Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Neoplasms and EWSR1[original query] |
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| Evaluation of polymorphisms in EWSR1 and risk of Ewing sarcoma: a report from the Childhood Cancer Survivor Study. Pediatric blood & cancer 2012 Jul 59 (1): 52-6. DuBois Steven G, Goldsby Robert, Segal Mark, Woo Jonathan, Copren Kirsten, Kane John P, Pullinger Clive R, Matthay Katherine K, Witte John, Lessnick Stephen L, Robison Leslie L, Bhatia Smita, Strong Louise |
| Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations. Cancer discovery 2014 Nov 4 (11): 1342-53. Tirode Franck, Surdez Didier, Ma Xiaotu, Parker Matthew, Le Deley Marie Cécile, Bahrami Armita, Zhang Zhaojie, Lapouble Eve, Grossetête-Lalami Sandrine, Rusch Michael, Reynaud Stéphanie, Rio-Frio Thomas, Hedlund Erin, Wu Gang, Chen Xiang, Pierron Gaelle, Oberlin Odile, Zaidi Sakina, Lemmon Gordon, Gupta Pankaj, Vadodaria Bhavin, Easton John, Gut Marta, Ding Li, Mardis Elaine R, Wilson Richard K, Shurtleff Sheila, Laurence Valérie, Michon Jean, Marec-Bérard Perrine, Gut Ivo, Downing James, Dyer Michael, Zhang Jinghui, Delattre Olivier, |
| Frequency and outcome of pediatric acute lymphoblastic leukemia with ZNF384 gene rearrangements including a novel translocation resulting in an ARID1B/ZNF384 gene fusion. Pediatric blood & cancer 2016 11 63 (11): 1915-21. Shago Mary, Abla Oussama, Hitzler Johann, Weitzman Sheila, Abdelhaleem Moham |
| Whole-exome sequencing identifies a somatic missense mutation of NBN in clear cell sarcoma of the salivary gland. Oncology reports 2016 Apr . Zhang Lei, Jia Zhen, Mao Fengbiao, Shi Yueyi, Bu Rong Fa, Zhang Baoro |
| Comprehensive Genomic Profiling of 282 Pediatric Low- and High-Grade Gliomas Reveals Genomic Drivers, Tumor Mutational Burden, and Hypermutation Signatures. The oncologist 2017 9 22 (12): 1478-1490. Johnson Adrienne, Severson Eric, Gay Laurie, Vergilio Jo-Anne, Elvin Julia, Suh James, Daniel Sugganth, Covert Mandy, Frampton Garrett M, Hsu Sigmund, Lesser Glenn J, Stogner-Underwood Kimberly, Mott Ryan T, Rush Sarah Z, Stanke Jennifer J, Dahiya Sonika, Sun James, Reddy Prasanth, Chalmers Zachary R, Erlich Rachel, Chudnovsky Yakov, Fabrizio David, Schrock Alexa B, Ali Siraj, Miller Vincent, Stephens Philip J, Ross Jeffrey, Crawford John R, Ramkissoon Shakti |
| Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients. Genes, chromosomes & cancer 2017 Jun . Busse Tracy M, Roth Jacquelyn J, Wilmoth Donna, Wainwright Luanne, Tooke Laura, Biegel Jaclyn |
| The Role of Molecular Testing in the Differential Diagnosis of Salivary Gland Carcinomas. The American journal of surgical pathology 2017 10 42 (2): e11-e27. Skálová Alena, Stenman Göran, Simpson Roderick H W, Hellquist Henrik, Slouka David, Svoboda Tomas, Bishop Justin A, Hunt Jennifer L, Nibu Ken-Ichi, Rinaldo Alessandra, Vander Poorten Vincent, Devaney Kenneth O, Steiner Petr, Ferlito Alf |
Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility.
Nature communications 2018 08 9 (1): 3184. Machiela Mitchell J, Grünewald Thomas G P, Surdez Didier, Reynaud Stephanie, Mirabeau Olivier, Karlins Eric, Rubio Rebeca Alba, Zaidi Sakina, Grossetete-Lalami Sandrine, Ballet Stelly, Lapouble Eve, Laurence Valérie, Michon Jean, Pierron Gaelle, Kovar Heinrich, Gaspar Nathalie, Kontny Udo, González-Neira Anna, Picci Piero, Alonso Javier, Patino-Garcia Ana, Corradini Nadège, Bérard Perrine Marec, Freedman Neal D, Rothman Nathaniel, Dagnall Casey L, Burdett Laurie, Jones Kristine, Manning Michelle, Wyatt Kathleen, Zhou Weiyin, Yeager Meredith, Cox David G, Hoover Robert N, Khan Javed, Armstrong Gregory T, Leisenring Wendy M, Bhatia Smita, Robison Leslie L, Kulozik Andreas E, Kriebel Jennifer, Meitinger Thomas, Metzler Markus, Hartmann Wolfgang, Strauch Konstantin, Kirchner Thomas, Dirksen Uta, Morton Lindsay M, Mirabello Lisa, Tucker Margaret A, Tirode Franck, Chanock Stephen J, Delattre Olivi |
| High prevalence of TERT aberrations in myxoid liposarcoma: TERT reactivation may play a crucial role in tumorigenesis. Cancer science 2021 12 113 (3): 1078-1089. Kunieda Junko, Yamashita Kyoko, Togashi Yuki, Baba Satoko, Sakata Seiji, Inamura Kentaro, Ae Keisuke, Matsumoto Seiichi, Machinami Rikuo, Kitagawa Masanobu, Takeuchi Ken |
| Molecular Analysis of Colorectal Cancers Suggests a High Frequency of Lynch Syndrome in Indonesia. Cancers 2021 12 13 (24): . Susanti Susanti, Wibowo Satrio, Akbariani Gilang, Yoshuantari Naomi, Heriyanto Didik Setyo, Ridwanuloh Asep Muhamad, Hariyatun Hariyatun, Handaya Adeodatus Yuda, Kurnianda Johan, Hutajulu Susanna Hilda, Ilyas Mohamm |
| High Probability of Lynch Syndrome Among Colorectal Cancer Patients Is Associated With Higher Occurrence of KRAS and PIK3CA Mutations. World journal of oncology 2024 7 15 (4): 612-624. Didik Setyo Heriyanto, Naomi Yoshuantari, Gilang Akbariani, Vincent Lau, Hanifa Hanini, Zulfa Hidayati, Muhammad Zulfikar Arief, Andrew Nobiantoro Gunawan, Asep Muhamad Ridwanuloh, Wien Kusharyoto, Adeodatus Yuda Handaya, Mohammad Ilyas, Johan Kurnianda, Susanna Hilda Hutajulu, Susanti Susan |
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