Works by Schenck, Annette

Results: 36

Epigenetic Regulation of Learning and Memory by Drosophila EHMT/G9a.

Published in:

PLoS Biology, 2011, v. 9, n. 1, p. 1, doi. 10.1371/journal.pbio.1000569

By:

Kramer, Jamie M.;
Kochinke, Korinna;
Oortveld, Merel A. W.;
Marks, Hendrik;
Kramer, Daniela;
de Jong, Eiko K.;
Asztalos, Zoltan;
Westwood, J. Timothy;
Stunnenberg, Hendrik G.;
Sokolowski, Marla B.;
Keleman, Krystyna;
Huiqing Zhou;
van Bokhoven, Hans;
Schenck, Annette

Publication type:

Article

Growth, body composition, and endocrine‐metabolic profiles of individuals with Kleefstra syndrome provide directions for clinical management and translational studies.

Published in:

American Journal of Medical Genetics. Part A, 2024, v. 194, n. 5, p. 1, doi. 10.1002/ajmg.a.63472

By:

Bouman, Arianne;
Geelen, Joyce M.;
Kummeling, Joost;
Schenck, Annette;
van der Zwan, Yvonne G.;
Klein, Willemijn M.;
Kleefstra, Tjitske

Publication type:

Article

Phosphorylation of WAVE1 regulates actin polymerization and dendritic spine morphology.

Published in:

Nature, 2006, v. 442, n. 7104, p. 814, doi. 10.1038/nature04976

By:

Yong Kim;
Jee Young Sung;
Ceglia, Ilaria;
Ko-Woon Lee;
Jung-Hyuck Ahn;
Halford, Jonathan M.;
Kim, Amie M.;
Kwak, Seung P.;
Jong Bae Park;
Sung Ho Ryu;
Schenck, Annette;
Bardoni, Barbara;
Scott, John D.;
Nairn, Angus C.;
Greengard, Paul

Publication type:

Article

Human Intellectual Disability Genes Form Conserved Functional Modules in <i>Drosophila</i>.

Published in:

PLoS Genetics, 2013, v. 9, n. 10, p. 1, doi. 10.1371/journal.pgen.1003911

By:

Oortveld, Merel A. W.;
Keerthikumar, Shivakumar;
Oti, Martin;
Nijhof, Bonnie;
Fernandes, Ana Clara;
Kochinke, Korinna;
Castells-Nobau, Anna;
van Engelen, Eva;
Ellenkamp, Thijs;
Eshuis, Lilian;
Galy, Anne;
van Bokhoven, Hans;
Habermann, Bianca;
Brunner, Han G.;
Zweier, Christiane;
Verstreken, Patrik;
Huynen, Martijn A.;
Schenck, Annette

Publication type:

Article

The histone methyltransferase G9a regulates tolerance to oxidative stress–induced energy consumption.

Published in:

PLoS Biology, 2019, v. 17, n. 3, p. 1, doi. 10.1371/journal.pbio.2006146

By:

Riahi, Human;
Brekelmans, Carlijn;
Foriel, Sarah;
Merkling, Sarah H.;
Lyons, Taylor A.;
Itskov, Pavel M.;
Kleefstra, Tjitske;
Ribeiro, Carlos;
van Rij, Ronald P.;
Kramer, Jamie M.;
Schenck, Annette

Publication type:

Article

FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 6, p. 835, doi. 10.1093/hmg/ddi077

By:

Castets, Marie;
Schaeffer, Céline;
Bechara, Elias;
Schenck, Annette;
Khandjian, Edward W.;
Luche, Sylvie;
Moine, Hervé;
Rabilloud, Thierry;
Mandel, Jean-Louis;
Bardoni, Barbara

Publication type:

Article

82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 14, p. 1689, doi. 10.1093/hmg/ddg181

By:

Bardoni, Barbara;
Castets, Marie;
Huot, Marc-Etienne;
Schenck, Annette;
Adinolfi, Salvatore;
Corbin, François;
Pastore, Annalisa;
Khandjian, Edouard W.;
Mandel, Jean-Louis

Publication type:

Article

A novel RNA-binding nuclear protein that interacts with the frgile X mental retardation (FMR1) protein.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 13, p. 2557, doi. 10.1093/hmg/8.13.2557

By:

Bardoni, Barbara;
Schenck, Annette;
Mandel, Jean Louise

Publication type:

Article

Converging evidence does not support GIT1 as an ADHD risk gene.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 6, p. 492, doi. 10.1002/ajmg.b.32327

By:

Klein, Marieke;
van der Voet, Monique;
Harich, Benjamin;
van Hulzen, Kimm J. E.;
Onnink, A. Marten H.;
Hoogman, Martine;
Guadalupe, Tulio;
Zwiers, Marcel;
Groothuismink, Johanne M.;
Verberkt, Alicia;
Nijhof, Bonnie;
Castells‐Nobau, Anna;
Faraone, Stephen V.;
Buitelaar, Jan K.;
Schenck, Annette;
Arias‐Vasquez, Alejandro;
Franke, Barbara

Publication type:

Article

The epigenetic regulator G9a attenuates stress-induced resistance and metabolic transcriptional programs across different stressors and species.

Published in:

BMC Biology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s12915-021-01025-0

By:

Riahi, Human;
Fenckova, Michaela;
Goruk, Kayla J.;
Schenck, Annette;
Kramer, Jamie M.

Publication type:

Article

BOD1 Is Required for Cognitive Function in Humans and Drosophila.

Published in:

PLoS Genetics, 2016, v. 12, n. 5, p. 1, doi. 10.1371/journal.pgen.1006022

By:

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.

Publication type:

Article

Restoring polyamines protects from age-induced memory impairment in an autophagy-dependent manner.

Published in:

Nature Neuroscience, 2013, v. 16, n. 10, p. 1453, doi. 10.1038/nn.3512

By:

Gupta, Varun K;
Scheunemann, Lisa;
Eisenberg, Tobias;
Mertel, Sara;
Bhukel, Anuradha;
Koemans, Tom S;
Kramer, Jamie M;
Liu, Karen S Y;
Schroeder, Sabrina;
Stunnenberg, Hendrik G;
Sinner, Frank;
Magnes, Christoph;
Pieber, Thomas R;
Dipt, Shubham;
Fiala, André;
Schenck, Annette;
Schwaerzel, Martin;
Madeo, Frank;
Sigrist, Stephan J

Publication type:

Article

The Epigenetic Regulator G9a Mediates Tolerance to RNA Virus Infection in Drosophila.

Published in:

PLoS Pathogens, 2015, v. 11, n. 4, p. 1, doi. 10.1371/journal.ppat.1004692

By:

Merkling, Sarah H.;
Bronkhorst, Alfred W.;
Overheul, Gijs J.;
Van Rij, Ronald P.;
Kramer, Jamie M.;
Schenck, Annette

Publication type:

Article

Investigating cytosolic 5′-nucleotidase II family genes as candidates for neuropsychiatric disorders in Drosophila (114/150 chr).

Published in:

Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-020-01149-x

By:

Singgih, Euginia L.;
van der Voet, Monique;
Schimmel-Naber, Marlies;
Brinkmann, Emma L.;
Schenck, Annette;
Franke, Barbara

Publication type:

Article

Peroxisome-associated Sgroppino links fat metabolism with survival after RNA virus infection in Drosophila.

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-38559-x

By:

Merkling, Sarah H.;
Riahi, Human;
Overheul, Gijs J.;
Schenck, Annette;
van Rij, Ronald P.

Publication type:

Article

Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila.

Published in:

PLoS ONE, 2019, v. 14, n. 2, p. 1, doi. 10.1371/journal.pone.0211652

By:

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

Publication type:

Article

Intellectual disability-associated disruption of O-GlcNAc cycling impairs habituation learning in Drosophila.

Published in:

PLoS Genetics, 2022, v. 18, n. 5, p. 1, doi. 10.1371/journal.pgen.1010159

By:

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.

Publication type:

Article

A New Fiji-Based Algorithm That Systematically Quantifies Nine Synaptic Parameters Provides Insights into Drosophila NMJ Morphometry.

Published in:

PLoS Computational Biology, 2016, v. 12, n. 3, p. 1, doi. 10.1371/journal.pcbi.1004823

By:

Nijhof, Bonnie;
Castells-Nobau, Anna;
Wolf, Louis;
Scheffer-de Gooyert, Jolanda M.;
Monedero, Ignacio;
Torroja, Laura;
Coromina, Lluis;
van der Laak, Jeroen A. W. M.;
Schenck, Annette

Publication type:

Article

CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation.

Published in:

Human Genetics, 2010, v. 128, n. 3, p. 281, doi. 10.1007/s00439-010-0848-x

By:

Mukhopadhyay, Arijit;
Kramer, Jamie M.;
Merkx, Gerard;
Lugtenberg, Dorien;
Smeets, Dominique F.;
Oortveld, Merel A. W.;
Blokland, Ellen A.W.;
Agrawal, Jyoti;
Schenck, Annette;
van Bokhoven, Hans;
Huys, Erik;
Schoenmakers, Eric F.;
van Kessel, Ad Geurts;
van Nouhuys, C. Erik;
Cremers, Frans P. M.

Publication type:

Article

KDM5-mediated transcriptional activation of ribosomal protein genes alters translation efficiency to regulate mitochondrial metabolism in neurons.

Published in:

Nucleic Acids Research, 2024, v. 52, n. 11, p. 6201, doi. 10.1093/nar/gkae261

By:

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

Publication type:

Article

HSPC300 and its role in neuronal connectivity.

Published in:

Neural Development, 2007, v. 2, p. 18, doi. 10.1186/1749-8104-2-18

By:

Qurashi, Abrar;
Sahin, H. Bahar;
Carrera, Pilar;
Gautreau, Alexis;
Schenck, Annette;
Giangrande, Angela

Publication type:

Article

Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxia.

Published in:

2021

By:

Rebelo, Adriana P;
Eidhof, Ilse;
Cintra, Vivian P;
Guillot-Noel, Léna;
Pereira, Claudia V;
Timmann, Dagmar;
Traschütz, Andreas;
Schöls, Ludger;
Coarelli, Giulia;
Durr, Alexandra;
Anheim, Mathieu;
Tranchant, Christine;
van de Warrenburg, Bart;
Guissart, Claire;
Koenig, Michel;
Howell, Jack;
Moraes, Carlos T;
Schenck, Annette;
Stevanin, Giovanni;
Züchner, Stephan

Publication type:

journal article

Reply: A homozygous GDAP2 loss-of-function variant in a patient with adult-onset cerebellar ataxia; and Novel GDAP2 pathogenic variants cause autosomal recessive spinocerebellar ataxia-27 (SCAR27) in a Chinese family.

Published in:

2020

By:

Eidhof, Ilse;
Baets, Jonathan;
Kamsteeg, Erik-Jan;
Schenck, Annette;
Warrenburg, Bart P van de;
van de Warrenburg, Bart P

Publication type:

Letter

GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxia.

Published in:

2018

By:

Eidhof, Ilse;
Baets, Jonathan;
Kamsteeg, Erik-Jan;
Deconinck, Tine;
Ninhuijs, Lisa van;
Martin, Jean-Jacques;
Schüle, Rebecca;
Züchner, Stephan;
Jonghe, Peter De;
Schenck, Annette;
van Ninhuijs, Lisa;
De Jonghe, Peter;
van de Warrenburg, Bart P

Publication type:

journal article

Protein complexes containing CYFIP/Sra/PIR121 coordinate Arf1 and Rac1 signalling during clathrin–AP-1-coated carrier biogenesis at the TGN.

Published in:

2010

By:

Anitei, Mihaela;
Stange, Christoph;
Parshina, Irina;
Baust, Thorsten;
Schenck, Annette;
Raposo, Graça;
Kirchhausen, Tomas;
Hoflack, Bernard

Publication type:

Correction Notice

Protein complexes containing CYFIP/Sra/PIR121 coordinate Arf1 and Rac1 signalling during clathrin–AP-1-coated carrier biogenesis at the TGN.

Published in:

Nature Cell Biology, 2010, v. 12, n. 4, p. 330, doi. 10.1038/ncb2034

By:

Anitei, Mihaela;
Stange, Christoph;
Parshina, Irina;
Baust, Thorsten;
Schenck, Annette;
Raposo, Graça;
Kirchhausen, Tomas;
Hoflack, Bernard

Publication type:

Article

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

Published in:

PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0081791

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

Publication type:

Article

Analysis of Adhesion Molecules and Basement Membrane Contributions to Synaptic Adhesion at the Drosophila Embryonic NMJ.

Published in:

PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0036339

By:

Koper, Andre;
Schenck, Annette;
Prokop, Andreas

Publication type:

Article

Ataxia-associated DNA repair genes protect the Drosophila mushroom body and locomotor function against glutamate signaling-associated damage.

Published in:

Frontiers in Neural Circuits, 2023, p. 1, doi. 10.3389/fncir.2023.1148947

By:

Eidhof, Ilse;
Krebbers, Alina;
van de Warrenburg, Bart;
Schenck, Annette

Publication type:

Article

Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder.

Published in:

PLoS Genetics, 2017, v. 13, n. 10, p. 1, doi. 10.1371/journal.pgen.1006864

By:

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.

Publication type:

Article

Altered GPM6A/M6 Dosage Impairs Cognition and Causes Phenotypes Responsive to Cholesterol in Human and Drosophila.

Published in:

Human Mutation, 2014, v. 35, n. 12, p. 1495, doi. 10.1002/humu.22697

By:

Gregor, Anne;
Kramer, Jamie M.;
Voet, Monique;
Schanze, Ina;
Uebe, Steffen;
Donders, Rogier;
Reis, André;
Schenck, Annette;
Zweier, Christiane

Publication type:

Article

Genome sequencing identifies major causes of severe intellectual disability.

Published in:

Nature, 2014, v. 511, n. 7509, p. 344, doi. 10.1038/nature13394

By:

Gilissen, Christian;
Hehir-Kwa, Jayne Y.;
Thung, Djie Tjwan;
van de Vorst, Maartje;
van Bon, Bregje W. M.;
Willemsen, Marjolein H.;
Kwint, Michael;
Janssen, Irene M.;
Hoischen, Alexander;
Schenck, Annette;
Leach, Richard;
Klein, Robert;
Tearle, Rick;
Bo, Tan;
Pfundt, Rolph;
Yntema, Helger G.;
de Vries, Bert B. A.;
Kleefstra, Tjitske;
Brunner, Han G.;
Vissers, Lisenka E. L. M.

Publication type:

Article

From man to fly – convergent evidence links FBXO25 to ADHD and comorbid psychiatric phenotypes.

Published in:

Journal of Child Psychology & Psychiatry, 2020, v. 61, n. 5, p. 545, doi. 10.1111/jcpp.13161

By:

Harich, Benjamin;
Klein, Marieke;
Ockeloen, Charlotte W.;
Voet, Monique;
Schimmel‐Naber, Marlies;
Leeuw, Nicole;
Schenck, Annette;
Franke, Barbara

Publication type:

Article

A Drosophila Mitochondrial Complex I Deficiency Phenotype Array.

Published in:

Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00245

By:

Foriel, Sarah;
Renkema, G. Herma;
Lasarzewski, Yvonne;
Berkhout, Job;
Rodenburg, Richard J.;
Smeitink, Jan A. M.;
Beyrath, Julien;
Schenck, Annette

Publication type:

Article

SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 12, p. 2257, doi. 10.1093/hmg/ddp161

By:

Cliffe, Simon T.;
Kramer, Jamie M.;
Hussain, Khalid;
Robben, Joris H.;
de Jong, Eiko K.;
de Brouwer, Arjan P.;
Nibbeling, Esther;
Kamsteeg, Erik-Jan;
Wong, Melanie;
Prendiville, Julie;
James, Chela;
Padidela, Raja;
Becknell, Charlie;
van Bokhoven, Hans;
Deen, Peter M.T.;
Hennekam, Raoul C.M.;
Lindeman, Robert;
Schenck, Annette;
Roscioli, Tony;
Buckley, Michael F.

Publication type:

Article

CYFIP2 is highly abundant in CD4.

Published in:

European Journal of Immunology, 2004, v. 34, n. 4, p. 1217, doi. 10.1002/eji.200324726

By:

Mayne, Michael;
Moffatt, Teri;
Kong, Hong;
McLaren, Paul J.;
Fowke, Keith R.;
Becker, Kevin G.;
Namaka, Mike;
Schenck, Annette;
Bardoni, Barbara;
Bernstein, Charles N.;
Melanson, Maria

Publication type:

Article