Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: Breast Neoplasms and meta-analysis and ATM[original query] |
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The association between ATM D1853N polymorphism and breast cancer susceptibility: a meta-analysis. Journal of experimental & clinical cancer research : CR 2010 29 117. Gao Lin-Bo, Pan Xin-Min, Sun Hong, Wang Xia, Rao Li, Li Li-Juan, Liang Wei-Bo, Lv Mei-Li, Yang Wen-Zhong, Zhang L |
Association between polymorphisms of the ataxia telangiectasia mutated gene and breast cancer risk: evidence from the current studies. Breast cancer research and treatment 2011 Feb 126 (1): 141-8. Lu Pei-Hua, Wei Mu-Xin, Si Shu-Ping, Liu Xiao, Shen Wei, Tao Guo-Qing, Chen Min-B |
Lack of association between ATM C.1066-6T > G mutation and breast cancer risk: a meta-analysis of 8,831 cases and 4,957 controls. Breast cancer research and treatment 2011 Jan 125 (2): 473-7. Ding Hong, Mao Chen, Li Shui-Ming, Liu Qu, Lin Lin, Chen Qi |
Association between ATM 5557G>A polymorphism and breast cancer risk: a meta-analysis. Molecular biology reports 2012 Feb 39 (2): 1113-8. Mao Chen, Chung Vincent C H, He Ben-Fu, Luo Rong-Cheng, Tang Jin-Li |
Association between ATM polymorphisms and cancer risk: a meta-analysis. Molecular biology reports 2012 May 39 (5): 5719-25. Shen Li, Yin Zhi-Hua, Wan Yan, Zhang Yue, Li Kun, Zhou Bao-S |
The association between ATM IVS 22-77 T>C and cancer risk: a meta-analysis. PloS one 2012 7 (1): e29479. Zhao Lin, Gu Aihua, Ji Guixiang, Zou Peng, Zhao Peng, Lu Ail |
Protein-truncating variants in moderate-risk breast cancer susceptibility genes: a meta-analysis of high-risk case-control screening studies. Cancer genetics 2015 Sep 208 (9): 455-63. Aloraifi Fatima, McCartan Damian, McDevitt Trudi, Green Andrew J, Bracken Adrian, Geraghty Jam |
Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5456 breast and prostate cancer patients. Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology 2016 12 121 (3): 431-439. Andreassen Christian Nicolaj, Rosenstein Barry S, Kerns Sarah L, Ostrer Harry, De Ruysscher Dirk, Cesaretti Jamie A, Barnett Gillian C, Dunning Alison M, Dorling Leila, West Catharine M L, Burnet Neil G, Elliott Rebecca, Coles Charlotte, Hall Emma, Fachal Laura, Vega Ana, Gómez-Caamaño Antonio, Talbot Christopher J, Symonds R Paul, De Ruyck Kim, Thierens Hubert, Ost Piet, Chang-Claude Jenny, Seibold Petra, Popanda Odilia, Overgaard Marie, Dearnaley David, Sydes Matthew R, Azria David, Koch Christine Anne, Parliament Matthew, Blackshaw Michael, Sia Michael, Fuentes-Raspall Maria J, Ramon Y Cajal Teresa, Barnadas Agustin, Vesprini Danny, Gutiérrez-Enríquez Sara, Mollà Meritxell, Díez Orland, Yarnold John R, Overgaard Jens, Bentzen Søren M, Alsner Jan, |
Effect of ATM-111 (G>A) Polymorphism on Cancer Risk: A Meta-Analysis. Genetic testing and molecular biomarkers 2016 May . Huang Senlin, Zhang Yuzhao, Zeng T |
Penetrance of ATM Gene Mutations in Breast Cancer: A Meta-Analysis of Different Measures of Risk. Genetic epidemiology 2016 Apr . Marabelli Monica, Cheng Su-Chun, Parmigiani Giovan |
Network Meta-Analysis on the Effects of DNA Damage Response-Related Gene Mutations on Overall Survival of Breast Cancer Based on TCGA Database. Journal of cellular biochemistry 2017 May . Liu Chang, Chang Hong, Li Xiao-Han, Qi Ya-Fei, Wang Jin-Ou, Zhang Ying, Yang Xiang-Ho |
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.
Nature communications 2018 Sep 9 (1): 3636. Rafnar Thorunn, Gunnarsson Bjarni, Stefansson Olafur A, Sulem Patrick, Ingason Andres, Frigge Michael L, Stefansdottir Lilja, Sigurdsson Jon K, Tragante Vinicius, Steinthorsdottir Valgerdur, Styrkarsdottir Unnur, Stacey Simon N, Gudmundsson Julius, Arnadottir Gudny A, Oddsson Asmundur, Zink Florian, Halldorsson Gisli, Sveinbjornsson Gardar, Kristjansson Ragnar P, Davidsson Olafur B, Salvarsdottir Anna, Thoroddsen Asgeir, Helgadottir Elisabet A, Kristjansdottir Katrin, Ingthorsson Orri, Gudmundsson Valur, Geirsson Reynir T, Arnadottir Ragnheidur, Gudbjartsson Daniel F, Masson Gisli, Asselbergs Folkert W, Jonasson Jon G, Olafsson Karl, Thorsteinsdottir Unnur, Halldorsson Bjarni V, Thorleifsson Gudmar, Stefansson Ka |
Agnostic Pathway/Gene Set Analysis of Genome-Wide Association Data Identifies Associations for Pancreatic Cancer.
Journal of the National Cancer Institute 2018 Dec . Walsh Naomi, Zhang Han, Hyland Paula L, Yang Qi, Mocci Evelina, Zhang Mingfeng, Childs Erica J, Collins Irene, Wang Zhaoming, Arslan Alan A, Beane-Freeman Laura, Bracci Paige M, Brennan Paul, Canzian Federico, Duell Eric J, Gallinger Steven, Giles Graham G, Goggins Michael, Goodman Gary E, Goodman Phyllis J, Hung Rayjean J, Kooperberg Charles, Kurtz Robert C, Malats Núria, LeMarchand Loic, Neale Rachel E, Olson Sara H, Scelo Ghislaine, Shu Xiao O, Van Den Eeden Stephen K, Visvanathan Kala, White Emily, Zheng Wei, , Albanes Demetrius, Andreotti Gabriella, Babic Ana, Bamlet William R, Berndt Sonja I, Borgida Ayelet, Boutron-Ruault Marie-Christine, Brais Lauren, Brennan Paul, Bueno-de-Mesquita Bas, Buring Julie, Chaffee Kari G, Chanock Stephen, Cleary Sean, Cotterchio Michelle, Foretova Lenka, Fuchs Charles, M Gaziano J Michael, Giovannucci Edward, Goggins Michael, Hackert Thilo, Haiman Christopher, Hartge Patricia, Hasan Manal, Helzlsouer Kathy J, Herman Joseph, Holcatova Ivana, Holly Elizabeth A, Hoover Robert, Hung Rayjean J, Janout Vladimir, Klein Eric A, Kurtz Robert C, Laheru Daniel, Lee I-Min, Lu Lingeng, Malats Núria, Mannisto Satu, Milne Roger L, Oberg Ann L, Orlow Irene, Patel Alpa V, Peters Ulrike, Porta Miquel, Real Francisco X, Rothman Nathaniel, Sesso Howard D, Severi Gianluca, Silverman Debra, Strobel Oliver, Sund Malin, Thornquist Mark D, Tobias Geoffrey S, Wactawski-Wende Jean, Wareham Nick, Weiderpass Elisabete, Wentzensen Nicolas, Wheeler William, Yu Herbert, Zeleniuch-Jacquotte Anne, Kraft Peter, Li Donghui, Jacobs Eric J, Petersen Gloria M, Wolpin Brian M, Risch Harvey A, Amundadottir Laufey T, Yu Kai, Klein Alison P, Stolzenberg-Solomon Rachael |
Association between ATM rs1801516 polymorphism and cancer susceptibility: a meta-analysis involving 12,879 cases and 18,054 controls. BMC cancer 2018 Nov 18 (1): 1060. Gu Yulu, Shi Jikang, Qiu Shuang, Qiao Yichun, Zhang Xin, Cheng Yi, Liu Yaw |
Prevalence of pathogenic variants and variants of unknown significance in patients at high risk of breast cancer: A systematic review and meta-analysis of gene-panel data. Critical reviews in oncology/hematology 2018 11 132 138-144. van Marcke C, Collard A, Vikkula M, Duhoux F |
ATM rs189037 (G?>?A) polymorphism increased the risk of cancer: an updated meta-analysis. BMC medical genetics 2019 Feb 20 (1): 28. Zhao Zhi-Liang, Xia Lu, Zhao Cong, Yao J |
Impact of ATM rs1801516 on late skin reactions of radiotherapy for breast cancer: Evidences from a cohort study and a trial sequential meta-analysis. PloS one 2019 14 (11): e0225685. Terrazzino Salvatore, Cargnin Sarah, Deantonio Letizia, Pisani Carla, Masini Laura, Canonico Pier Luigi, Genazzani Armando A, Krengli Mar |
The prevalence of ataxia telangiectasia mutated (ATM) variants in patients with breast cancer patients: a systematic review and meta-analysis. Cancer cell international 2021 Sep 21 (1): 474. Moslemi Masoumeh, Vafaei Maryam, Khani Pouria, Soheili Marzieh, Nedaeinia Reza, Manian Mostafa, Moradi Yousef, Sohrabi Ehs |
The association between ATM variants and risk of breast cancer: a systematic review and meta-analysis. BMC cancer 2021 Jan 21 (1): 27. Moslemi Masoumeh, Moradi Yousef, Dehghanbanadaki Hojat, Afkhami Hamed, Khaledi Mansoor, Sedighimehr Najmeh, Fathi Javad, Sohrabi Ehs |
A comprehensive literature review and meta-analysis of the prevalence of pan-cancer BRCA mutations, homologous recombination repair gene mutations, and homologous recombination deficiencies. Environmental and molecular mutagenesis 2022 Jul 63 (6): 308-316. Shao Changxia, Wan Jun, Lam Fred C, Tang Huilin, Marley Andrew R, Song Yiqing, Miller Chelsey, Brown Madeline, Han Jiali, Adeboyeje Gboye |
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk. Nature genetics 2023 8 . Naomi Wilcox, Martine Dumont, Anna González-Neira, Sara Carvalho, Charles Joly Beauparlant, Marco Crotti, Craig Luccarini, Penny Soucy, Stéphane Dubois, Rocio Nuñez-Torres, Guillermo Pita, Eugene J Gardner, Joe Dennis, M Rosario Alonso, Nuria Álvarez, Caroline Baynes, Annie Claude Collin-Deschesnes, Sylvie Desjardins, Heiko Becher, Sabine Behrens, Manjeet K Bolla, Jose E Castelao, Jenny Chang-Claude, Sten Cornelissen, Thilo Dörk, Christoph Engel, Manuela Gago-Dominguez, Pascal Guénel, Andreas Hadjisavvas, Eric Hahnen, Mikael Hartman, Belén Herráez, , Audrey Jung, Renske Keeman, Marion Kiechle, Jingmei Li, Maria A Loizidou, Michael Lush, Kyriaki Michailidou, Mihalis I Panayiotidis, Xueling Sim, Soo Hwang Teo, Jonathan P Tyrer, Lizet E van der Kolk, Cecilia Wahlström, Qin Wang, John R B Perry, Javier Benitez, Marjanka K Schmidt, Rita K Schmutzler, Paul D P Pharoah, Arnaud Droit, Alison M Dunning, Anders Kvist, Peter Devilee, Douglas F Easton, Jacques Sima |
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- Page last updated:May 06, 2024
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