Works by Kramer, Jamie M.

Results: 24
    1

    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
    2

    Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.

    Published in:
    Nature Genetics, 2012, v. 44, n. 6, p. 639, doi. 10.1038/ng.2262
    By:
    • Koolen, David A;
    • Kramer, Jamie M;
    • Neveling, Kornelia;
    • Nillesen, Willy M;
    • Moore-Barton, Heather L;
    • Elmslie, Frances V;
    • Toutain, Annick;
    • Amiel, Jeanne;
    • Malan, Valérie;
    • Tsai, Anne Chun-Hui;
    • Cheung, Sau Wai;
    • Gilissen, Christian;
    • Verwiel, Eugene T P;
    • Martens, Sarah;
    • Feuth, Ton;
    • Bongers, Ernie M H F;
    • de Vries, Petra;
    • Scheffer, Hans;
    • Vissers, Lisenka E L M;
    • de Brouwer, Arjan P M
    Publication type:
    Article
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    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
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    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
    12
    13

    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
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    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
    18
    19

    Identification of a novel synaptic protein, TMTC3, involved in periventricular nodular heterotopia with intellectual disability and epilepsy.

    Published in:
    Human Molecular Genetics, 2017, v. 26, n. 21, p. 4278, doi. 10.1093/hmg/ddx316
    By:
    • Farhan, Sali M. K.;
    • Nixon, Kevin C. J.;
    • Everest, Michelle;
    • Edwards, Tara N.;
    • Long, Shirley;
    • Segal, Dmitri;
    • Knip, Maria J.;
    • Arts, Heleen H.;
    • Chakrabarti, Rana;
    • Jian Wang;
    • Robinson, John F.;
    • Lee, Donald;
    • Mirsattari, Seyed M.;
    • Rupar, C. Anthony;
    • Siu, Victoria M.;
    • Poulter, Michael O.;
    • Hegele, Robert A.;
    • Kramer, Jamie M.
    Publication type:
    Article
    20

    Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration.

    Published in:
    Human Molecular Genetics, 2015, v. 24, n. 23, p. 6736, doi. 10.1093/hmg/ddv380
    By:
    • Dubos, Aline;
    • Castells-Nobau, Anna;
    • Meziane, Hamid;
    • Oortveld, Merel A. W.;
    • Houbaert, Xander;
    • Iacono, Giovanni;
    • Martin, Christelle;
    • Mittelhaeuser, Christophe;
    • Lalanne, Valérie;
    • Kramer, Jamie M.;
    • Bhukel, Anuradha;
    • Quentin, Christine;
    • Slabbert, Jan;
    • Verstreken, Patrik;
    • Sigrist, Stefan J.;
    • Messaddeq, Nadia;
    • Birling, Marie-Christine;
    • Selloum, Mohammed;
    • Stunnenberg, Henk G.;
    • Humeau, Yann
    Publication type:
    Article
    21

    CEP89 is required for mitochondrial metabolism and neuronal function in man and fly.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 15, p. 3138, doi. 10.1093/hmg/ddt170
    By:
    • 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.
    Publication type:
    Article
    22

    Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 10, p. 1960, doi. 10.1093/hmg/ddt043
    By:
    • Iqbal, Zafar;
    • Vandeweyer, Geert;
    • van der Voet, Monique;
    • Waryah, Ali Muhammad;
    • Zahoor, Muhammad Yasir;
    • Besseling, Judith A.;
    • Roca, Laura Tomas;
    • Vulto-van Silfhout, Anneke T.;
    • Nijhof, Bonnie;
    • Kramer, Jamie M.;
    • Van der Aa, Nathalie;
    • Ansar, Muhammad;
    • Peeters, Hilde;
    • Helsmoortel, Céline;
    • Gilissen, Christian;
    • Vissers, Lisenka E. L. M.;
    • Veltman, Joris A.;
    • de Brouwer, Arjan P. M.;
    • Kooy, R. Frank;
    • Riazuddin, Sheikh
    Publication type:
    Article
    23

    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
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