sabbe, Bernard G.C.

Volltext

Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness von Johnstone, Mandy, Maclean, Alan, Heyrman, Lien, Lenaerts, An-Sofie, Nordin, Annelie, Nilsson, Lars-Göran, De Rijk, Peter, Goossens, Dirk, Adolfsson, Rolf, St. Clair, David M., Hall, Jeremy, Lawrie, Stephen M., McIntosh, Andrew M., Del-Favero, Jurgen, Blackwood, Douglas H.R., Pickard, Benjamin S.

Volltext

Lack of association of an insertion/deletion polymorphism in the G protein-coupled receptor 50 with bipolar disorder in a Northern Swedish population von Alaerts, Maaike, Venken, Tine, Lenaerts, An-Sofie, De Zutter, Sonia, Norrback, Karl-Fredrik, Adolfsson, Rolf, Del-Favero, Jurgen

Volltext

Support for NRG1 as a Susceptibility Factor for Schizophrenia in a Northern Swedish Isolated Population von Alaerts, Maaike, Ceulemans, Shana, Forero, Diego, Moens, Lotte N, De Zutter, Sonia, Heyrman, Lien, Lenaerts, An-Sofie, Norrback, Karl-Fredrik, De Rijk, Peter, Nilsson, Lars-Göran, Goossens, Dirk, Adolfsson, Rolf, Del-Favero, Jurgen

Volltext

The SMAD2/3 interactome reveals that TGFβ controls m^sup 6^A mRNA methylation in pluripotency von Bertero, Alessandro, Brown, Stephanie, Madrigal, Pedro, Osnato, Anna, Ortmann, Daniel, Yiangou, Loukia, Kadiwala, Juned, Hubner, Nina C, de los Mozos, Igor Ruiz, Sadée, Christoph, Lenaerts, An-Sofie, Nakanoh, Shota, Grandy, Rodrigo, Farnell, Edward, Ule, Jernej, Stunnenberg, Hendrik G, Mendjan, Sasha, Vallier, Ludovic

Volltext

The SMAD2/3 interactome reveals that TGF controls m6A mRNA methylation in pluripotency von Bertero, Alessandro, Brown, Stephanie, Madrigal, Pedro, Osnato, Anna, Ortmann, Daniel, Yiangou, Loukia, Kadiwala, Juned, Hubner, Nina C, de los Mozos, Igor Ruiz, Sade, Christoph, Lenaerts, An-Sofie, Nakanoh, Shota, Grandy, Rodrigo, Farnell, Edward, Ule, Jernej, Stunnenberg, Hendrik G, Mendjan, Sasha, Vallier, Ludovic

Volltext