Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Lung Neoplasms and CHEK2[original query] |
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| A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2006 Dec 15 (12): 2542-5. Thompson Deborah, Seal Sheila, Schutte Mieke, McGuffog Lesley, Barfoot Rita, Renwick Anthony, Eeles Rosalind, Sodha Nayanta, Houlston Richard, Shanley Susan, Klijn Jan, Wasielewski Marijke, Chang-Claude Jenny, Futreal P Andrew, Weber Barbara L, Nathanson Katherine L, Stratton Michael, Meijers-Heijboer Hanne, Rahman Nazneen, Easton Douglas |
| Uncommon CHEK2 mis-sense variant and reduced risk of tobacco-related cancers: case control study. Human molecular genetics 2007 Aug 16 (15): 1794-801. Brennan Paul, McKay James, Moore Lee, Zaridze David, Mukeria Anush, Szeszenia-Dabrowska Neonilia, Lissowska Jolanta, Rudnai Peter, Fabianova Eleonora, Mates Dana, Bencko Vladimir, Foretova Lenka, Janout Vladimir, Chow Wong-Ho, Rothman Nathanial, Chabrier Amelie, Gaborieau Valerie, Odefrey Fabrice, Southey Melissa, Hashibe Mia, Hall Janet, Boffetta Paolo, Peto Julian, Peto Richard, Hung Rayjean |
| Inherited predisposition of lung cancer: a hierarchical modeling approach to DNA repair and cell cycle control pathways. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007 Dec 16 (12): 2736-44. Hung Rayjean J, Baragatti Meili, Thomas Duncan, McKay James, Szeszenia-Dabrowska Neonila, Zaridze David, Lissowska Jolanta, Rudnai Peter, Fabianova Eleonora, Mates Dana, Foretova Lenka, Janout Vladimir, Bencko Vladimir, Chabrier Amelie, Moullan Norman, Canzian Federico, Hall Janet, Boffetta Paolo, Brennan Pa |
| Constitutional CHEK2 mutations are associated with a decreased risk of lung and laryngeal cancers. Carcinogenesis 2008 Apr 29 (4): 762-5. Cybulski Cezary, Masojc Bartlomiej, Oszutowska Dorota, Jaworowska Ewa, Grodzki Tomasz, Waloszczyk Piotr, Serwatowski Piotr, Pankowski Juliusz, Huzarski Tomasz, Byrski Tomasz, Górski Bohdan, Jakubowska Anna, Debniak Tadeusz, Wokolorczyk Dominika, Gronwald Jacek, Tarnowska Czeslawa, Serrano-Fernández Pablo, Lubinski Jan, Narod Steven |
| A variant in the CHEK2 promoter at a methylation site relieves transcriptional repression and confers reduced risk of lung cancer. Carcinogenesis 2010 Jul 31 (7): 1251-8. Zhang Shuyu, Lu Juan, Zhao Xueying, Wu Wenting, Wang Huibo, Lu Jun, Wu Qihan, Chen Xin, Fan Weiwei, Chen Hongyan, Wang Feng, Hu Zhibin, Jin Li, Wei Qingyi, Shen Hongbing, Huang Wei, Lu Da |
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, |
| CHEK2*1100delC homozygosity in the Netherlands--prevalence and risk of breast and lung cancer. European journal of human genetics : EJHG 2014 Jan 22 (1): 46-51. Huijts Petra E A, Hollestelle Antoinette, Balliu Brunilda, Houwing-Duistermaat Jeanine J, Meijers Caro M, Blom Jannet C, Ozturk Bahar, Krol-Warmerdam Elly M M, Wijnen Juul, Berns Els M J J, Martens John W M, Seynaeve Caroline, Kiemeney Lambertus A, van der Heijden Henricus F, Tollenaar Rob A E M, Devilee Peter, van Asperen Christi |
| Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.
Nature genetics 2014 Jul 46 (7): 736-41. Wang Yufei, McKay James D, Rafnar Thorunn, Wang Zhaoming, Timofeeva Maria N, Broderick Peter, Zong Xuchen, Laplana Marina, Wei Yongyue, Han Younghun, Lloyd Amy, Delahaye-Sourdeix Manon, Chubb Daniel, Gaborieau Valerie, Wheeler William, Chatterjee Nilanjan, Thorleifsson Gudmar, Sulem Patrick, Liu Geoffrey, Kaaks Rudolf, Henrion Marc, Kinnersley Ben, Vallée Maxime, LeCalvez-Kelm Florence, Stevens Victoria L, Gapstur Susan M, Chen Wei V, 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, Benhamou Simone, Vooder Tonu, Välk Kristjan, Nelis Mari, Metspalu Andres, Lener Marcin, Lubi?ski Jan, Johansson Mattias, Vineis Paolo, Agudo Antonio, Clavel-Chapelon Francoise, Bueno-de-Mesquita H Bas, Trichopoulos Dimitrios, Khaw Kay-Tee, Johansson Mikael, Weiderpass Elisabete, Tjønneland Anne, Riboli Elio, Lathrop Mark, Scelo Ghislaine, Albanes Demetrius, Caporaso Neil E, Ye Yuanqing, Gu Jian, Wu Xifeng, Spitz Margaret R, Dienemann Hendrik, Rosenberger Albert, Su Li, Matakidou Athena, Eisen Timothy, Stefansson Kari, Risch Angela, Chanock Stephen J, Christiani David C, Hung Rayjean J, Brennan Paul, Landi Maria Teresa, Houlston Richard S, Amos Christopher |
| Rare variants in BRCA2 and CHEK2 are associated with the risk of urinary tract cancers. Scientific reports 2016 6 33542. Ge Yuqiu, Wang Yunyan, Shao Wei, Jin Jing, Du Mulong, Ma Gaoxiang, Chu Haiyan, Wang Meilin, Zhang Zhengdo |
| Prevalence of the CHEK2 R95* germline mutation. Hereditary cancer in clinical practice 2016 14 19. Knappskog Stian, Leirvaag Beryl, Gansmo Liv B, Romundstad Pål, Hveem Kristian, Vatten Lars, Lønning Per |
| Association of CHEK2 polymorphisms with the efficacy of platinum-based chemotherapy for advanced non-small-cell lung cancer in Chinese never-smoking women. Journal of thoracic disease 2016 Sep 8 (9): 2519-2529. Xu Wen, Liu Di, Yang Yang, Ding Xi, Sun Yifeng, Zhang Baohong, Xu Jinfu, Su |
| Germline Mutations in DNA Repair Genes in Lung Adenocarcinoma. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2017 11 12 (11): 1673-1678. Parry Erin M, Gable Dustin L, Stanley Susan E, Khalil Sara E, Antonescu Valentin, Florea Liliana, Armanios Ma |
| Spectrum of Pathogenic Germline Mutations in Chinese Lung Cancer Patients through Next-Generation Sequencing. Pathology oncology research : POR 2019 11 26 (1): 109-114. Tian Panwen, Cheng Xiangyang, Zhao Zhengyi, Zhang Yuzi, Bao Celimuge, Wang Yanyan, Cai Shangli, Ma Guowei, Huang Yi |
| The contribution of hereditary cancer-related germline mutations to lung cancer susceptibility. Translational lung cancer research 2020 7 9 (3): 646-658. Liu Mengyuan, Liu Xinyi, Suo Peisu, Gong Yuan, Qu Baolin, Peng Xiumei, Xiao Wenhua, Li Yuemin, Chen Yan, Zeng Zhen, Lu Yinying, Huang Tanxiao, Zhao Yingshen, Liu Ming, Li Lifeng, Chen Yaru, Zhou Yanqing, Liu Guifeng, Yao Jianfei, Chen Shifu, Song Le |
| Mutation profile of non-small cell lung cancer revealed by next generation sequencing. Respiratory research 2021 Jan 22 (1): 3. Chang Ya-Sian, Tu Siang-Jyun, Chen Yu-Chia, Liu Ting-Yuan, Lee Ya-Ting, Yen Ju-Chen, Fang Hsin-Yuan, Chang Jan-Gow |
| Germline Pathogenic Variants Impact Clinicopathology of Advanced Lung Cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2022 4 31 (7): 1450-1459. Mukherjee Semanti, Bandlamudi Chaitanya, Hellmann Matthew D, Kemel Yelena, Drill Esther, Rizvi Hira, Tkachuk Kaitlyn, Khurram Aliya, Walsh Michael F, Zauderer Marjorie G, Mandelker Diana, Topka Sabine, Zehir Ahmet, Srinivasan Preethi, Esai Selvan Myvizhi, Carlo Maria I, Cadoo Karen A, Latham Alicia, Hamilton Jada G, Liu Ying L, Lipkin Steven M, Belhadj Sami, Bond Gareth L, Gümü? Zeynep H, Klein Robert J, Ladanyi Marc, Solit David B, Robson Mark E, Jones David R, Kris Mark G, Vijai Joseph, Stadler Zsofia K, Amos Christopher I, Taylor Barry S, Berger Michael F, Rudin Charles M, Offit Kenne |
| Association of Reported Candidate Monogenic Genes With Lung Cancer Risk. Clinical lung cancer 2023 2 . Rifkin Andrew S, Less Ethan M, Wei Jun, Shi Zhuqing, Zheng Siqun Lilly, Helfand Brian T, Hulick Peter J, Krantz Seth B, Xu Jianfe |
| Rate of Pathogenic Germline Variants in Patients With Lung Cancer. JCO precision oncology 2023 11 7 e2300190. Steven Sorscher, Jaclyn LoPiccolo, Brandie Heald, Elaine Chen, Sara L Bristow, Scott T Michalski, Sarah M Nielsen, Alix Lacoste, Emil Keyder, Hayan Lee, Robert L Nussbaum, Renato Martins, Edward D Espl |
| Prevalence of pathogenic or likely pathogenic germline variants in cancer predisposition genes among selected patients with lung adenocarcinoma: The GERMLUNG study. Lung cancer (Amsterdam, Netherlands) 2024 6 194 107864. Oscar Arrieta, Enrique Caballé-Pérez, Norma Hernández-Pedro, Eunice Romero-Nuñez, José Lucio-Lozada, Cesar Castillo-Ruiz, Karla Acevedo-Castillo, Rosa María Álvarez-Gómez, Carolina Molina-Garay, Marco Jiménez-Olivares, Karol Carrillo-Sánchez, Elvia Cristina Mendoza-Caamal, Andrés F Cardona, Jordi Remon, Carmen Alaez-Vers |
| Checkpoint Kinase 2 (CHEK2) Gene Mutation in a Patient With Breast and Prostate Cancer: A Unique Presentation of a Rare Disease. Cureus 2024 1 15 (11): e49710. Samar N Ekram, Nasser Al Shanbari, Bassam M Bin Laswad, Abdulrahman Alharthi, Waseem Tayeb, Abdulbari Bah |
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