Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: MLLT10[original query] |
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Common variation at 10p12.31 near MLLT10 influences meningioma risk.
Nature genetics 2011 Sep 43 (9): 825-7. Dobbins Sara E, Broderick Peter, Melin Beatrice, Feychting Maria, Johansen Christoffer, Andersson Ulrika, Brännström Thomas, Schramm Johannes, Olver Bianca, Lloyd Amy, Ma Yussanne P, Hosking Fay J, Lönn Stefan, Ahlbom Anders, Henriksson Roger, Schoemaker Minouk J, Hepworth Sarah J, Hoffmann Per, Mühleisen Thomas W, Nöthen Markus M, Moebus Susanne, Eisele Lewin, Kosteljanetz Michael, Muir Kenneth, Swerdlow Anthony, Simon Matthias, Houlston Richard |
Brain tumor risk according to germ-line variation in the MLLT10 locus. European journal of human genetics : EJHG 2015 Jan 23 (1): 132-4. Egan Kathleen M, Baskin Rebekah, Nabors L Burton, Thompson Reid C, Olson Jeffrey J, Browning James E, Madden Melissa H, Monteiro Alvaro |
Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat.
International journal of obesity (2005) 2016 Apr 40 (4): 662-74. Sung Y J, Pérusse L, Sarzynski M A, Fornage M, Sidney S, Sternfeld B, Rice T, Terry J G, Jacobs D R, Katzmarzyk P, Curran J E, Jeffrey Carr J, Blangero J, Ghosh S, Després J-P, Rankinen T, Rao D C, Bouchard |
Comprehensive genetic analysis of donor cell derived leukemia with KMT2A rearrangement. Pediatric blood & cancer 2017 9 65 (2): . Taniguchi Rieko, Muramatsu Hideki, Okuno Yusuke, Suzuki Kyogo, Obu Satoshi, Nakatochi Masahiro, Shimamura Teppei, Takahashi Yoshiyuki, Horikoshi Yasuo, Watanabe Kenichiro, Kojima Sei |
Molecular studies reveal MLL-MLLT10/AF10 and ARID5B-MLL gene fusions displaced in a case of infantile acute lymphoblastic leukemia with complex karyotype. Oncology letters 2017 8 14 (2): 2295-2299. Hiwatari Mitsuteru, Seki Masafumi, Akahoshi Shogo, Yoshida Kenichi, Miyano Satoru, Shiraishi Yuichi, Tanaka Hiroko, Chiba Kenichi, Ogawa Seishi, Takita Jun |
Genetic variants and increased risk of meningioma: an updated meta-analysis. OncoTargets and therapy 2017 10 1875-1888. Han Xiao-Yong, Wang Wei, Wang Lei-Lei, Wang Xi-Rui, Li Ga |
Accurate and Sensitive Analysis of Minimal Residual Disease in Acute Myeloid Leukemia Using Deep Sequencing of Single Nucleotide Variations. The Journal of molecular diagnostics : JMD 2018 10 21 (1): 149-162. Delsing Malmberg Erik, Rehammar Anna, Pereira Mariana B, Abrahamsson Jonas, Samuelsson Tore, Ståhlman Sara, Asp Julia, Tierens Anne, Palmqvist Lars, Kristiansson Erik, Fogelstrand Lin |
Fusion partner-specific mutation profiles and KRAS mutations as adverse prognostic factors in MLL-rearranged AML. Blood advances 2020 9 4 (19): 4623-4631. Matsuo Hidemasa, Yoshida Kenichi, Nakatani Kana, Harata Yutarou, Higashitani Moe, Ito Yuri, Kamikubo Yasuhiko, Shiozawa Yusuke, Shiraishi Yuichi, Chiba Kenichi, Tanaka Hiroko, Okada Ai, Nannya Yasuhito, Takeda June, Ueno Hiroo, Kiyokawa Nobutaka, Tomizawa Daisuke, Taga Takashi, Tawa Akio, Miyano Satoru, Meggendorfer Manja, Haferlach Claudia, Ogawa Seishi, Adachi Souic |
Diverse mutations and structural variations contribute to Notch signaling deregulation in paediatric T-cell lymphoblastic lymphoma. Pediatric blood & cancer 2022 Aug e29926. Salmerón-Villalobos Julia, Ramis-Zaldivar Joan Enric, Balagué Olga, Verdú-Amorós Jaime, Celis Verónica, Sábado Constantino, Garrido Marta, Mato Sara, Uriz Javier, Ortega M José, Gutierrez-Camino Angela, Sinnett Daniel, Illarregi Unai, Carron Máxime, Regueiro Alexandra, Galera Ana, Gonzalez-Farré Blanca, Campo Elias, Garcia Noelia, Colomer Dolors, Astigarraga Itziar, Andrés Mara, Llavador Margarita, Martin-Guerrero Idoia, Salaverria Itzi |
Pleiotropic MLLT10 variation confers risk of meningioma and estrogen-mediated cancers. Neuro-oncology advances 0 4 (1): vdac044. Walsh Kyle M, Zhang Chenan, Calvocoressi Lisa, Hansen Helen M, Berchuck Andrew, Schildkraut Joellen M, Bondy Melissa L, Wrensch Margaret, Wiemels Joseph L, Claus Elizabeth |
Genome-Wide Association Study of Chronic Dizziness in the Elderly Identifies Loci Implicating MLLT10, BPTF, LINC01224, and ROS1. Journal of the Association for Research in Otolaryngology : JARO 2023 11 . Royce Clifford, Daniel Munro, Daniel Dochtermann, Poornima Devineni, Saiju Pyarajan, , Francesca Telese, Abraham A Palmer, Pejman Mohammadi, Rick Friedm |
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
Nature genetics 2023 3 55 (3): 423-436. Rahmioglu Nilufer, Mortlock Sally, Ghiasi Marzieh, Møller Peter L, Stefansdottir Lilja, Galarneau Geneviève, Turman Constance, Danning Rebecca, Law Matthew H, Sapkota Yadav, Christofidou Paraskevi, Skarp Sini, Giri Ayush, Banasik Karina, Krassowski Michal, Lepamets Maarja, Marciniak B?a?ej, Nõukas Margit, Perro Danielle, Sliz Eeva, Sobalska-Kwapis Marta, Thorleifsson Gudmar, Topbas-Selcuki Nura F, Vitonis Allison, Westergaard David, Arnadottir Ragnheidur, Burgdorf Kristoffer S, Campbell Archie, Cheuk Cecilia S K, Clementi Caterina, Cook James, De Vivo Immaculata, DiVasta Amy, Dorien O, Donoghue Jacqueline F, Edwards Todd, Fontanillas Pierre, Fung Jenny N, Geirsson Reynir T, Girling Jane E, Harkki Paivi, Harris Holly R, Healey Martin, Heikinheimo Oskari, Holdsworth-Carson Sarah, Hostettler Isabel C, Houlden Henry, Houshdaran Sahar, Irwin Juan C, Jarvelin Marjo-Riitta, Kamatani Yoichiro, Kennedy Stephen H, Kepka Ewa, Kettunen Johannes, Kubo Michiaki, Kulig Bartosz, Kurra Venla, Laivuori Hannele, Laufer Marc R, Lindgren Cecilia M, MacGregor Stuart, Mangino Massimo, Martin Nicholas G, Matalliotaki Charoula, Matalliotakis Michail, Murray Alison D, Ndungu Anne, Nezhat Camran, Olsen Catherine M, Opoku-Anane Jessica, Padmanabhan Sandosh, Paranjpe Manish, Peters Maire, Polak Grzegorz, Porteous David J, Rabban Joseph, Rexrode Kathyrn M, Romanowicz Hanna, Saare Merli, Saavalainen Liisu, Schork Andrew J, Sen Sushmita, Shafrir Amy L, Siewierska-Górska Anna, S?omka Marcin, Smith Blair H, Smolarz Beata, Szaflik Tomasz, Szy??o Krzysztof, Takahashi Atsushi, Terry Kathryn L, Tomassetti Carla, Treloar Susan A, Vanhie Arne, Vincent Katy, Vo Kim C, Werring David J, Zeggini Eleftheria, Zervou Maria I, , , , , , Adachi Sosuke, Buring Julie E, Ridker Paul M, D'Hooghe Thomas, Goulielmos George N, Hapangama Dharani K, Hayward Caroline, Horne Andrew W, Low Siew-Kee, Martikainen Hannu, Chasman Daniel I, Rogers Peter A W, Saunders Philippa T, Sirota Marina, Spector Tim, Strapagiel Dominik, Tung Joyce Y, Whiteman David C, Giudice Linda C, Velez-Edwards Digna R, Uimari Outi, Kraft Peter, Salumets Andres, Nyholt Dale R, Mägi Reedik, Stefansson Kari, Becker Christian M, Yurttas-Beim Piraye, Steinthorsdottir Valgerdur, Nyegaard Mette, Missmer Stacey A, Montgomery Grant W, Morris Andrew P, Zondervan Krina |
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