Works matching IS 09646906 AND DT 2009 AND VI 18 AND IP 6

Results: 22
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    Subscription Page.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 6, p. NP, doi. 10.1093/hmg/ddp097
    Publication type:
    Article
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    Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 6, p. 1110, doi. 10.1093/hmg/ddp008
    By:
    • Asai-Coakwell, Mika;
    • French, Curtis R.;
    • Ye, Ming;
    • Garcha, Kamal;
    • Bigot, Karin;
    • Perera, Anoja G.;
    • Staehling-Hampton, Karen;
    • Mema, Silvina C.;
    • Chanda, Bhaskar;
    • Mushegian, Arcady;
    • Bamforth, Steven;
    • Doschak, Michael R.;
    • Li, Guang;
    • Dobbs, Matthew B.;
    • Giampietro, Philip F.;
    • Brooks, Brian P.;
    • Vijayalakshmi, Perumalsamy;
    • Sauvé, Yves;
    • Abitbol, Marc;
    • Sundaresan, Periasamy
    Publication type:
    Article
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    Editorial Board.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 6, p. NP, doi. 10.1093/hmg/ddp096
    Publication type:
    Article
    10

    Evaluation of imputation-based association in and around the integrin-α-M (ITGAM) gene and replication of robust association between a non-synonymous functional variant within ITGAM and systemic lupus erythematosus (SLE).

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 6, p. 1171, doi. 10.1093/hmg/ddp007
    By:
    • Han, Shizhong;
    • Kim-Howard, Xana;
    • Deshmukh, Harshal;
    • Kamatani, Yoichiro;
    • Viswanathan, Parvathi;
    • Guthridge, Joel M.;
    • Thomas, Kenaz;
    • Kaufman, Kenneth M.;
    • Ojwang, Joshua;
    • Rojas-Villarraga, Adriana;
    • Baca, Vicente;
    • Orozco, Lorena;
    • Rhodes, Benjamin;
    • Choi, Chan-Bum;
    • Gregersen, Peter K.;
    • Merrill, Joan T.;
    • James, Judith A.;
    • Gaffney, Patrick M.;
    • Moser, Kathy L.;
    • Jacob, Chaim O.
    Publication type:
    Article
    11

    Association of ESR1 gene tagging SNPs with breast cancer risk.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 6, p. 1131, doi. 10.1093/hmg/ddn429
    By:
    • Dunning, Alison M.;
    • Healey, Catherine S.;
    • Baynes, Caroline;
    • Maia, Ana-Teresa;
    • Scollen, Serena;
    • Vega, Ana;
    • Rodríguez, Raquel;
    • Barbosa-Morais, Nuno L.;
    • Ponder, Bruce A.J.;
    • Low, Yen-Ling;
    • Bingham, Sheila;
    • Haiman, Christopher A.;
    • Le Marchand, Loic;
    • Broeks, Annegien;
    • Schmidt, Marjanka K.;
    • Hopper, John;
    • Southey, Melissa;
    • Beckmann, Matthias W.;
    • Fasching, Peter A.;
    • Peto, Julian
    Publication type:
    Article
    12

    Contents Page.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 6, p. NP, doi. 10.1093/hmg/ddp094
    Publication type:
    Article
    13

    Association study of the IL18RAP locus in three European populations with coeliac disease.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 6, p. 1148, doi. 10.1093/hmg/ddn438
    By:
    • Koskinen, Lotta L.E.;
    • Einarsdottir, Elisabet;
    • Dukes, Emma;
    • Heap, Graham A. R.;
    • Dubois, Patrick;
    • Korponay-Szabo, Ilma R.;
    • Kaukinen, Katri;
    • Kurppa, Kalle;
    • Ziberna, Fabiana;
    • Vatta, Serena;
    • Not, Tarcisio;
    • Ventura, Alessandro;
    • Sistonen, Pertti;
    • Ádány, Róza;
    • Pocsai, Zsuzsa;
    • Széles, György;
    • Mäki, Markku;
    • Kere, Juha;
    • Wijmenga, Cisca;
    • van Heel, David A.
    Publication type:
    Article
    14
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    Expansion of the human μ-opioid receptor gene architecture: novel functional variants.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 6, p. 1037, doi. 10.1093/hmg/ddn439
    By:
    • Shabalina, Svetlana A.;
    • Zaykin, Dmitri V.;
    • Gris, Pavel;
    • Ogurtsov, Aleksey Y.;
    • Gauthier, Josee;
    • Shibata, Kyoko;
    • Tchivileva, Inna E.;
    • Belfer, Inna;
    • Mishra, Bikashkumar;
    • Kiselycznyk, Carly;
    • Wallace, Margaret R.;
    • Staud, Roland;
    • Spiridonov, Nikolay A.;
    • Max, Mitchell B.;
    • Goldman, David;
    • Fillingim, Roger B.;
    • Maixner, William;
    • Diatchenko, Luda
    Publication type:
    Article
    16
    17

    Cover Page.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 6, p. NP, doi. 10.1093/hmg/ddp095
    Publication type:
    Article
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    Efhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibility.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 6, p. 1099, doi. 10.1093/hmg/ddp006
    By:
    • Suzuki, Toshimitsu;
    • Miyamoto, Hiroyuki;
    • Nakahari, Takashi;
    • Inoue, Ikuyo;
    • Suemoto, Takahiro;
    • Jiang, Bin;
    • Hirota, Yuki;
    • Itohara, Shigeyoshi;
    • Saido, Takaomi C.;
    • Tsumoto, Tadaharu;
    • Sawamoto, Kazunobu;
    • Hensch, Takao K.;
    • Delgado-Escueta, Antonio V.;
    • Yamakawa, Kazuhiro
    Publication type:
    Article
    22

    MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 6, p. 1065, doi. 10.1093/hmg/ddn443
    By:
    • Xiong, Lan;
    • Catoire, Hélène;
    • Dion, Patrick;
    • Gaspar, Claudia;
    • Lafrenière, Ronald G.;
    • Girard, Simon L.;
    • Levchenko, Anastasia;
    • Rivière, Jean-Baptiste;
    • Fiori, Laura;
    • St-Onge, Judith;
    • Bachand, Isabelle;
    • Thibodeau, Pascale;
    • Allen, Richard;
    • Earley, Christopher;
    • Turecki, Gustavo;
    • Montplaisir, Jacques;
    • Rouleau, Guy A.
    Publication type:
    Article