HuGE Literature Finder
Records
1
-
29
Adult diffuse glioma GWAS by molecular subtype identifies variants in D2HGDH and FAM20C.
![]() Neuro-oncology 2020 May . Eckel-Passow Jeanette E, Drucker Kristen L, Kollmeyer Thomas M, Kosel Matt L, Decker Paul A, Molinaro Annette M, Rice Terri, Praska Corinne E, Clark Lauren, Caron Alissa, Abyzov Alexej, Batzler Anthony, Song Jun S, Pekmezci Melike, Hansen Helen M, McCoy Lucie S, Bracci Paige M, Wiemels Joseph, Wiencke John K, Francis Stephen, Burns Terry C, Giannini Caterina, Lachance Daniel H, Wrensch Margaret, Jenkins Robert |
The Genetic Architecture of Gliomagenesis-Genetic Risk Variants Linked to Specific Molecular Subtypes. Cancers 2019 Dec 11 (12): . Wu Wendy Yi-Ying, Johansson Gunnar, Wibom Carl, Brännström Thomas, Malmström Annika, Henriksson Roger, Golovleva Irina, Bondy Melissa L, Andersson Ulrika, Dahlin Anna M, Melin Beatri |
Association analysis of RTEL1 variants with risk of adult gliomas in a Korean population. PloS one 2018 13 (11): e0207660. Namgoong Suhg, Cheong Hyun Sub, Kim Jeong-Hyun, Kim Lyoung Hyo, Seo Jung Yeon, Kang Seok-Gu, Yoon Seon-Jin, Kim Se Hoon, Chang Jong Hee, Shin Hyoung D |
The effects of gene polymorphisms on glioma prognosis. The journal of gene medicine 2017 Oct . Cui Ying, Li Guolin, Yan Mengdan, Li Jing, Jin Tianbo, Li Shanqu, Mu Shij |
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 |
The role of the RTEL1 rs2297440 polymorphism in the risk of glioma development: a meta-analysis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2016 Mar . Zhang Cuiping, Lu Yu, Zhang Xiaolian, Yang Dongmei, Shang Shuxin, Liu Denghe, Jiang Kongmei, Huang Weiqia |
CCDC26, CDKN2BAS, RTEL1 and TERT Polymorphisms in pediatric brain tumor susceptibility. Carcinogenesis 2015 Aug 36 (8): 876-82. Adel Fahmideh Maral, Lavebratt Catharina, Schüz Joachim, Röösli Martin, Tynes Tore, Grotzer Michael A, Johansen Christoffer, Kuehni Claudia E, Lannering Birgitta, Prochazka Michaela, Schmidt Lisbeth S, Feychting Mar |
Investigation of established genetic risk variants for glioma in prediagnostic samples from a population-based nested case-control study. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2015 May 24 (5): 810-6. Wibom Carl, Späth Florentin, Dahlin Anna M, Langseth Hilde, Hovig Eivind, Rajaraman Preetha, Johannesen Tom Børge, Andersson Ulrika, Melin Beatri |
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 |
Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk.
![]() Nature genetics 2014 Jul 46 (7): 731-5. Walsh Kyle M, Codd Veryan, Smirnov Ivan V, Rice Terri, Decker Paul A, Hansen Helen M, Kollmeyer Thomas, Kosel Matthew L, Molinaro Annette M, McCoy Lucie S, Bracci Paige M, Cabriga Belinda S, Pekmezci Melike, Zheng Shichun, Wiemels Joseph L, Pico Alexander R, Tihan Tarik, Berger Mitchell S, Chang Susan M, Prados Michael D, Lachance Daniel H, O'Neill Brian Patrick, Sicotte Hugues, Eckel-Passow Jeanette E, , van der Harst Pim, Wiencke John K, Samani Nilesh J, Jenkins Robert B, Wrensch Margaret |
Regulator of telomere elongation helicase 1 (RTEL1) rs6010620 polymorphism contribute to increased risk of glioma. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2014 Jun 35 (6): 5259-66. Zhao Wei, Bian Yusong, Zhu Wei, Zou Peng, Tang Guot |
Associations between the rs6010620 polymorphism in RTEL1 and risk of glioma: a meta-analysis of 20,711 participants. Asian Pacific journal of cancer prevention : APJCP 2014 15 (17): 7163-7. Wu Yao, Tong Xiang, Tang Ling-Li, Zhou Kai, Zhong Chuan-Hong, Jiang S |
The RTEL1 rs6010620 polymorphism and glioma risk: a meta-analysis based on 12 case-control studies. Asian Pacific journal of cancer prevention : APJCP 2014 15 (23): 10175-9. Du Shu-Li, Geng Ting-Ting, Feng Tian, Chen Cui-Ping, Jin Tian-Bo, Chen Ch |
RTEL1 and TERT polymorphisms are associated with astrocytoma risk in the Chinese Han population. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2013 Dec 34 (6): 3659-66. Jin Tian-Bo, Zhang Jia-Yi, Li Gang, Du Shu-Li, Geng Ting-Ting, Gao Jing, Liu Qian-Ping, Gao Guo-Dong, Kang Long-Li, Chen Chao, Li Shan- |
Telomere length and risk of glioma. Cancer epidemiology 2013 Dec 37 (6): 935-8. Walcott Farzana, Rajaraman Preetha, Gadalla Shahinaz M, Inskip Peter D, Purdue Mark P, Albanes Demetrius, Orr Esther, De Vivo Immaculata, Savage Sharon |
Genetic variants in telomerase-related genes are associated with an older age at diagnosis in glioma patients: evidence for distinct pathways of gliomagenesis. Neuro-oncology 2013 Aug 15 (8): 1041-7. Walsh Kyle M, Rice Terri, Decker Paul A, Kosel Matthew L, Kollmeyer Thomas, Hansen Helen M, Zheng Shichun, McCoy Lucie S, Bracci Paige M, Anderson Erik, Hsuang George, Wiemels Joe L, Pico Alexander R, Smirnov Ivan, Molinaro Annette M, Tihan Tarik, Berger Mitchell S, Chang Susan M, Prados Michael D, Lachance Daniel H, Sicotte Hugues, Eckel-Passow Jeanette E, Wiencke John K, Jenkins Robert B, Wrensch Margaret |
Known glioma risk loci are associated with glioma with a family history of brain tumours -- a case-control gene association study. International journal of cancer. Journal international du cancer 2013 May 132 (10): 2464-8. Melin Beatrice, Dahlin Anna M, Andersson Ulrika, Wang Zhaoming, Henriksson Roger, Hallmans Göran, Bondy Melissa L, Johansen Christoffer, Feychting Maria, Ahlbom Anders, Kitahara Cari M, Wang Sophia S, Ruder Avima M, Carreón Tania, Butler Mary Ann, Inskip Peter D, Purdue Mark, Hsing Ann W, Mechanic Leah, Gillanders Elizabeth, Yeager Meredith, Linet Martha, Chanock Stephen J, Hartge Patricia, Rajaraman Preet |
Analysis of 60 reported glioma risk SNPs replicates published GWAS findings but fails to replicate associations from published candidate-gene studies. Genetic epidemiology 2013 Feb 37 (2): 2. Walsh KM, Anderson E, Hansen HM, Decker PA, Kosel ML, Kollmeyer T, Rice T, Zheng S, Xiao Y, Chang JS, McCoy LS, Bracci PM, Wiemels JL, Pico AR, Smirnov I, Lachance DH, Sicotte H, Eckel-Passow JE, Wiencke JK, Jenkins RB, Wrensch MR |
RTEL1 tagging SNPs and haplotypes were associated with glioma development. Diagnostic pathology 2013 8 83. Li Gang, Jin Tianbo, Liang Hongjuan, Zhang Zhiguo, He Shiming, Tu Yanyang, Yang Haixia, Geng Tingting, Cui Guangbin, Chen Chao, Gao Guodo |
Association between glioma susceptibility loci and tumour pathology defines specific molecular etiologies. Neuro-oncology 2012 Nov . Di Stefano AL, Enciso-Mora V, Marie Y, Desestret V, Labussière M, Boisselier B, Mokhtari K, Idbaih A, Hoang-Xuan K, Delattre JY, Houlston RS, Sanson M |
Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: a novel candidate SNP approach. Frontiers in genetics 2012 3 . Jacobs DI, Walsh KM, Wrensch M, Wiencke J, Jenkins R, Houlston RS, Bondy M, Simon M, Sanson M, Gousias K, Schramm J, Labussière M, Di Stefano AL, Wichmann HE, Müller-Nurasyid M, Schreiber S, Franke A, Moebus S, Eisele L, Dewan AT, Dubrow R |
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 |
Associations of high-grade glioma with glioma risk alleles and histories of allergy and smoking. American journal of epidemiology 2011 Sep 174 (5): 574-81. Lachance Daniel H, Yang Ping, Johnson Derek R, Decker Paul A, Kollmeyer Thomas M, McCoy Lucie S, Rice Terri, Xiao Yuanyuan, Ali-Osman Francis, Wang Frances, Stoddard Shawn M, Sprau Debra J, Kosel Matthew L, Wiencke John K, Wiemels Joseph L, Patoka Joseph S, Davis Faith, McCarthy Bridget, Rynearson Amanda L, Worra Joel B, Fridley Brooke L, O'Neill Brian Patrick, Buckner Jan C, Il'yasova Dora, Jenkins Robert B, Wrensch Margaret |
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 |
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 |
Genetic risk profiles identify different molecular etiologies for glioma. Clinical cancer research : an official journal of the American Association for Cancer Research 2010 Nov 16 (21): 5252-9. Simon Matthias, Hosking Fay J, Marie Yannick, Gousias Konstantinos, Boisselier Blandine, Carpentier Catherine, Schramm Johannes, Mokhtari Karima, Hoang-Xuan Khe, Idbaih Ahmed, Delattre Jean-Yves, Lathrop Mark, Robertson Lindsay B, Houlston Richard S, Sanson Ma |
Interaction between 5 genetic variants and allergy in glioma risk. American journal of epidemiology 2010 Jun 171 (11): 1165-73. Schoemaker Minouk J, Robertson Lindsay, Wigertz Annette, Jones Michael E, Hosking Fay J, Feychting Maria, Lönn Stefan, McKinney Patricia A, Hepworth Sarah J, Muir Kenneth R, Auvinen Anssi, Salminen Tiina, Kiuru Anne, Johansen Christoffer, Houlston Richard S, Swerdlow Anthony |
Genome-wide association study identifies five susceptibility loci for glioma.
![]() Nature genetics 2009 Aug 41 (8): 899-904. Shete Sanjay, Hosking Fay J, Robertson Lindsay B, Dobbins Sara E, Sanson Marc, Malmer Beatrice, Simon Matthias, Marie Yannick, Boisselier Blandine, Delattre Jean-Yves, Hoang-Xuan Khe, El Hallani Soufiane, Idbaih Ahmed, Zelenika Diana, Andersson Ulrika, Henriksson Roger, Bergenheim A Tommy, Feychting Maria, Lönn Stefan, Ahlbom Anders, Schramm Johannes, Linnebank Michael, Hemminki Kari, Kumar Rajiv, Hepworth Sarah J, Price Amy, Armstrong Georgina, Liu Yanhong, Gu Xiangjun, Yu Robert, Lau Ching, Schoemaker Minouk, Muir Kenneth, Swerdlow Anthony, Lathrop Mark, Bondy Melissa, Houlston Richard |
Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
![]() 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 |
- Page last reviewed:Oct 1, 2021
- Page last updated:Jun 22, 2022
- Content source: