Works matching IS 03406717 AND DT 2010 AND VI 127 AND IP 5

Results: 15
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    Analysis of the indel at the ARMS2 3′UTR in age-related macular degeneration.

    Published in:
    Human Genetics, 2010, v. 127, n. 5, p. 595, doi. 10.1007/s00439-010-0805-8
    By:
    • Gaofeng Wang;
    • Spencer, Kylee L.;
    • Scott, William K.;
    • Whitehead, Patrice;
    • Court, Brenda L.;
    • Ayala-Haedo, Juan;
    • Ping Mayo;
    • Schwartz, Stephen G.;
    • Kovach, Jaclyn L.;
    • Gallins, Paul;
    • Polk, Monica;
    • Agarwal, Anita;
    • Postel, Eric A.;
    • Haines, Jonathan L.;
    • Pericak-Vance, Margaret A.
    Publication type:
    Article
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    Kalirin: a novel genetic risk factor for ischemic stroke.

    Published in:
    Human Genetics, 2010, v. 127, n. 5, p. 513, doi. 10.1007/s00439-010-0790-y
    By:
    • Krug, Tiago;
    • Manso, Helena;
    • Gouveia, Liliana;
    • Sobral, João;
    • Xavier, Joana M.;
    • Albergaria, Isabel;
    • Gaspar, Gisela;
    • Correia, Manuel;
    • Viana-Baptista, Miguel;
    • Simões, Rita Moiron;
    • Pinto, Amélia Nogueira;
    • Taipa, Ricardo;
    • Ferreira, Carla;
    • Fontes, João Ramalho;
    • Silva, Mário Rui;
    • Gabriel, João Paulo;
    • Matos, Ilda;
    • Lopes, Gabriela;
    • Ferro, José M.;
    • Vicente, Astrid M.
    Publication type:
    Article
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    Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.

    Published in:
    Human Genetics, 2010, v. 127, n. 5, p. 525, doi. 10.1007/s00439-010-0789-4
    By:
    • Zuvich, Rebecca L.;
    • McCauley, Jacob L.;
    • Oksenberg, Jorge R.;
    • Sawcer, Stephen J.;
    • De Jager, Philip L.;
    • Aubin, Cristin;
    • Cross, Anne H.;
    • Piccio, Laura;
    • Aggarwal, Neelum T.;
    • Evans, Denis;
    • Hafler, David A.;
    • Compston, Alastair;
    • Hauser, Stephen L.;
    • Pericak-Vance, Margaret A.;
    • Haines, Jonathan L.
    Publication type:
    Article
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    Identification of 28 novel mutations in the Bardet–Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease.

    Published in:
    Human Genetics, 2010, v. 127, n. 5, p. 583, doi. 10.1007/s00439-010-0804-9
    By:
    • Muller, Jean;
    • Stoetzel, C.;
    • Vincent, M. C.;
    • Leitch, C. C.;
    • Laurier, V.;
    • Danse, J. M.;
    • Hellé, S.;
    • Marion, V.;
    • Bennouna-Greene, V.;
    • Vicaire, S.;
    • Megarbane, A.;
    • Kaplan, J.;
    • Drouin-Garraud, V.;
    • Hamdani, M.;
    • Sigaudy, S.;
    • Francannet, C.;
    • Roume, J.;
    • Bitoun, P.;
    • Goldenberg, A.;
    • Philip, N.
    Publication type:
    Article