Works matching IS 09646906 AND DT 2013 AND VI 22 AND IP 7

Results: 23
    1

    GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 7, p. 1457, doi. 10.1093/hmg/dds534
    By:
    • Li, Jin;
    • Glessner, Joseph T.;
    • Zhang, Haitao;
    • Hou, Cuiping;
    • Wei, Zhi;
    • Bradfield, Jonathan P.;
    • Mentch, Frank D.;
    • Guo, Yiran;
    • Kim, Cecilia;
    • Xia, Qianghua;
    • Chiavacci, Rosetta M.;
    • Thomas, Kelly A.;
    • Qiu, Haijun;
    • Grant, Struan F.A.;
    • Furth, Susan L.;
    • Hakonarson, Hakon;
    • Sleiman, Patrick M.A.
    Publication type:
    Article
    2
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    Subscription Page.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 7, p. NP, doi. 10.1093/hmg/ddt124
    Publication type:
    Article
    5

    Patient-specific induced-pluripotent stem cells-derived cardiomyocytes recapitulate the pathogenic phenotypes of dilated cardiomyopathy due to a novel DES mutation identified by whole exome sequencing.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 7, p. 1395, doi. 10.1093/hmg/dds556
    By:
    • Tse, Hung-Fat;
    • Ho, Jenny C. Y.;
    • Choi, Shing-Wan;
    • Lee, Yee-Ki;
    • Butler, Amy W.;
    • Ng, Kwong-Man;
    • Siu, Chung-Wah;
    • Simpson, Michael A.;
    • Lai, Wing-Hon;
    • Chan, Yau-Chi;
    • Au, Ka-Wing;
    • Zhang, Jinqiu;
    • Lay, Kenneth W. J.;
    • Esteban, Miguel A.;
    • Nicholls, John M.;
    • Colman, Alan;
    • Sham, Pak C.
    Publication type:
    Article
    6
    7

    Molecular and functional analysis of the C-terminal region of human erythroid-specific 5-aminolevulinic synthase associated with X-linked dominant protoporphyria (XLDPP).

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 7, p. 1280, doi. 10.1093/hmg/dds531
    By:
    • Ducamp, Sarah;
    • Schneider-Yin, Xiaoye;
    • de Rooij, Felix;
    • Clayton, Jerome;
    • Fratz, Erica J.;
    • Rudd, Alice;
    • Ostapowicz, George;
    • Varigos, George;
    • Lefebvre, Thibaud;
    • Deybach, Jean-Charles;
    • Gouya, Laurent;
    • Wilson, Paul;
    • Ferreira, Gloria C.;
    • Minder, Elisabeth I.;
    • Puy, Hervé
    Publication type:
    Article
    8

    Contents Page.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 7, p. NP, doi. 10.1093/hmg/ddt128
    Publication type:
    Article
    9
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    14

    A genome-wide association study of early menopause and the combined impact of identified variants.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 7, p. 1465, doi. 10.1093/hmg/dds551
    By:
    • Perry, John R. B.;
    • Corre, Tanguy;
    • Esko, Tõnu;
    • Chasman, Daniel I.;
    • Fischer, Krista;
    • Franceschini, Nora;
    • He, Chunyan;
    • Kutalik, Zoltan;
    • Mangino, Massimo;
    • Rose, Lynda M.;
    • Vernon Smith, Albert;
    • Stolk, Lisette;
    • Sulem, Patrick;
    • Weedon, Michael N.;
    • Zhuang, Wei V.;
    • Arnold, Alice;
    • Ashworth, Alan;
    • Bergmann, Sven;
    • Buring, Julie E.;
    • Burri, Andrea
    Publication type:
    Article
    15
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    Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 7, p. 1417, doi. 10.1093/hmg/dds558
    By:
    • Smith, Katherine R.;
    • Dahl, Hans-Henrik M.;
    • Canafoglia, Laura;
    • Andermann, Eva;
    • Damiano, John;
    • Morbin, Michela;
    • Bruni, Amalia C.;
    • Giaccone, Giorgio;
    • Cossette, Patrick;
    • Saftig, Paul;
    • Grötzinger, Joachim;
    • Schwake, Michael;
    • Andermann, Frederick;
    • Staropoli, John F.;
    • Sims, Katherine B.;
    • Mole, Sara E.;
    • Franceschetti, Silvana;
    • Alexander, Noreen A.;
    • Cooper, Jonathan D.;
    • Chapman, Harold A.
    Publication type:
    Article
    18
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    Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 7, p. 1473, doi. 10.1093/hmg/dds552
    By:
    • Cordell, Heather J.;
    • Töpf, Ana;
    • Mamasoula, Chrysovalanto;
    • Postma, Alex V.;
    • Bentham, Jamie;
    • Zelenika, Diana;
    • Heath, Simon;
    • Blue, Gillian;
    • Cosgrove, Catherine;
    • Granados Riveron, Javier;
    • Darlay, Rebecca;
    • Soemedi, Rachel;
    • Wilson, Ian J.;
    • Ayers, Kristin L.;
    • Rahman, Thahira J.;
    • Hall, Darroch;
    • Mulder, Barbara J.M.;
    • Zwinderman, Aelko H.;
    • van Engelen, Klaartje;
    • Brook, J. David
    Publication type:
    Article
    21

    Cover Page.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 7, p. NP, doi. 10.1093/hmg/ddt122
    Publication type:
    Article
    22

    Editorial Board.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 7, p. NP, doi. 10.1093/hmg/ddt123
    Publication type:
    Article
    23