HuGE Literature Finder
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| [Analysis of Gene Mutation Characteristics and Prognosis of Elderly Patients with Acute Myeloid Leukemia]. Zhongguo shi yan xue ye xue za zhi 2022 Jun 30 (3): 755-759. Zhou Nai-Cen, Li Guo-Hui, Qin Wei-Wei, Wang Wen-Qing, Guo Huai-Peng, Liu Cong, Liu |
| Clinical implications and genetic features of clonal cytopenia of undetermined significance compared to lower-risk myelodysplastic syndrome. British journal of haematology 2022 May . Choi Eun-Ji, Cho Young-Uk, Hur Eun-Hye, Park Han-Seung, Choi Yunsuk, Lee Jung-Hee, Lee Kyoo-Hyung, Kim Miyoung, Hwang Sang-Hyun, Jang Seongsoo, Park Chan-Jeoung, Seo Eul-Ju, Lee Je-Hw |
| Gender-related differences in the outcomes and genomic landscape of patients with myelodysplastic syndrome/myeloproliferative neoplasm overlap syndromes. British journal of haematology 2021 May . Karantanos Theodoros, Gondek Lukasz P, Varadhan Ravi, Moliterno Alison R, DeZern Amy E, Jones Richard J, Jain Tan |
| [Significance of Targeted Sequencing Assay for Patients with Suspected Myeloid Malignancies]. Zhongguo shi yan xue ye xue za zhi 2020 Dec 28 (6): 1985-1990. Zhang Li-Juan, Shi Yu-Ye, Chen Yue, Deng Yuan, Ding Yi-Han, Li Zan, Chen Kan-Kan, Ding Bang-He, Wang Chun-Ling, Yu Liang, He Zheng-M |
| Molecular basis of ETV6-mediated predisposition to childhood acute lymphoblastic leukemia. Blood 2020 Jul . Nishii Rina, Baskin-Doerfler Rebekah, Yang Wentao, Oak Ninad, Zhao Xujie, Yang Wenjian, Hoshitsuki Keito, Bloom Mackenzie, Verbist Katherine C, Burns Melissa A, Li Zhenhua, Lin Ting-Nien, Qian Maoxiang, Moriyama Takaya, Gastier-Foster Julie M, Rabin Karen R, Raetz Elizabeth, Mullighan Charles G, Pui Ching-Hon, Yeoh Allen Eng Juh, Zhang Jinghui, Metzger Monika, Klco Jeffery M, Hunger Stephen P, Newman Scott, Wu Gang, Loh Mignon L, Nichols Kim E, Yang Jun |
| [Analysis of RUNX1 Gene Mutation in Patients with Myelodysplastic Syndrome]. Zhongguo shi yan xue ye xue za zhi 2020 Feb 28 (1): 202-208. Cai Xiao-Hui, Chen Mei-Yu, Chao Hong-Ying, Jiang Nai-Ke, Lu Xu-Zhang, Han Wen-Min, Qin Wei, Jia Zhu-X |
| A 4-gene leukemic stem cell score can independently predict the prognosis of myelodysplastic syndrome patients. Blood advances 2020 Feb 4 (4): 644-654. Wang Yu-Hung, Lin Chien-Chin, Yao Chi-Yuan, Hsu Chia-Lang, Hou Hsin-An, Tsai Cheng-Hong, Chou Wen-Chien, Tien Hwei-Fa |
| Integration Analysis of JAK2 or RUNX1 Mutation With Bone Marrow Blast Can Improve Risk Stratification in the Patients With Lower Risk Myelodysplastic Syndrome. Frontiers in oncology 2020 10 610525. Fang Ying, Guo Juan, Wu Dong, Wu Ling-Yun, Song Lu-Xi, Zhang Zheng, Zhao You-Shan, Chang Chun-Ka |
| Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity. Breast cancer research : BCR 2018 Aug 20 (1): 87. Penkert Judith, Schmidt Gunnar, Hofmann Winfried, Schubert Stephanie, Schieck Maximilian, Auber Bernd, Ripperger Tim, Hackmann Karl, Sturm Marc, Prokisch Holger, Hille-Betz Ursula, Mark Dorothea, Illig Thomas, Schlegelberger Brigitte, Steinemann Dor |
| Prognostic tumor sequencing panels frequently identify germ line variants associated with hereditary hematopoietic malignancies. Blood advances 2018 01 2 (2): 146-150. Drazer Michael W, Kadri Sabah, Sukhanova Madina, Patil Sushant A, West Allison H, Feurstein Simone, Calderon Dalein A, Jones Matthew F, Weipert Caroline M, Daugherty Christopher K, Ceballos-López Adrián A, Raca Gordana, Lingen Mark W, Li Zejuan, Segal Jeremy P, Churpek Jane E, Godley Lucy |
| Clinical Outcomes and Co-Occurring Mutations in Patients with RUNX1-Mutated Acute Myeloid Leukemia. International journal of molecular sciences 2017 Jul 18 (8): . Khan Maliha, Cortes Jorge, Kadia Tapan, Naqvi Kiran, Brandt Mark, Pierce Sherry, Patel Keyur P, Borthakur Gautam, Ravandi Farhad, Konopleva Marina, Kornblau Steven, Kantarjian Hagop, Bhalla Kapil, DiNardo Courtney |
| Idiopathic hypereosinophilia is clonal disorder? Clonality identified by targeted sequencing. PloS one 2017 12 (10): e0185602. Lee Jee-Soo, Seo Heewon, Im Kyongok, Park Si Nae, Kim Sung-Min, Lee Eun Kyoung, Kim Jung-Ah, Lee Joon-Hee, Kwon Sunghoon, Kim Miyoung, Koh Insong, Hwang Seungwoo, Park Heung-Woo, Kang Hye-Ryun, Park Kyoung Soo, Kim Ju Han, Lee Dong So |
| Impact of genotype on leukaemic transformation in polycythaemia vera and essential thrombocythaemia. British journal of haematology 2017 09 178 (5): 764-771. Alvarez-Larrán Alberto, Senín Alicia, Fernández-Rodríguez Concepción, Pereira Arturo, Arellano-Rodrigo Eduardo, Gómez Montse, Ferrer-Marin Francisca, Martínez-López Joaquín, Camacho Laura, Colomer Dolors, Angona Anna, Navarro Blanca, Cervantes Francisco, Besses Carlos, Bellosillo Beatriz, Hernández-Boluda Juan Carl |
| RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features. Leukemia 2016 May . Gaidzik V I, Teleanu V, Papaemmanuil E, Weber D, Paschka P, Hahn J, Wallrabenstein T, Kolbinger B, Köhne C-H, Horst H A, Brossart P, Held G, Kündgen A, Ringhoffer M, Götze K, Rummel M, Gerstung M, Campbell P, Kraus J M, Kestler H A, Thol F, Heuser M, Schlegelberger B, Ganser A, Bullinger L, Schlenk R F, Döhner K, Döhner |
| The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes. British journal of haematology 2016 Mar . Olsson Linda, Zettermark Sofia, Biloglav Andrea, Castor Anders, Behrendtz Mikael, Forestier Erik, Paulsson Kajsa, Johansson Bert |
| Splicing factor mutations predict poor prognosis in patients with de novo acute myeloid leukemia. Oncotarget 2016 Jan . Hou Hsin-An, Liu Chieh-Yu, Kuo Yuan-Yeh, Chou Wen-Chien, Tsai Cheng-Hong, Lin Chien-Chin, Lin Liang-In, Tseng Mei-Hsuan, Chiang Ying-Chieh, Liu Ming-Chih, Liu Chia-Wen, Tang Jih-Luh, Yao Ming, Li Chi-Cheng, Huang Shang-Yi, Ko Bor-Sheng, Hsu Szu-Chun, Chen Chien-Yuan, Lin Chien-Ting, Wu Shang-Ju, Tsay Woei, Tien Hwei-Fa |
| Molecular Characterization of Pediatric Acute Myeloid Leukemia: Results of a Multicentric Study in Brazil. Archives of medical research 2016 11 47 (8): 656-667. Andrade Francianne Gomes, Noronha Elda Pereira, Brisson Gisele Dallapicola, Dos Santos Vicente Bueno Filipe, Cezar Ingrid Sardou, Terra-Granado Eugênia, Thuler Luiz Claudio Santos, Pombo-de-Oliveira Maria S, |
| Mutations in RAD21 disrupt regulation of APOB in patients with chronic intestinal pseudo-obstruction. Gastroenterology 2015 Apr 148 (4): 771-782.e11. Bonora Elena, Bianco Francesca, Cordeddu Lina, Bamshad Michael, Francescatto Ludmila, Dowless Dustin, Stanghellini Vincenzo, Cogliandro Rosanna F, Lindberg Greger, Mungan Zeynel, Cefle Kivanc, Ozcelik Tayfun, Palanduz Sukru, Ozturk Sukru, Gedikbasi Asuman, Gori Alessandra, Pippucci Tommaso, Graziano Claudio, Volta Umberto, Caio Giacomo, Barbara Giovanni, D'Amato Mauro, Seri Marco, Katsanis Nicholas, Romeo Giovanni, De Giorgio Rober |
| Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity. Haematologica 2015 Jan 100 (1): 42-8. Zhang Michael Y, Keel Siobán B, Walsh Tom, Lee Ming K, Gulsuner Suleyman, Watts Amanda C, Pritchard Colin C, Salipante Stephen J, Jeng Michael R, Hofmann Inga, Williams David A, Fleming Mark D, Abkowitz Janis L, King Mary-Claire, Shimamura Aki |
| Somatic mutations predict poor outcome in patients with myelodysplastic syndrome after hematopoietic stem-cell transplantation. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2014 Sep 32 (25): 2691-8. Bejar Rafael, Stevenson Kristen E, Caughey Bennett, Lindsley R Coleman, Mar Brenton G, Stojanov Petar, Getz Gad, Steensma David P, Ritz Jerome, Soiffer Robert, Antin Joseph H, Alyea Edwin, Armand Philippe, Ho Vincent, Koreth John, Neuberg Donna, Cutler Corey S, Ebert Benjamin |
| SF3B1 mutations in patients with myelodysplastic syndromes: the mutation is stable during disease evolution. American journal of hematology 2014 Aug 89 (8): E109-15. Lin Chien-Chin, Hou Hsin-An, Chou Wen-Chien, Kuo Yuan-Yeh, Wu Shang-Ju, Liu Chieh-Yu, Chen Chien-Yuan, Tseng Mei-Hsuan, Huang Chi-Fei, Lee Fen-Yu, Liu Ming-Chih, Liu Chia-Wen, Tang Jih-Luh, Yao Ming, Huang Shang-Yi, Hsu Szu-Chun, Ko Bor-Sheng, Tsay Woei, Chen Yao-Chang, Tien Hwei-Fa |
| Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis. Blood 2014 Apr 123 (14): 2229-37. Skokowa Julia, Steinemann Doris, Katsman-Kuipers Jenny E, Zeidler Cornelia, Klimenkova Olga, Klimiankou Maksim, Unalan Murat, Kandabarau Siarhei, Makaryan Vahagn, Beekman Renee, Behrens Kira, Stocking Carol, Obenauer Julia, Schnittger Susanne, Kohlmann Alexander, Valkhof Marijke G, Hoogenboezem Remco, Göhring Gudrun, Reinhardt Dirk, Schlegelberger Brigitte, Stanulla Martin, Vandenberghe Peter, Donadieu Jean, Zwaan C Michel, Touw Ivo P, van den Heuvel-Eibrink Marry M, Dale David C, Welte Ka |
| Clonal leukemic evolution in myelodysplastic syndromes with TET2 and IDH1/2 mutations. Haematologica 2014 Jan 99 (1): 28-36. Lin Tung-Liang, Nagata Yasunobu, Kao Hsiao-Wen, Sanada Masashi, Okuno Yusuke, Huang Chein-Fuang, Liang Der-Cherng, Kuo Ming-Chung, Lai Chang-Liang, Lee En-Hui, Shih Yu-Shu, Tanaka Hiroko, Shiraishi Yuichi, Chiba Kenichi, Lin Tung-Huei, Wu Jin-Hou, Miyano Satoru, Ogawa Seishi, Shih Lee-Yu |
| Dynamics of ASXL1 mutation and other associated genetic alterations during disease progression in patients with primary myelodysplastic syndrome. Blood cancer journal 2014 4 e177. Chen T-C, Hou H-A, Chou W-C, Tang J-L, Kuo Y-Y, Chen C-Y, Tseng M-H, Huang C-F, Lai Y-J, Chiang Y-C, Lee F-Y, Liu M-C, Liu C-W, Liu C-Y, Yao M, Huang S-Y, Ko B-S, Hsu S-C, Wu S-J, Tsay W, Chen Y-C, Tien H |
| AML1/RUNX1 gene point mutations in childhood myeloid malignancies. Pediatric blood & cancer 2011 Oct 57 (4): 583-7. Migas Alexandr, Savva Natallia, Mishkova Olga, Aleinikova Olga |
| Association of variants within APOE, SORL1, RUNX1, BACE1 and ALDH18A1 with dementia in Alzheimer's disease in subjects with Down syndrome. Neuroscience letters 2011 Jan 487 (2): 144-8. Patel Ashok, Rees Simon D, Kelly M Ann, Bain Steven C, Barnett Anthony H, Thalitaya Deepak, Prasher Vee |
| Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease. Gastroenterology 2010 Jul 139 (1): 130-9.e24. Roberts Kari E, Kawut Steven M, Krowka Michael J, Brown Robert S, Trotter James F, Shah Vijay, Peter Inga, Tighiouart Hocine, Mitra Nandita, Handorf Elizabeth, Knowles James A, Zacks Steven, Fallon Michael B, |
| A variant allele of Growth Factor Independence 1 (GFI1) is associated with acute myeloid leukemia. Blood 2010 Mar 115 (12): 2462-72. Khandanpour Cyrus, Thiede Christian, Valk Peter J M, Sharif-Askari Ehssan, Nückel Holger, Lohmann Dietmar, Horsthemke Bernhard, Siffert Winfried, Neubauer Andreas, Grzeschik Karl-Heinz, Bloomfield Clara D, Marcucci Guido, Maharry Kati, Slovak Marilyn L, van der Reijden Bert A, Jansen Joop H, Schackert Hans K, Afshar Khashayar, Schnittger Susanne, Peeters Justine K, Kroschinsky Frank, Ehninger Gerhard, Lowenberg Bob, Dührsen Ulrich, Möröy Tar |
| AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: prognostic implication and interaction with other gene alterations. Blood 2009 Dec 114 (26): 5352-61. Tang Jih-Luh, Hou Hsin-An, Chen Chien-Yuan, Liu Chieh-Yu, Chou Wen-Chien, Tseng Mei-Hsuan, Huang Chi-Fei, Lee Fen-Yu, Liu Ming-Chih, Yao Ming, Huang Shang-Yi, Ko Bor-Sheng, Hsu Szu-Chun, Wu Shang-Ju, Tsay Woei, Chen Yao-Chang, Lin Liang-In, Tien Hwei-Fa |
| Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype. Haematologica 2009 Feb 94 (2): 213-23. Akagi Tadayuki, Ogawa Seishi, Dugas Martin, Kawamata Norihiko, Yamamoto Go, Nannya Yasuhito, Sanada Masashi, Miller Carl W, Yung Amanda, Schnittger Susanne, Haferlach Torsten, Haferlach Claudia, Koeffler H Phill |
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- Page last updated:Jun 28, 2022
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