Found: 8

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  • The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.

    Published in:
    Nature Genetics, 2013, v. 45, n. 5, p. 522, doi. 10.1038/ng.2583
    By:
    • Weinhold, Niels;
    • Johnson, David C;
    • Chubb, Daniel;
    • Chen, Bowang;
    • Försti, Asta;
    • Hosking, Fay J;
    • Broderick, Peter;
    • Ma, Yussanne P;
    • Dobbins, Sara E;
    • Hose, Dirk;
    • Walker, Brian A;
    • Davies, Faith E;
    • Kaiser, Martin F;
    • Li, Ni L;
    • Gregory, Walter A;
    • Jackson, Graham H;
    • Witzens-Harig, Mathias;
    • Neben, Kai;
    • Hoffmann, Per;
    • Nöthen, Markus M
    Publication type:
    Article

  • Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 58, doi. 10.1038/ng.993
    By:
    • Broderick, Peter;
    • Chubb, Daniel;
    • Johnson, David C;
    • Weinhold, Niels;
    • Försti, Asta;
    • Lloyd, Amy;
    • Olver, Bianca;
    • Ma, Yussanne P;
    • Dobbins, Sara E;
    • Walker, Brian A;
    • Davies, Faith E;
    • Gregory, Walter A;
    • Child, J Anthony;
    • Ross, Fiona M;
    • Jackson, Graham H;
    • Neben, Kai;
    • Jauch, Anna;
    • Hoffmann, Per;
    • Mühleisen, Thomas W;
    • Nöthen, Markus M
    Publication type:
    Article

  • Common variation at 10p12.31 near MLLT10 influences meningioma risk.

    Published in:
    Nature Genetics, 2011, v. 43, n. 9, p. 825, doi. 10.1038/ng.879
    By:
    • Dobbins, Sara E.;
    • Broderick, Peter;
    • Melin, Beatrice;
    • Feychting, Maria;
    • Johansen, Christoffer;
    • Andersson, Ulrika;
    • Brännström, Thomas;
    • Schramm, Johannes;
    • Olver, Bianca;
    • Lloyd, Amy;
    • Ma, Yussanne P;
    • Hosking, Fay J.;
    • Lönn, Stefan;
    • Ahlbom, Anders;
    • Henriksson, Roger;
    • Schoemaker, Minouk J.;
    • Hepworth, Sarah J.;
    • Hoffmann, Per;
    • Mühleisen, Thomas W.;
    • Nöthen, Markus M.
    Publication type:
    Article

  • JAGuaR: Junction Alignments to Genome for RNA-Seq Reads.

    Published in:
    PLoS ONE, 2014, v. 9, n. 7, p. 1, doi. 10.1371/journal.pone.0102398
    By:
    • Butterfield, Yaron S.;
    • Kreitzman, Maayan;
    • Thiessen, Nina;
    • Corbett, Richard D.;
    • Li, Yisu;
    • Pang, Johnson;
    • Ma, Yussanne P.;
    • Jones, Steven J. M.;
    • Birol, İnanç
    Publication type:
    Article

  • Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer.

    Published in:
    Nature Communications, 2016, v. 7, n. 6, p. 11883, doi. 10.1038/ncomms11883
    By:
    • Chubb, Daniel;
    • Broderick, Peter;
    • Dobbins, Sara E.;
    • Frampton, Matthew;
    • Kinnersley, Ben;
    • Penegar, Steven;
    • Price, Amy;
    • Ma, Yussanne P.;
    • Sherborne, Amy L.;
    • Palles, Claire;
    • Timofeeva, Maria N.;
    • Bishop, D. Timothy;
    • Dunlop, Malcolm G.;
    • Tomlinson, Ian;
    • Houlston, Richard S.
    Publication type:
    Article

  • Whole genome and whole transcriptome genomic profiling of a metastatic eccrine porocarcinoma.

    Published in:
    NPJ Precision Oncology, 2018, v. 2, n. 1, p. N.PAG, doi. 10.1038/s41698-018-0050-5
    By:
    • Thibodeau, My Linh;
    • Bonakdar, Melika;
    • Zhao, Eric;
    • Mungall, Karen L.;
    • Reisle, Caralyn;
    • Zhang, Wei;
    • Bye, Morgan H.;
    • Thiessen, Nina;
    • Bleile, Dustin;
    • Mungall, Andrew J.;
    • Ma, Yussanne P.;
    • Jones, Martin R.;
    • Renouf, Daniel J.;
    • Lim, Howard J.;
    • Yip, Stephen;
    • Ng, Tony;
    • Ho, Cheryl;
    • Laskin, Janessa;
    • Marra, Marco A.;
    • Schrader, Kasmintan A.
    Publication type:
    Article

  • The silent mutational landscape of infant MLL-AF4 pro-B acute lymphoblastic leukemia.

    Published in:
    Genes, Chromosomes & Cancer, 2013, v. 52, n. 10, p. 954, doi. 10.1002/gcc.22090
    By:
    • Dobbins, Sara E.;
    • Sherborne, Amy L.;
    • Ma, Yussanne P.;
    • Bardini, Michela;
    • Biondi, Andrea;
    • Cazzaniga, Giovanni;
    • Lloyd, Amy;
    • Chubb, Daniel;
    • Greaves, Mel F.;
    • Houlston, Richard S.
    Publication type:
    Article

  • Genomic and Cytogenetic Characterization of a Balanced Translocation Disrupting NUP98.

    Published in:
    Cytogenetic & Genome Research, 2017, v. 152, n. 3, p. 117, doi. 10.1159/000479463
    By:
    • Thibodeau, My Linh;
    • Steinraths, Michelle;
    • Brown, Lindsay;
    • Zong, Zheyuan;
    • Shomer, Naomi;
    • Taubert, Stefan;
    • Mungall, Karen L.;
    • Ma, Yussanne P.;
    • Mueller, Rosemary;
    • Birol, Inanc;
    • Lehman, anna
    Publication type:
    Article