HuGE Literature Finder
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| Characteristics of BRCA1/2 pathogenic germline mutations in chinese NSCLC patients and a comparison with HBOC. Hereditary cancer in clinical practice 2021 Feb 19 (1): 16. Xu Zheyuan, Wang Yang, Wang Lan, Cui Fengxian, Zhang Libin, Xiong Jian, Peng H |
| Tumor Mutation Burden and Differentially Mutated Genes Among Immune Phenotypes in Patients with Lung Adenocarcinoma. OncoTargets and therapy 2021 14 2953-2965. Wang Hao, Chen Shanhao, Meng Die, Wu Chunyan, Zhu Junjie, Jiang Minlin, Ning Jing, Wu Shengyu, Wu Lijia, Li Jingjie, Chen Bin, Zhao Sha, Li Wei, Yu Jia, Fang Qiyu, Zhu Jun, Zhao Wencheng, He Yayi, Zhou Caic |
| Clinical characteristics and prognostic implications of BRCA-associated tumors in males: a pan-tumor survey. BMC cancer 2020 Oct 20 (1): 994. Sun Peng, Li Yue, Chao Xue, Li Jibin, Luo Rongzhen, Li Mei, He Jieh |
| Polymorphisms and rare variants identified by next-generation sequencing confer risk for lung cancer in han Chinese population. Pathology, research and practice 2020 Feb 152873. Li Xiaoqi, Liu Jinsheng, Wang Ke, Zhou Juan, Zhang Hang, Zhang Mancang, Shi Yongyo |
| Detection of Genetic Mutations by Next-Generation Sequencing for Predicting Prognosis of Extensive-Stage Small-Cell Lung Cancer. Journal of oncology 2020 2020 8811487. Chen Dongfang, Xu Jianlin, Qiao Rong, Zhao Yizhuo, Chu Tianqing, Han Baohui, Zhong Run |
| Homologous recombination in lung cancer, germline and somatic mutations, clinical and phenotype characterization. Lung cancer (Amsterdam, Netherlands) 2019 Sep 137 48-51. Kadouri Luna, Rottenberg Yakir, Zick Aviad, Hamburger Tamar, Lipson Doron, Peretz Tamar, Nechushtan Hov |
| Association of BRCA2 K3326* With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin. Journal of the National Cancer Institute 2018 Sep 110 (9): 967-974. Rafnar Thorunn, Sigurjonsdottir Gudbjorg R, Stacey Simon N, Halldorsson Gisli, Sulem Patrick, Pardo Luba M, Helgason Hannes, Sigurdsson Stefan T, Gudjonsson Thorkell, Tryggvadottir Laufey, Olafsdottir Gudridur H, Jonasson Jon G, Alexiusdottir Kristin, Sigurdsson Asgeir, Gudmundsson Julius, Saemundsdottir Jona, Sigurdsson Jon K, Johannsdottir Hrefna, Uitterlinden Andre, Vermeulen Sita H, Galesloot Tessel E, Allain Dawn C, Lacko Martin, Sigurgeirsson Bardur, Thorisdottir Kristin, Johannsson Oskar T, Sigurdsson Fridbjorn, Ragnarsson Gunnar B, Isaksson Helgi, Hardardottir Hronn, Gudbjartsson Tomas, Gudbjartsson Daniel F, Masson Gisli, Kiemeney Lambertus A M L, Ewart Toland Amanda, Nijsten Tamar, Peters Wilbert H M, Olafsson Jon H, Jonsson Steinn, Thorsteinsdottir Unnur, Thorleifsson Gudmar, Stefansson Ka |
| Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2018 Jul . Liu Yanhong, Lusk Christine M, Cho Michael H, Silverman Edwin K, Qiao Dandi, Zhang Ruyang, Scheurer Michael E, Kheradmand Farrah, Wheeler David A, Tsavachidis Spiridon, Armstrong Georgina, Zhu Dakai, Wistuba Ignacio I, Chow Chi-Wan B, Behrens Carmen, Pikielny Claudio W, Neslund-Dudas Christine, Pinney Susan M, Anderson Marshall, Kupert Elena, Bailey-Wilson Joan, Gaba Colette, Mandal Diptasri, You Ming, de Andrade Mariza, Yang Ping, Field John K, Liloglou Triantafillos, Davies Michael, Lissowska Jolanta, Swiatkowska Beata, Zaridze David, Mukeriya Anush, Janout Vladimir, Holcatova Ivana, Mates Dana, Milosavljevic Sasa, Scelo Ghislaine, Brennan Paul, McKay James, Liu Geoffrey, Hung Rayjean J, , Christiani David C, Schwartz Ann G, Amos Christopher I, Spitz Margaret |
Genome-wide association study of familial lung cancer.
Carcinogenesis 2018 Jun . Byun Jinyoung, Schwartz Ann G, Lusk Christine, Wenzlaff Angela S, de Andrade Mariza, Mandal Diptasri, Gaba Colette, Yang Ping, You Ming, Kupert Elena Y, Anderson Marshall W, Han Younghun, Li Yafang, Qian David, Stilp Adrienne, Laurie Cathy, Nelson Sarah, Zheng Wenying, Hung Rayjean J, Gaborieau Valerie, Mckay James, Brennan Paul, Caporaso Neil E, Landi Maria Teresa, Wu Xifeng, McLaughlin John R, Brhane Yonathan, Bossé Yohan, Pinney Susan M, Bailey-Wilson Joan E, Amos Christopher |
| 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 |
| A randomized Phase II study of veliparib with temozolomide or carboplatin/paclitaxel versus placebo with carboplatin/paclitaxel in BRCA1/2 metastatic breast cancer: design and rationale. Future oncology (London, England) 2016 Oct . Isakoff Steven J, Puhalla Shannon, Domchek Susan M, Friedlander Michael, Kaufman Bella, Robson Mark, Telli Melinda L, Diéras Véronique, Han Hyo Sook, Garber Judy E, Johnson Eric F, Maag David, Qin Qin, Giranda Vincent L, Shepherd Stacie |
| Polymorphisms of the centrosomal gene (FGFR1OP) and lung cancer risk: a meta-analysis of 14,463 cases and 44,188 controls. Carcinogenesis 2016 Mar 37 (3): 280-289. Kang Xiaozheng, Liu Hongliang, Onaitis Mark W, Liu Zhensheng, Owzar Kouros, Han Younghun, Su Li, Wei Yongyue, Hung Rayjean J, Brhane Yonathan, McLaughlin John, Brennan Paul, Bickeböller Heike, Rosenberger Albert, Houlston Richard S, Caporaso Neil, Landi Maria Teresa, Heinrich Joachim, Risch Angela, Wu Xifeng, Ye Yuanqing, Christiani David C, Amos Christopher I, Wei Qingyi, |
| Polymorphism rs144848 in BRCA2 may reduce lung cancer risk in women: a case-control study in southeast China. Tumori 2016 Feb 0. Lin Yong, He Fei, Zhang Xin, Yu Tingting, Liu Zhiqiang, Cai L |
| 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 |
| The BRCA2 polymorphic stop codon: stuff or nonsense? Journal of medical genetics 2015 Sep 52 (9): 642-5. Higgs J E, Harkness E F, Bowers N L, Howard E, Wallace A J, Lalloo F, Newman W G, Evans D |
| Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis. European journal of human genetics : EJHG 2015 Aug . Kinnersley Ben, Kamatani Yoichiro, Labussière Marianne, Wang Yufei, Galan Pilar, Mokhtari Karima, Delattre Jean-Yves, Gousias Konstantinos, Schramm Johannes, Schoemaker Minouk J, Swerdlow Anthony, Fleming Sarah J, Herms Stefan, Heilmann Stefanie, Nöthen Markus M, Simon Matthias, Sanson Marc, Lathrop Mark, Houlston Richard |
| 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 |
| The poly(ADP-ribose) polymerase inhibitor niraparib (MK4827) in BRCA mutation carriers and patients with sporadic cancer: a phase 1 dose-escalation trial. The Lancet. Oncology 2013 Aug 14 (9): 882-92. Sandhu Shahneen K, Schelman William R, Wilding George, Moreno Victor, Baird Richard D, Miranda Susana, Hylands Lucy, Riisnaes Ruth, Forster Martin, Omlin Aurelius, Kreischer Nathan, Thway Khin, Gevensleben Heidrun, Sun Linda, Loughney John, Chatterjee Manash, Toniatti Carlo, Carpenter Christopher L, Iannone Robert, Kaye Stan B, de Bono Johann S, Wenham Robert |
| Prevalence of the variant allele rs61764370 T>G in the 3'UTR of KRAS among Dutch BRCA1, BRCA2 and non-BRCA1/BRCA2 breast cancer families. Breast cancer research and treatment 2011 Jul 128 (1): 79-84. Hollestelle Antoinette, Pelletier Cory, Hooning Maartje, Crepin Ellen, Schutte Mieke, Look Maxime, Collee J Margriet, Nieuwlaat Anja, Dorssers Lambert C J, Seynaeve Caroline, Aulchenko Yurii S, Martens John W M, van den Ouweland Ans M W, Weidhaas Joanne |
| Elevated lung cancer risk is associated with deficiencies in cell cycle checkpoints: genotype and phenotype analyses from a case-control study. International journal of cancer. Journal international du cancer 2010 May 126 (9): 2199-210. Zheng Yun-Ling, Kosti Ourania, Loffredo Christopher A, Bowman Elise, Mechanic Leah, Perlmutter Donna, Jones Raymond, Shields Peter G, Harris Curtis |
| A field synopsis on low-penetrance variants in DNA repair genes and cancer susceptibility. Journal of the National Cancer Institute 2009 Jan 101 (1): 24-36. Vineis Paolo, Manuguerra Maurizio, Kavvoura Fotini K, Guarrera Simonetta, Allione Alessandra, Rosa Fabio, Di Gregorio Alessandra, Polidoro Silvia, Saletta Federica, Ioannidis John P A, Matullo Giusep |
| Genetic variation in the DNA repair genes is predictive of outcome in lung cancer. Human molecular genetics 2007 Oct 16 (19): 2333-40. Matakidou Athena, el Galta Rachid, Webb Emily L, Rudd Matthew F, Bridle Helen, , Eisen Tim, Houlston Richard |
| 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 GH-IGF axis confer susceptibility to lung cancer. Genome research 2006 Jun 16 (6): 693-701. Rudd Matthew F, Webb Emily L, Matakidou Athena, Sellick Gabrielle S, Williams Richard D, Bridle Helen, Eisen Tim, Houlston Richard S, |
| Screening of homologous recombination gene polymorphisms in lung cancer patients reveals an association of the NBS1-185Gln variant and p53 gene mutations. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2003 Aug 12 (8): 699-704. Medina Pedro P, Ahrendt Steven A, Pollan Marina, Fernandez Paloma, Sidransky David, Sanchez-Cespedes Montserr |
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- Page last updated:Oct 25, 2021
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