Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Syndrome and ETV6[original query] |
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| 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 |
| Germline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: a systematic genetic study. The Lancet. Oncology 2015 Oct . Moriyama Takaya, Metzger Monika L, Wu Gang, Nishii Rina, Qian Maoxiang, Devidas Meenakshi, Yang Wenjian, Cheng Cheng, Cao Xueyuan, Quinn Emily, Raimondi Susana, Gastier-Foster Julie M, Raetz Elizabeth, Larsen Eric, Martin Paul L, Bowman W Paul, Winick Naomi, Komada Yoshihiro, Wang Shuoguo, Edmonson Michael, Xu Heng, Mardis Elaine, Fulton Robert, Pui Ching-Hon, Mullighan Charles, Evans William E, Zhang Jinghui, Hunger Stephen P, Relling Mary V, Nichols Kim E, Loh Mignon L, Yang Jun |
| Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy. Nature genetics 2015 1 47 (2): 180-5. Zhang Michael Y, Churpek Jane E, Keel Siobán B, Walsh Tom, Lee Ming K, Loeb Keith R, Gulsuner Suleyman, Pritchard Colin C, Sanchez-Bonilla Marilyn, Delrow Jeffrey J, Basom Ryan S, Forouhar Melissa, Gyurkocza Boglarka, Schwartz Bradford S, Neistadt Barbara, Marquez Rafael, Mariani Christopher J, Coats Scott A, Hofmann Inga, Lindsley R Coleman, Williams David A, Abkowitz Janis L, Horwitz Marshall S, King Mary-Claire, Godley Lucy A, Shimamura Aki |
| Favorable impact of allogeneic stem cell transplantation in patients with therapy-related myelodysplasia regardless of TP53 mutational status. Haematologica 2017 10 102 (12): 2030-2038. Aldoss Ibrahim, Pham Anh, Li Sierra Min, Gendzekhadze Ketevan, Afkhami Michelle, Telatar Milhan, Hong Hao, Padeganeh Abbas, Bedell Victoria, Cao Thai, Khaled Samer K, Malki Monzr M Al, Salhotra Amandeep, Ali Haris, Aribi Ahmed, Palmer Joycelynne, Aoun Patricia, Spielberger Ricardo, Stein Anthony S, Snyder David, O'Donnell Margaret R, Murata-Collins Joyce, Senitzer David, Weisenburger Dennis, Forman Stephen J, Pullarkat Vinod, Marcucci Guido, Pillai Raju, Nakamura Ryota |
| 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 |
| A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome. Aging clinical and experimental research 2020 9 33 (7): 1987-1992. Ferrari Silvia, Regazzo Daniela, Omenetto Elisabetta, Scaroni Carla, Semenzato Gianpietro, Fabris Fabrizio, Vianello Fabriz |
| Evolution of histomorphologic, cytogenetic, and genetic abnormalities in an untreated patient with MIRAGE syndrome. Cancer genetics 2020 7 245 42-48. Rentas Stefan, Pillai Vinodh, Wertheim Gerald B, Akgumus Gozde T, Nichols Kim E, Deardorff Matthew A, Conlin Laura K, Li Marilyn M, Olson Timothy S, Luo Minj |
| 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, Burns Melissa, Li Zhenhua, Lin Ting-Nien, Qian Maoxiang, Moriyama Takaya, Gastier-Foster Julie M, Rabin Karen R, Raetz Elizabeth, Mullighan Charles, Pui Ching-Hon, Yeoh Allen Eng-Juh, Zhang Jinghui, Metzger Monika L, Klco Jeffery M, Hunger Stephen P, Newman Scott, Wu Gang, Loh Mignon L, Nichols Kim E, Yang Jun |
| Genetic alterations in Thai adult patients with acute myeloid leukemia and myelodysplastic syndrome-excess blasts detected by next-generation sequencing technique. Annals of hematology 2021 Apr . Owattanapanich Weerapat, Herzig Julia, Jahn Nikolaus, Panina Ekaterina, Ruchutrakool Theera, Kungwankiattichai Smith, Issaragrisil Surapol, Döhner Hartmut, Döhner Konstan |
| Mutations Encountered in Acute Lymphoblastic Leukemia: A Retrospective Study in a Teaching Hospital in Jeddah, Saudi Arabia. Cureus 2021 2 13 (1): e12426. Qari Mohamad H, Alattas Ali Alawi, Binkuddah Sultan Mohammed, Almarri Abdullah K, Shafy Suhayb, Alsulami Salem Khalifah, Alzuhayri Juma |
| 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 |
| The clinical and molecular spectrum of ETV6 mutated myeloid neoplasms. British journal of haematology 2023 5 . Mark Gurney, Ismahene Chekkaf, Anmol Baranwal, Rami Basmaci, Bahga Katamesh, Patricia Greipp, James M Foran, Talha Badar, Abhishek A Mangaonkar, Kebede H Begna, Naseema Gangat, Mrinal M Patnaik, Mark R Litzow, Mithun V Shah, David S Viswanatha, Rong He, Hassan B Alkhateeb, Aref Al-Ka |
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