Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: Leukemia and BRCA2[original query] |
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Multi-factor dimensionality reduction applied to a large prospective investigation on gene-gene and gene-environment interactions. Carcinogenesis 2007 Feb 28 (2): 414-22. Manuguerra M, Matullo G, Veglia F, Autrup H, Dunning A M, Garte S, Gormally E, Malaveille C, Guarrera S, Polidoro S, Saletta F, Peluso M, Airoldi L, Overvad K, Raaschou-Nielsen O, Clavel-Chapelon F, Linseisen J, Boeing H, Trichopoulos D, Kalandidi A, Palli D, Krogh V, Tumino R, Panico S, Bueno-De-Mesquita H B, Peeters P H, Lund E, Pera G, Martinez C, Amiano P, Barricarte A, Tormo M J, Quiros J R, Berglund G, Janzon L, Jarvholm B, Day N E, Allen N E, Saracci R, Kaaks R, Ferrari P, Riboli E, Vineis |
Variants in the ATM-BRCA2-CHEK2 axis predispose to chronic lymphocytic leukemia. Blood 2006 Jul 108 (2): 638-44. Rudd Matthew F, Sellick Gabrielle S, Webb Emily L, Catovsky Daniel, Houlston Richard |
Risk of acute promyelocytic leukemia in multiple sclerosis: coding variants of DNA repair genes. Neurology 2011 Mar 76 (12): 1059-65. Hasan S K, Buttari F, Ottone T, Voso M T, Hohaus S, Marasco E, Mantovani V, Garagnani P, Sanz M A, Cicconi L, Bernardi G, Centonze D, Lo-Coco |
Haplotypes of DNA repair and cell cycle control genes, X-ray exposure, and risk of childhood acute lymphoblastic leukemia. Cancer causes & control : CCC 2011 Dec 22 (12): 1721-30. Chokkalingam Anand P, Bartley Karen, Wiemels Joseph L, Metayer Catherine, Barcellos Lisa F, Hansen Helen M, Aldrich Melinda C, Guha Neela, Urayama Kevin Y, Scélo Ghislaine, Chang Jeffrey S, Month Stacy R, Wiencke John K, Buffler Patricia |
Association between the RAD51 135 G>C polymorphism and risk of cancer: a meta-analysis of 19,068 cases and 22,630 controls. PloS one 2013 8 (9): e75153. Wang Wei, Li Jia-Lin, He Xiao-Feng, Li An-Ping, Cai Yong-Lin, Xu Na, Sun Shu-Mei, Wu Bing- |
TP53 p.R337H prevalence in a series of Brazilian hereditary breast cancer families. Hereditary cancer in clinical practice 2014 12 (1): 8. Cury Nathalia M, Ferraz Victor Ef, Silva Wilson |
Inherited mutations in cancer susceptibility genes are common among survivors of breast cancer who develop therapy-related leukemia. Cancer 2015 Dec . Churpek Jane E, Marquez Rafael, Neistadt Barbara, Claussen Kimberly, Lee Ming K, Churpek Matthew M, Huo Dezheng, Weiner Howard, Bannerjee Mekhala, Godley Lucy A, Le Beau Michelle M, Pritchard Colin C, Walsh Tom, King Mary-Claire, Olopade Olufunmilayo I, Larson Richard |
Mutational landscape of gastric adenocarcinoma in Chinese: implications for prognosis and therapy. Proceedings of the National Academy of Sciences of the United States of America 2015 Jan 112 (4): 1107-12. Chen Kexin, Yang Da, Li Xiangchun, Sun Baocun, Song Fengju, Cao Wenfeng, Brat Daniel J, Gao Zhibo, Li Haixin, Liang Han, Zhao Yanrui, Zheng Hong, Li Miao, Buckner Jan, Patterson Scott D, Ye Xiang, Reinhard Christoph, Bhathena Anahita, Joshi Deepa, Mischel Paul S, Croce Carlo M, Wang Yi Michael, Raghavakaimal Sreekumar, Li Hui, Lu Xin, Pan Yang, Chang Han, Ba Sujuan, Luo Longhai, Cavenee Webster K, Zhang Wei, Hao Xish |
Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin. Molecular cytogenetics 2018 1 11 6. La Starza Roberta, Pierini Tiziana, Pastorino Lorenza, Albi Elisa, Matteucci Caterina, Crescenzi Barbara, Sportoletti Paolo, Covarelli Piero, Falzetti Franca, Roti Giovanni, Ascani Stefano, Mecucci Cristi |
Estimated number of adult survivors of childhood cancer in United States with cancer-predisposing germline variants. Pediatric blood & cancer 2019 11 67 (2): e28047. Wilson Carmen L, Wang Zhaoming, Liu Qi, Ehrhardt Matthew J, Mostafavi Roya, Easton John, Mulder Heather, Hedges Dale J, Wang Shuoguo, Rusch Michael, Edmonson Michael, Levy Shawn, Lanctot Jennifer Q, Currie Kelsey, Lear Matthew, Patel Aman, Sapkota Yadav, Brooke Russell J, Moon Wonjong, Chang Ti-Cheng, Chen Wenan, Kesserwan Chimene A, Wu Gang, Nichols Kim E, Hudson Melissa M, Zhang Jinghui, Robison Leslie L, Yasui Yuta |
Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia. Scientific reports 2020 9 10 (1): 14297. Kim Borahm, Yun Woobin, Lee Seung-Tae, Choi Jong Rok, Yoo Keon Hee, Koo Hong Hoe, Jung Chul Won, Kim Sun H |
Frequency of pathogenic/likely pathogenic germline variants in cancer-related genes among children with acute leukemia in Saudi Arabia. Pediatric blood & cancer 2020 5 67 (7): e28340. Alsultan Abdulrahman, Essa Mohammed, Aljefri Abdullah, Ayas Mouhab, Alharbi Musa, Alkhayat Nawaf, Al-Anzi Faisal, Yassin Fawwaz, Alkasim Fawaz, Alharbi Qasim, Abdullah Shaker, Jastaniah Was |
Family history of early onset acute lymphoblastic leukemia is suggesting genetic associations. Scientific reports 2021 Jun 11 (1): 12370. Li Xinjun, Sundquist Kristina, Sundquist Jan, Försti Asta, Hemminki Ka |
Fanconi anemia gene-associated germline predisposition in aplastic anemia and hematologic malignancies. Frontiers of medicine 2021 Nov . Nie Daijing, Zhang Jing, Wang Fang, Li Xvxin, Liu Lili, Zhang Wei, Cao Panxiang, Chen Xue, Zhang Yang, Chen Jiaqi, Ma Xiaoli, Zhou Xiaosu, Wu Qisheng, Liu Ming, Liu Mingyue, Tian Wenjun, Liu Hongxi |
Genotype-cancer association in patients with Fanconi anemia due to pathogenic variants in FANCD1 (BRCA2) or FANCN (PALB2). Cancer genetics 2021 10 258-259 101-109. McReynolds Lisa J, Biswas Kajal, Giri Neelam, Sharan Shyam K, Alter Blanche |
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort. Haematologica 2022 4 108 (1): 69-82. Altintas Burak, Giri Neelam, McReynolds Lisa J, Best Ana, Alter Blanche |
Mutations of BRCA1/2 Genes in the West of Turkey and Genotype-Phenotype Correlations. Clinical laboratory 2022 1 68 (1): . Gun-Bilgic Dilek, Aydin-Gumus Aydeniz, Bilgic Abdulkadir, Cam Fethi |
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- Page last updated:Mar 25, 2024
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