Works matching AU null, null


Results: 3399
    1
    2
    3
    5
    9
    11
    12
    13
    14
    15
    18
    20
    21
    26
    27
    28
    29
    31
    32

    Analysis of genetically driven alternative splicing identifies FBXO38 as a novel COPD susceptibility gene.

    Published in:
    PLoS Genetics, 2019, v. 15, n. 7, p. 1, doi. 10.1371/journal.pgen.1008229
    By:
    • Saferali, Aabida;
    • Yun, Jeong H.;
    • Parker, Margaret M.;
    • Sakornsakolpat, Phuwanat;
    • Chase, Robert P.;
    • Lamb, Andrew;
    • Hobbs, Brian D.;
    • Boezen, Marike H.;
    • Dai, Xiangpeng;
    • de Jong, Kim;
    • Beaty, Terri H.;
    • Wei, Wenyi;
    • Zhou, Xiaobo;
    • Silverman, Edwin K.;
    • Cho, Michael H.;
    • Castaldi, Peter J.;
    • Hersh, Craig P.;
    • null, null
    Publication type:
    Article
    33

    Genetic architecture of human thinness compared to severe obesity.

    Published in:
    PLoS Genetics, 2019, v. 15, n. 1, p. 1, doi. 10.1371/journal.pgen.1007603
    By:
    • Riveros-McKay, Fernando;
    • Mistry, Vanisha;
    • Bounds, Rebecca;
    • Hendricks, Audrey;
    • Keogh, Julia M.;
    • Thomas, Hannah;
    • Henning, Elana;
    • Corbin, Laura J.;
    • null, null;
    • O’Rahilly, Stephen;
    • Zeggini, Eleftheria;
    • Wheeler, Eleanor;
    • Barroso, Inês;
    • Farooqi, I. Sadaf
    Publication type:
    Article
    34
    35
    36

    Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.

    Published in:
    PLoS Genetics, 2018, v. 14, n. 7, p. 1, doi. 10.1371/journal.pgen.1007394
    By:
    • Huusko, Johanna M.;
    • Karjalainen, Minna K.;
    • Graham, Britney E.;
    • Zhang, Ge;
    • Farrow, Emily G.;
    • Miller, Neil A.;
    • Jacobsson, Bo;
    • Eidem, Haley R.;
    • Murray, Jeffrey C.;
    • Bedell, Bruce;
    • Breheny, Patrick;
    • Brown, Noah W.;
    • Bødker, Frans L.;
    • Litterman, Nadia K.;
    • Jiang, Pan-Pan;
    • Russell, Laura;
    • Hinds, David A.;
    • Hu, Youna;
    • null, null;
    • Rokas, Antonis
    Publication type:
    Article
    37

    De novo and inherited private variants in MAP1B in periventricular nodular heterotopia.

    Published in:
    PLoS Genetics, 2018, v. 14, n. 5, p. 1, doi. 10.1371/journal.pgen.1007281
    By:
    • Heinzen, Erin L.;
    • O'Neill, Adam C.;
    • Zhu, Xiaolin;
    • Allen, Andrew S.;
    • Bahlo, Melanie;
    • Chelly, Jamel;
    • Dobyns, William B.;
    • Freytag, Saskia;
    • Guerrini, Renzo;
    • Leventer, Richard J.;
    • Poduri, Annapurna;
    • Robertson, Stephen P.;
    • Walsh, Christopher A.;
    • Zhang, Mengqi;
    • null, null
    Publication type:
    Article
    38
    39
    40
    41
    42
    43
    44

    Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human disease.

    Published in:
    PLoS Computational Biology, 2018, v. 14, n. 3, p. 1, doi. 10.1371/journal.pcbi.1005934
    By:
    • Baillie, J. Kenneth;
    • Bretherick, Andrew;
    • Haley, Christopher S.;
    • Clohisey, Sara;
    • Gray, Alan;
    • Neyton, Lucile P. A.;
    • Barrett, Jeffrey;
    • Stahl, Eli A.;
    • Tenesa, Albert;
    • Andersson, Robin;
    • Brown, J. Ben;
    • Faulkner, Geoffrey J.;
    • Lizio, Marina;
    • Schaefer, Ulf;
    • Daub, Carsten;
    • Itoh, Masayoshi;
    • Kondo, Naoto;
    • Lassmann, Timo;
    • Kawai, Jun;
    • null, null
    Publication type:
    Article
    45
    49