Hakutulokset - Bailey Gallinger
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PhenomeCentral: A Portal for Phenotypic and Genotypic Matchmaking of Patients with Rare Genetic Diseases Tekijä Orion J. Buske, Marta Gîrdea, Sergiu Dumitriu, Bailey Gallinger, Taila Hartley, Heather Trang, Andriy Misyura, Tal Friedman, Chandree L. Beaulieu, William P. Bone, Amanda E. Links, Nicole L. Washington, Melissa Haendel, Peter N. Robinson, Cornelius F. Boerkoel, David R. Adams, William A. Gahl, Kym M. Boycott, Michael Brudno
Julkaistu 2015Artigo -
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The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations Tekijä Anita Villani, Scott Davidson, Nisha Kanwar, Winnie Lo, Yisu Li, Sarah Cohen‐Gogo, Fabio Fuligni, Lisa-Monique Edward, Nicholas Light, Mehdi Layeghifard, Ricardo Harripaul, Larissa Waldman, Bailey Gallinger, Federico Comitani, Ledia Brunga, Reid Hayes, Nathaniel D. Anderson, Arun Ramani, Kyoko E. Yuki, Sasha Blay, Brittney Johnstone, Cara Inglese, Rawan Hammad, Catherine Goudie, Andrew Y. Shuen, Jonathan D. Wasserman, Rosemarie E. Venier, Marianne Eliou, Miranda Lorenti, Carol Ann Ryan, Michael Braga, Meagan Gloven-Brown, Jianan Han, P. Montero, Famida Spatare, James A. Whitlock, Stephen W. Scherer, Kathy Chun, Martin J. Somerville, Cynthia Hawkins, Mohamed Abdelhaleem, Vijay Ramaswamy, Gino R. Somers, Lianna Kyriakopoulou, Johann Hitzler, Mary Shago, Daniel A. Morgenstern, Uri Tabori, M. Stephen Meyn, Meredith S. Irwin, David Malkin, Adam Shlien
Julkaistu 2022Artigo -
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Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance Tekijä Carol Durno, Ayse B. Ercan, Vanessa Bianchi, Melissa Edwards, Melyssa Aronson, Melissa A. Galati, Eshetu G. Atenafu, Gadi Abebe‐Campino, Abeer Al-Battashi, Musa Alharbi, Vahid Fallah Azad, Hagit Baris, Donald Basel, Raymond Bedgood, Anne Bendel, Shay Ben‐Shachar, Deborah T. Blumenthal, Maude L. Blundell, Miriam Bornhorst, Annika Bronsema, Elizabeth Cairney, Sara Rhode, Shani Caspi, Aghiad Chamdin, Stefano Chiaravalli, Shlomi Constantini, Bruce Crooks, Anirban Das, Rina Dvir, Roula Farah, William D. Foulkes, Z Frenkel, Bailey Gallinger, Sharon L. Gardner, David Gass, Mithra Ghalibafian, Catherine Gilpin, Yael Goldberg, Catherine Goudie, Syed Ahmer Hamid, Heather Hampel, Jordan R. Hansford, Craig Harlos, Nobuko Hijiya, Saunders Hsu, Junne Kamihara, Rejin Kebudi, Jeffrey Knipstein, Carl Koschmann, Christian P. Kratz, Valérie Larouche, Álvaro Lassaletta, Scott Lindhorst, Simon C. Ling, Michael P. Link, Rebecca Loret De Mola, Rebecca C. Luiten, Michal Lurye, Jamie L. Maciaszek, Vanan MagimairajanIssai, Ossama Maher, Maura Massimino, Rose B. McGee, Naureen Mushtaq, Gary Mason, Monica Newmark, Garth Nicholas, Kim E. Nichols, Theodore Nicolaides, Enrico Opocher, Michael Osborn, Benjamin Oshrine, Rachel Pearlman, Daniel Pettee, Jan Rapp, Mohsin Rashid, Alyssa Reddy, Lara Reichman, Marc Remke, Gabriel Robbins, Sumita Roy, Magnus Sabel, David Samuel, Isabelle Scheers, Kami Wolfe Schneider, Santanu Sen, Duncan Stearns, David Sumerauer, Carol J. Swallow, Leslie M. Taylor, Gregory A. Thomas, Helen Toledano, Patrick Tomboc, An Van Damme, Ira Winer, Michal Yalon, Yi‐Yen Lee, Michal Zápotocký, Shayna Zelcer, David S. Ziegler
Julkaistu 2021Artigo
Työkalut:
Liittyvät aiheet
Medicine
Bioinformatics
Biology
Cancer
Computational biology
Gene
Genetics
Internal medicine
Oncology
Childhood cancer
Cohort
Disease
Exome
Exome sequencing
Gastroenterology
Genome
Genomics
Germline
Germline mutation
Mutation
Pathology
Phenotype
Precision medicine
Precision oncology
Rare disease
Somatic cell
Surgery