X-linked mental retardation and epigenetics

por Froyen, Guy, Bauters, Marijke, Voet, Thierry, Marynen, Peter
Publicado 2006

Diagnostic Validation of a Comprehensive Targeted Panel for Broad Mutational and Biomarker Analysis in Solid Tumors

por Froyen, Guy, Geerdens, Ellen, Berden, Severine, Cruys, Bert, Maes, Brigitte
Publicado 2022

Liquid Biopsy in Early-Stage Lung Cancer: Current and Future Clinical Applications

por Vandekerckhove, Olivia, Cuppens, Kristof, Pat, Karin, Du Pont, Bert, Froyen, Guy, Maes, Brigitte
Publicado 2023

Mapping the landscape of tandem repeat variability by targeted long read single molecule sequencing in familial X-linked intellectual disability

por Zablotskaya, Alena, Van Esch, Hilde, Verstrepen, Kevin J., Froyen, Guy, Vermeesch, Joris R.
Publicado 2018

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

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

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

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

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

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

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

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

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

por 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
Publicado 2013

The Dynamics of Nucleotide Variants in the Progression from Low–Intermediate Myeloma Precursor Conditions to Multiple Myeloma: Studying Serial Samples with a Targeted Sequencing Ap...

por Oben, Bénedith, Cosemans, Charlotte, Geerdens, Ellen, Linsen, Loes, Vanhees, Kimberly, Maes, Brigitte, Theunissen, Koen, Cruys, Bert, Lionetti, Marta, Arijs, Ingrid, Bolli, Niccolò, Froyen, Guy, Rummens, Jean-Luc
Publicado 2022

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

por 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
Publicado 2015

Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing

por Hu, Hao, Wrogemann, Klaus, Kalscheuer, Vera, Tzschach, Andreas, Richard, Hugues, Haas, Stefan A., Menzel, Corinna, Bienek, Melanie, Froyen, Guy, Raynaud, Martine, Van Bokhoven, Hans, Chelly, Jamel, Ropers, Hilger, Chen, Wei
Publicado 2010

Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing

por Hu, Hao, Wrogemann, Klaus, Kalscheuer, Vera, Tzschach, Andreas, Richard, Hugues, Haas, Stefan A., Menzel, Corinna, Bienek, Melanie, Froyen, Guy, Raynaud, Martine, Van Bokhoven, Hans, Chelly, Jamel, Ropers, Hilger, Chen, Wei
Publicado 2010

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

por 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
Publicado 2013

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

por 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
Publicado 2014

Impaired oxidative stress response characterizes HUWE1-promoted X-linked intellectual disability

por Bosshard, Matthias, Aprigliano, Rossana, Gattiker, Cristina, Palibrk, Vuk, Markkanen, Enni, Backe, Paul Hoff, Pellegrino, Stefania, Raymond, F. Lucy, Froyen, Guy, Altmeyer, Matthias, Bjørås, Magnar, Dianov, Grigory L., van Loon, Barbara
Publicado 2017

Publisher Correction: Impaired oxidative stress response characterizes HUWE1-promoted X-linked intellectual disability

por Bosshard, Matthias, Aprigliano, Rossana, Gattiker, Cristina, Palibrk, Vuk, Markkanen, Enni, Backe, Paul Hoff, Pellegrino, Stefania, Raymond, F. Lucy, Froyen, Guy, Altmeyer, Matthias, Bjørås, Magnar, Dianov, Grigory L., Loon, Barbara van
Publicado 2018

Standardization of Somatic Variant Classifications in Solid and Haematological Tumours by a Two-Level Approach of Biological and Clinical Classes: An Initiative of the Belgian ComP...

por Froyen, Guy, Le Mercier, Marie, Lierman, Els, Vandepoele, Karl, Nollet, Friedel, Boone, Elke, Van der Meulen, Joni, Jacobs, Koen, Lambin, Suzan, Vander Borght, Sara, Van Valckenborgh, Els, Antoniou, Aline, Hébrant, Aline
Publicado 2019

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

por 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
Publicado 2014

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

por 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
Publicado 2013