Human Genome Epidemiology Literature Finder
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Records 1 - 18 (of 18 Records) |
| Query Trace: Syndrome and GATA2[original query] |
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| Acquired ASXL1 mutations are common in patients with inherited GATA2 mutations and correlate with myeloid transformation. Haematologica 2014 Feb 99 (2): 276-81. West Robert R, Hsu Amy P, Holland Steven M, Cuellar-Rodriguez Jennifer, Hickstein Dennis |
| 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 |
| 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 |
| Lethal Influenza in Two Related Adults with Inherited GATA2 Deficiency. Journal of clinical immunology 2018 6 38 (4): 513-526. Sologuren Ithaisa, Martínez-Saavedra María Teresa, Solé-Violán Jordi, de Borges de Oliveira Edgar, Betancor Eva, Casas Inmaculada, Oleaga-Quintas Carmen, Martínez-Gallo Mónica, Zhang Shen-Ying, Pestano Jose, Colobran Roger, Herrera-Ramos Estefanía, Pérez Carmen, López-Rodríguez Marta, Ruiz-Hernández José Juan, Franco Nieves, Ferrer José María, Bilbao Cristina, Andújar-Sánchez Miguel, Álvarez Fernández Mercedes, Ciancanelli Michael J, Rodríguez de Castro Felipe, Casanova Jean-Laurent, Bustamante Jacinta, Rodríguez-Gallego Carl |
| 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 |
| Reanalysing genomic data by normalized coverage values uncovers CNVs in bone marrow failure gene panels. NPJ genomic medicine 2019 4 30. Lauhasurayotin Supanun, Cuvelier Geoff D, Klaassen Robert J, Fernandez Conrad V, Pastore Yves D, Abish Sharon, Rayar Meera, Steele MacGregor, Jardine Lawrence, Breakey Vicky R, Brossard Josee, Sinha Roona, Silva Mariana, Goodyear Lisa, Lipton Jeffrey H, Michon Bruno, Corriveau-Bourque Catherine, Sung Lillian, Shabanova Iren, Li Hongbing, Zlateska Bozana, Dhanraj Santhosh, Cada Michaela, Scherer Stephen W, Dror Yig |
| Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7. British journal of haematology 2020 8 191 (5): 835-843. Yoshida Masanori, Tanase-Nakao Kanako, Shima Hirohito, Shirai Ryota, Yoshida Kaoru, Osumi Tomoo, Deguchi Takao, Mori Makiko, Arakawa Yuki, Takagi Masatoshi, Miyamura Takako, Sakaguchi Kimiyoshi, Toyoda Hidemi, Ishida Hisashi, Sakata Naoki, Imamura Toshihiko, Kawahara Yuta, Morimoto Akira, Koike Takashi, Yagasaki Hiroshi, Ito Shuichi, Tomizawa Daisuke, Kiyokawa Nobutaka, Narumi Satoshi, Kato Motohi |
| Comparison of Outcomes of Myeloablative Allogeneic Stem Cell Transplantation for Pediatric Patients with Bone Marrow Failure, Myelodysplastic Syndrome and Acute Myeloid Leukemia with and without Germline GATA2 Mutations. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2020 2 26 (6): 1124-1130. Hofmann Inga, Avagyan Serine, Stetson Alyssa, Guo Dongjing, Al-Sayegh Hasan, London Wendy B, Lehmann Lesl |
| 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 |
| [Predisposition and progression of myelodysplastic syndromes]. [Rinsho ketsueki] The Japanese journal of clinical hematology 2021 5 62 (4): 278-288. Makishima Hide |
| Comparison of myeloid neoplasms with nonclassic 3q26.2/MECOM versus classic inv(3)/t(3;3) rearrangements reveals diverse clinicopathologic features, genetic profiles, and molecular mechanisms of MECOM activation. Genes, chromosomes & cancer 2021 10 61 (2): 71-80. Gao Juehua, Gurbuxani Sandeep, Zak Taylor, Kocherginsky Masha, Ji Peng, Wehbe Firas, Chen Qing, Chen Yi-Hua, Lu Xinyan, Jennings Lawrence, Frankfurt Olga, Altman Jessica, Sukhanova Madi |
| 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 |
| Somatic mutational landscape of hereditary hematopoietic malignancies caused by germ line RUNX1, GATA2, and DDX41 variants. Blood advances 2023 7 . Claire C Homan, Michael W Drazer, Kai Yu, David Michael Lawrence, Jinghua Feng, Luis Alberto Arriola-Martinez, Matthew J Pozsgai, Kelsey E McNeely, Thuong Thi Ha, Parvathy Venugopal, Peer Arts, Sarah King-Smith, Jesse Jc Cheah, Mark Armstrong, Paul Wang, Csaba Bödör, Alan B Cantor, Mario Cazzola, Erin S Degelman, Courtney D DiNardo, Nicolas Duployez, Rémi Favier, Stefan Fröhling, Ana Rio-Machin, Jeffery M Klco, Alwin Krämer, Mineo Kurokawa, Joanne Lee, Luca Malcovati, Neil V Morgan, Natsoulis Georges, Carolyn Owen, Keyur P Patel, Claude Preudhomme, Hana Raslova, Hugh Young Rienhoff, Tim Ripperger, Rachael R Schulte, Kiran Tawana, Elvira Velloso, Yan Benedict, Erika Mijin Kwon Kim, Raman Sood, Amy P Hsu, Steven M Holland, Kerry Phillips, Nicola Poplawski, Milena Babic, Andrew H Wei, Cecily J Forsyth, Helen Mar Fan, Ian Lewis, Julian P Cooney, Rachel Susman, Lucy C Fox, Piers Blombery, Deepak Singhal, Devendra K Hiwase, Belinda Phipson, Andreas W Schreiber, Christopher N Hahn, Hamish S Scott, Paul P Liu, Lucy A Godley, Anna L Bro |
| 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 |
| Gene mutation analysis using next-generation sequencing and its clinical significance in patients with myeloid neoplasm: A multi-center study from China. Cancer medicine 2023 2 . Li Junnan, Pei Li, Liang Simin, Xu Shuangnian, Wang Yi, Wang Xiao, Liao Yi, Zhan Qian, Cheng Wei, Yang Zesong, Tang Xiaoqiong, Zhang Hongbin, Xiao Qing, Chen Jianbin, Liu Lin, Wang |
| Genetic Characteristics of Patients with Young-Onset Myelodysplastic Neoplasms. Journal of clinical medicine 2023 12 12 (24): . Hyun-Young Kim, Keon Hee Yoo, Chul Won Jung, Hee-Jin Kim, Sun-Hee K |
| Gata2 Noncoding Genetic Variation as a Determinant of Hematopoietic Stem/Progenitor Cell Mobilization Efficiency. Blood advances 2023 10 . Alexandra A Soukup, Emery H Bresni |
| Influence of genetic co-mutation on chemotherapeutic outcome in NPM1-mutated and FLT3-ITD wild-type AML patients. Cancer medicine 2024 8 13 (15): e70102. Quan Wu, Yujiao Zhang, Baoyi Yuan, Yun Huang, Ling Jiang, Fang Liu, Ping Yan, Jiaying Cheng, Zhiquan Long, Xuejie Jia |
- Page last reviewed:Feb 1, 2024
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