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| Molecular Landscape and Validation of New Genomic Classification in 2668 Adult AML Patients: Real Life Data from the PETHEMA Registry. Cancers 2023 1 15 (2): . Sargas Claudia, Ayala Rosa, Larráyoz María José, Chillón María Carmen, Carrillo-Cruz Estrella, Bilbao-Sieyro Cristina, Prados de la Torre Esther, Martínez-Cuadrón David, Rodríguez-Veiga Rebeca, Boluda Blanca, Gil Cristina, Bernal Teresa, Bergua Juan Miguel, Algarra Lorenzo, Tormo Mar, Martínez-Sánchez Pilar, Soria Elena, Serrano Josefina, Alonso-Domínguez Juan Manuel, García-Boyero Raimundo, Amigo María Luz, Herrera-Puente Pilar, Sayas María José, Lavilla-Rubira Esperanza, Martínez-López Joaquín, Calasanz María José, García-Sanz Ramón, Pérez-Simón José Antonio, Gómez-Casares María Teresa, Sánchez-García Joaquín, Barragán Eva, Montesinos Pau, On Behalf Of Pethema Grou |
| [Clinical Significance of RAS Gene Mutations in Patients with Acute Myeloid Leukemia]. Zhongguo shi yan xue ye xue za zhi 2022 Oct 30 (5): 1391-1396. Wei Ji-Feng, Qiu Hui-Ying, Chen Ze, Miao Lei, Wang Ying, Zhao Li-Dong, Cai Zhi-M |
| Clinical and Genomic Profiles of Korean Patients with MECOM Rearrangement and the t(3;21)(q26.2;q22.1) Translocation. Annals of laboratory medicine 2022 4 42 (5): 590-596. Lee Jikyo, Kim Sung Min, Kim Soonok, Yun Jiwon, Jeong Dajeong, Lee Young Eun, Roh Eun-Youn, Lee Dong So |
| The Prognostic Ability of RAS Pathway-Related Gene Mutations in Patients with Myeloid Neoplasms Treated with Hypomethylating Agents. Acta haematologica 2021 Jul 1-11. Park Hee Sue, Son Bo Ra, Shin Kyeong Seob, Byeon Seonggyu, Kim Hee Kyung, Yang Yaewon, Jeong Yusook, Han Hye Sook, Lee Ki Hyeong, Kwon Jihy |
| CSF3R T618I, SETBP1 G870S, SRSF2 P95H, and ASXL1 Q780* tetramutation co-contribute to myeloblast transformation in a chronic neutrophilic leukemia. Annals of hematology 2021 Apr . Qian Yi, Chen Yan, Li Xiaomi |
| Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia. Haematologica 2021 Mar . Kaburagi Taeko, Yamato Genki, Shiba Norio, Yoshida Kenichi, Hara Yusuke, Tabuchi Ken, Shiraishi Yuichi, Ohki Kentaro, Sotomatsu Manabu, Arakawa Hirokazu, Matsuo Hidemasa, Shimada Akira, Taki Tomohiko, Kiyokawa Nobutaka, Tomizawa Daisuke, Horibe Keizo, Miyano Satoru, Taga Takashi, Adachi Souichi, Ogawa Seishi, Hayashi Yasuhi |
| Genomic analysis of primary and secondary myelofibrosis redefines the prognostic impact of ASXL1 mutations: a FIM study. Blood advances 2021 Mar 5 (5): 1442-1451. Luque Paz Damien, Riou Jérémie, Verger Emmanuelle, Cassinat Bruno, Chauveau Aurélie, Ianotto Jean-Christophe, Dupriez Brigitte, Boyer Françoise, Renard Maxime, Mansier Olivier, Murati Anne, Rey Jérôme, Etienne Gabriel, Mansat-De Mas Véronique, Tavitian Suzanne, Nibourel Olivier, Girault Stéphane, Le Bris Yannick, Girodon François, Ranta Dana, Chomel Jean-Claude, Cony-Makhoul Pascale, Sujobert Pierre, Robles Margot, Ben Abdelali Raouf, Kosmider Olivier, Cottin Laurane, Roy Lydia, Sloma Ivan, Vacheret Fabienne, Wemeau Mathieu, Mossuz Pascal, Slama Borhane, Cussac Vincent, Denis Guillaume, Walter-Petrich Anouk, Burroni Barbara, Jézéquel Nathalie, Giraudier Stéphane, Lippert Eric, Socié Gérard, Kiladjian Jean-Jacques, Ugo Valér |
| Clinical Impact of Inherited and Acquired Genetic Variants in Mastocytosis. International journal of molecular sciences 2021 1 22 (1): . Nedoszytko Boguslaw, Arock Michel, Lyons Jonathan J, Bachelot Guillaume, Schwartz Lawrence B, Reiter Andreas, Jawhar Mohamad, Schwaab Juliana, Lange Magdalena, Greiner Georg, Hoermann Gregor, Niedoszytko Marek, Metcalfe Dean D, Valent Pet |
| Mutations in chronic myelomonocytic leukemia and their prognostic relevance. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2021 4 23 (9): 1731-1742. Jian J, Qiao Y, Li Y, Guo Y, Ma H, Liu |
| RAS Pathway Mutation Patterns in Patients With Juvenile Myelomonocytic Leukemia: A Developing Country Single-center Experience. Clinical lymphoma, myeloma & leukemia 2020 Feb . Hamdy Nayera, Bokhary Hossam, Elsayed Amr, Hozayn Walaa, Soliman Sonya, Salem Sherine, Alsheshtawi Khaled, Abdalla Amr, Hafez Hanafy, Hammad Mahmo |
| Cytogenetic and molecular landscape and its potential clinical significance in Hispanic CMML patients from Puerto Rico. Oncotarget 2020 12 11 (47): 4411-4420. Jiang Zeju, Sun Xinlai, Wu Zhao, Alhatem Albert, Zheng Ruifang, Liu Dongfang, Wang Yaqun, Kumar Dibyendu, Xia Changqing, You Bei, Wang He, Liu Chen, Jiang Jie-G |
| Juvenile myelomonocytic leukemia - A bona fide RASopathy syndrome. Best practice & research. Clinical haematology 2020 5 33 (2): 101171. Lasho Terra, Patnaik Mrinal |
| Myeloid malignancies with isolated 7q deletion can be further characterized by their accompanying molecular mutations. Genes, chromosomes & cancer 2019 Apr . Hartmann Luise, Haferlach Claudia, Meggendorfer Manja, Kern Wolfgang, Haferlach Torsten, Stengel An |
| Incorporation of mutations in five genes in the revised International Prognostic Scoring System can improve risk stratification in the patients with myelodysplastic syndrome. Blood cancer journal 2018 Apr 8 (4): 39. Hou Hsin-An, Tsai Cheng-Hong, Lin Chien-Chin, Chou Wen-Chien, Kuo Yuan-Yeh, Liu Chieh-Yu, Tseng Mei-Hsuan, Peng Yen-Ling, Liu Ming-Chih, Liu Chia-Wen, Liao Xiu-Wen, Lin Liang-In, Yao Ming, Tang Jih-Luh, Tien Hwei-Fa |
| Prognostic Role of Gene Mutations in Chronic Myelomonocytic Leukemia Patients Treated With Hypomethylating Agents. EBioMedicine 2018 Apr . Duchmann Matthieu, Yalniz Fevzi F, Sanna Alessandro, Sallman David, Coombs Catherine C, Renneville Aline, Kosmider Olivier, Braun Thorsten, Platzbecker Uwe, Willems Lise, Adès Lionel, Fontenay Michaela, Rampal Raajit, Padron Eric, Droin Nathalie, Preudhomme Claude, Santini Valeria, Patnaik Mrinal M, Fenaux Pierre, Solary Eric, Itzykson Rapha |
| Determination of CEBPA mutations by next generation sequencing in pediatric acute leukemia. Bratislavske lekarske listy 2018 119 (6): 366-372. Akin D F, Oner D A, Kurekci E, Akar |
| The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions. Nature medicine 2017 Dec . Bolouri Hamid, Farrar Jason E, Triche Timothy, Ries Rhonda E, Lim Emilia L, Alonzo Todd A, Ma Yussanne, Moore Richard, Mungall Andrew J, Marra Marco A, Zhang Jinghui, Ma Xiaotu, Liu Yu, Liu Yanling, Auvil Jaime M Guidry, Davidsen Tanja M, Gesuwan Patee, Hermida Leandro C, Salhia Bodour, Capone Stephen, Ramsingh Giridharan, Zwaan Christian Michel, Noort Sanne, Piccolo Stephen R, Kolb E Anders, Gamis Alan S, Smith Malcolm A, Gerhard Daniela S, Meshinchi Sohe |
| Targeted next-generation sequencing identifies clinically relevant mutations in patients with chronic neutrophilic leukemia at diagnosis and blast crisis. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2017 Jul . Langabeer S E, Haslam K, Kelly J, Quinn J, Morrell R, Conneally |
| Mutational profiling of acute myeloid leukemia with normal cytogenetics in Brazilian patients: the value of next-generation sequencing for genomic classification. Journal of investigative medicine : the official publication of the American Federation for Clinical Research 2017 9 65 (8): 1155-1158. de Noronha Thiago Rodrigo, Mitne-Neto Miguel, Chauffaille Maria de Lourd |
| RAS-pathway mutation patterns define epigenetic subclasses in juvenile myelomonocytic leukemia. Nature communications 2017 12 8 (1): 2126. Lipka Daniel B, Witte Tania, Toth Reka, Yang Jing, Wiesenfarth Manuel, Nöllke Peter, Fischer Alexandra, Brocks David, Gu Zuguang, Park Jeongbin, Strahm Brigitte, Wlodarski Marcin, Yoshimi Ayami, Claus Rainer, Lübbert Michael, Busch Hauke, Boerries Melanie, Hartmann Mark, Schönung Maximilian, Kilik Umut, Langstein Jens, Wierzbinska Justyna A, Pabst Caroline, Garg Swati, Catalá Albert, De Moerloose Barbara, Dworzak Michael, Hasle Henrik, Locatelli Franco, Masetti Riccardo, Schmugge Markus, Smith Owen, Stary Jan, Ussowicz Marek, van den Heuvel-Eibrink Marry M, Assenov Yassen, Schlesner Matthias, Niemeyer Charlotte, Flotho Christian, Plass Christo |
| Next-generation sequencing in systemic mastocytosis: Derivation of a mutation-augmented clinical prognostic model for survival. American journal of hematology 2016 May . Pardanani Animesh, Lasho Terra, Elala Yoseph, Wassie Emnet, Finke Christy, Reichard Kaaren K, Chen Dong, Hanson Curtis A, Ketterling Rhett P, Tefferi Ayal |
| Targeted next-generation sequencing identifies a subset of idiopathic hypereosinophilic syndrome with features similar to chronic eosinophilic leukemia, not otherwise specified. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2016 May . Wang Sa A, Tam Wayne, Tsai Albert G, Arber Daniel A, Hasserjian Robert P, Geyer Julia T, George Tracy I, Czuchlewski David R, Foucar Kathryn, Rogers Heesun J, Hsi Eric D, Bryan Rea B, Bagg Adam, Dal Cin Paola, Zhao Chong, Kelley Todd W, Verstovsek Srdan, Bueso-Ramos Carlos, Orazi Attil |
| Incidences and Prognostic Impact of c-KIT, WT1, CEBPA, and CBL Mutations, and Mutations Associated With Epigenetic Modification in Core Binding Factor Acute Myeloid Leukemia: A Multicenter Study in a Korean Population. Annals of laboratory medicine 2015 May 35 (3): 288-97. Park Sang Hyuk, Lee Hyun Ji, Kim In-Suk, Kang Jeong-Eun, Lee Eun Yup, Kim Hyeoung-Joon, Kim Yeo-Kyeoung, Won Jong-Ho, Bang Soo Mee, Kim Hawk, Song Moo-Kon, Chung Joo Seop, Shin Ho-J |
| Next-generation sequencing of acute myeloid leukemia identifies the significance of TP53, U2AF1, ASXL1, and TET2 mutations. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2015 May 28 (5): 706-14. Ohgami Robert S, Ma Lisa, Merker Jason D, Gotlib Jason R, Schrijver Iris, Zehnder James L, Arber Daniel |
| CALR mutation screening in pediatric primary myelofibrosis. Pediatric blood & cancer 2014 Dec 61 (12): 2256-62. An Wenbin, Wan Yang, Guo Ye, Chen Xiaojuan, Ren Yuanyuan, Zhang Jingliao, Chang Lixian, Wei Wei, Zhang Peihong, Zhu Xiaof |
| High number of additional genetic lesions in acute myeloid leukemia with t(8;21)/RUNX1-RUNX1T1: frequency and impact on clinical outcome. Leukemia 2014 Jul 28 (7): 1449-58. Krauth M-T, Eder C, Alpermann T, Bacher U, Nadarajah N, Kern W, Haferlach C, Haferlach T, Schnittger |
| TET2 gene mutation is unfavorable prognostic factor in cytogenetically normal acute myeloid leukemia patients with NPM1+ and FLT3-ITD - mutations. International journal of hematology 2014 Jul 100 (1): 96-104. Tian Xiaopeng, Xu Yang, Yin Jia, Tian Hong, Chen Suning, Wu Depei, Sun Aini |
| SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations. Leukemia 2013 Sep 27 (9): 1852-60. Meggendorfer M, Bacher U, Alpermann T, Haferlach C, Kern W, Gambacorti-Passerini C, Haferlach T, Schnittger |
| The importance of relative mutant level for evaluating impact on outcome of KIT, FLT3 and CBL mutations in core-binding factor acute myeloid leukemia. Leukemia 2013 Sep 27 (9): 1891-901. Allen C, Hills R K, Lamb K, Evans C, Tinsley S, Sellar R, O'Brien M, Yin J L, Burnett A K, Linch D C, Gale R |
| Prognostic score including gene mutations in chronic myelomonocytic leukemia. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2013 Jul 31 (19): 2428-36. Itzykson Raphaël, Kosmider Olivier, Renneville Aline, Gelsi-Boyer Véronique, Meggendorfer Manja, Morabito Margot, Berthon Céline, Adès Lionel, Fenaux Pierre, Beyne-Rauzy Odile, Vey Norbert, Braun Thorsten, Haferlach Torsten, Dreyfus François, Cross Nicholas C P, Preudhomme Claude, Bernard Olivier A, Fontenay Michaela, Vainchenker William, Schnittger Susanne, Birnbaum Daniel, Droin Nathalie, Solary Er |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 22, 2023
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