Human Genome Epidemiology Literature Finder
|
Records 1 - 28 (of 28 Records) |
| Query Trace: Disease and STAG2[original query] |
|---|
| 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 |
| Deep Sequencing in Conjunction with Expression and Functional Analyses Reveals Activation of FGFR1 in Ewing Sarcoma. Clinical cancer research : an official journal of the American Association for Cancer Research 2015 Jul . Agelopoulos Konstantin, Richter Günther H S, Schmidt Eva, Dirksen Uta, von Heyking Kristina, Moser Benjamin, Klein Hans-Ulrich, Kontny Udo, Dugas Martin, Poos Kathrin, Korsching Eberhard, Buch Thorsten, Weckesser Matthias, Schulze Isabell, Besoke Regina, Witten Anika, Stoll Monika, Köhler Gabriele, Hartmann Wolfgang, Wardelmann Eva, Rossig Claudia, Baumhoer Daniel, Jürgens Heribert, Burdach Stefan, Berdel Wolfgang E, Müller-Tidow Carst |
| The Mutational Landscape of Acute Promyelocytic Leukemia Reveals an Interacting Network of Co-Occurrences and Recurrent Mutations. PloS one 2016 11 (2): e0148346. Ibáñez Mariam, Carbonell-Caballero José, García-Alonso Luz, Such Esperanza, Jiménez-Almazán Jorge, Vidal Enrique, Barragán Eva, López-Pavía María, LLop Marta, Martín Iván, Gómez-Seguí Inés, Montesinos Pau, Sanz Miguel A, Dopazo Joaquín, Cervera Jo |
| Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia. British journal of haematology 2016 Jul . Shiba Norio, Yoshida Kenichi, Shiraishi Yuichi, Okuno Yusuke, Yamato Genki, Hara Yusuke, Nagata Yasunobu, Chiba Kenichi, Tanaka Hiroko, Terui Kiminori, Kato Motohiro, Park Myoung-Ja, Ohki Kentaro, Shimada Akira, Takita Junko, Tomizawa Daisuke, Kudo Kazuko, Arakawa Hirokazu, Adachi Souichi, Taga Takashi, Tawa Akio, Ito Etsuro, Horibe Keizo, Sanada Masashi, Miyano Satoru, Ogawa Seishi, Hayashi Yasuhi |
| The evolving genomic landscape of urothelial carcinoma. Nature reviews. Urology 2017 Feb . Glaser Alexander P, Fantini Damiano, Shilatifard Ali, Schaeffer Edward M, Meeks Joshua |
| Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies. Genetics in medicine : official journal of the American College of Medical Genetics 2018 8 21 (3): 663-675. Yuan Bo, Neira Juanita, Pehlivan Davut, Santiago-Sim Teresa, Song Xiaofei, Rosenfeld Jill, Posey Jennifer E, Patel Vipulkumar, Jin Weihong, Adam Margaret P, Baple Emma L, Dean John, Fong Chin-To, Hickey Scott E, Hudgins Louanne, Leon Eyby, Madan-Khetarpal Suneeta, Rawlins Lettie, Rustad Cecilie F, Stray-Pedersen Asbjørg, Tveten Kristian, Wenger Olivia, Diaz Jullianne, Jenkins Laura, Martin Laura, McGuire Marianne, Pietryga Marguerite, Ramsdell Linda, Slattery Leah, , Abid Farida, Bertuch Alison A, Grange Dorothy, Immken LaDonna, Schaaf Christian P, Van Esch Hilde, Bi Weimin, Cheung Sau Wai, Breman Amy M, Smith Janice L, Shaw Chad, Crosby Andrew H, Eng Christine, Yang Yaping, Lupski James R, Xiao Rui, Liu Pengf |
| An integrative bioinformatics approach reveals coding and non-coding gene variants associated with gene expression profiles and outcome in breast cancer molecular subtypes. British journal of cancer 2018 Mar . Gy?rffy Balázs, Pongor L?rinc, Bottai Giulia, Li Xiaotong, Budczies Jan, Szabó András, Hatzis Christos, Pusztai Lajos, Santarpia Libe |
| Risk stratification by somatic mutation burden in Ewing sarcoma. Cancer 2019 1 125 (8): 1357-1364. Liu Kevin X, Lamba Nayan, Hwang William L, Niemierko Andrzej, DuBois Steven G, Haas-Kogan Daphne |
| Co-occurrence of cohesin complex and Ras signaling mutations during progression from myelodysplastic syndromes to secondary acute myeloid leukemia. Haematologica 2020 Jul . Martín-Izquierdo Marta, Abáigar María, Hernández-Sánchez Jesús M, Tamborero David, López-Cadenas Félix, Ramos Fernando, Lumbreras Eva, Madinaveitia-Ochoa Andrés, Megido Marta, Labrador Jorge, Sánchez-Real Javier, Olivier Carmen, Dávila Julio, Aguilar Carlos, Rodríguez Juan N, Martín-Nuñez Guillermo, Santos-Mínguez Sandra, Miguel-García Cristina, Benito Rocío, Díez-Campelo María, Hernández-Rivas Jesús |
| Novel Genetic Variations in Acute Myeloid Leukemia in Pakistani Population. Frontiers in genetics 2020 11 560. Shahid Saba, Shakeel Muhammad, Siddiqui Saima, Ahmed Shariq, Sohail Misha, Khan Ishtiaq Ahmad, Abid Aiysha, Shamsi Tah |
| Added prognostic value of secondary AML-like gene mutations in ELN intermediate-risk older AML: ALFA-1200 study results. Blood advances 2020 May 4 (9): 1942-1949. Gardin Claude, Pautas Cécile, Fournier Elise, Itzykson Raphaël, Lemasle Emilie, Bourhis Jean-Henri, Adès Lionel, Marolleau Jean-Pierre, Malfuson Jean-Valère, Gastaud Lauris, Raffoux Emmanuel, Lambert Juliette, Braun Thorsten, Thomas Xavier, Chantepie Sylvain, Cluzeau Thomas, de Botton Stéphane, Berthon Céline, Boissel Nicolas, Duployez Nicolas, Terré Christine, Peffault de Latour Régis, Michallet Mauricette, Celli-Lebras Karine, Preudhomme Claude, Dombret Her |
| Muscle-invasive Urothelial Cancer: Association of Mutational Status with Metastatic Pattern and Survival. Radiology 2020 4 295 (3): 572-580. Alessandrino Francesco, Williams Kristin, Nassar Amin H, Gujrathi Rahul, Silverman Stuart G, Sonpavde Guru, Shinagare Atul |
| [Clinical Characteristics and Prognostic Significance of BCOR/BCORL1 Gene Mutation in Patients with Myelodysplastic Syndromes]. Zhongguo shi yan xue ye xue za zhi 2020 Dec 28 (6): 2004-2010. Cen Yan-Xia, Li Y |
| Co-mutation pattern, clonal hierarchy, and clone size concur to determine disease phenotype of SRSF2-mutated neoplasms. Leukemia 2020 12 35 (8): 2371-2381. Todisco Gabriele, Creignou Maria, Gallì Anna, Guglielmelli Paola, Rumi Elisa, Roncador Marco, Rizzo Ettore, Nannya Yasuhito, Pietra Daniela, Elena Chiara, Bono Elisa, Molteni Elisabetta, Rosti Vittorio, Catricalá Silvia, Sarchi Martina, Dimitriou Marios, Ungerstedt Johanna, Vannucchi Alessandro Maria, Hellström-Lindberg Eva, Ogawa Seishi, Cazzola Mario, Malcovati Lu |
| ASXL1 and STAG2 are common mutations in GATA2 deficiency patients with bone marrow disease and myelodysplastic syndrome. Blood advances 2021 9 6 (3): 793-807. West Robert R, Calvo Katherine R, Embree Lisa J, Wang Weixin, Tuschong Laura M, Bauer Thomas R, Tillo Desiree, Lack Justin, Droll Stephenie, Hsu Amy P, Holland Steven M, Hickstein Dennis |
| STAG2 as a prognostic biomarker in low-grade non-muscle invasive bladder cancer. Urologic oncology 2021 3 39 (7): 438.e1-438.e9. Taber Ann, Park Youngrok, Lelo Alana, Prip Frederik, Xiao Jerry, Berry Deborah L, Chaldekas Krysta, Jensen Jørgen Bjerggaard, Philips George, Kim Jung-Sik, Harris Brent T, Dyrskjøt Lars, Waldman To |
| Genomic Sequencing for Bladder Urothelial Carcinoma and Its Clinical Implications for Immunotherapy. Cancer research and treatment 2021 11 54 (3): 894-906. Kim Ryul, Hong Jung Yong, Lee Jeeyun, Kwon Ghee Young, Jeong Byong Chang, Park Se Ho |
| Clinical and genomic characterization of patients diagnosed with the provisional entity acute myeloid leukemia with BCR-ABL1, a Swedish population-based study. Genes, chromosomes & cancer 2021 Jan . Orsmark-Pietras Christina, Landberg Niklas, Lorenz Fryderyk, Uggla Bertil, Höglund Martin, Lehmann Sören, Derolf Åsa, Deneberg Stefan, Antunovic Petar, Cammenga Jörg, Möllgård Lars, Wennström Lovisa, Lilljebjörn Henrik, Rissler Marianne, Fioretos Thoas, Lazarevic Vladimir |
| Distinct genetic landscapes and their clinical implications in younger and older patients with myelodysplastic syndromes. Hematological oncology 2022 11 . Lee Wan-Hsuan, Lin Chien-Chin, Wang Yu-Hung, Yao Chi-Yuan, Kuo Yuan-Yeh, Tseng Mei-Hsuan, Peng Yen-Ling, Hsu Cheng-An, Sun Hsun-I, Chuang Yi-Kuang, Hsu Chia-Lang, Tien Feng-Ming, Tsai Cheng-Hong, Chou Wen-Chien, Hou Hsin-An, Tien Hwei-Fa |
| Adverse prognostic impact of the loss of STAG2 protein expression in patients with newly diagnosed localised Ewing sarcoma: A report from the Children's Oncology Group. British journal of cancer 2022 Oct . Shulman David S, Chen Sonja, Hall David, Nag Anwesha, Thorner Aaron R, Lessnick Stephen L, Stegmaier Kimberly, Janeway Katherine A, DuBois Steven G, Krailo Mark D, Barkauskas Donald A, Church Alanna J, Crompton Brian |
| STAG2 Protein Expression in Non-muscle-invasive Bladder Cancer: Associations with Sex, Genomic and Transcriptomic Changes, and Clinical Outcomes. European urology open science 2022 Apr 38 88-95. Gordon Naheema S, Humayun-Zakaria Nada, Goel Anshita, Abbotts Ben, Zeegers Maurice P, Cheng K K, James Nicholas D, Arnold Roland, Bryan Richard T, Ward Douglas |
| Association of social deprivation with survival in younger adult patients with AML: an Alliance study. Blood advances 2023 5 . Melanie Rebechi, Jessica Kohlschmidt, Krzysztof Mrózek, Deedra Nicolet, Alice S Mims, James S Blachly, Shelley Orwick, Karilyn Larkin, Christopher C Oakes, Andrew Hantel, Andrew J Carroll, William Blum, Bayard L Powell, Geoffrey L Uy, Richard M Stone, Richard A Larson, John C Byrd, Electra D Paskett, Jesse J Plascak, Ann-Kathrin Eisfe |
| NEXT-GENERATION SEQUENCING-BASED GENOMIC PROFILING OF CHILDREN WITH ACUTE MYELOID LEUKEMIA. The Journal of molecular diagnostics : JMD 2023 4 . Szilvia Krizsán, Borbála Péterffy, Bálint Egyed, Tibor Nagy, Endre Sebestyén, Lajos László Hegyi, Zsuzsanna Jakab, Dániel J Erdélyi, Judit Müller, György Péter, Krisztina Csanádi, Krisztián Kállay, Gergely Kriván, Gábor Barna, Gábor Bedics, Irén Haltrich, Gábor Ottóffy, Katalin Csernus, Ágnes Vojcek, Lilla Györgyi Tiszlavicz, Krisztina Mita Gábor, Ágnes Kelemen, Péter Hauser, Zsuzsanna Gaál, István Szegedi, Anikó Ujfalusi, Béla Kajtár, Csongor Kiss, András Matolcsy, Botond Tímár, Gábor Kovács, Donát Alpár, Csaba Böd |
| Interplay between chronic inflammation and clonal haematopoiesis of indeterminate potential in Behçet's disease. Arthritis research & therapy 2023 3 25 (1): 33. Park Jihye, An Hongyul, Lim Jiwoo, Park I Seul, Kim Mi Hyun, Kim Ji Hyung, Kim Seung Won, Koh Young Il, Lee Eun Young, Cheon Jae H |
| Comprehensive genomic profiling reveals molecular subsets of ASXL1-mutated myeloid neoplasms. Leukemia & lymphoma 2023 11 1-10. Steven M Johnson, James Haberberger, Jonathan Galeotti, Lori Ramkissoon, Catherine C Coombs, Daniel R Richardson, Matthew C Foster, Daniel Duncan, Nathan D Montgomery, Naomi L Ferguson, Joshua F Zeidn |
| High BM plasma S100A8/A9 is associated with a perturbed microenvironment and poor prognosis in myelodysplastic syndromes. Blood advances 2023 1 . Wang Yu-Hung, Lin Chien-Chin, Yao Chi-Yuan, Amaral Fabio, Yu Shan-Chi, Kao Chein-Jun, Shih Pin-Tsen, Hou Hsin-An, Chou Wen-Chien, Tien Hwei-Fa |
| The clinical implications of BCOR mutations in a large cohort of acute myeloid leukemia patients: a 5-year single-center retrospective study. Leukemia & lymphoma 2024 8 1-10. Deyuan Hu, Kai Shen, YuSha Guo, Xie Bing Bao, Ningzheng Dong, Suning Ch |
| [Clinical characteristics of myeloid tumors combined with the proliferation of large granular lymphocytes]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2024 7 45 (4): 396-400. C X Du, G P Xiang, L Peng, X Y Xiao, G S Teng, Y H Zhang, Y Wang, Y F Duan, Z H Shao, J B |
- Page last reviewed:Feb 1, 2024
- Content source: