Found: 3

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  • MYO9B polymorphisms in multiple sclerosis.

    Published in:
    European Journal of Human Genetics, 2009, v. 17, n. 6, p. 840, doi. 10.1038/ejhg.2008.251
    By:
    • Kemppinen, Anu;
    • Suvela, Minna;
    • Tienari, Pentti J.;
    • Elovaara, Irina;
    • Koivisto, Keijo;
    • Pirttilä, Tuula;
    • Reunanen, Mauri;
    • Rautakorpi, Ilkka;
    • Hillert, Jan;
    • Lundmark, Frida;
    • Oturai, Annette;
    • Ryder, Lars;
    • Harbo, Hanne F.;
    • Celius, Elisabeth G.;
    • Palotie, Aarno;
    • Daly, Mark;
    • Peltonen, Leena;
    • Saarela, Janna
    Publication type:
    Article

  • Increased Mutational Burden and Alterations to DNA Damage Repair Genes are Associated With Poor Prognosis and Sensitivity to PI3K-mTOR Inhibitors in Multiple Myeloma.

    Published in:
    Clinical Lymphoma, Myeloma & Leukemia, 2017, v. 17, p. e2, doi. 10.1016/j.clml.2017.03.004
    By:
    • Majumder, Muntasir Mamun;
    • Tamborero, David;
    • Anttila, Pekka;
    • Silvennoinen, Raija;
    • Lievonen, Juha;
    • Eldfors, Samuli;
    • Kumar, Ashwini;
    • Parsons, Alun;
    • Suvela, Minna;
    • Jantunen, Esa;
    • Porkka, Kimmo;
    • Heckman, Caroline
    Publication type:
    Article

  • Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 9, p. 1670, doi. 10.1093/hmg/ddp073
    By:
    • Kallio, Suvi P.;
    • Jakkula, Eveliina;
    • Purcell, Shaun;
    • Suvela, Minna;
    • Koivisto, Keijo;
    • Tienari, Pentti J.;
    • Elovaara, Irina;
    • Pirttilä, Tuula;
    • Reunanen, Mauri;
    • Bronnikov, Denis;
    • Viander, Markku;
    • Meri, Seppo;
    • Hillert, Jan;
    • Lundmark, Frida;
    • Harbo, Hanne F.;
    • Lorentzen, Åslaug R.;
    • De Jager, Philip L.;
    • Daly, Mark J.;
    • Hafler, David A.;
    • Palotie, Aarno
    Publication type:
    Article