X-linked mental retardation and epigenetics

by Froyen, Guy, Bauters, Marijke, Voet, Thierry, Marynen, Peter
Published 2006

Nxf7 deficiency impairs social exploration and spatio-cognitive abilities as well as hippocampal synaptic plasticity in mice

by Callaerts-Vegh, Zsuzsanna, Ahmed, Tariq, Vermaercke, Ben, Marynen, Peter, Balschun, Detlef, Froyen, Guy, D’Hooge, Rudi
Published 2015

Telomere length homeostasis and telomere position effect on a linear human artificial chromosome are dictated by the genetic background

by Weuts, An, Voet, Thierry, Verbeeck, Jelle, Lambrechts, Nathalie, Wirix, Evelyne, Schoonjans, Luc, Danloy, Sophie, Marynen, Peter, Froyen, Guy
Published 2012

Large-scale analysis of tandem repeat variability in the human genome

by Duitama, Jorge, Zablotskaya, Alena, Gemayel, Rita, Jansen, An, Belet, Stefanie, Vermeesch, Joris R., Verstrepen, Kevin J., Froyen, Guy
Published 2014

Validation and Application of a Custom-Designed Targeted Next-Generation Sequencing Panel for the Diagnostic Mutational Profiling of Solid Tumors

by Froyen, Guy, Broekmans, An, Hillen, Femke, Pat, Karin, Achten, Ruth, Mebis, Jeroen, Rummens, Jean-Luc, Willemse, Johan, Maes, Brigitte
Published 2016

Generation and Characterization of an Nxf7 Knockout Mouse to Study NXF5 Deficiency in a Patient with Intellectual Disability

by Vanmarsenille, Lieselot, Verbeeck, Jelle, Belet, Stefanie, Roebroek, Anton J., Van de Putte, Tom, Nevelsteen, Joke, Callaerts-Vegh, Zsuzsanna, D’Hooge, Rudi, Marynen, Peter, Froyen, Guy
Published 2013

A novel fragile X syndrome mutation reveals a conserved role for the carboxy-terminus in FMRP localization and function

by Okray, Zeynep, de Esch, Celine EF, Van Esch, Hilde, Devriendt, Koen, Claeys, Annelies, Yan, Jiekun, Verbeeck, Jelle, Froyen, Guy, Willemsen, Rob, de Vrij, Femke MS, Hassan, Bassem A
Published 2015

Ubiquitin Ligase HUWE1 Regulates Axon Branching through the Wnt/β-Catenin Pathway in a Drosophila Model for Intellectual Disability

by Vandewalle, Joke, Langen, Marion, Zschaetzsch, Marlen, Nijhof, Bonnie, Kramer, Jamie M., Brems, Hilde, Bauters, Marijke, Lauwers, Elsa, Srahna, Mohammed, Marynen, Peter, Verstreken, Patrik, Schenck, Annette, Hassan, Bassem A., Froyen, Guy
Published 2013

X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypes

by Philips, Anju K, Sirén, Auli, Avela, Kristiina, Somer, Mirja, Peippo, Maarit, Ahvenainen, Minna, Doagu, Fatma, Arvio, Maria, Kääriäinen, Helena, Van Esch, Hilde, Froyen, Guy, Haas, Stefan A, Hu, Hao, Kalscheuer, Vera M, Järvelä, Irma
Published 2014

Correction: Ubiquitin Ligase HUWE1 Regulates Axon Branching through the Wnt/β-Catenin Pathway in a Drosophila Model for Intellectual Disability

by Vandewalle, Joke, Langen, Marion, Zschaetzsch, Marlen, Nijhof, Bonnie, Kramer, Jamie M., Brems, Hilde, Bauters, Marijke, Lauwers, Elsa, Srahna, Mohammed, Marynen, Peter, Verstreken, Patrik, Schenck, Annette, Hassan, Bassem A., Froyen, Guy
Published 2014

Rer1p maintains ciliary length and signaling by regulating γ-secretase activity and Foxj1a levels

by Jurisch-Yaksi, Nathalie, Rose, Applonia J., Lu, Huiqi, Raemaekers, Tim, Munck, Sebastian, Baatsen, Pieter, Baert, Veerle, Vermeire, Wendy, Scales, Suzie J., Verleyen, Daphne, Vandepoel, Roel, Tylzanowski, Przemko, Yaksi, Emre, de Ravel, Thomy, Yost, H. Joseph, Froyen, Guy, Arrington, Cammon B., Annaert, Wim
Published 2013

Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins

by Carmi, Shai, Hui, Ken Y., Kochav, Ethan, Liu, Xinmin, Xue, James, Grady, Fillan, Guha, Saurav, Upadhyay, Kinnari, Ben-Avraham, Dan, Mukherjee, Semanti, Bowen, B. Monica, Thomas, Tinu, Vijai, Joseph, Cruts, Marc, Froyen, Guy, Lambrechts, Diether, Plaisance, Stéphane, Van Broeckhoven, Christine, Van Damme, Philip, Van Marck, Herwig, Barzilai, Nir, Darvasi, Ariel, Offit, Kenneth, Bressman, Susan, Ozelius, Laurie J., Peter, Inga, Cho, Judy H., Ostrer, Harry, Atzmon, Gil, Clark, Lorraine N., Lencz, Todd, Pe’er, Itsik
Published 2014