HuGE Literature Finder
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| Clinical relevance of clonal hematopoiesis in the oldest-old population. Blood 2021 Jun . Rossi Marianna, Meggendorfer Manja, Zampini Matteo, Tettamanti Mauro, Riva Emma, Travaglino Erica, Bersanelli Matteo, Mandelli Sara, Galbussera Alessia Antonella, Mosca Ettore, Saba Elena, Chiereghin Chiara, Manes Nicla, Milanesi Chiara, Ubezio Marta, Morabito Lucio, Peano Clelia, Soldà Giulia, Asselta Rosanna, Duga Stefano, Selmi Carlo, De Santis Maria, Malik Karolina, Maggioni Giulia, Bicchieri Maria Elena, Campagna Alessia, Tentori Cristina Astrid, Russo Antonio, Civilini Efrem, Allavena Paola, Piazza Rocco, Corrao Giovanni, Sala Claudia, Termanini Alberto, Giordano Laura, Detoma Paolo, Malabaila Aurelio, Sala Luca, Rosso Stefano, Zanetti Roberto, Saitta Claudia, Riva Elena, Condorelli Gianluigi, Passamonti Francesco, Santoro Armando, Sole Francesc, Platzbecker Uwe, Fenaux Pierre, Bolli Niccolo, Castellani Gastone, Kern Wolfgang, Vassiliou George, Haferlach Torsten, Lucca Ugo, Della Porta Matteo |
Clonal myelopoiesis in the UK Biobank cohort: ASXL1 mutations are strongly associated with smoking.
Leukemia 2020 Oct 34 (10): 2660-2672. Dawoud Ahmed A Z, Tapper William J, Cross Nicholas C |
| [Detection and Diagnostic Values of JAK2, CALR, MPL Gene Mutations in 208 Cases of BCR/ABL1 Negative Chronic Myeloproliferative Diseases]. Zhongguo shi yan xue ye xue za zhi 2018 Aug 26 (4): 1122-1128. Li Zhen-Ling, Gao Li, Zhang Hui, Zhang Chun-Xia, Chen Yan-Rong, Huang Fan-Zhou, Gong Ming, Gao Ya-Yue, Tang Yin, Ma Yi-G |
| Driver mutations of young lung adenocarcinoma patients with malignant pleural effusion. Genes, chromosomes & cancer 2018 Aug . Wu Shang-Gin, Liu Yi-Nan, Yu Chong-Jen, Yang James Chih-Hsin, Shih Jin-Yu |
| Copy number abnormality of acute lymphoblastic leukemia cell lines based on their genetic subtypes. International journal of hematology 2018 May . Tomoyasu Chihiro, Imamura Toshihiko, Tomii Toshihiro, Yano Mio, Asai Daisuke, Goto Hiroaki, Shimada Akira, Sanada Masashi, Iwamoto Shotaro, Takita Junko, Minegishi Masayoshi, Inukai Takeshi, Sugita Kanji, Hosoi Haji |
| High Frequency of Copy-Neutral Loss of Heterozygosity in Patients with Myelofibrosis. Cytogenetic and genome research 2018 Mar . Rego de Paula Junior Milton, Nonino Alexandre, Minuncio Nascimento Juliana, Bonadio Raphael S, Pic-Taylor Aline, de Oliveira Silviene F, Wellerson Pereira Rinaldo, do Couto Mascarenhas Cintia, Forte Mazzeu Julia |
| [The clinical characteristics, gene mutations and prognosis of chronic neutrophilic leukemia]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2017 Jan 38 (1): 28-32. Cui Y J, Jiang Q, Liu J Q, Li B, Xu Z F, Qin T J, Zhang Y, Cai W Y, Zhang H L, Fang L W, Pan L J, Hu N B, Qu S Q, Xiao Z |
| pSTAT3/pSTAT5 Signaling Patterns in Molecularly Defined Subsets of Myeloproliferative Neoplasms. Applied immunohistochemistry & molecular morphology : AIMM / official publication of the Society for Applied Immunohistochemistry 2016 Jun . Sakr Hany, Clark Schneider Kelli, Murugesan Gurunathan, Bodo Juraj, Hsi Eric D, Cook James |
| The 5q deletion size in myeloid malignancies is correlated to additional chromosomal aberrations and to TP53 mutations. Genes, chromosomes & cancer 2016 May . Stengel Anna, Kern Wolfgang, Haferlach Torsten, Meggendorfer Manja, Haferlach Claud |
| Molecular biomarkers of thrombosis in myeloproliferative neoplasms. Thrombosis research 2016 Apr 140 Suppl 1 S71-5. Barbui Tiziano, Falanga An |
| Detection of mutations in JAK2 exons 12-15 by Sanger sequencing. International journal of laboratory hematology 2015 Sep . Alghasham N, Alnouri Y, Abalkhail H, Khalil |
| JAK2 V617F, MPL, and CALR Mutations in Korean Patients with Essential Thrombocythemia and Primary Myelofibrosis. Journal of Korean medical science 2015 Jul 30 (7): 882-8. Kim Bo Hyun, Cho Young-Uk, Bae Mi-Hyun, Jang Seongsoo, Seo Eul-Ju, Chi Hyun-Sook, Choi Yunsuk, Kim Dae-Young, Lee Jung-Hee, Lee Je-Hwan, Lee Kyoo-Hyung, Park Young-Mi, Lee Jong-Keuk, Park Chan-Jeou |
| Next-generation sequencing of acute myeloid leukemia identifies the significance of TP53, U2AF1, ASXL1, and TET2 mutations. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2015 May 28 (5): 706-14. Ohgami Robert S, Ma Lisa, Merker Jason D, Gotlib Jason R, Schrijver Iris, Zehnder James L, Arber Daniel |
| A compendium of cytogenetic abnormalities in myelofibrosis: molecular and phenotypic correlates in 826 patients. British journal of haematology 2015 Apr 169 (1): 71-6. Wassie Emnet, Finke Christy, Gangat Naseema, Lasho Terra L, Pardanani Animesh, Hanson Curtis A, Ketterling Rhett P, Tefferi Ayal |
| Initial experience with genomic profiling of heavily pretreated breast cancers. Annals of surgical oncology 2014 Oct 21 (10): 3216-22. Staren Edgar D, Braun Donald, Tan Bradford, Gupta Digant, Kim Seungchan, Kramer Kim, Markman Maur |
| High number of additional genetic lesions in acute myeloid leukemia with t(8;21)/RUNX1-RUNX1T1: frequency and impact on clinical outcome. Leukemia 2014 Jul 28 (7): 1449-58. Krauth M-T, Eder C, Alpermann T, Bacher U, Nadarajah N, Kern W, Haferlach C, Haferlach T, Schnittger |
| MET and EGFR mutations identified in ALK-rearranged pulmonary adenocarcinoma: molecular analysis of 25 ALK-positive cases. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2013 May 8 (5): 574-81. Boland Jennifer M, Jang Jin Sung, Li Jun, Lee Adam M, Wampfler Jason A, Erickson-Johnson Michele R, Soares Ibere, Yang Ping, Jen Jin, Oliveira Andre M, Yi Eunhee |
| Outcome in children with Down's syndrome and acute lymphoblastic leukemia: role of IKZF1 deletions and CRLF2 aberrations. Leukemia 2012 Oct 26 (10): 2204-11. Buitenkamp T D, Pieters R, Gallimore N E, van der Veer A, Meijerink J P P, Beverloo H B, Zimmermann M, de Haas V, Richards S M, Vora A J, Mitchell C D, Russell L J, Schwab C, Harrison C J, Moorman A V, van den Heuvel-Eibrink M M, den Boer M L, Zwaan C |
| Absence of JAK2V617F mutation in patients with beta-thalassemia major and thrombocytosis due to splenectomy. Molecular biology reports 2012 May 39 (5): 6101-5. Vlachaki E, Kalogeridis A, Neokleous N, Perifanis V, Klonizakis F, Ioannidou E, Klonizakis |
| Genetic analysis of patients with leukemic transformation of myeloproliferative neoplasms shows recurrent SRSF2 mutations that are associated with adverse outcome. Blood 2012 May 119 (19): 4480-5. Zhang Su-Jiang, Rampal Raajit, Manshouri Taghi, Patel Jay, Mensah Nana, Kayserian Andrew, Hricik Todd, Heguy Adriana, Hedvat Cyrus, Gönen Mithat, Kantarjian Hagop, Levine Ross L, Abdel-Wahab Omar, Verstovsek Srd |
| Association of JAK2 mutation status and cytogenetic abnormalities in myeloproliferative neoplasms and myelodysplastic/myeloproliferative neoplasms. American journal of clinical pathology 2011 May 135 (5): 709-19. Dunlap Jennifer, Kelemen Katalin, Leeborg Nicky, Braziel Rita, Olson Susan, Press Richard, Huang James, Gatter Ken, Loriaux Marc, Fan Gua |
| CBL, CBLB, TET2, ASXL1, and IDH1/2 mutations and additional chromosomal aberrations constitute molecular events in chronic myelogenous leukemia. Blood 2011 May 117 (21): e198-206. Makishima Hideki, Jankowska Anna M, McDevitt Michael A, O'Keefe Christine, Dujardin Simon, Cazzolli Heather, Przychodzen Bartlomiej, Prince Courtney, Nicoll John, Siddaiah Harish, Shaik Mohammed, Szpurka Hadrian, Hsi Eric, Advani Anjali, Paquette Ronald, Maciejewski Jaroslaw |
| Impact of JAK2V617F mutation status, allele burden, and clearance after allogeneic stem cell transplantation for myelofibrosis. Blood 2010 Nov 116 (18): 3572-81. Alchalby Haefaa, Badbaran Anita, Zabelina Tatjana, Kobbe Guido, Hahn Joachim, Wolff Daniel, Bornhäuser Martin, Thiede Christian, Baurmann Herrad, Bethge Wolfgang, Hildebrandt York, Bacher Ulrike, Fehse Boris, Zander Axel R, Kröger Nicola |
| JAK2 V617F mutation in myelodysplastic syndrome, myelodysplastic syndrome/myeloproliferative neoplasm, unclassifiable, refractory anemia with ring sideroblasts with thrombocytosis, and acute myeloid leukemia. The Korean journal of hematology 2010 Mar 45 (1): 46-50. Jekarl Dong Wook, Han Sang Bong, Kim Myungshin, Lim Jihyang, Oh Eun-Jee, Kim Yonggoo, Kim Hee-Je, Min Woo-Sung, Han Kyung |
| Genetic changes including gene copy number alterations and their relation to prognosis in childhood acute myeloid leukemia. Leukemia & lymphoma 2010 Jan 51 (1): 114-24. Armengol Gemma, Canellas Anna, Alvarez Yolanda, Bastida Pilar, Toledo José Sánchez De, Pérez-Iribarne Maria Del Mar, Camós Mireia, Tuset Esperanza, Estella Jesús, Coll María Dolores, Caballín María Rosa, Knuutila Saka |
| Quantitative assay for the detection of the V617F variant in the Janus kinase 2 (JAK2) gene using the Luminex xMAP technology. BMC medical genetics 2010 11 (1): 54. Paradis François W, Simard Raynald, Gaudet Dani |
| Prevalence and clinical correlates of JAK2 mutations in Down syndrome acute lymphoblastic leukaemia. British journal of haematology 2009 Mar 144 (6): 930-2. Gaikwad Amos, Rye Cassia L, Devidas Meenakshi, Heerema Nyla A, Carroll Andrew J, Izraeli Shai, Plon Sharon E, Basso Giuseppe, Pession Andrea, Rabin Karen |
| 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:Oct 20, 2021
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