Intellectual disability-associated disruption of O-GlcNAc cycling impairs habituation learning in Drosophila
Fenckova, Michaela, Muha, Villo, Mariappa, Daniel, Catinozzi, Marica, Czajewski, Ignacy, Blok, Laura E R, Ferenbach, Andrew T, Storkebaum, Erik, Schenck, Annette, van Aalten, Daan M F
Published in PLoS genetics (02.05.2022)
Published in PLoS genetics (02.05.2022)
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Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila
Castells-Nobau, Anna, Eidhof, Ilse, Fenckova, Michaela, Brenman-Suttner, Dova B, Scheffer-de Gooyert, Jolanda M, Christine, Sheren, Schellevis, Rosa L, van der Laan, Kiran, Quentin, Christine, van Ninhuijs, Lisa, Hofmann, Falko, Ejsmont, Radoslaw, Fisher, Simon E, Kramer, Jamie M, Sigrist, Stephan J, Simon, Anne F, Schenck, Annette
Published in PloS one (12.02.2019)
Published in PloS one (12.02.2019)
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BOD1 Is Required for Cognitive Function in Humans and Drosophila
Esmaeeli-Nieh, Sahar, Fenckova, Michaela, Porter, Iain M, Motazacker, M Mahdi, Nijhof, Bonnie, Castells-Nobau, Anna, Asztalos, Zoltan, Weißmann, Robert, Behjati, Farkhondeh, Tzschach, Andreas, Felbor, Ute, Scherthan, Harry, Sayfati, Seyed Morteza, Ropers, H Hilger, Kahrizi, Kimia, Najmabadi, Hossein, Swedlow, Jason R, Schenck, Annette, Kuss, Andreas W
Published in PLoS genetics (11.05.2016)
Published in PLoS genetics (11.05.2016)
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KDM5-mediated transcriptional activation of ribosomal protein genes alters translation efficiency to regulate mitochondrial metabolism in neurons
Yheskel, Matanel, Hatch, Hayden A M, Pedrosa, Erika, Terry, Bethany K, Siebels, Aubrey A, Zheng, Xiang Yu, Blok, Laura E R, Fencková, Michaela, Sidoli, Simone, Schenck, Annette, Zheng, Deyou, Lachman, Herbert M, Secombe, Julie
Published in Nucleic acids research (10.04.2024)
Published in Nucleic acids research (10.04.2024)
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Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules
Kochinke, Korinna, Zweier, Christiane, Nijhof, Bonnie, Fenckova, Michaela, Cizek, Pavel, Honti, Frank, Keerthikumar, Shivakumar, Oortveld, Merel A.W., Kleefstra, Tjitske, Kramer, Jamie M., Webber, Caleb, Huynen, Martijn A., Schenck, Annette
Published in American journal of human genetics (07.01.2016)
Published in American journal of human genetics (07.01.2016)
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From Rare Copy Number Variants to Biological Processes in ADHD
Harich, Benjamin, van der Voet, Monique, Klein, Marieke, Čížek, Pavel, Fenckova, Michaela, Schenck, Annette, Franke, Barbara
Published in The American journal of psychiatry (01.09.2020)
Published in The American journal of psychiatry (01.09.2020)
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Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Stessman, Holly A F, Xiong, Bo, Coe, Bradley P, Wang, Tianyun, Hoekzema, Kendra, Fenckova, Michaela, Kvarnung, Malin, Gerdts, Jennifer, Trinh, Sandy, Cosemans, Nele, Vives, Laura, Lin, Janice, Turner, Tychele N, Santen, Gijs, Ruivenkamp, Claudia, Kriek, Marjolein, van Haeringen, Arie, Aten, Emmelien, Friend, Kathryn, Liebelt, Jan, Barnett, Christopher, Haan, Eric, Shaw, Marie, Gecz, Jozef, Anderlid, Britt-Marie, Nordgren, Ann, Lindstrand, Anna, Schwartz, Charles, Kooy, R Frank, Vandeweyer, Geert, Helsmoortel, Celine, Romano, Corrado, Alberti, Antonino, Vinci, Mirella, Avola, Emanuela, Giusto, Stefania, Courchesne, Eric, Pramparo, Tiziano, Pierce, Karen, Nalabolu, Srinivasa, Amaral, David G, Scheffer, Ingrid E, Delatycki, Martin B, Lockhart, Paul J, Hormozdiari, Fereydoun, Harich, Benjamin, Castells-Nobau, Anna, Xia, Kun, Peeters, Hilde, Nordenskjöld, Magnus, Schenck, Annette, Bernier, Raphael A, Eichler, Evan E
Published in Nature genetics (01.04.2017)
Published in Nature genetics (01.04.2017)
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Habituation Learning Is a Widely Affected Mechanism in Drosophila Models of Intellectual Disability and Autism Spectrum Disorders
Fenckova, Michaela, Blok, Laura E.R., Asztalos, Lenke, Goodman, David P., Cizek, Pavel, Singgih, Euginia L., Glennon, Jeffrey C., IntHout, Joanna, Zweier, Christiane, Eichler, Evan E., von Reyn, Catherine R., Bernier, Raphael A., Asztalos, Zoltan, Schenck, Annette
Published in Biological psychiatry (1969) (15.08.2019)
Published in Biological psychiatry (1969) (15.08.2019)
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Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder
Koemans, Tom S, Kleefstra, Tjitske, Chubak, Melissa C, Stone, Max H, Reijnders, Margot R F, de Munnik, Sonja, Willemsen, Marjolein H, Fenckova, Michaela, Stumpel, Connie T R M, Bok, Levinus A, Sifuentes Saenz, Margarita, Byerly, Kyna A, Baughn, Linda B, Stegmann, Alexander P A, Pfundt, Rolph, Zhou, Huiqing, van Bokhoven, Hans, Schenck, Annette, Kramer, Jamie M
Published in PLoS genetics (25.10.2017)
Published in PLoS genetics (25.10.2017)
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Disruption of an EHMT1-Associated Chromatin-Modification Module Causes Intellectual Disability
Kleefstra, Tjitske, Kramer, Jamie M., Neveling, Kornelia, Willemsen, Marjolein H., Koemans, Tom S., Vissers, Lisenka E.L.M., Wissink-Lindhout, Willemijn, Fenckova, Michaela, van den Akker, Willem M.R., Kasri, Nael Nadif, Nillesen, Willy M., Prescott, Trine, Clark, Robin D., Devriendt, Koenraad, van Reeuwijk, Jeroen, de Brouwer, Arjan P.M., Gilissen, Christian, Zhou, Huiqing, Brunner, Han G., Veltman, Joris A., Schenck, Annette, van Bokhoven, Hans
Published in American journal of human genetics (13.07.2012)
Published in American journal of human genetics (13.07.2012)
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Neuroinformatic analyses of common and distinct genetic components associated with major neuropsychiatric disorders
Lotan, Amit, Fenckova, Michaela, Bralten, Janita, Alttoa, Aet, Dixson, Luanna, Williams, Robert W, van der Voet, Monique
Published in Frontiers in neuroscience (06.11.2014)
Published in Frontiers in neuroscience (06.11.2014)
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Journal Article
GATAD2B loss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth in Drosophila
Willemsen, Marjolein H, Nijhof, Bonnie, Fenckova, Michaela, Nillesen, Willy M, Bongers, Ernie M H F, Castells-Nobau, Anna, Asztalos, Lenke, Viragh, Erika, van Bon, Bregje W M, Tezel, Emre, Veltman, Joris A, Brunner, Han G, de Vries, Bert B A, de Ligt, Joep, Yntema, Helger G, van Bokhoven, Hans, Isidor, Bertrand, Le Caignec, Cédric, Lorino, Elsa, Asztalos, Zoltan, Koolen, David A, Vissers, Lisenka E L M, Schenck, Annette, Kleefstra, Tjitske
Published in Journal of medical genetics (01.08.2013)
Published in Journal of medical genetics (01.08.2013)
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Increased extracellular adenosine in Drosophila that are deficient in adenosine deaminase activates a release of energy stores leading to wasting and death
Zuberova, Monika, Fenckova, Michaela, Simek, Petr, Janeckova, Lucie, Dolezal, Tomas
Published in Disease models & mechanisms (01.11.2010)
Published in Disease models & mechanisms (01.11.2010)
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CEP89 is required for mitochondrial metabolism and neuronal function in man and fly
van Bon, Bregje W M, Oortveld, Merel A W, Nijtmans, Leo G, Fenckova, Michaela, Nijhof, Bonnie, Besseling, Judith, Vos, Melissa, Kramer, Jamie M, de Leeuw, Nicole, Castells-Nobau, Anna, Asztalos, Lenke, Viragh, Erika, Ruiter, Mariken, Hofmann, Falko, Eshuis, Lillian, Collavin, Licio, Huynen, Martijn A, Asztalos, Zoltan, Verstreken, Patrik, Rodenburg, Richard J, Smeitink, Jan A, de Vries, Bert B A, Schenck, Annette
Published in Human molecular genetics (01.08.2013)
Published in Human molecular genetics (01.08.2013)
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