HuGE Literature Finder
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A multi-omic approach identifies an autism spectrum disorder (ASD) regulatory complex of functional epimutations in placentas from children born preterm. Autism research : official journal of the International Society for Autism Research 2023 3 . Freedman Anastasia N, Clark Jeliyah, Eaves Lauren A, Roell Kyle, Oran Ali, Koval Lauren, Rager Julia, Santos Hudson P, Kuban Karl, Joseph Robert M, Frazier Jean, Marsit Carmen J, Burt Amber A, O'Shea T Michael, Fry Rebecca |
Combined low-pass whole genome and targeted sequencing in liquid biopsies for pediatric solid tumors. NPJ precision oncology 2023 2 7 (1): 21. Christodoulou Eirini, Yellapantula Venkata, O'Halloran Katrina, Xu Liya, Berry Jesse L, Cotter Jennifer A, Zdanowicz Anya, Mascarenhas Leo, Amatruda James F, Ostrow Dejerianne, Bootwalla Moiz, Gai Xiaowu, Navid Fariba, Biegel Jaclyn |
Keratin-positive fibrotic extraskeletal myxoid chondrosarcoma: a close mimic of myoepithelial tumour. Histopathology 2023 2 . Sugino Hirokazu, Iwata Shintaro, Satomi Kaishi, Mori Taisuke, Nobusawa Sumihito, Nagashima Toshiteru, Matsushita Yuko, Yatabe Yasushi, Ichimura Koichi, Kawai Akira, Yoshida Akihi |
Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding. American journal of human genetics 2023 2 110 (3): 427-441. Lee Olivia W, Rodrigues Calvin, Lin Shu-Hong, Luo Wen, Jones Kristine, Brown Derek W, Zhou Weiyin, Karlins Eric, Khan Sairah M, Baulande Sylvain, Raynal Virginie, Surdez Didier, Reynaud Stephanie, Rubio Rebeca Alba, Zaidi Sakina, Grossetête Sandrine, Ballet Stelly, Lapouble Eve, Laurence Valérie, Pierron Gaelle, Gaspar Nathalie, Corradini Nadège, Marec-Bérard Perrine, Rothman Nathaniel, Dagnall Casey L, Burdett Laurie, Manning Michelle, Wyatt Kathleen, Yeager Meredith, Chari Raj, Leisenring Wendy M, Kulozik Andreas E, Kriebel Jennifer, Meitinger Thomas, Strauch Konstantin, Kirchner Thomas, Dirksen Uta, Mirabello Lisa, Tucker Margaret A, Tirode Franck, Armstrong Gregory T, Bhatia Smita, Robison Leslie L, Yasui Yutaka, Romero-Pérez Laura, Hartmann Wolfgang, Metzler Markus, Diver W Ryan, Lori Adriana, Freedman Neal D, Hoover Robert N, Morton Lindsay M, Chanock Stephen J, Grünewald Thomas G P, Delattre Olivier, Machiela Mitchell |
Mutational landscape of primary and recurrent Ewing sarcoma. Contemporary oncology (Poznan, Poland) 2022 1 25 (4): 241-248. Jagodzi?ska-Mucha Paulina, Sobczuk Pawe?, Miku?a Micha?, Raciborska Anna, Dawidowska Anna, Kulecka Maria, Bilska Katarzyna, Szumera-Cie?kiewicz Anna, Kluska Anna, Pi?tkowska Magdalena, Ba?abas Anna, Rutkowski Piotr, ?ugowska Iwo |
Identification of novel SSX1 fusions in synovial sarcoma. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2021 9 35 (2): 228-239. Yoshida Akihiko, Arai Yasuhito, Satomi Kaishi, Kubo Takashi, Ryo Eijitsu, Matsushita Yuko, Hama Natsuko, Sudo Kazuki, Komiyama Motokiyo, Yatabe Yasushi, Shibata Tatsuhiro, Ichikawa Hitoshi, Ichimura Koichi, Kawai Akira, Mori Taisu |
Intracranial mesenchymal tumors with FET-CREB fusion are composed of at least two epigenetic subgroups distinct from meningioma and extracranial sarcomas. Brain pathology (Zurich, Switzerland) 2021 11 32 (4): e13037. Sloan Emily A, Gupta Rohit, Koelsche Christian, Chiang Jason, Villanueva-Meyer Javier E, Alexandrescu Sanda, Eschbacher Jennifer M, Wang Wesley, Mafra Manuela, Ud Din Nasir, Carr-Boyd Emily, Watson Michael, Punsoni Michael, Oviedo Angelica, Gilani Ahmed, Kleinschmidt-DeMasters Bette K, Coss Dylan J, Lopes M Beatriz, Reddy Alyssa, Mueller Sabine, Cho Soo-Jin, Horvai Andrew E, Lee Julieann C, Pekmezci Melike, Tihan Tarik, Bollen Andrew W, Rodriguez Fausto J, Ellison David W, Perry Arie, von Deimling Andreas, Chang Susan M, Berger Mitchel S, Solomon David |
Lupus susceptibility region containing CTLA4 rs17268364 functionally reduces CTLA4 expression by binding EWSR1 and correlates IFN-? signature. Arthritis research & therapy 2021 11 23 (1): 279. Qi Yuan-Yuan, Zhao Xin-Yu, Liu Xin-Ran, Wang Yan-Na, Zhai Ya-Ling, Zhang Xiao-Xue, Wang Xiao-Yang, Zhang Li-Jie, Zhao Ya-Fei, Cui Yan, Ning Xiang-Hui, Zhou Xu-J |
Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma.
![]() PloS one 2020 15 (9): e0237792. Lin Shu-Hong, Sampson Joshua N, Grünewald Thomas G P, Surdez Didier, Reynaud Stephanie, Mirabeau Olivier, Karlins Eric, Rubio Rebeca Alba, Zaidi Sakina, Grossetête-Lalami Sandrine, Ballet Stelly, Lapouble Eve, Laurence Valérie, Michon Jean, Pierron Gaelle, Kovar Heinrich, Kontny Udo, González-Neira Anna, Alonso Javier, Patino-Garcia Ana, Corradini Nadège, Bérard Perrine Marec, Miller Jeremy, Freedman Neal D, Rothman Nathaniel, Carter Brian D, 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, Krumbholz Manuela, Hartmann Wolfgang, Strauch Konstantin, Kirchner Thomas, Dirksen Uta, Mirabello Lisa, Tucker Margaret A, Tirode Franck, Morton Lindsay M, Chanock Stephen J, Delattre Olivier, Machiela Mitchell |
Recurrent secondary genomic alterations in desmoplastic small round cell tumors. BMC medical genetics 2020 5 21 (1): 101. Chow Warren A, Yee Jiing-Kuan, Tsark Walter, Wu Xiwei, Qin Hanjun, Guan Min, Ross Jeffrey S, Ali Siraj M, Millis Sherri |
The spectrum of rare central nervous system (CNS) tumors with EWSR1-non-ETS fusions: experience from three pediatric institutions with review of the literature. Brain pathology (Zurich, Switzerland) 2020 9 31 (1): 70-83. Lopez-Nunez Oscar, Cafferata Barbara, Santi Mariarita, Ranganathan Sarangarajan, Pearce Thomas M, Kulich Scott M, Bailey Kelly M, Broniscer Alberto, Rossi Sabrina, Zin Angelica, Nasrallah MacLean P, Li Marilyn M, Zhong Yiming, Miele Evelina, Alaggio Rita, Surrey Lea |
DNA Methylation-Based Classifier for Accurate Molecular Diagnosis of Bone Sarcomas. JCO precision oncology 2018 1 2017 . Wu S Peter, Cooper Benjamin T, Bu Fang, Bowman Christopher J, Killian J Keith, Serrano Jonathan, Wang Shiyang, Jackson Twana M, Gorovets Daniel, Shukla Neerav, Meyers Paul A, Pisapia David J, Gorlick Richard, Ladanyi Marc, Thomas Kristen, Snuderl Matija, Karajannis Matthias |
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 |
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 |
Comparison of clinical features and outcomes in patients with extraskeletal versus skeletal localized Ewing sarcoma: A report from the Children's Oncology Group. Pediatric blood & cancer 2016 10 63 (10): 1771-9. Cash Thomas, McIlvaine Elizabeth, Krailo Mark D, Lessnick Stephen L, Lawlor Elizabeth R, Laack Nadia, Sorger Joel, Marina Neyssa, Grier Holcombe E, Granowetter Linda, Womer Richard B, DuBois Steven |
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, |
The genomic landscape of the Ewing Sarcoma family of tumors reveals recurrent STAG2 mutation. PLoS genetics 2014 Jul 10 (7): e1004475. Brohl Andrew S, Solomon David A, Chang Wendy, Wang Jianjun, Song Young, Sindiri Sivasish, Patidar Rajesh, Hurd Laura, Chen Li, Shern Jack F, Liao Hongling, Wen Xinyu, Gerard Julia, Kim Jung-Sik, Lopez Guerrero Jose Antonio, Machado Isidro, Wai Daniel H, Picci Piero, Triche Timothy, Horvai Andrew E, Miettinen Markku, Wei Jun S, Catchpool Daniel, Llombart-Bosch Antonio, Waldman Todd, Khan Jav |
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 |
Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.
![]() Nature genetics 2012 Mar 44 (3): 323-7. Postel-Vinay Sophie, Véron Amélie S, Tirode Franck, Pierron Gaelle, Reynaud Stéphanie, Kovar Heinrich, Oberlin Odile, Lapouble Eve, Ballet Stelly, Lucchesi Carlo, Kontny Udo, González-Neira Anna, Picci Piero, Alonso Javier, Patino-Garcia Ana, de Paillerets Brigitte Bressac, Laud Karine, Dina Christian, Froguel Philippe, Clavel-Chapelon Françoise, Doz Francois, Michon Jean, Chanock Stephen J, Thomas Gilles, Cox David G, Delattre Olivi |
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- Page last updated:Mar 30, 2023
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