Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: CUX1[original query] |
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Clinical significance of genetic aberrations in secondary acute myeloid leukemia. American journal of hematology 2012 Nov 87 (11): 1010-6. Milosevic Jelena D, Puda Ana, Malcovati Luca, Berg Tiina, Hofbauer Michael, Stukalov Alexey, Klampfl Thorsten, Harutyunyan Ashot S, Gisslinger Heinz, Gisslinger Bettina, Burjanivova Tatiana, Rumi Elisa, Pietra Daniela, Elena Chiara, Vannucchi Alessandro M, Doubek Michael, Dvorakova Dana, Robesova Blanka, Wieser Rotraud, Koller Elisabeth, Suvajdzic Nada, Tomin Dragica, Tosic Natasa, Colinge Jacques, Racil Zdenek, Steurer Michael, Pavlovic Sonja, Cazzola Mario, Kralovics Robe |
Possible association of CUX1 gene polymorphisms with antidepressant response in major depressive disorder.
The pharmacogenomics journal 2013 Aug 13 (4): 354-8. Sasayama D, Hiraishi A, Tatsumi M, Kamijima K, Ikeda M, Umene-Nakano W, Yoshimura R, Nakamura J, Iwata N, Kunugi |
A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study. PLoS genetics 2013 Jan 9 (1): 1. Peters U, North KE, Sethupathy P, Buyske S, Haessler J, Jiao S, Fesinmeyer MD, Jackson RD, Kuller LH, Rajkovic A, Lim U, Cheng I, Schumacher F, Wilkens L, Li R, Monda K, Ehret G, Nguyen KD, Cooper R, Lewis CE, Leppert M, Irvin MR, Gu CC, Houston D, Buzkova P, Ritchie M, Matise TC, Le Marchand L, Hindorff LA, Crawford DC, Haiman CA, Kooperberg C |
Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.
Autism research : official journal of the International Society for Autism Research 2015 Aug . Liu Xiaoxi, Shimada Takafumi, Otowa Takeshi, Wu Yu-Yu, Kawamura Yoshiya, Tochigi Mamoru, Iwata Yasuhide, Umekage Tadashi, Toyota Tomoko, Maekawa Motoko, Iwayama Yoshimi, Suzuki Katsuaki, Kakiuchi Chihiro, Kuwabara Hitoshi, Kano Yukiko, Nishida Hisami, Sugiyama Toshiro, Kato Nobumasa, Chen Chia-Hsiang, Mori Norio, Yamada Kazuo, Yoshikawa Takeo, Kasai Kiyoto, Tokunaga Katsushi, Sasaki Tsukasa, Gau Susan Shur-F |
Hypomorphism of Fto and Rpgrip1l causes obesity in mice. The Journal of clinical investigation 2016 Apr . Stratigopoulos George, Burnett Lisa Cole, Rausch Richard, Gill Richard, Penn David Barth, Skowronski Alicja A, LeDuc Charles A, Lanzano Anthony J, Zhang Pumin, Storm Daniel R, Egli Dieter, Leibel Rudolph |
Copy number variants in Ebstein anomaly. PloS one 2017 12 (12): e0188168. Giannakou Andreas, Sicko Robert J, Zhang Wei, Romitti Paul, Browne Marilyn L, Caggana Michele, Brody Lawrence C, Jelliffe-Pawlowski Laura, Shaw Gary M, Kay Denise M, Mills James |
[Clinical Characteristic of "triple-negative" Essential Thrombocythaemia Patients and Mutation Analysis by Targeted Sequencing]. Zhongguo shi yan xue ye xue za zhi 2018 Aug 26 (4): 1137-1145. Ju Man-Kai, Fu Rong-Feng, Li Hui-Yuan, Liu Xiao-Fan, Xue Feng, Chen Yun-Fei, Huang Yue-Ting, Zhang Li-Yan, Yang Ren-Chi, Zhang L |
Haploinsufficiency of CUX1 Causes Nonsyndromic Global Developmental Delay With Possible Catch-up Development. Annals of neurology 2018 7 84 (2): 200-207. Platzer Konrad, Cogné Benjamin, Hague Jennifer, Marcelis Carlo L, Mitter Diana, Oberndorff Katrin, Park Soo-Mi, Ploos van Amstel Hans K, Simonic Ingrid, van der Smagt Jasper J, Stegmann Alexander P A, Stevens Servi J C, Stumpel Constance T R M, Vincent Marie, Lemke Johannes R, Jamra Ra |
Next-generation sequencing with a 54-gene panel identified unique mutational profile and prognostic markers in Chinese patients with myelofibrosis. Annals of hematology 2019 Apr 98 (4): 869-879. Gill Harinder, Ip Ho-Wan, Yim Rita, Tang Wing-Fai, Pang Herbert H, Lee Paul, Leung Garret M K, Li Jamilla, Tang Karen, So Jason C C, Leung Rock Y Y, Li Jun, Panagioutou Gianni, Lam Clarence C K, Kwong Yok-L |
Chromothripsis 18 in multiple myeloma patient with rapid extramedullary relapse. Molecular cytogenetics 2018 11 7. Smetana Jan, Oppelt Jan, Štork Martin, Pour Lud?k, Kuglík Pe |
Intratumoral heterogeneity for inactivating frameshift mutation of CUX1 and SIRT1 genes in gastric and colorectal cancers. Polish journal of pathology : official journal of the Polish Society of Pathologists 2017 68 (3): 258-260. Jo Yun Sol, Kim Min Sung, Yoo Nam Jin, Lee Sug Hyu |
Distinct clinical and biological implications of CUX1 in myeloid neoplasms. Blood advances 2019 7 3 (14): 2164-2178. Aly Mai, Ramdzan Zubaidah M, Nagata Yasunobu, Balasubramanian Suresh K, Hosono Naoko, Makishima Hideki, Visconte Valeria, Kuzmanovic Teodora, Adema Vera, Nazha Aziz, Przychodzen Bartlomiej P, Kerr Cassandra M, Sekeres Mikkael A, Abazeed Mohamed E, Nepveu Alain, Maciejewski Jaroslaw |
Copy number alterations and copy-neutral loss of heterozygosity in Ukrainian patients with primary myelofibrosis. Experimental oncology 2019 Mar 41 (1): 53-56. Poluben L, Bryke Ch R, Hsu Y, Shumeiko O, Neumerzhitska L, Klimuk B, Rybchenko L, Klymenko S, Balk S P, Fraenkel P |
Integrative Genomic Analysis Reveals Cancer-Associated Gene Mutations in Chronic Myeloid Leukemia Patients with Resistance or Intolerance to Tyrosine Kinase Inhibitor. OncoTargets and therapy 2020 9 13 8581-8591. Wu Waner, Xu Na, Zhou Xuan, Liu Liang, Tan Yaxian, Luo Jie, Huang Jixian, Qin Jiayue, Wang Juan, Li Zhimin, Yin Changxin, Zhou Lingling, Liu Xiao |
Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan.
The journal of headache and pain 2021 Aug 22 (1): 89. Tsai Chia-Kuang, Liang Chih-Sung, Lin Guan-Yu, Tsai Chia-Lin, Lee Jiunn-Tay, Sung Yueh-Feng, Lin Yu-Kai, Hung Kuo-Sheng, Chen Wei-Liang, Yang Fu-C |
Clinical, biological, and prognostic implications of SF3B1 co-occurrence mutations in very low/low- and intermediate-risk MDS patients. Annals of hematology 2021 Jan . Janusz Kamila, Izquierdo Marta Martín, Cadenas Félix López, Ramos Fernando, Sánchez Jesús María Hernández, Lumbreras Eva, Robledo Cristina, Del Real Javier Sánchez, Caballero Juan Carlos, Collado Rosa, Bernal Teresa, Pedro Carme, Insunza Andrés, de Paz Raquel, Xicoy Blanca, Salido Eduardo, García Joaquín Sánchez, Mínguez Sandra Santos, García Cristina Miguel, Muñoz Ana María Simón, Barba Mercedes Sánchez, Rivas Jesús María Hernández, Abáigar María, Campelo María Dí |
Clonal haematopoiesis of indeterminate potential-related mutations and outcome in dilated and ischaemic cardiomyopathy. ESC heart failure 2022 Aug . Wu Jasmine M F, Bekfani Tarek, Hinze Anna, Westphal Julian Georg, Steinacker Berit, Zeller Max, Hartmann Charlotte, Möbius-Winkler Sven, Hochhaus Andreas, Schulze P Christian, Ernst Thom |
Identifying selection signatures and runs of homozygosity for spine curvature in Chinese indigenous pigs. Animal genetics 2022 5 53 (4): 513-517. Jiayuan Mo, Yujie Lu, Kuirong Chen, Siran Zhu, Wenjing Qi, Lingli Feng, Xiaoxiao Liu, Liang Liang, Ganqiu Lan, Jing Lia |
Regulation of the Late Onset alzheimer's Disease Associated HLA-DQA1/DRB1 Expression. American journal of Alzheimer's disease and other dementias 2022 3 37 15333175221085066. Zhang Xiaoyu, Zou Meijaun, Wu Yuwei, Jiang Danli, Wu Ting, Zhao Yihan, Wu Di, Cui Jing, Li Ga |
Whole-exome sequencing of BRCA-negative breast cancer patients and case-control analyses identify variants associated with breast cancer susceptibility. Human genomics 2022 11 16 (1): 61. Lee Ning Yuan, Hum Melissa, Amali Aseervatham Anusha, Lim Wei Kiat, Wong Matthew, Myint Matthew Khine, Tay Ru Jin, Ong Pei-Yi, Samol Jens, Lim Chia Wei, Ang Peter, Tan Min-Han, Lee Soo-Chin, Lee Ann S |
NEXT-GENERATION SEQUENCING-BASED GENOMIC PROFILING OF CHILDREN WITH ACUTE MYELOID LEUKEMIA. The Journal of molecular diagnostics : JMD 2023 4 . Szilvia Krizsán, Borbála Péterffy, Bálint Egyed, Tibor Nagy, Endre Sebestyén, Lajos László Hegyi, Zsuzsanna Jakab, Dániel J Erdélyi, Judit Müller, György Péter, Krisztina Csanádi, Krisztián Kállay, Gergely Kriván, Gábor Barna, Gábor Bedics, Irén Haltrich, Gábor Ottóffy, Katalin Csernus, Ágnes Vojcek, Lilla Györgyi Tiszlavicz, Krisztina Mita Gábor, Ágnes Kelemen, Péter Hauser, Zsuzsanna Gaál, István Szegedi, Anikó Ujfalusi, Béla Kajtár, Csongor Kiss, András Matolcsy, Botond Tímár, Gábor Kovács, Donát Alpár, Csaba Böd |
Comprehensive genomic profiling reveals molecular subsets of ASXL1-mutated myeloid neoplasms. Leukemia & lymphoma 2023 11 1-10. Steven M Johnson, James Haberberger, Jonathan Galeotti, Lori Ramkissoon, Catherine C Coombs, Daniel R Richardson, Matthew C Foster, Daniel Duncan, Nathan D Montgomery, Naomi L Ferguson, Joshua F Zeidn |
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- Page last updated:Apr 22, 2024
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