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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Glioblastoma and RTEL1[original query]
Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. GWAS Catalog
Nature genetics 2009 Aug 41 (8): 905-8.
Wrensch Margaret, Jenkins Robert B, Chang Jeffrey S, Yeh Ru-Fang, Xiao Yuanyuan, Decker Paul A, Ballman Karla V, Berger Mitchel, Buckner Jan C, Chang Susan, Giannini Caterina, Halder Chandralekha, Kollmeyer Thomas M, Kosel Matthew L, LaChance Daniel H, McCoy Lucie, O'Neill Brian P, Patoka Joe, Pico Alexander R, Prados Michael, Quesenberry Charles, Rice Terri, Rynearson Amanda L, Smirnov Ivan, Tihan Tarik, Wiemels Joe, Yang Ping, Wiencke John
Distinct germ line polymorphisms underlie glioma morphologic heterogeneity.
Cancer genetics 2011 Jan 204 (1): 13-8.
Jenkins Robert B, Wrensch Margaret R, Johnson Derek, Fridley Brooke L, Decker Paul A, Xiao Yuanyuan, Kollmeyer Thomas M, Rynearson Amanda L, Fink Stephanie, Rice Terri, McCoy Lucie S, Halder Chandralekha, Kosel Matthew L, Giannini Caterina, Tihan Tarik, O'Neill Brian P, Lachance Daniel H, Yang Ping, Wiemels Joseph, Wiencke John
Association of sequence variants on chromosomes 20, 11, and 5 (20q13.33, 11q23.3, and 5p15.33) with glioma susceptibility in a Chinese population.
American journal of epidemiology 2011 Apr 173 (8): 915-22.
Chen Hongyan, Chen Yuanyuan, Zhao Yao, Fan Weiwei, Zhou Keke, Liu Yanhong, Zhou Liangfu, Mao Ying, Wei Qingyi, Xu Jianfeng, Lu Da
Cancer susceptibility variants and the risk of adult glioma in a US case-control study.
Journal of neuro-oncology 2011 1 104 (2): 535-42.
Egan Kathleen M, Thompson Reid C, Nabors L B, Olson Jeffrey J, Brat Daniel J, Larocca Renato V, Brem Steven, Moots Paul L, Madden Melissa H, Browning James E, Ann Chen
Fine mapping analysis of a region of 20q13.33 identified five independent susceptibility loci for glioma in a Chinese Han population.
Carcinogenesis 2012 May 33 (5): 1065-71.
Song Xiao, Zhou Keke, Zhao Yingjie, Huai Cong, Zhao Yao, Yu Hongjie, Chen Yuanyuan, Chen Gong, Chen Hongyan, Fan Weiwei, Mao Ying, Lu Da
Analysis of difference of association between polymorphisms in the XRCC5, RPA3 and RTEL1 genes and glioma, astrocytoma and glioblastoma.
American journal of cancer research 2015 5 (7): 2294-300.
Jin Tianbo, Wang Yuan, Li Gang, Du Shuli, Yang Hua, Geng Tingting, Hou Peng, Gong Yongku
Genetic risk variants in the CDKN2A/B, RTEL1 and EGFR genes are associated with somatic biomarkers in glioma.
Journal of neuro-oncology 2016 May 127 (3): 483-92.
Ghasimi Soma, Wibom Carl, Dahlin Anna M, Brännström Thomas, Golovleva Irina, Andersson Ulrika, Melin Beatri
A functional variant on 20q13.33 related to glioma risk alters enhancer activity and modulates expression of multiple genes.
Human mutation 2020 11 42 (1): 77-88.
Ali Mourad Wagdy, Patro C Pawan K, Zhu Jacqueline Jufen, Dampier Christopher H, Plummer Sarah J, Kuscu Cem, Adli Mazhar, Lau Ching, Lai Rose K, Casey Grah
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