Found: 8

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  • Difficult Delivery and Neonatal Resuscitation: A Novel Simulation for Emergency Medicine Residents.

    Published in:
    Western Journal of Emergency Medicine: Integrating Emergency Care with Population Health, 2020, v. 21, n. 1, p. 102, doi. 10.5811/westjem.2019.10.43913
    By:
    • Nickerson, Jillian Elizabeth;
    • Webb, Taryn;
    • Boehm, Lorraine;
    • Neher, Hayley;
    • Wong, Lillian;
    • LaMonica, Julia;
    • Bentley, Suzanne
    Publication type:
    Article

  • Systematic genomic and translational efficiency studies of uveal melanoma.

    Published in:
    PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0178189
    By:
    • Johnson, Chelsea Place;
    • Kim, Ivana K.;
    • Esmaeli, Bita;
    • Amin-Mansour, Ali;
    • Treacy, Daniel J.;
    • Carter, Scott L.;
    • Hodis, Eran;
    • Wagle, Nikhil;
    • Seepo, Sara;
    • Yu, Xiaoxing;
    • Lane, Anne Marie;
    • Gragoudas, Evangelos S.;
    • Vazquez, Francisca;
    • Nickerson, Elizabeth;
    • Cibulskis, Kristian;
    • McKenna, Aaron;
    • Gabriel, Stacey B.;
    • Getz, Gad;
    • Van Allen, Eliezer M.;
    • ‘t Hoen, Peter A. C.
    Publication type:
    Article

  • Landscape of genomic alterations in cervical carcinomas.

    Published in:
    Nature, 2014, v. 506, n. 7488, p. 371, doi. 10.1038/nature12881
    By:
    • Ojesina, Akinyemi I.;
    • Lichtenstein, Lee;
    • Freeman, Samuel S.;
    • Pedamallu, Chandra Sekhar;
    • Imaz-Rosshandler, Ivan;
    • Pugh, Trevor J.;
    • Cherniack, Andrew D.;
    • Ambrogio, Lauren;
    • Cibulskis, Kristian;
    • Bertelsen, Bjørn;
    • Romero-Cordoba, Sandra;
    • Treviño, Victor;
    • Vazquez-Santillan, Karla;
    • Guadarrama, Alberto Salido;
    • Wright, Alexi A.;
    • Rosenberg, Mara W.;
    • Duke, Fujiko;
    • Kaplan, Bethany;
    • Wang, Rui;
    • Nickerson, Elizabeth
    Publication type:
    Article

  • Somatic mutation of CDKN1B in small intestine neuroendocrine tumors.

    Published in:
    Nature Genetics, 2013, v. 45, n. 12, p. 1483, doi. 10.1038/ng.2821
    By:
    • Francis, Joshua M;
    • Kiezun, Adam;
    • Ramos, Alex H;
    • Serra, Stefano;
    • Pedamallu, Chandra Sekhar;
    • Qian, Zhi Rong;
    • Banck, Michaela S;
    • Kanwar, Rahul;
    • Kulkarni, Amit A;
    • Karpathakis, Anna;
    • Manzo, Veronica;
    • Contractor, Tanupriya;
    • Philips, Juliet;
    • Nickerson, Elizabeth;
    • Pho, Nam;
    • Hooshmand, Susanne M;
    • Brais, Lauren K;
    • Lawrence, Michael S;
    • Pugh, Trevor;
    • McKenna, Aaron
    Publication type:
    Article

  • Phenotypic spectrum and prevalence of INPP5E mutations in Joubert Syndrome and related disorders.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 10, p. 1074, doi. 10.1038/ejhg.2012.305
    By:
    • Travaglini, Lorena;
    • Brancati, Francesco;
    • Silhavy, Jennifer;
    • Iannicelli, Miriam;
    • Nickerson, Elizabeth;
    • Elkhartoufi, Nadia;
    • Scott, Eric;
    • Spencer, Emily;
    • Gabriel, Stacey;
    • Thomas, Sophie;
    • Ben-Zeev, Bruria;
    • Bertini, Enrico;
    • Boltshauser, Eugen;
    • Chaouch, Malika;
    • Roberta Cilio, Maria;
    • de Jong, Mirjam M;
    • Kayserili, Hulya;
    • Ogur, Gonul;
    • Poretti, Andrea;
    • Signorini, Sabrina
    Publication type:
    Article

  • Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer.

    Published in:
    Nature Genetics, 2012, v. 44, n. 6, p. 685, doi. 10.1038/ng.2279
    By:
    • Barbieri, Christopher E;
    • Baca, Sylvan C;
    • Lawrence, Michael S;
    • Demichelis, Francesca;
    • Blattner, Mirjam;
    • Theurillat, Jean-Philippe;
    • White, Thomas A;
    • Stojanov, Petar;
    • Van Allen, Eliezer;
    • Stransky, Nicolas;
    • Nickerson, Elizabeth;
    • Chae, Sung-Suk;
    • Boysen, Gunther;
    • Auclair, Daniel;
    • Onofrio, Robert C;
    • Park, Kyung;
    • Kitabayashi, Naoki;
    • MacDonald, Theresa Y;
    • Sheikh, Karen;
    • Vuong, Terry
    Publication type:
    Article

  • Melanoma genome sequencing reveals frequent PREX2 mutations.

    Published in:
    Nature, 2012, v. 485, n. 7399, p. 502, doi. 10.1038/nature11071
    By:
    • Berger, Michael F.;
    • Hodis, Eran;
    • Heffernan, Timothy P.;
    • Deribe, Yonathan Lissanu;
    • Lawrence, Michael S.;
    • Protopopov, Alexei;
    • Ivanova, Elena;
    • Watson, Ian R.;
    • Nickerson, Elizabeth;
    • Ghosh, Papia;
    • Zhang, Hailei;
    • Zeid, Rhamy;
    • Ren, Xiaojia;
    • Cibulskis, Kristian;
    • Sivachenko, Andrey Y.;
    • Wagle, Nikhil;
    • Sucker, Antje;
    • Sougnez, Carrie;
    • Onofrio, Robert;
    • Ambrogio, Lauren
    Publication type:
    Article

  • Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing.

    Published in:
    Nature Medicine, 2006, v. 12, n. 7, p. 852, doi. 10.1038/nm1437
    By:
    • Thomas, Roman K;
    • Nickerson, Elizabeth;
    • Simons, Jan F;
    • Jänne, Pasi A;
    • Tengs, Torstein;
    • Yuza, Yuki;
    • Garraway, Levi A;
    • LaFramboise, Thomas;
    • Lee, Jeffrey C;
    • Shah, Kinjal;
    • O'Neill, Keith;
    • Sasaki, Hidefumi;
    • Lindeman, Neal;
    • Kwok-Kin Wong;
    • Borras, Ana M;
    • Gutmann, Edward J;
    • Dragnev, Konstantin H;
    • DeBiasi, Ralph;
    • Tzu-Hsiu Chen;
    • Glatt, Karen A
    Publication type:
    Article