Works matching IS 09646906 AND DT 2013 AND VI 22 AND IP 14

Results: 23
    1
    2
    3
    4
    5
    6
    7
    8

    Editorial Board.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 14, p. NP, doi. 10.1093/hmg/ddt305
    Publication type:
    Article
    9

    DNA polymerase ɛ and δ exonuclease domain mutations in endometrial cancer.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 14, p. 2820, doi. 10.1093/hmg/ddt131
    By:
    • Church, David N.;
    • Briggs, Sarah E.W.;
    • Palles, Claire;
    • Domingo, Enric;
    • Kearsey, Stephen J.;
    • Grimes, Jonathon M.;
    • Gorman, Maggie;
    • Martin, Lynn;
    • Howarth, Kimberley M.;
    • Hodgson, Shirley V.;
    • Kaur, Kulvinder;
    • Taylor, Jenny;
    • Tomlinson, Ian P.M.
    Publication type:
    Article
    10
    11

    Subscription Page.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 14, p. NP, doi. 10.1093/hmg/ddt306
    Publication type:
    Article
    12

    TRAP1 rescues PINK1 loss-of-function phenotypes.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 14, p. 2829, doi. 10.1093/hmg/ddt132
    By:
    • Zhang, Li;
    • Karsten, Peter;
    • Hamm, Sabine;
    • Pogson, Joe H.;
    • Müller-Rischart, A. Kathrin;
    • Exner, Nicole;
    • Haass, Christian;
    • Whitworth, Alexander J.;
    • Winklhofer, Konstanze F.;
    • Schulz, Jörg B.;
    • Voigt, Aaron
    Publication type:
    Article
    13

    Global increases in both common and rare copy number load associated with autism.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 14, p. 2870, doi. 10.1093/hmg/ddt136
    By:
    • Girirajan, Santhosh;
    • Johnson, Rebecca L.;
    • Tassone, Flora;
    • Balciuniene, Jorune;
    • Katiyar, Neerja;
    • Fox, Keolu;
    • Baker, Carl;
    • Srikanth, Abhinaya;
    • Yeoh, Kian Hui;
    • Khoo, Su Jen;
    • Nauth, Therese B.;
    • Hansen, Robin;
    • Ritchie, Marylyn;
    • Hertz-Picciotto, Irva;
    • Eichler, Evan E.;
    • Pessah, Isaac N.;
    • Selleck, Scott B.
    Publication type:
    Article
    14

    Cover Page.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 14, p. NP, doi. 10.1093/hmg/ddt304
    Publication type:
    Article
    15
    16
    17
    18
    19

    Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 14, p. 2973
    By:
    • Keller, Margaux F.;
    • Saad, Mohamad;
    • Bras, Jose;
    • Bettella, Francesco;
    • Nicolaou, Nayia;
    • Simón-Sánchez, Javier;
    • Mittag, Florian;
    • chel, Finja Bü;
    • Sharma, Manu;
    • Gibbs, J. Raphael;
    • Schulte, Claudia;
    • Moskvina, Valentina;
    • Durr, Alexandra;
    • Holmans, Peter;
    • Kilarski, Laura L.;
    • Guerreiro, Rita;
    • Hernandez, Dena G.;
    • Brice, Alexis;
    • Ylikotila, Pauli;
    • Stefánsson, Hreinn
    Publication type:
    Article
    20

    A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 14, p. 2941, doi. 10.1093/hmg/ddt141
    By:
    • Jones, Gregory T.;
    • Bown, Matthew J.;
    • Gretarsdottir, Solveig;
    • Romaine, Simon P.R.;
    • Helgadottir, Anna;
    • Yu, Grace;
    • Tromp, Gerard;
    • Norman, Paul E.;
    • Jin, Cao;
    • Baas, Annette F.;
    • Blankensteijn, Jan D.;
    • Kullo, Iftikhar J.;
    • Phillips, L. Victoria;
    • Williams, Michael J.A.;
    • Topless, Ruth;
    • Merriman, Tony R.;
    • Vasudevan, Thodor M.;
    • Lewis, David R.;
    • Blair, Ross D.;
    • Hill, Andrew A.
    Publication type:
    Article
    21
    22

    Contents Page.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 14, p. NP, doi. 10.1093/hmg/ddt303
    Publication type:
    Article
    23