Výsledky vyhledávání - Ana Novokmet

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  1. 1
    Recurrent Focal Copy-Number Changes and Loss of Heterozygosity Implicate Two Noncoding RNAs and One Tumor Suppressor Gene at Chromosome 3q13.31 in Osteosarcoma

    Recurrent Focal Copy-Number Changes and Loss of Heterozygosity Implicate Two Noncoding RNAs and One Tumor Suppressor Gene at Chromosome 3q13.31 in Osteosarcoma Autor Ivan Pašić, Adam Shlien, Adam D. Durbin, Dimitrios J. Stavropoulos, Berivan Baskin, Peter N. Ray, Ana Novokmet, David Malkin

    Vydáno 2010
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  2. 2
    Prevalence and Functional Consequence of <i>TP53</i> Mutations in Pediatric Adrenocortical Carcinoma: A Children's Oncology Group Study

    Prevalence and Functional Consequence of <i>TP53</i> Mutations in Pediatric Adrenocortical Carcinoma: A Children's Oncology Group Study Autor Jonathan D. Wasserman, Ana Novokmet, Claudia Eichler-Jonsson, Raul C. Ribeiro, Carlos Rodríguez‐Galindo, Gerard P. Zambetti, David Malkin

    Vydáno 2015
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  3. 3
    Excessive genomic DNA copy number variation in the Li–Fraumeni cancer predisposition syndrome

    Excessive genomic DNA copy number variation in the Li–Fraumeni cancer predisposition syndrome Autor Adam Shlien, Uri Tabori, Christian R. Marshall, Małgorzata Pieńkowska, Lars Feuk, Ana Novokmet, Sonia Nanda, Harriet Druker, Stephen W. Scherer, David Malkin

    Vydáno 2008
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  4. 4
    Anaplastic rhabdomyosarcoma in <i>TP53</i> germline mutation carriers

    Anaplastic rhabdomyosarcoma in <i>TP53</i> germline mutation carriers Autor Simone Hettmer, Natasha M. Archer, Gino R. Somers, Ana Novokmet, Amy J. Wagers, Lisa Diller, Carlos Rodríguez‐Galindo, Lisa A. Teot, David Malkin

    Vydáno 2013
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  5. 5
    A Common Molecular Mechanism Underlies Two Phenotypically Distinct 17p13.1 Microdeletion Syndromes

    A Common Molecular Mechanism Underlies Two Phenotypically Distinct 17p13.1 Microdeletion Syndromes Autor Adam Shlien, Berivan Baskin, Maria Isabel Achatz, Dimitrios J. Stavropoulos, Kim E. Nichols, Louanne Hudgins, Chantal F. Morel, Margaret P Adam, Nataliya Zhukova, Lianne E. Rotin, Ana Novokmet, Harriet Druker, Mary Shago, Peter N. Ray, Pierre Hainaut, David Malkin

    Vydáno 2010
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  6. 6
    Monoallelic Expression Determines Oncogenic Progression and Outcome in Benign and Malignant Brain Tumors

    Monoallelic Expression Determines Oncogenic Progression and Outcome in Benign and Malignant Brain Tumors Autor Erin J. Walker, Cindy Zhang, Pedro Castelo‐Branco, Cynthia Hawkins, Wesley V. Wilson, Nataliya Zhukova, Noa Alon, Ana Novokmet, Berivan Baskin, Peter N. Ray, Christiane B. Knobbe‐Thomsen, Peter B. Dirks, Michael D. Taylor, Sidney Croul, David Malkin, Uri Tabori

    Vydáno 2011
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  7. 7
    DNA methylation signature is prognostic of choroid plexus tumor aggressiveness

    DNA methylation signature is prognostic of choroid plexus tumor aggressiveness Autor Małgorzata Pieńkowska, Sanaa Choufani, Andrei L. Turinsky, Tanya Guha, Diana M. Merino, Ana Novokmet, Michael Brudno, Rosanna Weksberg, Adam Shlien, Cynthia Hawkins, Éric Bouffet, Uri Tabori, Richard J. Gilbertson, Jonathan L. Finlay, Nada Jabado, Christian Thomas, Martin Sill, David Capper, Martin Hasselblatt, David Malkin

    Vydáno 2019
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  8. 8
    Parent decision‐making around the genetic testing of children for germline <i>TP53</i> mutations

    Parent decision‐making around the genetic testing of children for germline <i>TP53</i> mutations Autor Melissa A. Alderfer, Kristin Zelley, Robert B. Lindell, Ana Novokmet, L. Phuong, Judy E. Garber, Deepika Nathan, Sarah Scollon, Nicolette M. Chun, Andrea Farkas Patenaude, James M. Ford, Sharon E. Plon, Joshua D. Schiffman, Lisa Diller, Sharon A. Savage, David Malkin, Carol A. Ford, Kim E. Nichols

    Vydáno 2014
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  9. 9
    Molecular Characterization of Choroid Plexus Tumors Reveals Novel Clinically Relevant Subgroups

    Molecular Characterization of Choroid Plexus Tumors Reveals Novel Clinically Relevant Subgroups Autor Diana M. Merino, Adam Shlien, Anita Villani, Małgorzata Pieńkowska, Stephen C. Mack, Vijay Ramaswamy, David Shih, Ruth Tatevossian, Ana Novokmet, Sanaa Choufani, Rina Dvir, Myran Ben-Arush, Brent T. Harris, Eugene Hwang, Rishi Lulla, Stefan M. Pfister, Maria Isabel Achatz, Nada Jabado, Jonathan L. Finlay, Rosanna Weksberg, Éric Bouffet, Cynthia Hawkins, Michael D. Taylor, Uri Tabori, David W. Ellison, Richard J. Gilbertson, David Malkin

    Vydáno 2014
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  10. 10
    Genome-Wide DNA Methylation Analysis Reveals Epigenetic Dysregulation of MicroRNA-34A in <i>TP53</i>-Associated Cancer Susceptibility

    Genome-Wide DNA Methylation Analysis Reveals Epigenetic Dysregulation of MicroRNA-34A in <i>TP53</i>-Associated Cancer Susceptibility Autor Nardin Samuel, Gavin W. Wilson, Mathieu Lemire, Badr Id Said, Youliang Lou, Weili Li, Diana M. Merino, Ana Novokmet, James Tran, Kim E. Nichols, Jonathan L. Finlay, Sanaa Choufani, Marc Remke, Vijay Ramaswamy, Florence M.G. Cavalli, Christine Elser, Lynn Meister, Michael D. Taylor, Uri Tabori, Meredith S. Irwin, Rosanna Weksberg, Jonathan D. Wasserman, Andrew D. Paterson, Jordan R. Hansford, Maria Isabel Achatz, Thomas J. Hudson, David Malkin

    Vydáno 2016
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  11. 11
    Li-Fraumeni Exploration Consortium Data Coordinating Center: Building an Interactive Web-Based Resource for Collaborative International Cancer Epidemiology Research for a Rare Condition

    Li-Fraumeni Exploration Consortium Data Coordinating Center: Building an Interactive Web-Based Resource for Collaborative International Cancer Epidemiology Research for a Rare Cond... Autor L. Phuong, Sharon Sand, Neiladri Saha, Mauricio Oberti, Tom Dolafi, L. Digianni, Elizabeth J. Root, Xianhua Kong, Renée C. Bremer, Karina Miranda Santiago, Jasmina Bojadzieva, Derek Barley, Ana Novokmet, Karen A. Ketchum, Ngoc Thanh Nguyên, Shine Jacob, Kim E. Nichols, Christian P. Kratz, Joshua D. Schiffman, D. Gareth Evans, Maria Isabel Achatz, Louise C. Strong, Judy E. Garber, Sweta A. Ladwa, David Malkin, Jeffrey N. Weitzel

    Vydáno 2020
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  12. 12
    Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis

    Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis Autor Nicholas Light, Mehdi Layeghifard, Ayush Attery, Vallijah Subasri, Matthew Zatzman, Nathaniel D. Anderson, Rupal Hatkar, Sasha Blay, David Chen, Ana Novokmet, Fabio Fuligni, James Tran, Richard de Borja, Himanshi Agarwal, Larissa Waldman, Lisa M. Abegglen, Daniel J. Albertson, Jonathan L. Finlay, Jordan R. Hansford, Sam Behjati, Anita Villani, Moritz Gerstung, Ludmil B. Alexandrov, Gino R. Somers, Joshua D. Schiffman, Varda Rotter, David Malkin, Adam Shlien

    Vydáno 2023
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  13. 13
    Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors

    Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors Autor Nathaniel D. Anderson, Richard de Borja, Matthew D. Young, Fabio Fuligni, Andrej Rosic, Nicola D. Roberts, Simon Hajjar, Mehdi Layeghifard, Ana Novokmet, Paul E. Kowalski, Matthew Anaka, Scott Davidson, Mehdi Zarrei, Badr Id Said, Laura Schreiner, Remi Marchand, Joseph Sitter, Nalan Gökgöz, Ledia Brunga, Garrett T. Graham, Anthony Fullam, Nischalan Pillay, Jeffrey A. Toretsky, Akihiko Yoshida, Tatsuhiro Shibata, Markus Metzler, Gino R. Somers, Stephen W. Scherer, Adrienne M. Flanagan, Peter J. Campbell, Joshua D. Schiffman, Mary Shago, Ludmil B. Alexandrov, Jay S. Wunder, Irene L. Andrulis, David Malkin, Sam Behjati, Adam Shlien

    Vydáno 2018
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