HuGE Literature Finder
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| Intratumor Heterogeneity of Synchronous Anticancer research 2021 Aug 41 (8): 3779-3787. Kim Hayeon, Gim Jeong-An, Kim Chung-Yeul, Kim Aer |
| Only SF3B1 mutation involving K700E independently predicts overall survival in myelodysplastic syndromes. Cancer 2021 Jun . Kanagal-Shamanna Rashmi, Montalban-Bravo Guillermo, Sasaki Koji, Darbaniyan Faezeh, Jabbour Elias, Bueso-Ramos Carlos, Wei Yue, Chien Kelly, Kadia Tapan, Ravandi Farhad, Borthakur Gautam, Soltysiak Kelly A, Routbort Mark, Patel Keyur, Pierce Sherry, Medeiros L Jeffrey, Kantarjian Hagop, Garcia-Manero Guiller |
| A Novel 85-Gene Expression Signature Predicts Unfavorable Prognosis in Acute Myeloid Leukemia. Technology in cancer research & treatment 2021 15330338211004933. Lai Yanli, Sheng Lixia, Wang Jiaping, Zhou Miao, OuYang Guifa |
| Clinical and genomic characterization of patients diagnosed with the provisional entity acute myeloid leukemia with BCR-ABL1, a Swedish population-based study. Genes, chromosomes & cancer 2021 Jan . Orsmark-Pietras Christina, Landberg Niklas, Lorenz Fryderyk, Uggla Bertil, Höglund Martin, Lehmann Sören, Derolf Åsa, Deneberg Stefan, Antunovic Petar, Cammenga Jörg, Möllgård Lars, Wennström Lovisa, Lilljebjörn Henrik, Rissler Marianne, Fioretos Thoas, Lazarevic Vladimir |
| Mutation profile of non-small cell lung cancer revealed by next generation sequencing. Respiratory research 2021 Jan 22 (1): 3. Chang Ya-Sian, Tu Siang-Jyun, Chen Yu-Chia, Liu Ting-Yuan, Lee Ya-Ting, Yen Ju-Chen, Fang Hsin-Yuan, Chang Jan-Gow |
| Identification of two novel mutations in human acute myeloid leukemia cases. Leukemia & lymphoma 2020 Oct 1-8. O'Brien Gráinne, Zyla Joanna, Manola Kalliopi N, Pagoni Maria N, Polanska Joanna, Badie Christop |
| Landscape of driver mutations and their clinical impacts in pediatric B-cell precursor acute lymphoblastic leukemia. Blood advances 2020 Oct 4 (20): 5165-5173. Ueno Hiroo, Yoshida Kenichi, Shiozawa Yusuke, Nannya Yasuhito, Iijima-Yamashita Yuka, Kiyokawa Nobutaka, Shiraishi Yuichi, Chiba Kenichi, Tanaka Hiroko, Isobe Tomoya, Seki Masafumi, Kimura Shunsuke, Makishima Hideki, Nakagawa Masahiro M, Kakiuchi Nobuyuki, Kataoka Keisuke, Yoshizato Tetsuichi, Nishijima Dai, Deguchi Takao, Ohki Kentaro, Sato Atsushi, Takahashi Hiroyuki, Hashii Yoshiko, Tokimasa Sadao, Hara Junichi, Kosaka Yoshiyuki, Kato Koji, Inukai Takeshi, Takita Junko, Imamura Toshihiko, Miyano Satoru, Manabe Atsushi, Horibe Keizo, Ogawa Seishi, Sanada Masas |
| The Association of Modifiable Breast Cancer Risk Factors and Somatic Genomic Alterations in Breast Tumors: The Cancer Genome Atlas Network. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2020 Jan . Heng Yujing J, Hankinson Susan E, Wang Jun, Alexandrov Ludmil B, Ambrosone Christine B, Andrade Victor Piana de, Brufsky Adam M, Couch Fergus J, King Tari A, Modugno Francesmary, Vachon Celine M, Eliassen A Heather, Tamimi Rulla M, Kraft Pet |
| Mutation status and burden can improve prognostic prediction of patients with lower-risk myelodysplastic syndromes. Cancer science 2019 Dec . Jiang Lingxu, Luo Yingwan, Zhu Shuanghong, Wang Lu, Ma Liya, Zhang Hua, Shen Chuying, Yang Wenli, Ren Yanling, Zhou Xinping, Mei Chen, Ye Li, Xu Weilai, Yang Haiyang, Lu Chenxi, Jin Jie, Tong Hongy |
Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population.
Scientific reports 2019 Nov 9 (1): 17332. Low Siew-Kee, Chin Yoon Ming, Ito Hidemi, Matsuo Keitaro, Tanikawa Chizu, Matsuda Koichi, Saito Hiroko, Sakurai-Yageta Mika, Nakaya Naoki, Shimizu Atsushi, Nishizuka Satoshi S, Yamaji Taiki, Sawada Norie, Iwasaki Motoki, Tsugane Shoichiro, Takezaki Toshiro, Suzuki Sadao, Naito Mariko, Wakai Kenji, Kamatani Yoichiro, Momozawa Yukihide, Murakami Yoshinori, Inazawa Johji, Nakamura Yusuke, Kubo Michiaki, Katagiri Toyomasa, Miki Yosh |
| Association of genetic variants in CHEK2 with oesophageal squamous cell carcinoma in the South African Black population. Carcinogenesis 2019 Feb . Chen Wenlong C, Bye Hannah, Matejcic Marco, Amar Ariella, Govender Dhiren, Khew Yee Wen, Beynon Victoria, Kerr Robyn, Singh Elvira, Prescott Natalie J, Lewis Cathryn M, Babb de Villiers Chantal, Parker M Iqbal, Mathew Christopher |
| Novel susceptibility variants at the ERG locus for childhood acute lymphoblastic leukemia in Hispanics. Blood 2019 Feb 133 (7): 724-729. Qian Maoxiang, Xu Heng, Perez-Andreu Virginia, Roberts Kathryn G, Zhang Hui, Yang Wenjian, Zhang Shouyue, Zhao Xujie, Smith Colton, Devidas Meenakshi, Gastier-Foster Julie M, Raetz Elizabeth, Larsen Eric, Burchard Esteban G, Winick Naomi, Bowman W Paul, Martin Paul L, Borowitz Michael, Wood Brent, Antillon-Klussmann Federico, Pui Ching-Hon, Mullighan Charles G, Evans William E, Hunger Stephen P, Relling Mary V, Loh Mignon L, Yang Jun |
| An Association and Meta-Analysis of Esophageal Squamous Cell Carcinoma Risk Associated with PLCE1 rs2274223, C20orf54 rs13042395 and RUNX1 rs2014300 Polymorphisms. Pathology oncology research : POR 2019 Jan . Nariman-Saleh-Fam Ziba, Saadatian Zahra, Nariman-Saleh-Fam Lida, Ouladsahebmadarek Elaheh, Tavakkoly-Bazzaz Javad, Bastami Mil |
| Identification of Key Genes and Pathways Associated with RUNX1 Mutations in Acute Myeloid Leukemia Using Bioinformatics Analysis. Medical science monitor : international medical journal of experimental and clinical research 2018 Oct 24 7100-7108. Zhu Fangxiao, Huang Rui, Li Jing, Liao Xiwen, Huang Yumei, Lai Yongro |
| Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity. Breast cancer research : BCR 2018 Aug 20 (1): 87. Penkert Judith, Schmidt Gunnar, Hofmann Winfried, Schubert Stephanie, Schieck Maximilian, Auber Bernd, Ripperger Tim, Hackmann Karl, Sturm Marc, Prokisch Holger, Hille-Betz Ursula, Mark Dorothea, Illig Thomas, Schlegelberger Brigitte, Steinemann Dor |
| Genomic and outcome analyses of Ph-like ALL in NCI standard-risk patients: a report from the Children's Oncology Group. Blood 2018 Jul . Roberts Kathryn G, Reshmi Shalini C, Harvey Richard C, Chen I-Ming, Patel Kinnari, Stonerock Eileen, Jenkins Heather, Dai Yunfeng, Valentine Marc, Gu Zhaohui, Zhao Yaqi, Zhang Jinghui, Payne-Turner Debbie, Devidas Meenakshi, Heerema Nyla A, Carroll Andrew J, Raetz Elizabeth A, Borowitz Michael J, Wood Brent L, Mattano Leonard A, Maloney Kelly W, Carroll William L, Loh Mignon L, Willman Cheryl L, Gastier-Foster Julie M, Mullighan Charles G, Hunger Stephen |
| Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease. Blood 2018 Jul . Branford Susan, Wang Paul, Yeung David T, Thomson Daniel, Purins Adrian, Wadham Carol, Shahrin Nur Hezrin, Marum Justine E, Nataren Nathalie, Parker Wendy T, Geoghegan Joel, Feng Jinghua, Shanmuganathan Naranie, Mueller Martin C, Dietz Christian, Stangl Doris, Donaldson Zoe, Altamura Haley, Georgievski Jasmina, Braley Jodi, Brown Anna, Hahn Christopher, Walker Ieuan, Kim Soo-Hyun, Choi Soo-Young, Park Sa-Hee, Kim Dong-Wook, White Deborah L, Yong Agnes S M, Ross David M, Scott Hamish S, Schreiber Andreas W, Hughes Timothy |
| Clinical and Biological Implications of Mutational Spectrum in Acute Myeloid Leukemia of FAB Subtypes M0 and M1. Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2018 Jun 47 (5): 1853-1861. Cheng Zhiheng, Dai Yifeng, Pang Yifan, Jiao Yang, Zhao Hongmian, Wu Sun, Zhang Lingxiu, Zhang Yuan, Wang Xiufeng, Wang Lihua, Ma Dong, Qin Tong, Hu Ning, Zhang Yijie, Hu Kai, Zhang Qingyi, Shi Jinlong, Fu L |
| CSF3R Mutations are frequently associated with abnormalities of RUNX1, CBFB, CEBPA, and NPM1 genes in acute myeloid leukemia. Cancer 2018 Jun . Zhang Yang, Wang Fang, Chen Xue, Zhang Yu, Wang Mingyu, Liu Hong, Cao Panxiang, Ma Xiaoli, Wang Tong, Zhang Jianping, Zhang Xian, Lu Peihua, Liu Hongxi |
| Mutational spectrum and prognostic stratification of intermediate-risk acute myeloid leukemia. Cancer gene therapy 2018 Jun . Wu Sun, Dai Yifeng, Zhang Yuan, Wang Xiufeng, Wang Lihua, Ma Dong, Zhang Lingxiu, Pang Yifan, Jiao Yang, Niu Mingshan, Xu Kailin, Ke Xiaoyan, Shi Jinlong, Cheng Zhiheng, Fu L |
| Mutations in DNMT3A, U2AF1, and EZH2 identify intermediate-risk acute myeloid leukemia patients with poor outcome after CR1. Blood cancer journal 2018 Jan 8 (1): 4. Saygin Caner, Hirsch Cassandra, Przychodzen Bartlomiej, Sekeres Mikkael A, Hamilton Betty K, Kalaycio Matt, Carraway Hetty E, Gerds Aaron T, Mukherjee Sudipto, Nazha Aziz, Sobecks Ronald, Goebel Christopher, Abounader Donna, Maciejewski Jaroslaw P, Advani Anjali |
| Influence of TS (rs34743033) and RUNX1 (rs2014300) gene polymorphisms on survival outcomes of fluorouracil-based chemotherapy in Chinese advanced gastric cancer patients. Cancer management and research 2018 10 1429-1437. Han Rongbo, Wei Jingsun, Zhang Honghong, Su Xinyu, Chu Xia, Chen Yuetong, Gong Yang, Wang Xiujuan, Shi Junfeng, Chen Jinf |
| Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients. Genes, chromosomes & cancer 2017 Jun . Busse Tracy M, Roth Jacquelyn J, Wilmoth Donna, Wainwright Luanne, Tooke Laura, Biegel Jaclyn |
| Breast ductal carcinoma in situ carry mutational driver events representative of invasive breast cancer. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2017 Mar . Pang Jia-Min B, Savas Peter, Fellowes Andrew P, Mir Arnau Gisela, Kader Tanjina, Vedururu Ravikiran, Hewitt Chelsee, Takano Elena A, Byrne David J, Choong David Yh, Millar Ewan Ka, Lee C Soon, O'Toole Sandra A, Lakhani Sunil R, Cummings Margaret C, Mann G Bruce, Campbell Ian G, Dobrovic Alexander, Loi Sherene, Gorringe Kylie L, Fox Stephen |
| Functional germline variants in driver genes of breast cancer. Cancer causes & control : CCC 2017 Feb . Göhler Stella, Da Silva Filho Miguel Inacio, Johansson Robert, Enquist-Olsson Kerstin, Henriksson Roger, Hemminki Kari, Lenner Per, Försti As |
| Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
Oncotarget 2017 Jan 8 (5): 7891-7899. Lv Hongchao, Zhang Mingming, Shang Zhenwei, Li Jin, Zhang Shanshan, Lian Duan, Zhang Ruij |
| Correlates of Prenatal and Early-Life Tobacco Smoke Exposure and Frequency of Common Gene Deletions in Childhood Acute Lymphoblastic Leukemia. Cancer research 2017 04 77 (7): 1674-1683. de Smith Adam J, Kaur Maneet, Gonseth Semira, Endicott Alyson, Selvin Steve, Zhang Luoping, Roy Ritu, Shao Xiaorong, Hansen Helen M, Kang Alice Y, Walsh Kyle M, Dahl Gary V, McKean-Cowdin Roberta, Metayer Catherine, Wiemels Joseph |
| MEGSA: A Powerful and Flexible Framework for Analyzing Mutual Exclusivity of Tumor Mutations. American journal of human genetics 2016 Feb . Hua Xing, Hyland Paula L, Huang Jing, Song Lei, Zhu Bin, Caporaso Neil E, Landi Maria Teresa, Chatterjee Nilanjan, Shi Jianx |
| Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population. BMC cancer 2016 16 (1): 165. Marouf Chaymaa, Göhler Stella, Filho Miguel Inacio Da Silva, Hajji Omar, Hemminki Kari, Nadifi Sellama, Försti As |
| Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes. PloS one 2016 11 (10): e0164370. Abáigar María, Robledo Cristina, Benito Rocío, Ramos Fernando, Díez-Campelo María, Hermosín Lourdes, Sánchez-Del-Real Javier, Alonso Jose M, Cuello Rebeca, Megido Marta, Rodríguez Juan N, Martín-Núñez Guillermo, Aguilar Carlos, Vargas Manuel, Martín Ana A, García Juan L, Kohlmann Alexander, Del Cañizo M Consuelo, Hernández-Rivas Jesús |
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- Page last updated:Jan 12, 2022
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