Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Neoplasms and Ddx41[original query] |
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| DDX41 mutations in myeloid neoplasms are associated with male gender, TP53 mutations and high-risk disease. American journal of hematology 2019 4 94 (7): 757-766. Quesada Andrés E, Routbort Mark J, DiNardo Courtney D, Bueso-Ramos Carlos E, Kanagal-Shamanna Rashmi, Khoury Joseph D, Thakral Beenu, Zuo Zhuang, Yin C Cameron, Loghavi Sanam, Ok Chi Y, Wang Sa A, Tang Zhenya, Bannon Sarah A, Benton Christopher B, Garcia-Manero Guillermo, Kantarjian Hagop, Luthra Rajyalakshmi, Medeiros L Jeffrey, Patel Keyur |
| Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia. Scientific reports 2020 9 10 (1): 14297. Kim Borahm, Yun Woobin, Lee Seung-Tae, Choi Jong Rok, Yoo Keon Hee, Koo Hong Hoe, Jung Chul Won, Kim Sun H |
| Germ line variants in patients with acute myeloid leukemia without a suspicion of hereditary hematologic malignancy syndrome. Blood advances 2023 7 . Francesca Guijarro, Mònica López-Guerra, Jordi Morata, Alex Bataller, Sara Paz, Josep Maria Cornet-Masana, Antònia Banús-Mulet, Laia Cuesta-Casanovas, Josep Maria Carbó, Sandra Castaño-Díez, Carlos Jiménez-Vicente, Albert Cortés-Bullich, Ana Triguero, Alexandra Martínez-Roca, Daniel Esteban, Marta Gómez-Hernando, José Ramón Álamo Moreno, Irene López-Oreja, Marta Garrote, Ruth Muñoz Risueño, Raul Tonda, Ivo G Gut, Dolors Colomer, Marina Díaz-Beya, Jordi Este |
| Prevalence and clinical expression of germline predisposition to myeloid neoplasms in adults with marrow hypocellularity. Blood 2023 5 . Elisabetta Molteni, Elisa Bono, Anna Galli, Chiara Elena, Jacqueline Ferrari, Nicolas Fiorelli, Sara Pozzi, Virginia Valeria Ferretti, Martina Sarchi, Ettore Rizzo, Virginia Camilotto, Emanuela Boveri, Mario Cazzola, Luca Malcova |
| Analysis of clinical and genomic profiles of therapy-related myeloid neoplasm in Korea. Human genomics 2023 2 17 (1): 13. Yun Jiwon, Song Hyojin, Kim Sung-Min, Kim Soonok, Kwon Seok Ryun, Lee Young Eun, Jeong Dajeong, Park Jae Hyeon, Kwon Sunghoon, Yun Hongseok, Lee Dong So |
| The clinical and genomic landscape of patients with DDX41 variants identified during diagnostic sequencing. Blood advances 2023 10 . Anna Maierhofer, Nikita Mehta, Ryan A Chisholm, Stephan Hutter, Constance Baer, Niroshan Nadarajah, Christian Pohlkamp, Ella R Thompson, Paul A James, Wolfgang Kern, Claudia Haferlach, Manja Meggendorfer, Torsten Haferlach, Piers Blombe |
| Stagnation in quality of next-generation sequencing assays for the diagnosis of hereditary hematopoietic malignancies. Journal of genetic counseling 2023 1 . Roloff Gregory W, Shaw Reid, O'Connor Timothy E, Hathaway Feighanne, Drazer Michael |
| Case Report of a DDX41 Germline Mutation in a Family with Multiple Relatives Suffering from Leukemia. Biomedicines 2024 1 12 (1): . Jan Nicolai Wagner, Maximilian Al-Bazaz, Anika Forstreuter, Mohammad Ibrahim Hammada, Jurek Hille, Dzhoy Papingi, Carsten Bokemeyer, Walter Fiedl |
- Page last reviewed:Feb 1, 2024
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