Works matching AU Yip, Stephen


Results: 114
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    Establishing a Framework for the Clinical Translation of Germline Findings in Precision Oncology.

    Published in:
    JNCI Cancer Spectrum, 2020, v. 4, n. 5, p. 1, doi. 10.1093/jncics/pkaa045
    By:
    • Dixon, Katherine;
    • Young, Sean;
    • Shen, Yaoqing;
    • Thibodeau, My Linh;
    • Fok, Alexandra;
    • Pleasance, Erin;
    • Zhao, Eric;
    • Jones, Martin;
    • Aubert, Geraldine;
    • Armstrong, Linlea;
    • Virani, Alice;
    • Regier, Dean;
    • Gelmon, Karen;
    • Renouf, Dan;
    • Chia, Stephen;
    • Bosdet, Ian;
    • Rassekh, S Rod;
    • Deyell, Rebecca J;
    • Yip, Stephen;
    • Fisic, Ana
    Publication type:
    Article
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    Intratumoral heterogeneity in a minority of ovarian low-grade serous carcinomas.

    Published in:
    BMC Cancer, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2407-14-982
    By:
    • Tone, Alicia A.;
    • McConechy, Melissa K.;
    • Yang, Winnie;
    • Jiarui Ding;
    • Yip, Stephen;
    • Kong, Esther;
    • Kwong-Kwok Wong;
    • Gershenson, David M.;
    • Mackay, Helen;
    • Shah, Sohrab;
    • Gilks, Blake;
    • Tinker, Anna V.;
    • Clarke, Blaise;
    • McAlpine, Jessica N.;
    • Huntsman, David
    Publication type:
    Article
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    Personalized Oncogenomics: Clinical Experience with Malignant Peritoneal Mesothelioma Using Whole Genome Sequencing.

    Published in:
    PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0119689
    By:
    • Sheffield, Brandon S.;
    • Tinker, Anna V.;
    • Shen, Yaoqing;
    • Hwang, Harry;
    • Li-Chang, Hector H.;
    • Pleasance, Erin;
    • Ch’ng, Carolyn;
    • Lum, Amy;
    • Lorette, Julie;
    • McConnell, Yarrow J.;
    • Sun, Sophie;
    • Jones, Steven J. M.;
    • Gown, Allen M.;
    • Huntsman, David G.;
    • Schaeffer, David F.;
    • Churg, Andrew;
    • Yip, Stephen;
    • Laskin, Janessa;
    • Marra, Marco A.
    Publication type:
    Article
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    EZH2 expression is a prognostic factor in childhood intracranial ependymoma: A Canadian Pediatric Brain Tumor Consortium study.

    Published in:
    Cancer (0008543X), 2015, v. 121, n. 9, p. 1499, doi. 10.1002/cncr.29198
    By:
    • Li, Amanda M.;
    • Dunham, Christopher;
    • Tabori, Uri;
    • Carret, Anne‐Sophie;
    • McNeely, P. Daniel;
    • Johnston, Donna;
    • Lafay‐Cousin, Lucie;
    • Wilson, Beverly;
    • Eisenstat, David D.;
    • Jabado, Nada;
    • Zelcer, Shayna;
    • Silva, Mariana;
    • Scheinemann, Katrin;
    • Fryer, Christopher;
    • Hendson, Glenda;
    • Fotovati, Abbas;
    • Hawkins, Cynthia;
    • Yip, Stephen;
    • Dunn, Sandra E.;
    • Hukin, Juliette
    Publication type:
    Article
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    Fatal Congenital Hypertrophic Cardiomyopathy and a Pancreatic Nodule Morphologically Identical to Focal Lesion of Congenital Hyperinsulinism in an Infant with Costello Syndrome: Case Report and Review of the Literature.

    Published in:
    Pediatric & Developmental Pathology, 2015, v. 18, n. 3, p. 237, doi. 10.2350/14-07-1525-CR.1
    By:
    • SHEFFIELD, BRANDON S.;
    • YIP, STEPHEN;
    • RUCHELLI, EDUARDO D.;
    • DUNHAM, CHRISTOPHER P.;
    • SHERWIN, ELIZABETH;
    • BROOKS, PAUL A.;
    • SUR, AMITAVA;
    • SINGH, AVASH;
    • HUMAN, DEREK G.;
    • PATEL, MILLAN S.;
    • LEE, ANNA F.
    Publication type:
    Article
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    The role of resection alone in select children with intracranial ependymoma: the Canadian Pediatric Brain Tumour Consortium experience.

    Published in:
    Child's Nervous System, 2015, v. 31, n. 1, p. 57, doi. 10.1007/s00381-014-2575-4
    By:
    • Ailon, Tamir;
    • Dunham, Christopher;
    • Carret, Anne-Sophie;
    • Tabori, Uri;
    • Mcneely, P.;
    • Zelcer, Shayna;
    • Wilson, Beverley;
    • Lafay-Cousin, Lucie;
    • Johnston, Donna;
    • Eisenstat, David;
    • Silva, Marianna;
    • Jabado, Nada;
    • Goddard, Karen;
    • Fryer, Chris;
    • Hendson, Glenda;
    • Hawkins, Cynthia;
    • Dunn, Sandra;
    • Yip, Stephen;
    • Singhal, Ashutosh;
    • Hukin, Juliette
    Publication type:
    Article
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    G-quadruplexes mark alternative lengthening of telomeres.

    Published in:
    NAR Cancer, 2021, v. 3, n. 3, p. 1, doi. 10.1093/narcan/zcab031
    By:
    • Yang, Sunny Y.;
    • Chang, Emily Y. C.;
    • Lim, Joanne;
    • Kwan, Harwood H.;
    • Monchaud, David;
    • Yip, Stephen;
    • Stirling, Peter C.;
    • Wong, Judy M. Y.
    Publication type:
    Article
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    Novel targeted therapies in chordoma: an update.

    Published in:
    Therapeutics & Clinical Risk Management, 2015, v. 11, p. 873, doi. 10.2147/TCRM.S50526
    By:
    • Di Maio, Salvatore;
    • Yip, Stephen;
    • Al Zhrani, Gmaan A.;
    • Alotaibi, Fahad E.;
    • Al Turki, Abdulrahman;
    • Kong, Esther;
    • Rostomily, Robert C.
    Publication type:
    Article
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    Novel findings and expansion of phenotype in a mosaic RASopathy caused by somatic KRAS variants.

    Published in:
    American Journal of Medical Genetics. Part A, 2021, v. 185, n. 9, p. 2829, doi. 10.1002/ajmg.a.62356
    By:
    • Chang, Caitlin A.;
    • Perrier, Renee;
    • Kurek, Kyle C.;
    • Estrada‐Veras, Juvianee;
    • Lehman, Anna;
    • Yip, Stephen;
    • Hendson, Glenda;
    • Diamond, Carol;
    • Pinchot, Jason W.;
    • Tran, Jennifer M.;
    • Arkin, Lisa M.;
    • Drolet, Beth A.;
    • Napier, Melanie P.;
    • O'Neill, Sarah A.;
    • Balci, Tugce B.;
    • Keppler‐Noreuil, Kim M.
    Publication type:
    Article
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    Paternal uniparental disomy 11p15.5 in the pancreatic nodule of an infant with Costello syndrome: Shared mechanism for hyperinsulinemic hypoglycemia in neonates with Costello and Beckwith-Wiedemann syndrome and somatic loss of heterozygosity in Costello syndrome driving clonal expansion

    Published in:
    American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 3, p. 559, doi. 10.1002/ajmg.a.37471
    By:
    • Gripp, Karen W.;
    • Robbins, Katherine M.;
    • Sheffield, Brandon S.;
    • Lee, Anna F.;
    • Patel, Millan S.;
    • Yip, Stephen;
    • Doyle, Daniel;
    • Stabley, Deborah;
    • Sol‐Church, Katia
    Publication type:
    Article
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    Somatic mosaicism for the p.His1047Arg mutation in PIK3CA in a girl with mesenteric lipomatosis.

    Published in:
    American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 9, p. 2360, doi. 10.1002/ajmg.a.36622
    By:
    • Cohen, Ana S. A.;
    • Townsend, Katelin N.;
    • Xiang, Qing‐San;
    • Attariwala, Raj;
    • Borchers, Christof;
    • Senger, Christof;
    • Picker, Wayne;
    • Levi, Jasna;
    • Yewchuk, Lila;
    • Tan, Joelle;
    • Eydoux, Patrice;
    • Lum, Amy;
    • Yong, Siu‐Li;
    • McKinnon, Margaret L.;
    • Lear, Scott A.;
    • Everett, Robert;
    • Jones, Steven J. M.;
    • Yip, Stephen;
    • Gibson, William T.
    Publication type:
    Article
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    DNA hypermethylation and 1p Loss silence NHE-1 in oligodendroglioma.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 6, p. 845, doi. 10.1002/ana.23610
    By:
    • Blough, Michael D.;
    • Al-Najjar, Mohammad;
    • Chesnelong, Charles;
    • Binding, Carmen E.;
    • Rogers, Alexandra D.;
    • Luchman, H. Artee;
    • Kelly, John J.;
    • Fliegel, Larry;
    • Morozova, Olena;
    • Yip, Stephen;
    • Marra, Marco;
    • Weiss, Samuel;
    • Chan, Jennifer A.;
    • Cairncross, J. Gregory
    Publication type:
    Article
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    Enhancing clinical genomic accuracy with panelGC: a novel metric and tool for quantifying and monitoring GC biases in hybridization capture panel sequencing.

    Published in:
    Briefings in Bioinformatics, 2024, v. 25, n. 5, p. 1, doi. 10.1093/bib/bbae442
    By:
    • Cheng, Xuanjin;
    • Goktas, Murathan T;
    • Williamson, Laura M;
    • Krzywinski, Martin;
    • Mulder, David T;
    • Swanson, Lucas;
    • Slind, Jill;
    • Sihvonen, Jelena;
    • Chow, Cynthia R;
    • Carr, Amy;
    • Bosdet, Ian;
    • Tucker, Tracy;
    • Young, Sean;
    • Moore, Richard;
    • Mungall, Karen L;
    • Yip, Stephen;
    • Jones, Steven J M
    Publication type:
    Article
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