Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Breast Neoplasms and WRN[original query] |
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| Polymorphisms in DNA repair genes, ionizing radiation exposure and risk of breast cancer in U.S. Radiologic technologists. International journal of cancer. Journal international du cancer 2008 Jan 122 (1): 177-82. Bhatti Parveen, Struewing Jeffery P, Alexander Bruce H, Hauptmann Michael, Bowen Laura, Mateus-Pereira Lutecia H, Pineda Marbin A, Simon Steven L, Weinstock Robert M, Rosenstein Marvin, Stovall Marilyn, Preston Dale L, Linet Martha S, Doody Michele M, Sigurdson Alice |
| Genetic variation in the premature aging gene WRN: a case-control study on breast cancer susceptibility. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007 Feb 16 (2): 263-9. Ding Shian-ling, Yu Jyh-Cherng, Chen Shou-Tung, Hsu Giu-Cheng, Shen Chen-Ya |
| A polymorphism in Werner syndrome gene is associated with breast cancer susceptibility in Chinese women. Breast cancer research and treatment 2009 Nov 118 (1): 169-75. Wang Zhanwei, Xu Yan, Tang Jinhai, Ma Hongxia, Qin Jianwei, Lu Chen, Wang Xuechen, Hu Zhibin, Wang Xinru, Shen Hongbi |
| Association Between WRN Cys1367Arg (T>C) and Cancer Risk: A Meta-analysis. Technology in cancer research & treatment 2014 Dec . Wang Bo, Li Guifang, Sun Fei, Dong Nan, Sun Zhenguo, Jiang Deh |
| Association of the rs1346044 Polymorphism of the Werner Syndrome Gene RECQL2 with Increased Risk and Premature Onset of Breast Cancer. International journal of molecular sciences 2015 16 (12): 29643-53. Zins Karin, Frech Barbara, Taubenschuss Eva, Schneeberger Christian, Abraham Dietmar, Schreiber Mart |
| Analysis of DNA Repair Genes Polymorphisms in Breast Cancer. Pathology oncology research : POR 2016 Aug . Romanowicz Hanna, Pyziak ?ukasz, Jab?o?ski Filip, Bry? Magdalena, Forma Ewa, Smolarz Bea |
| Targeted exome sequencing of Korean triple-negative breast cancer reveals homozygous deletions associated with poor prognosis of adjuvant chemotherapy-treated patients. Oncotarget 2017 Sep 8 (37): 61538-61550. Jeong Hae Min, Kim Ryong Nam, Kwon Mi Jeong, Oh Ensel, Han Jinil, Lee Se Kyung, Choi Jong-Sun, Park Sara, Nam Seok Jin, Gong Gyung Yup, Nam Jin Wu, Choi Doo Ho, Lee Hannah, Nam Byung-Ho, Choi Yoon-La, Shin Young K |
| Recommendations for Preventive Care for Women with Rare Genetic Cause of Breast and Ovarian Cancer. Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti 2019 8 32 (Supplementum2): 6-13. Foretová Lenka, Navrátilová Marie, Svoboda Marek, Vaší?ková Petra, S?ahlová Eva Hrabincová, Házová Jana, Kleiblová Petra, Kleibl Zden?k, Machá?ková Eva, Palácová Markéta, Petráková Katarí |
| Werner Syndrome Protein Expression in Breast Cancer. Clinical breast cancer 2020 9 21 (1): 57-73.e7. Savva Constantinos, Sadiq Maaz, Sheikh Omar, Karim Syed, Trivedi Sachin, Green Andrew R, Rakha Emad A, Madhusudan Srinivasan, Arora Arvi |
| Gene Panel Testing in Hereditary Breast Cancer. Archives of Iranian medicine 2020 Mar 23 (3): 155-162. Rostami Parvin, Zendehdel Kazem, Shirkoohi Reza, Ebrahimi Elmira, Ataei Mitra, Imanian Hashem, Najmabadi Hossein, Akbari Mohammad Reza, Sanati Mohammad Hosse |
| Investigation of monogenic causes of familial breast cancer: data from the BEACCON case-control study. NPJ breast cancer 2021 Jun 7 (1): 76. Li Na, Lim Belle W X, Thompson Ella R, McInerny Simone, Zethoven Magnus, Cheasley Dane, Rowley Simone M, Wong-Brown Michelle W, Devereux Lisa, Gorringe Kylie L, Sloan Erica K, Trainer Alison, Scott Rodney J, James Paul A, Campbell Ian |
| Untangling the clinicopathological significance of MRE11-RAD50-NBS1 complex in sporadic breast cancers. NPJ breast cancer 2021 Nov 7 (1): 143. Alblihy Adel, Shoqafi Ahmed, Toss Michael S, Algethami Mashael, Harris Anna E, Jeyapalan Jennie N, Abdel-Fatah Tarek, Servante Juliette, Chan Stephen Y T, Green Andrew, Mongan Nigel P, Rakha Emad A, Madhusudan Srinivas |
| Co-Occurrence of Germline Genomic Variants and Copy Number Variations in Hereditary Breast and Colorectal Cancer Patients. Genes 2023 8 14 (8): . Luiza Côrtes, Tatiane Ramos Basso, Rolando André Rios Villacis, Jeferson Dos Santos Souza, Mads Malik Aagaard Jørgensen, Maria Isabel Achatz, Silvia Regina Rogat |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 18, 2023
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