Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Monosomy and TP53[original query] |
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| RAS, FLT3, and TP53 mutations in therapy-related myeloid malignancies with abnormalities of chromosomes 5 and 7. Genes, chromosomes & cancer 2004 1 39 (3): 217-23. Side Lucy E, Curtiss Nicole P, Teel Kathryn, Kratz Christian, Wang Pauline W, Larson Richard A, Le Beau Michelle M, Shannon Kevin |
| Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93%. Genes, chromosomes & cancer 2014 Jun 53 (6): 524-36. Mühlbacher Verena, Zenger Melanie, Schnittger Susanne, Weissmann Sandra, Kunze Franziska, Kohlmann Alexander, Bellos Frauke, Kern Wolfgang, Haferlach Torsten, Haferlach Claud |
| Association of the type of 5q loss with complex karyotype, clonal evolution, TP53 mutation status, and prognosis in acute myeloid leukemia and myelodysplastic syndrome. Genes, chromosomes & cancer 2014 May 53 (5): 402-10. Volkert Sarah, Kohlmann Alexander, Schnittger Susanne, Kern Wolfgang, Haferlach Torsten, Haferlach Claud |
| "Double-hit" chronic lymphocytic leukemia: An aggressive subgroup with 17p deletion and 8q24 gain. American journal of hematology 2017 Dec . Chapiro Elise, Lesty Claude, Gabillaud Clémentine, Durot Eric, Bouzy Simon, Armand Marine, Le Garff-Tavernier Magali, Bougacha Nadia, Struski Stéphanie, Bidet Audrey, Laharanne Elodie, Barin Carole, Veronese Lauren, Prié Nolwen, Eclache Virginie, Gaillard Baptiste, Michaux Lucienne, Lefebvre Christine, Gaillard Jean-Baptiste, Terré Christine, Penther Dominique, Bastard Christian, Nadal Nathalie, Fert-Ferrer Sandra, Auger Nathalie, Godon Catherine, Sutton Laurent, Tournilhac Olivier, Susin Santos A, Nguyen-Khac Florence, |
| Granular cell astrocytoma: an aggressive IDH-wildtype diffuse glioma with molecular genetic features of primary glioblastoma. Brain pathology (Zurich, Switzerland) 2018 Sep . Vizcaino M Adelita, Palsgrove Doreen N, Yuan Ming, Giannini Caterina, Cabrera-Aldana Eibar Ernesto, Pallavajjala Aparna, Burger Peter C, Rodriguez Fausto |
| EVI1 expression predicts outcome in higher-risk myelodysplastic syndrome patients. Leukemia & lymphoma 2018 5 59 (12): 2929-2940. Liu Lin, Wang Jinhuan, Jiang Yanan, Xie Huan, Tang Xiaoqiong, Li Qiubai, Wang Huaquan, Zou Ping, Miao Zhaoyi, Lv Yangyang, Wang Haitao, Cao Zeng, Zhao Zhiga |
| Chromothripsis 18 in multiple myeloma patient with rapid extramedullary relapse. Molecular cytogenetics 2018 11 7. Smetana Jan, Oppelt Jan, Štork Martin, Pour Lud?k, Kuglík Pe |
| Homogeneously staining region (hsr) on chromosome 11 is highly specific for KMT2A amplification in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). Cancer genetics 2019 Jul 238 18-22. Sakhdari Ali, Tang Zhenya, Ok Chi Young, Bueso-Ramos Carlos E, Medeiros L Jeffrey, Huh Yang |
| Evolutionary Routes in Metastatic Uveal Melanomas Depend on MBD4 Alterations. Clinical cancer research : an official journal of the American Association for Cancer Research 2019 6 25 (18): 5513-5524. Rodrigues Manuel, Mobuchon Lenha, Houy Alexandre, Alsafadi Samar, Baulande Sylvain, Mariani Odette, Marande Benjamin, Ait Rais Khadija, Van der Kooij Monique K, Kapiteijn Ellen, Gassama Sieta, Gardrat Sophie, Barnhill Raymond L, Servois Vincent, Dendale Rémi, Putterman Marc, Tick Sarah, Piperno-Neumann Sophie, Cassoux Nathalie, Pierron Gaëlle, Waterfall Joshua J, Roman-Roman Sergio, Mariani Pascale, Stern Marc-Hen |
| Distinct mutation spectrum, clinical outcome and therapeutic responses of typical complex/monosomy karyotype acute myeloid leukemia carrying TP53 mutations. American journal of hematology 2019 3 94 (6): 650-657. Leung Garret M K, Zhang Chunxiao, Ng Nelson K L, Yang Ning, Lam Stephen S Y, Au Chun H, Chan Tsun L, Ma Edmond S K, Tsui Sze P, Ip Ho W, So Jason C C, Ng Margaret H L, Cheng Kelvin C K, Wong Kit F, Siu Lisa L P, Yip Sze F, Lin Shek Y, Lau June S M, Luk Tsan H, Lee Harold K K, Lau Chi K, Kho Bonnie, Kwong Yok L, Leung Anskar Y |
| Hyperhaploid plasma cell myeloma characterized by poor outcome and monosomy 17 with frequently co-occurring TP53 mutations. Blood cancer journal 2019 2 9 (3): 20. Peterson Jess F, Rowsey Ross A, Marcou Cherisse A, Pearce Kathryn E, Williamson Cynthia M, Frederick Lori A, Greipp Patricia T, Ketterling Rhett P, Kumar Shaji, Viswanatha David S, Polley Mei-Yin, Fink James M, Reichard Kaaren K, Van Dyke Daniel L, Baughn Linda |
| Poor overall survival in hyperhaploid multiple myeloma is defined by double-hit bi-allelic inactivation of TP53. Oncotarget 2019 Jan 10 (7): 732-737. Ashby Cody, Tytarenko Ruslana G, Wang Yan, Weinhold Niels, Johnson Sarah K, Bauer Michael, Wardell Christopher P, Schinke Carolina, Thanendrarajan Sharmilan, Zangari Mauricio, van Rhee Frits, Davies Faith E, Sawyer Jeffrey R, Morgan Gareth J, Walker Brian |
| TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups. Leukemia 2019 Jan . Haase Detlef, Stevenson Kristen E, Neuberg Donna, Maciejewski Jaroslaw P, Nazha Aziz, Sekeres Mikkael A, Ebert Benjamin L, Garcia-Manero Guillermo, Haferlach Claudia, Haferlach Torsten, Kern Wolfgang, Ogawa Seishi, Nagata Yasunobu, Yoshida Kenichi, Graubert Timothy A, Walter Matthew J, List Alan F, Komrokji Rami S, Padron Eric, Sallman David, Papaemmanuil Elli, Campbell Peter J, Savona Michael R, Seegmiller Adam, Adès Lionel, Fenaux Pierre, Shih Lee-Yung, Bowen David, Groves Michael J, Tauro Sudhir, Fontenay Michaela, Kosmider Olivier, Bar-Natan Michal, Steensma David, Stone Richard, Heuser Michael, Thol Felicitas, Cazzola Mario, Malcovati Luca, Karsan Aly, Ganster Christina, Hellström-Lindberg Eva, Boultwood Jacqueline, Pellagatti Andrea, Santini Valeria, Quek Lynn, Vyas Paresh, Tüchler Heinz, Greenberg Peter L, Bejar Rafael, |
| Impact of somatic mutations in myelodysplastic patients with isolated partial or total loss of chromosome 7. Leukemia 2020 Feb . Crisà Elena, Kulasekararaj Austin G, Adema Vera, Such Esperanza, Schanz Julie, Haase Detlef, Shirneshan Katayoon, Best Steven, Mian Syed A, Kizilors Aytug, Cervera José, Lea Nicholas, Ferrero Dario, Germing Ulrich, Hildebrandt Barbara, Martínez Ana Belén Valencia, Santini Valeria, Sanz Guillermo F, Solé Francesc, Mufti Ghulam |
| RB1, p16, and Human Papillomavirus in Oropharyngeal Squamous Cell Carcinoma. Head and neck pathology 2021 4 15 (4): 1109-1118. Berdugo Jérémie, Rooper Lisa M, Chiosea Simion |
| Medulloblastoma in Adults: Cytogenetic Phenotypes Identify Prognostic Subgroups. Journal of neuropathology and experimental neurology 2021 Apr 80 (5): 419-430. Goschzik Tobias, Zur Muehlen Anja, Doerner Evelyn, Waha Andreas, Friedrich Carsten, Hau Peter, Pietsch Torst |
| 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 |
| TP53 mutation in newly diagnosed acute myeloid leukemia and myelodysplastic syndrome. Diagnostic pathology 2021 10 16 (1): 100. Niparuck Pimjai, Police Pornnapa, Noikongdee Phichchapha, Siriputtanapong Kanchana, Limsuwanachot Nittaya, Rerkamnuaychoke Budsaba, Chuncharunee Suporn, Siriboonpiputtana Teerapo |
| Differential characteristics of TP53 alterations in pure erythroid leukemia arising after exposure to cytotoxic therapy. Leukemia research 2022 5 118 106860. Tashakori Mehrnoosh, Wang Wei, Kadia Tapan M, Daver Naval G, Montalban-Bravo Guillermo, Loghavi Sanam, Wang Sa A, Medeiros L Jeffrey, Ravandi Farhad, Khoury Joseph |
| High-grade glioma with pleomorphic and pseudopapillary features (HPAP): a proposed type of circumscribed glioma in adults harboring frequent TP53 mutations and recurrent monosomy 13. Acta neuropathologica 2022 2 143 (3): 403-414. Pratt Drew, Abdullaev Zied, Papanicolau-Sengos Antonios, Ketchum Courtney, Panneer Selvam Pavalan, Chung Hye-Jung, Lee Ina, Raffeld Mark, Gilbert Mark R, Armstrong Terri S, Pytel Peter, Borys Ewa, Klonoski Joshua M, McCord Matthew, Horbinski Craig, Brat Daniel, Perry Arie, Solomon David, Eberhart Charles, Giannini Caterina, Quezado Martha, Aldape Kenne |
| Clinical features of complex karyotype in newly diagnosed acute myeloid leukemia. International journal of hematology 2022 12 . Yoshida Shota, Onozawa Masahiro, Miyashita Naoki, Kimura Hiroyuki, Takahashi Shogo, Yokoyama Shota, Matsukawa Toshihiro, Hirabayashi Shinsuke, Mori Akio, Hidaka Daisuke, Minauchi Koichiro, Shigematsu Akio, Hashiguchi Junichi, Igarashi Tetsuyuki, Kakinoki Yasutaka, Tsutsumi Yutaka, Ibata Makoto, Kobayashi Hajime, Haseyama Yoshihito, Fujimoto Katsuya, Ishihara Toshimichi, Sakai Hajime, Ota Shuichi, Kondo Takeshi, Teshima Takano |
| Genetic alterations of TP53 and OTX2 indicate increased risk of relapse in WNT medulloblastomas. Acta neuropathologica 2022 Oct . Goschzik Tobias, Mynarek Martin, Doerner Evelyn, Schenk Alina, Spier Isabel, Warmuth-Metz Monika, Bison Brigitte, Obrecht Denise, Struve Nina, Kortmann Rolf-Dieter, Schmid Matthias, Aretz Stefan, Rutkowski Stefan, Pietsch Torst |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
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