Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Disease and RAD52[original query] |
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| [Analysis of loss of heterozygosity and microsatellite instability RAD52, RAD54 and RAD54B gene and BRCA1 gene mutation in breast cancer]. Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego 2006 Dec 21 (126): 548-50. Romanowicz-Makowska Hanna, Smolarz Bea |
| RAD52 polymorphisms contribute to the development of papillary thyroid cancer susceptibility in Middle Eastern population. Journal of endocrinological investigation 2008 Oct 31 (10): 893-9. Siraj A K, Al-Rasheed M, Ibrahim M, Siddiqui K, Al-Dayel F, Al-Sanea O, Uddin S, Al-Kuraya |
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.
Human molecular genetics 2012 Nov 21 (22): 4980-95. Timofeeva Maria N, Hung Rayjean J, Rafnar Thorunn, Christiani David C, Field John K, Bickeböller Heike, Risch Angela, McKay James D, Wang Yufei, Dai Juncheng, Gaborieau Valerie, McLaughlin John, Brenner Darren, Narod Steven A, Caporaso Neil E, Albanes Demetrius, Thun Michael, Eisen Timothy, Wichmann H-Erich, Rosenberger Albert, Han Younghun, Chen Wei, Zhu Dakai, Spitz Margaret, Wu Xifeng, Pande Mala, Zhao Yang, Zaridze David, Szeszenia-Dabrowska Neonilia, Lissowska Jolanta, Rudnai Peter, Fabianova Eleonora, Mates Dana, Bencko Vladimir, Foretova Lenka, Janout Vladimir, Krokan Hans E, Gabrielsen Maiken Elvestad, Skorpen Frank, Vatten Lars, Njølstad Inger, Chen Chu, Goodman Gary, Lathrop Mark, Benhamou Simone, Vooder Tõnu, Välk Kristjan, Nelis Mari, Metspalu Andres, Raji Olaide, Chen Ying, Gosney John, Liloglou Triantafillos, Muley Thomas, Dienemann Hendrik, Thorleifsson Gudmar, Shen Hongbing, Stefansson Kari, Brennan Paul, Amos Christopher I, Houlston Richard, Landi Maria Teresa, |
| Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinoma. Cancer discovery 2012 Feb 2 (2): 131-9. Shi Jianxin, Chatterjee Nilanjan, Rotunno Melissa, Wang Yufei, Pesatori Angela C, Consonni Dario, Li Peng, Wheeler William, Broderick Peter, Henrion Marc, Eisen Timothy, Wang Zhaoming, Chen Wei, Dong Qiong, Albanes Demetrius, Thun Michael, Spitz Margaret R, Bertazzi Pier Alberto, Caporaso Neil E, Chanock Stephen J, Amos Christopher I, Houlston Richard S, Landi Maria Tere |
| DNA repair gene variants are associated with an increased risk of myelodysplastic syndromes in a Czech population. Journal of hematology & oncology 2013 6 9. Belickova Monika, Merkerova Michaela Dostalova, Stara Eliska, Vesela Jitka, Sponerova Dana, Mikulenkova Dana, Brdicka Radim, Neuwirtova Radana, Jonasova Anna, Cermak Jarosl |
| Targeted Resequencing of 30 Genes Improves the Detection of Deleterious Mutations in South Indian Women with Breast and/or Ovarian Cancers. Asian Pacific journal of cancer prevention : APJCP 2015 16 (13): 5211-7. Rajkumar Thangarajan, Meenakumari Balaiah, Mani Samson, Sridevi Veluswami, Sundersingh Shirl |
| Increased age-adjusted hazard of death associated with a common single nucleotide polymorphism of the human RAD52 gene in a cardiovascular cohort. Mechanisms of ageing and development 2017 10 167 56-63. Lenart Peter, Zlámal Filip, Machal Jan, Hlinomaz Ota, Groch Ladislav, Bienertová-Vašk? Jul |
| Assessment of DNA repair susceptibility genes identified by whole exome sequencing in head and neck cancer. DNA repair 2018 5 66-67 50-63. Das Raima, Kundu Sharbadeb, Laskar Shaheen, Choudhury Yashmin, Ghosh Sankar Kum |
| Characteristics of genomic alterations of lung adenocarcinoma in young never-smokers. International journal of cancer 2018 4 143 (7): 1696-1705. Luo Wenxin, Tian Panwen, Wang Yue, Xu Heng, Chen Lu, Tang Chao, Shu Yang, Zhang Shouyue, Wang Zhoufeng, Zhang Jun, Zhang Li, Jiang Lili, Liu Lunxu, Che Guowei, Guo Chenglin, Zhang Hong, Wang Jiali, Li Weim |
| Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility. PLoS genetics 2023 8 19 (8): e1010889. Timo A Kumpula, Sandra Vorimo, Taneli T Mattila, Luke O'Gorman, Galuh Astuti, Anna Tervasmäki, Susanna Koivuluoma, Tiina M Mattila, Mervi Grip, Robert Winqvist, Outi Kuismin, Jukka Moilanen, Alexander Hoischen, Christian Gilissen, Tuomo Mantere, Katri Pylk |
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