HuGE Literature Finder
Records 1-30
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Additional gene mutations may refine the 2017 European LeukemiaNet classification in adult patients with de novo acute myeloid leukemia aged?<60 years.
Leukemia 2020 May . Eisfeld Ann-Kathrin, Kohlschmidt Jessica, Mims Alice, Nicolet Deedra, Walker Christopher J, Blachly James S, Carroll Andrew J, Papaioannou Dimitrios, Kolitz Jonathan E, Powell Bayard E, Stone Richard M, de la Chapelle Albert, Byrd John C, Mrózek Krzysztof, Bloomfield Clara |
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[Characterization of mutational pattern of patients with core-binding factor acute myeloid leukemia].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 Jul 36 (7): 657-661. He Jinyuan, Chao Hongying, Zhou Min, Lu Xuzhang, Chen Tao, Yang Jianhe, Jiang Naike, Zhang |
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Targeted sequencing aids in identifying clonality in chronic myelomonocytic leukemia.
Leukemia research 2019 Jul 84 106190. Hwang Sang Mee, Kim Sung-Min, Nam Youngwon, Kim Jinhyun, Kim Sungsik, Ahn Yong-Oon, Park Yong, Yoon Sung-Soo, Shin Sue, Kwon Sunghoon, Lee Dong So |
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Mutational spectrum and associations with clinical features in patients with acute myeloid leukaemia based on next-generation sequencing.
Molecular medicine reports 2019 Mar . Li Ying, Lv Xiao, Ge Xueling, Yuan Dai, Ding Mei, Zhen Changqing, Zhao Wenbo, Liu Xin, Wang Xianghua, Xu Hongzhi, Li Ying, Wang X |
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Chronic neutrophilic leukemia: 2018 update on diagnosis, molecular genetics and management.
American journal of hematology 2018 Aug 93 (4): 578-587. Elliott Michelle A, Tefferi Ayal |
Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study.
Molecular medicine (Cambridge, Mass.) 2018 Jun 24 (1): 30. Chattopadhyay Subhayan, Thomsen Hauke, da Silva Filho Miguel Inacio, Weinhold Niels, Hoffmann Per, Nöthen Markus M, Marina Arendt, Jöckel Karl-Heinz, Schmidt Börge, Pechlivanis Sonali, Langer Christian, Goldschmidt Hartmut, Hemminki Kari, Försti As |
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Genomic alterations of plasma cell-free DNAs in small cell lung cancer and their clinical relevance.
Lung cancer (Amsterdam, Netherlands) 2018 Jun 120 113-121. Du Meijun, Thompson Jonathan, Fisher Hannah, Zhang Peng, Huang Chiang-Ching, Wang Lia |
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Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China.
Pediatrics and neonatology 2018 Mar . Wang Rongyue, Lei Tingying, Fu Fang, Li Ru, Jing Xiangyi, Yang Xin, Liu Juan, Li Dongzhi, Liao C |
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SETBP1 mutations in Chinese patients with acute myeloid leukemia and myelodysplastic syndrome.
Pathology, research and practice 2018 Mar . Yao Xin-Yu, Zhou Jing-Dong, Yang Jing, Zhang Wei, Ma Ji-Chun, Wen Xiang-Mei, Yao Dong-Ming, Xu Zi-Jun, Wu De-Hong, He Pin-Fang, Qian Jun, Lin Jia |
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Only SETBP1 hotspot mutations are associated with refractory disease in myeloid malignancies.
Journal of cancer research and clinical oncology 2017 Sep . Winkelmann Nils, Schäfer Vivien, Rinke Jenny, Kaiser Alexander, Ernst Philipp, Scholl Sebastian, Hochhaus Andreas, Ernst Thom |
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Targeted next-generation sequencing in myelodysplastic syndromes and prognostic interaction between mutations and IPSS-R.
American journal of hematology 2017 Sep . Tefferi Ayalew, Lasho Terra L, Patnaik Mrinal M, Saeed Lyla, Mudireddy Mythri, Idossa Dame, Finke Christy, Ketterling Rhett P, Pardanani Animesh, Gangat Nasee |
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Genetic variations in cancer-related significantly mutated genes and lung cancer susceptibility.
Annals of oncology : official journal of the European Society for Medical Oncology 2017 Jul 28 (7): 1625-1630. Zhang Y, Zhang L, Li R, Chang D W, Ye Y, Minna J D, Roth J A, Han B, Wu |
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Targeted next-generation sequencing identifies clinically relevant mutations in patients with chronic neutrophilic leukemia at diagnosis and blast crisis.
Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2017 Jul . Langabeer S E, Haslam K, Kelly J, Quinn J, Morrell R, Conneally |
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Targeted next generation sequencing and identification of risk factors in World Health Organization defined atypical chronic myeloid leukemia.
American journal of hematology 2017 Mar . Patnaik Mrinal M, Barraco Daniela, Lasho Terra L, Finke Christy M, Reichard Kaaren, Hoversten Katherine P, Ketterling Rhett P, Gangat Naseema, Tefferi Ayal |
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Clinical significance of CSF3R, SRSF2 and SETBP1 mutations in chronic neutrophilic leukemia and chronic myelomonocytic leukemia.
Oncotarget 2017 Feb . Ouyang Yuan, Qiao Chun, Chen Yu, Zhang Su-Jia |
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[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 |
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Prognostic significance of SETBP1 mutations in myelodysplastic syndromes, chronic myelomonocytic leukemia, and chronic neutrophilic leukemia: A meta-analysis.
PloS one 2017 12 (2): e0171608. Shou Li-Hong, Cao Dan, Dong Xiao-Hui, Fang Qiu, Wu Ying, Zhang Yan, Fei Ju-Ping, Xu Bao-Li |
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[Characterization of mutational pattern in patients with Ph negative myeloproliferative neoplasms].
Zhonghua bing li xue za zhi = Chinese journal of pathology 2016 Sep 45 (9): 626-30. Xing F, Lin Y N, Sun Q, Qin L, Jia Y J, Zhang D L, Ru |
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Fine-mapping, Novel Loci Identification, and SNP Association Transferability in a Genome-Wide Association Study of QRS Duration in African Americans.
Human molecular genetics 2016 Aug . Evans Daniel S, Avery Christy L, Nalls Mike A, Li Guo, Barnard John, Smith Erin N, Tanaka Toshiko, Butler Anne M, Buxbaum Sarah G, Alonso Alvaro, Arking Dan E, Berenson Gerald S, Bis Joshua C, Buyske Steven, Carty Cara L, Chen Wei, Chung Mina K, Cummings Steven R, Deo Rajat, Eaton Charles B, Fox Ervin R, Heckbert Susan R, Heiss Gerardo, Hindorff Lucia A, Hsueh Wen-Chi, Isaacs Aaron, Jamshidi Yalda, Kerr Kathleen F, Liu Felix, Liu Yongmei, Lohman Kurt K, Magnani Jared W, Maher Joseph F, Mehra Reena, Meng Yan A, Musani Solomon K, Newton-Cheh Christopher, North Kari E, Psaty Bruce M, Redline Susan, Rotter Jerome I, Schnabel Renate B, Schork Nicholas J, Shohet Ralph V, Singleton Andrew B, Smith Jonathan D, Soliman Elsayed Z, Srinivasan Sathanur R, Taylor Herman A, Van Wagoner David R, Wilson James G, Young Taylor, Zhang Zhu-Ming, Zonderman Alan B, Evans Michele K, Ferrucci Luigi, Murray Sarah S, Tranah Gregory J, Whitsel Eric A, Reiner Alex P, , Sotoodehnia No |
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Integrating clinical features and genetic lesions in the risk assessment of patients with chronic myelomonocytic leukemia.
Blood 2016 Jul . Elena Chiara, Gallì Anna, Such Esperanza, Meggendorfer Manja, Germing Ulrich, Rizzo Ettore, Cervera Jose, Molteni Elisabetta, Fasan Annette, Schuler Esther, Ambaglio Ilaria, Lopez-Pavia Maria, Zibellini Silvia, Kuendgen Andrea, Travaglino Erica, Sancho-Tello Reyes, Catricalà Silvia, Vicente Ana I, Haferlach Torsten, Haferlach Claudia, Sanz Guillermo F, Malcovati Luca, Cazzola Mar |
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Targeted next-generation sequencing identifies a subset of idiopathic hypereosinophilic syndrome with features similar to chronic eosinophilic leukemia, not otherwise specified.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2016 May . Wang Sa A, Tam Wayne, Tsai Albert G, Arber Daniel A, Hasserjian Robert P, Geyer Julia T, George Tracy I, Czuchlewski David R, Foucar Kathryn, Rogers Heesun J, Hsi Eric D, Bryan Rea B, Bagg Adam, Dal Cin Paola, Zhao Chong, Kelley Todd W, Verstovsek Srdan, Bueso-Ramos Carlos, Orazi Attil |
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Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.
Pediatrics 2016 Apr 137 (4): . Kornilov Sergey A, Rakhlin Natalia, Koposov Roman, Lee Maria, Yrigollen Carolyn, Caglayan Ahmet Okay, Magnuson James S, Mane Shrikant, Chang Joseph T, Grigorenko Elena |
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Predictors of survival in refractory anemia with ring sideroblasts and thrombocytosis (RARS-T) and the role of next-generation sequencing.
American journal of hematology 2016 Feb . Patnaik Mrinal M, Lasho Terra L, Finke Christy M, Hanson Curtis A, King Rebecca L, Ketterling Rhett P, Gangat Naseema, Tefferi Ayal |
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Prognostic interaction between ASXL1 and TET2 mutations in chronic myelomonocytic leukemia.
Blood cancer journal 2016 6 e385. Patnaik M M, Lasho T L, Vijayvargiya P, Finke C M, Hanson C A, Ketterling R P, Gangat N, Tefferi |
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Investigation of the 53 Markers in a DNA-Based Prognostic Test Revealing New Predisposition Genes for Adolescent Idiopathic Scoliosis.
Spine 2015 Jul 40 (14): 1086-91. Xu Leilei, Huang Shushu, Qin Xiaodong, Mao Saihu, Qiao Jun, Qian Bang-Ping, Qiu Yong, Zhu Zezha |
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Blast transformation in chronic myelomonocytic leukemia: Risk factors, genetic features, survival, and treatment outcome.
American journal of hematology 2015 May 90 (5): 411-6. Patnaik Mrinal M, Wassie Emnet A, Lasho Terra L, Hanson Curtis A, Ketterling Rhett, Tefferi Ayal |
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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 |
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Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer.
Nature genetics 2015 Apr 47 (4): 373-80. Michailidou Kyriaki, Beesley Jonathan, Lindstrom Sara, Canisius Sander, Dennis Joe, Lush Michael J, Maranian Mel J, Bolla Manjeet K, Wang Qin, Shah Mitul, Perkins Barbara J, Czene Kamila, Eriksson Mikael, Darabi Hatef, Brand Judith S, Bojesen Stig E, Nordestgaard Børge G, Flyger Henrik, Nielsen Sune F, Rahman Nazneen, Turnbull Clare, , Fletcher Olivia, Peto Julian, Gibson Lorna, dos-Santos-Silva Isabel, Chang-Claude Jenny, Flesch-Janys Dieter, Rudolph Anja, Eilber Ursula, Behrens Sabine, Nevanlinna Heli, Muranen Taru A, Aittomäki Kristiina, Blomqvist Carl, Khan Sofia, Aaltonen Kirsimari, Ahsan Habibul, Kibriya Muhammad G, Whittemore Alice S, John Esther M, Malone Kathleen E, Gammon Marilie D, Santella Regina M, Ursin Giske, Makalic Enes, Schmidt Daniel F, Casey Graham, Hunter David J, Gapstur Susan M, Gaudet Mia M, Diver W Ryan, Haiman Christopher A, Schumacher Fredrick, Henderson Brian E, Le Marchand Loic, Berg Christine D, Chanock Stephen J, Figueroa Jonine, Hoover Robert N, Lambrechts Diether, Neven Patrick, Wildiers Hans, van Limbergen Erik, Schmidt Marjanka K, Broeks Annegien, Verhoef Senno, Cornelissen Sten, Couch Fergus J, Olson Janet E, Hallberg Emily, Vachon Celine, Waisfisz Quinten, Meijers-Heijboer Hanne, Adank Muriel A, van der Luijt Rob B, Li Jingmei, Liu Jianjun, Humphreys Keith, Kang Daehee, Choi Ji-Yeob, Park Sue K, Yoo Keun-Young, Matsuo Keitaro, Ito Hidemi, Iwata Hiroji, Tajima Kazuo, Guénel Pascal, Truong Thérèse, Mulot Claire, Sanchez Marie, Burwinkel Barbara, Marme Frederik, Surowy Harald, Sohn Christof, Wu Anna H, Tseng Chiu-chen, Van Den Berg David, Stram Daniel O, González-Neira Anna, Benitez Javier, Zamora M Pilar, Perez Jose Ignacio Arias, Shu Xiao-Ou, Lu Wei, Gao Yu-Tang, Cai Hui, Cox Angela, Cross Simon S, Reed Malcolm W R, Andrulis Irene L, Knight Julia A, Glendon Gord, Mulligan Anna Marie, Sawyer Elinor J, Tomlinson Ian, Kerin Michael J, Miller Nicola, , , Lindblom Annika, Margolin Sara, Teo Soo Hwang, Yip Cheng Har, Taib Nur Aishah Mohd, Tan Gie-Hooi, Hooning Maartje J, Hollestelle Antoinette, Martens John W M, Collée J Margriet, Blot William, Signorello Lisa B, Cai Qiuyin, Hopper John L, Southey Melissa C, Tsimiklis Helen, Apicella Carmel, Shen Chen-Yang, Hsiung Chia-Ni, Wu Pei-Ei, Hou Ming-Feng, Kristensen Vessela N, Nord Silje, Alnaes Grethe I Grenaker, , Giles Graham G, Milne Roger L, McLean Catriona, Canzian Federico, Trichopoulos Dimitrios, Peeters Petra, Lund Eiliv, Sund Malin, Khaw Kay-Tee, Gunter Marc J, Palli Domenico, Mortensen Lotte Maxild, Dossus Laure, Huerta Jose-Maria, Meindl Alfons, Schmutzler Rita K, Sutter Christian, Yang Rongxi, Muir Kenneth, Lophatananon Artitaya, Stewart-Brown Sarah, Siriwanarangsan Pornthep, Hartman Mikael, Miao Hui, Chia Kee Seng, Chan Ching Wan, Fasching Peter A, Hein Alexander, Beckmann Matthias W, Haeberle Lothar, Brenner Hermann, Dieffenbach Aida Karina, Arndt Volker, Stegmaier Christa, Ashworth Alan, Orr Nick, Schoemaker Minouk J, Swerdlow Anthony J, Brinton Louise, Garcia-Closas Montserrat, Zheng Wei, Halverson Sandra L, Shrubsole Martha, Long Jirong, Goldberg Mark S, Labrèche France, Dumont Martine, Winqvist Robert, Pylkäs Katri, Jukkola-Vuorinen Arja, Grip Mervi, Brauch Hiltrud, Hamann Ute, Brüning Thomas, , Radice Paolo, Peterlongo Paolo, Manoukian Siranoush, Bernard Loris, Bogdanova Natalia V, Dörk Thilo, Mannermaa Arto, Kataja Vesa, Kosma Veli-Matti, Hartikainen Jaana M, Devilee Peter, Tollenaar Robert A E M, Seynaeve Caroline, Van Asperen Christi J, Jakubowska Anna, Lubinski Jan, Jaworska Katarzyna, Huzarski Tomasz, Sangrajrang Suleeporn, Gaborieau Valerie, Brennan Paul, McKay James, Slager Susan, Toland Amanda E, Ambrosone Christine B, Yannoukakos Drakoulis, Kabisch Maria, Torres Diana, Neuhausen Susan L, Anton-Culver Hoda, Luccarini Craig, Baynes Caroline, Ahmed Shahana, Healey Catherine S, Tessier Daniel C, Vincent Daniel, Bacot Francois, Pita Guillermo, Alonso M Rosario, Álvarez Nuria, Herrero Daniel, Simard Jacques, Pharoah Paul P D P, Kraft Peter, Dunning Alison M, Chenevix-Trench Georgia, Hall Per, Easton Douglas |
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Impact of TET2, SRSF2, ASXL1 and SETBP1 mutations on survival of patients with chronic myelomonocytic leukemia.
Experimental hematology & oncology 2015 4 14. Cui Yajuan, Tong Hongyan, Du Xin, Li Bing, Gale Robert Peter, Qin Tiejun, Liu Jinqin, Xu Zefeng, Zhang Yue, Huang Gang, Jin Jie, Fang Liwei, Zhang Hongli, Pan Lijuan, Hu Naibo, Qu Shiqiang, Xiao Zhiji |
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De novo mutations in moderate or severe intellectual disability.
PLoS genetics 2014 Oct 10 (10): e1004772. Hamdan Fadi F, Srour Myriam, Capo-Chichi Jose-Mario, Daoud Hussein, Nassif Christina, Patry Lysanne, Massicotte Christine, Ambalavanan Amirthagowri, Spiegelman Dan, Diallo Ousmane, Henrion Edouard, Dionne-Laporte Alexandre, Fougerat Anne, Pshezhetsky Alexey V, Venkateswaran Sunita, Rouleau Guy A, Michaud Jacques |
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- Page last updated:Feb 24, 2021
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