HuGE Literature Finder
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| Prognostic impact of the adverse molecular-genetic profile on long-term outcomes following allogeneic hematopoietic stem cell transplantation in acute myeloid leukemia. Bone marrow transplantation 2021 Mar . Daher-Reyes Georgina, Kim TaeHyung, Novitzky-Basso Igor, Kim Kyuoung Ha, Smith Adam, Stockley Tracy, Capochichi Jose-Mario, Al-Shaibani Zeyad, Pasic Ivan, Law Arjun, Lam Wilson, Michelis Fotios V, Gerbitz Armin, Viswabandya Auro, Lipton Jeffrey, Kumar Rajat, Mattsson Jonas, Schimmer Aaron, McNamara Caroline, Murphy Tracy, Maze Dawn, Gupta Vikas, Sibai Hassan, Chan Steven, Yee Karen, Minden Mark, Zhang Zhaolei, Schuh Andre, Kim Dennis D |
| Clinicopathologic Characterization of Hypocellular Acute Myeloid Leukemia (AML) Showed Fewer Genetic Abnormalities Involving Cell Proliferation and NPM1 When Compared With Nonhypocellular AML. American journal of clinical pathology 2020 Oct . Carlsen Eric, Bailey Nathanael G, Aggarwal Nidhi, Illar Gwendolyn M, Wild Matthew, Yatsenko Svetlana A, Rea Bryan, Liu Yen-Ch |
| Outcomes of adult patients with acute myeloid leukemia and unsuccessful cytogenetic analysis undergoing allogeneic hematopoietic stem cell transplantation. Hematology/oncology and stem cell therapy 2020 Oct . Nampoothiri Ram Vasudevan, Chen Shiyi, Pasic Ivan, Al-Shaibani Zeyad, Lam Wilson, Michelis Fotios V, Kim Dennis Dong Hwan, Viswabandya Auro, Gerbitz Armin, Lipton Jeffrey Howard, Kumar Rajat, Mattsson Jonas, Law Arjun Da |
| Analysis of SNP Array Abnormalities in Patients with DE NOVO Acute Myeloid Leukemia with Normal Karyotype. Scientific reports 2020 Apr 10 (1): 5904. Ibáñez Mariam, Such Esperanza, Onecha Esther, Gómez-Seguí Inés, Liquori Alessandro, Sellés Jorge, Hervás-Marín David, Barragán Eva, Ayala Rosa, LLop Marta, López-Pavía María, Rapado Inmaculada, Neef Alex, Sanjuan-Pla Alejandra, Sargas Claudia, Gonzalez-Romero Elisa, Boluda-Navarro Mireia, Andreu Rafa, Senent Leonor, Montesinos Pau, Martínez-López Joaquín, Angel Sanz Miguel, Sanz Guillermo, Cervera Jo |
| [Significance of detecting minimal/measurable residual disease utilizing genetic mutations in acute myeloid leukemia]. [Rinsho ketsueki] The Japanese journal of clinical hematology 2020 61 (8): 965-970. Yamaguchi Hiro |
| Gene mutational analysis by NGS and its clinical significance in patients with myelodysplastic syndrome and acute myeloid leukemia. Experimental hematology & oncology 2020 9 2. Yu Jifeng, Li Yingmei, Li Tao, Li Yafei, Xing Haizhou, Sun Hui, Sun Ling, Wan Dingming, Liu Yanfang, Xie Xinsheng, Jiang Zhongxi |
| [Characterizing the molecular cytogenetics in acute monocytic leukemia]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 Jun 36 (6): 556-560. Zhou Feng, Chao Hongying, Lu Xuzhang, Chen Tao, Yang Jianhe, Jiang Naike, Cen Ling, Zhou M |
| The genetics and clinical characteristics of children morphologically diagnosed as acute promyelocytic leukemia. Leukemia 2019 Jun 33 (6): 1387-1399. Zhao Jie, Liang Jian-Wei, Xue Hui-Liang, Shen Shu-Hong, Chen Jing, Tang Yan-Jing, Yu Li-Sha, Liang Huan-Huan, Gu Long-Jun, Tang Jing-Yan, Li Ben-Sha |
| The combination of NPM1, DNMT3A, and IDH1/2 mutations leads to inferior overall survival in AML. American journal of hematology 2019 May . Dunlap Jennifer B, Leonard Jessica, Rosenberg Mara, Cook Rachel, Press Richard, Fan Guang, Raess Philipp, Druker Brian J, Traer El |
| Identification of FLT3 and NPM1 Mutations in Patients with Acute Myeloid Leukaemia. Asian Pacific journal of cancer prevention : APJCP 2019 06 20 (6): 1749-1755. Mat Yusoff Yuslina, Abu Seman Zahidah, Othman Norodiyah, Kamaluddin Nor Rizan, Esa Ezalia, Zulkiply Nor Amalina, Abdullah Julia, Zakaria Zubaid |
| Presence of copy number aberration and clinical prognostic factors in patients with acute myeloid leukemia: an analysis of effect modification. Polish archives of internal medicine 2019 12 . Banescu Claudia, Tripon Florin, Trifa Adrian P, Crauciuc Andrei G, Bogli? Alina, Lazar Erzsebet, Dima Delia, Macarie Ioan, Duicu Carmen, Iancu Mihae |
| CSF3R Mutations are frequently associated with abnormalities of RUNX1, CBFB, CEBPA, and NPM1 genes in acute myeloid leukemia. Cancer 2018 Jun . Zhang Yang, Wang Fang, Chen Xue, Zhang Yu, Wang Mingyu, Liu Hong, Cao Panxiang, Ma Xiaoli, Wang Tong, Zhang Jianping, Zhang Xian, Lu Peihua, Liu Hongxi |
| Association of mutations with morphological dysplasia in de novo acute myeloid leukemia without 2016 WHO Classification-defined cytogenetic abnormalities. Haematologica 2018 Jan . Weinberg Olga K, Gibson Christopher J, Blonquist Traci M, Neuberg Donna, Pozdnyakova Olga, Kuo Frank, Ebert Benjamin L, Hasserjian Robert |
| Prognostic utility of six mutated genes for older patients with acute myeloid leukemia. International journal of cancer 2018 04 142 (8): 1664-1670. Wang Jinghan, Ma Zhixin, Wang Qinrong, Guo Qi, Huang Jiansong, Yu Wenjuan, Wang Huanping, Huang Jingwen, Washington Shao Yang, Chen Suning, Jin J |
| [EVI1 expression, clinical and cytogenetical characteristics in 447 patients with acute myeloid leukemia]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2016 Nov 37 (11): 936-941. He X F, Wang Q R, Cen J N, Qiu H Y, Sun A N, Chen S N, Wu D |
| Examination of the FLT3 and NPM1 mutational status in patients with acute myeloid leukemia from southeastern Poland. Archives of medical science : AMS 2016 Feb 12 (1): 120-8. Koczkodaj Dorota, Zmorzy?ski Szymon, Michalak-Wojnowska Ma?gorzata, W?sik-Szczepanek Ewa, Filip Agata |
| 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 |
| The Prognostic Relevance of BAALC and ERG Expression Levels in Cytogenetically Normal Pediatric Acute Myeloid Leukemia. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2015 Mar 31 (1): 21-8. Aref Salah, Al Khodary Tawfik, Zeed Tarek Abou, El Sadiek Amre, El Menshawy Nadia, Al Ashery Ras |
| 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 |
| Double CEBPA mutations are prognostically favorable in non-M3 acute myeloid leukemia patients with wild-type NPM1 and FLT3-ITD. International journal of clinical and experimental pathology 2014 7 (10): 6832-40. Wen Xiang-Mei, Lin Jiang, Yang Jing, Yao Dong-Ming, Deng Zhao-Qun, Tang Chun-Yan, Xiao Gao-Fei, Yang Lei, Ma Ji-Chun, Hu Jia-Bo, Qian Wei, Qian J |
| Potential application of IDH1 and IDH2 mutations as prognostic indicators in non-promyelocytic acute myeloid leukemia: a meta-analysis. Leukemia & lymphoma 2012 Dec 53 (12): 2423-9. Zhou Kuang-Guo, Jiang Li-Jun, Shang Zhen, Wang Jue, Huang Liang, Zhou Jian-Fe |
| Rapid screening of ASXL1, IDH1, IDH2, and c-CBL mutations in de novo acute myeloid leukemia by high-resolution melting. The Journal of molecular diagnostics : JMD 2012 Aug . Ibañez M, Such E, Cervera J, Luna I, Gomez-Seguí I, Lopez-Pavía M, Dolz S, Barragan E, Fuster O, Llop M, Rodriguez-Veiga R, Avaria A, Oltra S, Leonor Senent M, Moscardó F, Montesinos P, Martinez-Cuadrón D, Martín G, Sanz MA |
| ETV6 rearrangements are recurrent in myeloid malignancies and are frequently associated with other genetic events. Genes, chromosomes & cancer 2012 Apr 51 (4): 328-37. Haferlach Claudia, Bacher Ulrike, Schnittger Susanne, Alpermann Tamara, Zenger Melanie, Kern Wolfgang, Haferlach Torst |
| Genetic and epigenetic similarities and differences between childhood and adult AML. Pediatric blood & cancer 2012 Apr 58 (4): 525-31. Juhl-Christensen Caroline, Ommen Hans Beier, Aggerholm Anni, Lausen Birgitte, Kjeldsen Eigil, Hasle Henrik, Hokland Pet |
| Molecular alterations of isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) metabolic genes and additional genetic mutations in newly diagnosed acute myeloid leukemia patients. Journal of hematology & oncology 2012 5 (1): 5. Chotirat Sadudee, Thongnoppakhun Wanna, Promsuwicha Orathai, Boonthimat Chetsada, Auewarakul Chirayu |
| Gene mutation patterns and their prognostic impact in a cohort of 1185 patients with acute myeloid leukemia. Blood 2011 Nov 118 (20): 5593-603. Shen Yang, Zhu Yong-Mei, Fan Xing, Shi Jing-Yi, Wang Qin-Rong, Yan Xiao-Jing, Gu Zhao-Hui, Wang Yan-Yan, Chen Bing, Jiang Chun-Lei, Yan Han, Chen Fei-Fei, Chen Hai-Min, Chen Zhu, Jin Jie, Chen Sai-Ju |
| FLT3 and NPM1 mutations in myelodysplastic syndromes: Frequency and potential value for predicting progression to acute myeloid leukemia. American journal of clinical pathology 2011 Jan 135 (1): 62-9. Bains Ashish, Luthra Rajyalakshmi, Medeiros L Jeffrey, Zuo Zhua |
| Transcription factor mutations in myelodysplastic/myeloproliferative neoplasms. Haematologica 2010 Sep 95 (9): 1473-80. Ernst Thomas, Chase Andrew, Zoi Katerina, Waghorn Katherine, Hidalgo-Curtis Claire, Score Joannah, Jones Amy, Grand Francis, Reiter Andreas, Hochhaus Andreas, Cross Nicholas C |
| FLT3 internal tandem duplication and FLT3-D835 mutation in 80 AML patients categorized into cytogenetic risk groups. Post?py higieny i medycyny do?wiadczalnej (Online) 2010 64 466-70. Ma?y Ewa, Przyborsk Marta, Nowak Tomasz, Nowak Jerzy, Januszkiewicz Danu |
| Clinico-Haematologic association and prognostic relevance of NPM1 and FLT3-ITD mutations in acute Myeloid Leukaemia. Pakistan journal of medical sciences 0 35 (1): 23-28. Mahmood Rafia, Altaf Chaudhry, Malik Hamid Saeed, Khan Saleem Ahm |
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- Page last updated:Oct 20, 2021
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