Found: 5

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  • Association of Bone Morphogenetic Proteins With Otosclerosis.

    Published in:
    Journal of Bone & Mineral Research, 2008, v. 23, n. 4, p. 507, doi. 10.1359/JBMR.071112
    By:
    • Schrauwen, Isabelle;
    • Thys, Melissa;
    • Vanderstraeten, Kathleen;
    • Fransen, Erik;
    • Dieltjens, Nele;
    • Huyghe, Jeroen R.;
    • Ealy, Megan;
    • Claustres, Mireille;
    • Cremers, Cor R. W. J.;
    • Dhooge, Ingeborg;
    • Declau, Frank;
    • Van De Heyning, Paul;
    • Vincent, Robert;
    • Somers, Thomas;
    • Offeciers, Erwin;
    • Smith, Richard J. H.;
    • Van Camp, Guy
    Publication type:
    Article

  • Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations.

    Published in:
    Human Genetics, 2010, v. 127, n. 2, p. 155, doi. 10.1007/s00439-009-0754-2
    By:
    • Schrauwen, Isabelle;
    • Ealy, Megan;
    • Fransen, Erik;
    • Vanderstraeten, Kathleen;
    • Thys, Melissa;
    • Meyer, Nicole C.;
    • Cosgarea, Marcel;
    • Huber, Alex;
    • Mazzoli, Manuela;
    • Pfister, Markus;
    • Smith, Richard J. H.;
    • Van Camp, Guy
    Publication type:
    Article

  • A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9.

    Published in:
    Human Genetics, 2008, v. 123, n. 3, p. 267, doi. 10.1007/s00439-008-0470-3
    By:
    • Ali, Insaf Bel Hadj;
    • Thys, Melissa;
    • Beltaief, Najeh;
    • Schrauwen, Isabelle;
    • Hilgert, Nele;
    • Vanderstraeten, Kathleen;
    • Dieltjens, Nele;
    • Mnif, Emna;
    • Hachicha, Slah;
    • Besbes, Ghazi;
    • Arab, Saïda Ben;
    • Van Camp, Guy
    Publication type:
    Article

  • A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13–16.1.

    Published in:
    European Journal of Human Genetics, 2007, v. 15, n. 3, p. 362, doi. 10.1038/sj.ejhg.5201761
    By:
    • Thys, Melissa;
    • Van Den Bogaert, Kris;
    • Iliadou, Vassiliki;
    • Vanderstraeten, Kathleen;
    • Dieltjens, Nele;
    • Schrauwen, Isabelle;
    • Chen, Wenjie;
    • Eleftheriades, Nikolaos;
    • Grigoriadou, Maria;
    • Pauw, Robert Jan;
    • Cremers, Cor R. W. J.;
    • Smith, Richard J. H.;
    • Petersen, Michael B.;
    • Van Camp, Guy
    Publication type:
    Article

  • The coding polymorphism T263I in TGF-β1 is associated with otosclerosis in two independent populations.

    Published in:
    Human Molecular Genetics, 2007, v. 16, n. 17, p. 2021, doi. 10.1093/hmg/ddm150
    By:
    • Thys, Melissa;
    • Schrauwen, Isabelle;
    • Vanderstraeten, Kathleen;
    • Janssens, Katrien;
    • Dieltjens, Nele;
    • Van Den Bogaert, Kris;
    • Fransen, Erik;
    • Chen, Wenjie;
    • Ealy, Megan;
    • Claustres, Mireille;
    • Cremers, Cor R.W.J.;
    • Dhooge, Ingeborg;
    • Declau, Frank;
    • Claes, Jos;
    • Van de Heyning, Paul;
    • Vincent, Robert;
    • Somers, Thomas;
    • Offeciers, Erwin;
    • Smith, Richard J.H.;
    • Van Camp, Guy
    Publication type:
    Article