Works by Selloum, Mohammed


Results: 17
    1

    The Rogdi knockout mouse is a model for Kohlschütter–Tönz syndrome.

    Published in:
    Scientific Reports, 2024, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-50870-2
    By:
    • Jimenez-Armijo, Alexandra;
    • Morkmued, Supawich;
    • Ahumada, José Tomás;
    • Kharouf, Naji;
    • de Feraudy, Yvan;
    • Gogl, Gergo;
    • Riet, Fabrice;
    • Niederreither, Karen;
    • Laporte, Jocelyn;
    • Birling, Marie Christine;
    • Selloum, Mohammed;
    • Herault, Yann;
    • Hernandez, Magali;
    • Bloch-Zupan, Agnès
    Publication type:
    Article
    2

    Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models.

    Published in:
    Biomedicines, 2022, v. 10, n. 12, p. 3148, doi. 10.3390/biomedicines10123148
    By:
    • Meziane, Hamid;
    • Birling, Marie-Christine;
    • Wendling, Olivia;
    • Leblanc, Sophie;
    • Dubos, Aline;
    • Selloum, Mohammed;
    • Pavlovic, Guillaume;
    • Sorg, Tania;
    • Kalscheuer, Vera M.;
    • Billuart, Pierre;
    • Laumonnier, Frédéric;
    • Chelly, Jamel;
    • van Bokhoven, Hans;
    • Herault, Yann
    Publication type:
    Article
    3
    4

    A new mouse model of ARX dup24 recapitulates the patients behavioral and fine motor alterations.

    Published in:
    Human Molecular Genetics, 2018, v. 27, n. 12, p. 2138, doi. 10.1093/hmg/ddy122
    By:
    • Dubos, Aline;
    • Meziane, Hamid;
    • Iacono, Giovanni;
    • Curie, Aurore;
    • Riet, Fabrice;
    • Martin, Christelle;
    • Loaëc, Nade'ge;
    • Birling, Marie-Christine;
    • Selloum, Mohammed;
    • Normand, Elisabeth;
    • Pavlovic, Guillaume;
    • Sorg, Tania;
    • Stunnenberg, Henk G.;
    • Chelly, Jamel;
    • Humeau, Yann;
    • Friocourt, Gaë lle;
    • Hérault, Yann
    Publication type:
    Article
    5

    Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein.

    Published in:
    Genome Biology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s13059-023-03092-8
    By:
    • Kretz, Perrine F.;
    • Wagner, Christel;
    • Mikhaleva, Anna;
    • Montillot, Charlotte;
    • Hugel, Sylvain;
    • Morella, Ilaria;
    • Kannan, Meghna;
    • Fischer, Marie-Christine;
    • Milhau, Maxence;
    • Yalcin, Ipek;
    • Brambilla, Riccardo;
    • Selloum, Mohammed;
    • Herault, Yann;
    • Reymond, Alexandre;
    • Collins, Stephan C.;
    • Yalcin, Binnaz
    Publication type:
    Article
    6

    Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition.

    Published in:
    PLoS Genetics, 2017, v. 13, n. 7, p. 1, doi. 10.1371/journal.pgen.1006886
    By:
    • Arbogast, Thomas;
    • Iacono, Giovanni;
    • Chevalier, Claire;
    • Afinowi, Nurudeen O.;
    • Houbaert, Xander;
    • van Eede, Matthijs C.;
    • Laliberte, Christine;
    • Birling, Marie-Christine;
    • Linda, Katrin;
    • Meziane, Hamid;
    • Selloum, Mohammed;
    • Sorg, Tania;
    • Nadif Kasri, Nael;
    • Koolen, David A.;
    • Stunnenberg, Henk G.;
    • Henkelman, R. Mark;
    • Kopanitsa, Maksym;
    • Humeau, Yann;
    • De Vries, Bert B. A.;
    • Herault, Yann
    Publication type:
    Article
    7

    Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome.

    Published in:
    PLoS Genetics, 2021, v. 17, n. 9, p. 1, doi. 10.1371/journal.pgen.1009777
    By:
    • Brault, Véronique;
    • Nguyen, Thu Lan;
    • Flores-Gutiérrez, Javier;
    • Iacono, Giovanni;
    • Birling, Marie-Christine;
    • Lalanne, Valérie;
    • Meziane, Hamid;
    • Manousopoulou, Antigoni;
    • Pavlovic, Guillaume;
    • Lindner, Loïc;
    • Selloum, Mohammed;
    • Sorg, Tania;
    • Yu, Eugene;
    • Garbis, Spiros D.;
    • Hérault, Yann
    Publication type:
    Article
    8
    9
    10

    Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disability.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 11, p. 2314, doi. 10.1093/hmg/ddw102
    By:
    • Meziane, Hamid;
    • Khelfaoui, Malik;
    • Morello, Noemi;
    • Hiba, Bassem;
    • Calcagno, Eleonora;
    • Reibel-Foisset, Sophie;
    • Selloum, Mohammed;
    • Chelly, Jamel;
    • Humeau, Yann;
    • Riet, Fabrice;
    • Zanni, Ginevra;
    • Herault, Yann;
    • Bienvenu, Thierry;
    • Giustetto, Maurizio;
    • Billuart, Pierre
    Publication type:
    Article
    11

    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
    12
    13

    BAHD1 haploinsufficiency results in anxiety-like phenotypes in male mice.

    Published in:
    PLoS ONE, 2020, v. 15, n. 5, p. 1, doi. 10.1371/journal.pone.0232789
    By:
    • Pourpre, Renaud;
    • Naudon, Laurent;
    • Meziane, Hamid;
    • Lakisic, Goran;
    • Jouneau, Luc;
    • Varet, Hugo;
    • Legendre, Rachel;
    • Wendling, Olivia;
    • Selloum, Mohammed;
    • Proux, Caroline;
    • Coppée, Jean-Yves;
    • Herault, Yann;
    • Bierne, Hélène
    Publication type:
    Article
    14

    INFRAFRONTIER quality principles in systemic phenotyping.

    Published in:
    Mammalian Genome, 2022, v. 33, n. 1, p. 120, doi. 10.1007/s00335-021-09892-2
    By:
    • Ehlich, Hilke;
    • Cater, Heather L.;
    • Flenniken, Ann M.;
    • Goncalves Da Cruz, Isabelle;
    • Mura, Anne-Marie;
    • Ntafis, Vasileios;
    • Raess, Michael;
    • Selloum, Mohammed;
    • Stoeger, Claudia;
    • Suchanova, Sarka;
    • Vuolteenaho, Reetta;
    • Brown, Steve D. M.;
    • Hérault, Yann;
    • Hinttala, Reetta;
    • Hrabě de Angelis, Martin;
    • Kollias, George;
    • Kontoyiannis, Dimitris L.;
    • Malissen, Bernard;
    • McKerlie, Colin;
    • Sedláček, Radislav
    Publication type:
    Article
    15

    Genetic background determines metabolic phenotypes in the mouse.

    Published in:
    Mammalian Genome, 2008, v. 19, n. 5, p. 318, doi. 10.1007/s00335-008-9107-z
    By:
    • Champy, Marie-France;
    • Selloum, Mohammed;
    • Zeitler, Valérie;
    • Caradec, Claudia;
    • Jung, Barbara;
    • Rousseau, Stéphane;
    • Pouilly, Laurent;
    • Sorg, Tania;
    • Auwerx, Johan
    Publication type:
    Article
    16
    17

    ProMetIS, deep phenotyping of mouse models by combined proteomics and metabolomics analysis.

    Published in:
    Scientific Data, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41597-021-01095-3
    By:
    • Imbert, Alyssa;
    • Rompais, Magali;
    • Selloum, Mohammed;
    • Castelli, Florence;
    • Mouton-Barbosa, Emmanuelle;
    • Brandolini-Bunlon, Marion;
    • Chu-Van, Emeline;
    • Joly, Charlotte;
    • Hirschler, Aurélie;
    • Roger, Pierrick;
    • Burger, Thomas;
    • Leblanc, Sophie;
    • Sorg, Tania;
    • Ouzia, Sadia;
    • Vandenbrouck, Yves;
    • Médigue, Claudine;
    • Junot, Christophe;
    • Ferro, Myriam;
    • Pujos-Guillot, Estelle;
    • de Peredo, Anne Gonzalez
    Publication type:
    Article