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  • Integrative genetic analysis illuminates ALS heritability and identifies risk genes.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-022-35724-1
    By:
    • Megat, Salim;
    • Mora, Natalia;
    • Sanogo, Jason;
    • Roman, Olga;
    • Catanese, Alberto;
    • Alami, Najwa Ouali;
    • Freischmidt, Axel;
    • Mingaj, Xhuljana;
    • De Calbiac, Hortense;
    • Muratet, François;
    • Dirrig-Grosch, Sylvie;
    • Dieterle, Stéphane;
    • Van Bakel, Nick;
    • Müller, Kathrin;
    • Sieverding, Kirsten;
    • Weishaupt, Jochen;
    • Andersen, Peter Munch;
    • Weber, Markus;
    • Neuwirth, Christoph;
    • Margelisch, Markus
    Publication type:
    Article

  • Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes.

    Published in:
    2023
    By:
    • Megat, Salim;
    • Mora, Natalia;
    • Sanogo, Jason;
    • Roman, Olga;
    • Catanese, Alberto;
    • Alami, Najwa Ouali;
    • Freischmidt, Axel;
    • Mingaj, Xhuljana;
    • De Calbiac, Hortense;
    • Muratet, François;
    • Dirrig-Grosch, Sylvie;
    • Dieterle, Stéphane;
    • Van Bakel, Nick;
    • Müller, Kathrin;
    • Sieverding, Kirsten;
    • Weishaupt, Jochen;
    • Andersen, Peter Munch;
    • Weber, Markus;
    • Neuwirth, Christoph;
    • Margelisch, Markus
    Publication type:
    Correction Notice

  • Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by <italic>SHANK3</italic> point mutations.

    Published in:
    Molecular Autism, 2018, v. 9, n. 1, p. N.PAG, doi. 10.1186/s13229-018-0205-9
    By:
    • De Rubeis, Silvia;
    • Siper, Paige M.;
    • Durkin, Allison;
    • Weissman, Jordana;
    • Muratet, François;
    • Halpern, Danielle;
    • Trelles, Maria del Pilar;
    • Frank, Yitzchak;
    • Lozano, Reymundo;
    • Wang, A. Ting;
    • Holder, J. Lloyd;
    • Betancur, Catalina;
    • Buxbaum, Joseph D.;
    • Kolevzon, Alexander
    Publication type:
    Article

  • Prospective investigation of FOXP1 syndrome.

    Published in:
    Molecular Autism, 2017, v. 8, p. 1, doi. 10.1186/s13229-017-0172-6
    By:
    • Siper, Paige M.;
    • De Rubeis, Silvia;
    • del Pilar Trelles, Maria;
    • Durkin, Allison;
    • Di Marino, Daniele;
    • Muratet, François;
    • Frank, Yitzchak;
    • Lozano, Reymundo;
    • Eichler, Evan E.;
    • Kelly, Morgan;
    • Beighley, Jennifer;
    • Gerdts, Jennifer;
    • Wallace, Arianne S.;
    • Mefford, Heather C.;
    • Bernier, Raphael A.;
    • Kolevzon, Alexander;
    • Buxbaum, Joseph D.
    Publication type:
    Article