Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: Glioma and PHLDB1[original query] |
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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 |
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 |
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 |
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 |
Genome-wide association study of glioma and meta-analysis.
Human genetics 2012 Dec 131 (12): 1877-88. Rajaraman Preetha, Melin Beatrice S, Wang Zhaoming, McKean-Cowdin Roberta, Michaud Dominique S, Wang Sophia S, Bondy Melissa, Houlston Richard, Jenkins Robert B, Wrensch Margaret, Yeager Meredith, Ahlbom Anders, Albanes Demetrius, Andersson Ulrika, Freeman Laura E Beane, Buring Julie E, Butler Mary Ann, Braganza Melissa, Carreon Tania, Feychting Maria, Fleming Sarah J, Gapstur Susan M, Gaziano J Michael, Giles Graham G, Hallmans Goran, Henriksson Roger, Hoffman-Bolton Judith, Inskip Peter D, Johansen Christoffer, Kitahara Cari M, Lathrop Mark, Liu Chenwei, Le Marchand Loic, Linet Martha S, Lonn Stefan, Peters Ulrike, Purdue Mark P, Rothman Nathaniel, Ruder Avima M, Sanson Marc, Sesso Howard D, Severi Gianluca, Shu Xiao-Ou, Simon Matthias, Stampfer Meir, Stevens Victoria L, Visvanathan Kala, White Emily, Wolk Alicja, Zeleniuch-Jacquotte Anne, Zheng Wei, Decker Paul, Enciso-Mora Victor, Fridley Brooke, Gao Yu-Tang, Kosel Matthew, Lachance Daniel H, Lau Ching, Rice Terri, Swerdlow Anthony, Wiemels Joseph L, Wiencke John K, Shete Sanjay, Xiang Yong-Bing, Xiao Yuanyuan, Hoover Robert N, Fraumeni Joseph F, Chatterjee Nilanjan, Hartge Patricia, Chanock Stephen |
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 |
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 |
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 |
Fine mapping of a region of chromosome 11q23.3 reveals independent locus associated with risk of glioma. PloS one 2012 7 (12): e52864. Chen Hongyan, Sun Bing, Zhao Yingjie, Song Xiao, Fan Weiwei, Zhou Keke, Zhou Liangfu, Mao Ying, Lu Da |
The PHLDB1 rs498872 (11q23.3) polymorphism and glioma risk: A meta-analysis. Asia-Pacific journal of clinical oncology 2014 Jun . Gao Xingchun, Mi Yajing, Yan Aili, Sha Baoyong, Guo Na, Hu Zhifang, Zhang Ni, Jiang Fengliang, Gou Xingch |
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 |
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 |
Pleckstrin homology-like domain family B member 1 rs498872 polymorphism and glioma risk in Chinese Han population. Cellular and molecular biology (Noisy-le-Grand, France) 2017 Aug 63 (8): 7-9. Zhang J-W, Liu Z-H, Lin X-H, Du Y-P, Guo H |
A PHLDB1 variant associated with the nonfunctional pituitary adenoma. Journal of neuro-oncology 2019 Mar . Kim Lyoung Hyo, Kim Jeong-Hyun, Namgoong Suhg, Cheong Hyun Sub, Yoon Seon-Jin, Kim Eui Hyun, Kim Se Hoon, Kim Sun Ho, Chang Jong Hee, Shin Hyoung D |
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 |
Replication of GWAS identifies RTEL1, CDKN2A/B, and PHLDB1 SNPs as risk factors in Portuguese gliomas patients. Molecular biology reports 2019 11 47 (2): 877-886. Viana-Pereira Marta, Moreno Daniel Antunes, Linhares Paulo, Amorim Júlia, Nabiço Rui, Costa Sandra, Vaz Rui, Reis Rui Manu |
Australian genome-wide association study confirms higher female risk for adult glioma associated with variants in the region of CCDC26. Neuro-oncology 2022 12 . Alpen Karen, Vajdic Claire M, MacInnis Robert J, Milne Roger L, Koh Eng-Siew, Hovey Elizabeth, Harrup Rosemary, Bruinsma Fiona, Nguyen Tuong L, Li Shuai, Joseph David, Benke Geza, Dugué Pierre-Antoine, Southey Melissa C, Giles Graham G, Rosenthal Mark, Drummond Katharine J, Nowak Anna K, Hopper John L, Kapuscinski Miroslaw, Makalic En |
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