Výsledky vyhledávání - Catherine Clinton

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  1. 1
    Creating a scalable clinical pharmacogenomics service with automated interpretation and medical record result integration – experience from a pediatric tertiary care facility

    Creating a scalable clinical pharmacogenomics service with automated interpretation and medical record result integration – experience from a pediatric tertiary care facility Autor Shannon Manzi, Vincent A. Fusaro, Laura Chadwick, Catherine A. Brownstein, Catherine Clinton, Kenneth D. Mandl, Wendy A. Wolf, Jared B. Hawkins

    Vydáno 2016
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    Artigo
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  2. 2
    The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository

    The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository Autor Erin D. Harris, Sonja I. Ziniel, Jonathan G. Amatruda, Catherine Clinton, Sarah Savage, Patrick L. Taylor, Noelle Huntington, Robert C. Green, Ingrid A. Holm

    Vydáno 2012
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  3. 3
    Detection of Somatic Structural Variants Enables Quantification and Characterization of Circulating Tumor DNA in Children With Solid Tumors

    Detection of Somatic Structural Variants Enables Quantification and Characterization of Circulating Tumor DNA in Children With Solid Tumors Autor Kelly S. Klega, Alma Imamović, Gavin Ha, Andrea Clapp, Stephanie C. Meyer, Abigail Ward, Catherine Clinton, Anwesha Nag, Eliezer M. Van Allen, Elizabeth A. Mullen, Steven G. DuBois, Katherine A. Janeway, Matthew Meyerson, Aaron R. Thorner, Brian D. Crompton

    Vydáno 2018
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  4. 4
    Genomic and Immunologic Characterization of INI1-Deficient Pediatric Cancers

    Genomic and Immunologic Characterization of INI1-Deficient Pediatric Cancers Autor Suzanne J. Forrest, Alyaa Al‐Ibraheemi, Duong Doan, Abigail Ward, Catherine Clinton, Juan Putra, R. Seth Pinches, Cigall Kadoch, N. Susan, Steven G. DuBois, Patrick J. Leavey, Nicole R. LeBoeuf, Elizabeth A. Mullen, Natalie B. Collins, Alanna J. Church, Katherine A. Janeway

    Vydáno 2020
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  5. 5
    Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia

    Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia Autor Leana Doherty, Mee Rie Sheen, Adrianna Vlachos, Valérie Choesmel, Marie-Françoise O’Donohue, Catherine Clinton, Hal E. Schneider, Colin A. Sieff, Peter E. Newburger, Sarah E. Ball, Edyta Niewiadomska, Michał Matysiak, Bertil Glader, R.J. Arceci, Jason E. Farrar, Eva Atsidaftos, Jeffrey M. Lipton, Pierre‐Emmanuel Gleizes, Hanna T. Gazda

    Vydáno 2010
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  6. 6
    Belzutifan, a Potent HIF2α Inhibitor, in the Pacak–Zhuang Syndrome

    Belzutifan, a Potent HIF2α Inhibitor, in the Pacak–Zhuang Syndrome Autor Junne Kamihara, Kayla V. Hamilton, Jessica A. Pollard, Catherine Clinton, Jill A. Madden, Jasmine Lin, Alma Imamović, Catherine B. Wall, Ari J. Wassner, Brent R. Weil, Matthew M. Heeney, Sara O. Vargas, William G. Kaelin, Katherine A. Janeway, Rodolfo F. Perini, Naseem J. Zojwalla, Stephan D. Voss, Steven G. DuBois

    Vydáno 2021
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  7. 7
    DICER1-associated central nervous system sarcoma in children: comprehensive clinicopathologic and genetic analysis of a newly described rare tumor

    DICER1-associated central nervous system sarcoma in children: comprehensive clinicopathologic and genetic analysis of a newly described rare tumor Autor Junne Kamihara, Vera Paulson, Micheál Breen, Theodore W. Laetsch, Dinesh Rakheja, David S. Shulman, Michelle Long Schoettler, Catherine Clinton, Abigail Ward, Deirdre Reidy, R. Seth Pinches, Daniel A. Weiser, Elizabeth A. Mullen, Jaclyn Schienda, Paul A. Meyers, Steven G. DuBois, Jonathan A. Nowak, William D. Foulkes, Kris Ann P. Schultz, Katherine A. Janeway, Sara O. Vargas, Alanna J. Church

    Vydáno 2020
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  8. 8
    The ribosomal basis of diamond-blackfan anemia: mutation and database update

    The ribosomal basis of diamond-blackfan anemia: mutation and database update Autor Ilenia Boria, Emanuela Garelli, Hanna T. Gazda, Anna Aspesi, Paola Quarello, Elisa Pavesi, Daniela Ferrante, Joerg J Meerpohl, Mutlu Kartal‐Kaess, Lydie Da Costa, Alexis Proust, Thierry Leblanc, Maud Simansour, Niklas Dahl, Anne-Sophie Fröjmark, Dagmar Pospı́šilová, Radek Čmejla, Alan H. Beggs, Mee Rie Sheen, Michael Landowski, Christopher Buros, Catherine Clinton, Lori Dobson, Adrianna Vlachos, Eva Atsidaftos, Jeffrey M. Lipton, Steven R. Ellis, Ugo Ramenghi, Irma Dianzani

    Vydáno 2010
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  9. 9
    Renal medullary carcinomas depend upon SMARCB1 loss and are sensitive to proteasome inhibition

    Renal medullary carcinomas depend upon SMARCB1 loss and are sensitive to proteasome inhibition Autor Andrew L. Hong, Yuen‐Yi Tseng, Jeremiah A. Wala, Won‐Jun Kim, Bryan D. Kynnap, Mihir B. Doshi, Guillaume Kugener, Gabriel J. Sandoval, Thomas P. Howard, Ji Li, Xiaoping Yang, Michelle Tillgren, Mahmhoud Ghandi, Abeer Sayeed, Rebecca Deasy, Abigail Ward, Brian McSteen, Katherine Labella, Paula Keskula, Adam Tracy, Cora Connor, Catherine Clinton, Alanna J. Church, Brian D. Crompton, Katherine A. Janeway, Barbara Van Hare, David Sandak, Ole Gjoerup, Pratiti Bandopadhayay, Paul A. Clemons, Stuart L. Schreiber, David E. Root, Prafulla C. Gokhale, Susan Chi, Elizabeth A. Mullen, Charles W.M. Roberts, Cigall Kadoch, Rameen Beroukhim, Keith L. Ligon, Jesse S. Boehm, William C. Hahn

    Vydáno 2019
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  10. 10
    Matched Targeted Therapy for Pediatric Patients with Relapsed, Refractory, or High-Risk Leukemias: A Report from the LEAP Consortium

    Matched Targeted Therapy for Pediatric Patients with Relapsed, Refractory, or High-Risk Leukemias: A Report from the LEAP Consortium Autor Yana Pikman, Sarah K. Tasian, Maria Luisa Sulis, Kristen E. Stevenson, Traci M. Blonquist, Beth Apsel Winger, Todd M. Cooper, Melinda Pauly, Kelly W. Maloney, Michael J. Burke, Patrick A. Brown, Nathan Gossai, Jennifer L. McNeer, Neerav Shukla, Peter D. Cole, Justine M. Kahn, Jing Chen, Matthew J. Barth, Jeffrey A. Magee, Lisa Gennarini, Asmani A. Adhav, Catherine Clinton, Nicole Ocasio-Martinez, Giacomo Gotti, Yuting Li, Shan Lin, Alma Imamović, Cristina E. Tognon, Tasleema Patel, Haley L. Faust, Cristina F. Contreras, Anjali Cremer, Wilian A. Cortopassi, Diego Garrido Ruiz, Matthew P. Jacobson, Neekesh V. Dharia, Angela Su, Amanda L. Robichaud, Amy Saur Conway, Katherine Tarlock, Elliot Stieglitz, Andrew E. Place, Alexandre Puissant, Stephen P. Hunger, Annette S. Kim, Neal I. Lindeman, Lia Gore, Katherine A. Janeway, Lewis B. Silverman, Jeffrey W. Tyner, Marian H. Harris, Mignon L. Loh, Kimberly Stegmaier

    Vydáno 2021
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  11. 11
    Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes

    Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes Autor Catherine Goudie, Leora Witkowski, Noelle Cullinan, Lara Reichman, Ian Schiller, Melissa Tachdjian, Linlea Armstrong, Katherine A Blood, Josée Brossard, Ledia Brunga, Chantel Cacciotti, Kimberly Caswell, Sonia Cellot, M. Clark, Catherine Clinton, Hallie Coltin, Kathleen Felton, Conrad V. Fernandez, Adam Fleming, Noemi Fuentes-Bolanos, Paul Gibson, Ronald Grant, Rawan Hammad, Lynn W. Harrison, Meredith S. Irwin, Donna L. Johnston, Sarah Kane, Lucie Lafay‐Cousin, Irene Lara‐Corrales, Valérie Larouche, Natalie Mathews, M. Stephen Meyn, Orli Michaeli, Renée Perrier, Meghan Pike, Angela Punnett, Vijay Ramaswamy, Jemma Say, Gino R. Somers, Uri Tabori, My Linh Thibodeau, Annie-Kim Toupin, Katherine Tucker, Kalene van Engelen, Stéphanie Vairy, Nicolas Waespe, Meera Warby, Jonathan D. Wasserman, James A. Whitlock, Daniel Sinnett, Nada Jabado, Paul C. Nathan, Adam Shlien, Junne Kamihara, Rebecca Deyell, David S. Ziegler, Kim E. Nichols, Nandini Dendukuri, David Malkin, Anita Villani, William D. Foulkes

    Vydáno 2021
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