Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Disease and MLL2[original query] |
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| MYD88 L265P somatic mutation in Waldenström's macroglobulinemia. The New England journal of medicine 2012 Aug 367 (9): 9. Treon SP, Xu L, Yang G, Zhou Y, Liu X, Cao Y, Sheehy P, Manning RJ, Patterson CJ, Tripsas C, Arcaini L, Pinkus GS, Rodig SJ, Sohani AR, Harris NL, Laramie JM, Skifter DA, Lincoln SE, Hunter ZR |
| EZH2 mutations are frequent and represent an early event in follicular lymphoma. Blood 2013 Oct 122 (18): 3165-8. Bödör Csaba, Grossmann Vera, Popov Nikolay, Okosun Jessica, O'Riain Ciarán, Tan King, Marzec Jacek, Araf Shamzah, Wang Jun, Lee Abigail M, Clear Andrew, Montoto Silvia, Matthews Janet, Iqbal Sameena, Rajnai Hajnalka, Rosenwald Andreas, Ott German, Campo Elias, Rimsza Lisa M, Smeland Erlend B, Chan Wing C, Braziel Rita M, Staudt Louis M, Wright George, Lister T Andrew, Elemento Olivier, Hills Robert, Gribben John G, Chelala Claude, Matolcsy András, Kohlmann Alexander, Haferlach Torsten, Gascoyne Randy D, Fitzgibbon Ju |
| Clinical and molecular spectrum of renal malformations in Kabuki syndrome. The Journal of pediatrics 2013 Sep 163 (3): 742-6. Courcet Jean-Benoît, Faivre Laurence, Michot Caroline, Burguet Antoine, Perez-Martin Stéphanie, Alix Eudeline, Amiel Jeanne, Baumann Clarisse, Cordier Marie-Pierre, Cormier-Daire Valérie, Delrue Marie Ange, Gilbert-Dussardier Brigitte, Goldenberg Alice, Jacquemont Marie-Line, Jaquette Aurélia, Kayirangwa Honorine, Lacombe Didier, Le Merrer Martine, Toutain Annick, Odent Sylvie, Moncla Anne, Pelet Anna, Philip Nicole, Pinson Lucille, Poisson Sylvain, Kim-Han Le Quan Sang, Roume Joelle, Sanchez Elodie, Willems Marjolaine, Till Marianne, Vincent-Delorme Catherine, Mousson Christiane, Vinault Sandrine, Binquet Christine, Huet Frédéric, Sarda Pierre, Salomon Rémi, Lyonnet Stanislas, Sanlaville Damien, Geneviève Dav |
| CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma. Journal of neuro-oncology 2015 Aug . Dahlin Anna M, Hollegaard Mads V, Wibom Carl, Andersson Ulrika, Hougaard David M, Deltour Isabelle, Hjalmars Ulf, Melin Beatri |
| Exome sequencing identifies somatic mutations of DDX3X in natural killer/T-cell lymphoma. Nature genetics 2015 Sep 47 (9): 1061-6. Jiang Lu, Gu Zhao-Hui, Yan Zi-Xun, Zhao Xia, Xie Yin-Yin, Zhang Zi-Guan, Pan Chun-Ming, Hu Yuan, Cai Chang-Ping, Dong Ying, Huang Jin-Yan, Wang Li, Shen Yang, Meng Guoyu, Zhou Jian-Feng, Hu Jian-Da, Wang Jin-Fen, Liu Yuan-Hua, Yang Lin-Hua, Zhang Feng, Wang Jian-Min, Wang Zhao, Peng Zhi-Gang, Chen Fang-Yuan, Sun Zi-Min, Ding Hao, Shi Ju-Mei, Hou Jian, Yan Jin-Song, Shi Jing-Yi, Xu Lan, Li Yang, Lu Jing, Zheng Zhong, Xue Wen, Zhao Wei-Li, Chen Zhu, Chen Sai-Ju |
| Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene. Genes, chromosomes & cancer 2015 Sep 54 (9): 542-54. Juhlin C Christofer, Stenman Adam, Haglund Felix, Clark Victoria E, Brown Taylor C, Baranoski Jacob, Bilguvar Kaya, Goh Gerald, Welander Jenny, Svahn Fredrika, Rubinstein Jill C, Caramuta Stefano, Yasuno Katsuhito, Günel Murat, Bäckdahl Martin, Gimm Oliver, Söderkvist Peter, Prasad Manju L, Korah Reju, Lifton Richard P, Carling Tobi |
| The genetic landscape of dural marginal zone lymphomas. Oncotarget 2016 Jul 7 (28): 43052-43061. Ganapathi Karthik A, Jobanputra Vaidehi, Iwamoto Fabio, Jain Preti, Chen Jinli, Cascione Luciano, Nahum Odelia, Levy Brynn, Xie Yi, Khattar Pallavi, Hoehn Daniela, Bertoni Francesco, Murty Vundavalli V, Pittaluga Stefania, Jaffe Elaine S, Alobeid Bachir, Mansukhani Mahesh M, Bhagat Govi |
| Molecular genetic analysis in 14 Czech Kabuki syndrome patients is confirming the utility of phenotypic scoring. Clinical genetics 2016 09 90 (3): 230-7. Paderová J, Holubová A, Simandlová M, Puchmajerová A, Vlcková M, Malíková M, Pourová R, Vejvalková S, Havlovicová M, Šenkeríková M, Ptáková N, Drábová J, Geryk J, Maver A, Krepelová A, Macek |
| 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 |
| Targeted sequencing-based analyses of candidate gene variants in ulcerative colitis-associated colorectal neoplasia. British journal of cancer 2017 Jun 117 (1): 136-143. Chakrabarty Sanjiban, Varghese Vinay Koshy, Sahu Pranoy, Jayaram Pradyumna, Shivakumar Bhadravathi M, Pai Cannanore Ganesh, Satyamoorthy Kapaet |
| Mutation profiles in early-stage lung squamous cell carcinoma with clinical follow-up and correlation with markers of immune function. Annals of oncology : official journal of the European Society for Medical Oncology 2017 (1): 83-89. Choi M, Kadara H, Zhang J, Parra E R, Rodriguez-Canales J, Gaffney S G, Zhao Z, Behrens C, Fujimoto J, Chow C, Kim K, Kalhor N, Moran C, Rimm D, Swisher S, Gibbons D L, Heymach J, Kaftan E, Townsend J P, Lynch T J, Schlessinger J, Lee J, Lifton R P, Herbst R S, Wistuba I |
| Frequent somatic mutations of KMT2D (MLL2) and CARD11 genes in primary cold agglutinin disease. British journal of haematology 2017 12 183 (5): 838-842. Ma?ecka Agnieszka, Trøen Gunhild, Tierens Anne, Østlie Ingunn, Ma?ecki J?drzej, Randen Ulla, Wang Junbai, Berentsen Sigbjørn, Tjønnfjord Geir E, Delabie Jan M |
| KMT2D/MLL2 inactivation is associated with recurrence in adult-type granulosa cell tumors of the ovary. Nature communications 2018 Jun 9 (1): 2496. Hillman R Tyler, Celestino Joseph, Terranova Christopher, Beird Hannah C, Gumbs Curtis, Little Latasha, Nguyen Tri, Thornton Rebecca, Tippen Samantha, Zhang Jianhua, Lu Karen H, Gershenson David M, Rai Kunal, Broaddus Russell R, Futreal P Andr |
| KMT2D Mutation Is Associated With Poor Prognosis in Non-Small-Cell Lung Cancer. Clinical lung cancer 2018 07 19 (4): e489-e501. Ardeshir-Larijani Fatemeh, Bhateja Priyanka, Lipka Mary Beth, Sharma Neelesh, Fu Pingfu, Dowlati Afsh |
| Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations. Oncotarget 2018 1 8 (64): 108020-108030. Porkka Noora, Valo Satu, Nieminen Taina T, Olkinuora Alisa, Mäki-Nevala Satu, Eldfors Samuli, Peltomäki Päi |
| Genome-defined African ancestry is associated with distinct mutations and worse survival in patients with diffuse large B-cell lymphoma. Cancer 2020 May . Lee Michelle J, Koff Jean L, Switchenko Jeffrey M, Jhaney C Ileen, Harkins R Andrew, Patel Sharvil P, Dave Sandeep S, Flowers Christopher |
| Genomic Sequencing for Bladder Urothelial Carcinoma and Its Clinical Implications for Immunotherapy. Cancer research and treatment 2021 11 54 (3): 894-906. Kim Ryul, Hong Jung Yong, Lee Jeeyun, Kwon Ghee Young, Jeong Byong Chang, Park Se Ho |
| Early-onset metastatic and clinically advanced prostate cancer is a distinct clinical and molecular entity characterized by increased TMPRSS2-ERG fusions. Prostate cancer and prostatic diseases 2021 Jan . Chalmers Zachary R, Burns Michael C, Ebot Ericka M, Frampton Garrett M, Ross Jeffrey S, Hussain Maha H A, Abdulkadir Sarki |
| Genetic insights into thymic carcinomas and thymic neuroendocrine neoplasms denote prognosis signatures and pathways. Chinese medical journal 2023 9 . Shuyuan Wang, Zhitao Gu, Lei Zhu, Yuchen Han, Hong Yu, Wentao Fang, Baohui H |
| KMT2D suppresses Sonic hedgehog-driven medulloblastoma progression and metastasis. iScience 2023 10 26 (10): 107831. Reeti Mayur Sanghrajka, Richard Koche, Hector Medrano, Salsabiel El Nagar, Daniel N Stephen, Zhimin Lao, N Sumru Bayin, Kai Ge, Alexandra L Joyn |
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