Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 30 Records) |
| Query Trace: Neoplasms and PMS1[original query] |
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| Prevalence of germline mutations of MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer families from Spain. International journal of cancer. Journal international du cancer 2002 Apr 98 (5): 774-9. Caldes Trinidad, Godino Javier, de la Hoya Miguel, Garcia Carbonero Iciar, Perez Segura Pedro, Eng Charis, Benito Manuel, Diaz-Rubio Eduar |
| Polymorphisms and HNPCC: PMS2-MLH1 protein interactions diminished by single nucleotide polymorphisms. Human mutation 2002 1 19 (2): 108-13. Yuan Zi Qiang, Gottlieb Bruce, Beitel Lenore K, Wong Nora, Gordon Philip H, Wang Qing, Puisieux Alain, Foulkes William D, Trifiro Ma |
| Common variants in mismatch repair genes and risk of invasive ovarian cancer. Carcinogenesis 2006 Nov 27 (11): 2235-42. Song Honglin, Ramus Susan J, Quaye Lydia, DiCioccio Richard A, Tyrer Jonathan, Lomas Emma, Shadforth Danielle, Hogdall Estrid, Hogdall Claus, McGuire Valerie, Whittemore Alice S, Easton Douglas F, Ponder Bruce A J, Kjaer Susanne Kruger, Pharoah Paul D P, Gayther Simon |
| Polymorphism discovery in 62 DNA repair genes and haplotype associations with risks for lung and head and neck cancers. Carcinogenesis 2007 Aug 28 (8): 1731-9. Michiels Stefan, Danoy Patrick, Dessen Philippe, Bera Alex, Boulet Thomas, Bouchardy Christine, Lathrop Mark, Sarasin Alain, Benhamou Simo |
| Mismatch repair gene polymorphisms and survival in invasive ovarian cancer patients. European journal of cancer (Oxford, England : 1990) 2008 Oct 44 (15): 2259-65. Mann Andrea, Hogdall Estrid, Ramus Susan J, DiCioccio Richard A, Hogdall Claus, Quaye Lydia, McGuire Valerie, Whittemore Alice S, Shah Mitul, Greenberg David, Easton Douglas F, Ponder Bruce A J, Kjaer Susanne Krüger, Gayther Simon A, Thompson Deborah J, Pharoah Paul D P, Song Hongl |
| Common variants in mismatch repair genes and risk of colorectal cancer. Gut 2008 Aug 57 (8): 1097-101. Koessler T, Oestergaard M Z, Song H, Tyrer J, Perkins B, Dunning A M, Easton D F, Pharoah P D |
| Common germline variation in mismatch repair genes and survival after a diagnosis of colorectal cancer. International journal of cancer. Journal international du cancer 2009 Apr 124 (8): 1887-91. Koessler Thibaud, Azzato Elizabeth M, Perkins Barbara, Macinnis Robert J, Greenberg David, Easton Douglas F, Pharoah Paul D |
| Potentially functional polymorphisms in DNA repair genes and non-small-cell lung cancer survival: a pathway-based analysis. Molecular carcinogenesis 2012 Jul 51 (7): 546-52. Dong Jing, Hu Zhibin, Shu Yongqian, Pan Shiyang, Chen Wenping, Wang Yi, Hu Lingmin, Jiang Yue, Dai Juncheng, Ma Hongxia, Jin Guangfu, Shen Hongbi |
| The cumulative effects of polymorphisms in the DNA mismatch repair genes and tobacco smoking in oesophageal cancer risk. PloS one 2012 7 (5): e36962. Vogelsang Matjaz, Wang Yabing, Veber Nika, Mwapagha Lamech M, Parker M Iqb |
| Distinct cancer-specific survival in metastatic prostate cancer patients classified by a panel of single nucleotide polymorphisms of cancer-associated genes. Genes & cancer 2013 Jan 4 (1-2): 54-60. Tsuchiya Norihiko, Matsui Shigeyuki, Narita Shintaro, Kamba Tomomi, Mitsuzuka Koji, Hatakeyama Shingo, Horikawa Yohei, Inoue Takamitsu, Saito Seiichi, Ohyama Chikara, Arai Yoich, Ogawa Osamu, Habuchi Tomono |
| Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes. European journal of human genetics : EJHG 2014 Nov 22 (11): 1305-13. Castéra Laurent, Krieger Sophie, Rousselin Antoine, Legros Angélina, Baumann Jean-Jacques, Bruet Olivia, Brault Baptiste, Fouillet Robin, Goardon Nicolas, Letac Olivier, Baert-Desurmont Stéphanie, Tinat Julie, Bera Odile, Dugast Catherine, Berthet Pascaline, Polycarpe Florence, Layet Valérie, Hardouin Agnes, Frébourg Thierry, Vaur Dominiq |
| Advances in the diagnosis of hereditary kidney cancer: Initial results of a multigene panel test. Cancer 2017 Nov 123 (22): 4363-4371. Nguyen Kevin A, Syed Jamil S, Espenschied Carin R, LaDuca Holly, Bhagat Ansh M, Suarez-Sarmiento Alfredo, O'Rourke Timothy K, Brierley Karina L, Hofstatter Erin W, Shuch Bri |
| [High throughput-targeted sequencing panel for exploring radiosensitivity associated genes in esophageal squamous cell carcinoma]. Zhonghua zhong liu za zhi [Chinese journal of oncology] 2017 8 39 (8): 584-588. Qiao Y, Hu C X, Song D A, Li S Q, Zhou L H, Jiang X |
| Mismatch repair-deficient status associates with favorable prognosis of Eastern Chinese population with sporadic colorectal cancer. Oncology letters 2018 May 15 (5): 7007-7013. Gong Qing, Zhang Huan-Hu, Sun Sheng-Bo, Ge Wen-Min, Li Yue, Zhu Yong-Cun, Li Le-Pi |
| Mismatch repair single nucleotide polymorphisms and thyroid cancer susceptibility. Oncology letters 2018 May 15 (5): 6715-6726. Santos Luís S, Silva Susana N, Gil Octávia M, Ferreira Teresa C, Limbert Edward, Rueff Jo |
| Associations of Genetic Variations in Mismatch Repair Genes MSH3 and PMS1 with Acute Adverse Events and Survival in Patients with Rectal Cancer Receiving Postoperative Chemoradiotherapy. Cancer research and treatment 2019 Jul 51 (3): 1198-1206. Yang Jie, Huang Ying, Feng Yanru, Li Hongmin, Feng Ting, Chen Jinna, Yin Luxi, Wang Weihu, Wang Shulian, Liu Yueping, Song Yongwen, Li Yexiong, Jin Jing, Tan Wen, Lin Dongx |
| Germline and somatic mutations of multi-gene panel in Chinese patients with epithelial ovarian cancer: a prospective cohort study. Journal of ovarian research 2019 Aug 12 (1): 80. Li Wenhui, Shao Di, Li Lei, Wu Ming, Ma Shuiqing, Tan Xianjie, Zhong Sen, Guo Fengming, Wang Zhe, Ye Mingz |
| Germline investigation in male breast cancer of DNA repair genes by next-generation sequencing. Breast cancer research and treatment 2019 Sep . Scarpitta R, Zanna I, Aretini P, Gambino G, Scatena C, Mei B, Ghilli M, Rossetti E, Roncella M, Congregati C, Bonci F, Naccarato A G, Palli D, Caligo M |
| Molecular mutation characteristics of mismatch and homologous recombination repair genes in gastrointestinal cancer. Oncology letters 2019 8 18 (3): 2789-2798. Liu Xingcun, Yang Haiping, Wu Xiaohong, Huang Kai, Ma Paul, Jiang Pengpeng, Zheng Weiqing, Tang Tom, Liu Duju |
| [A single center study of colorectal cancer screening for Lynch syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 3 36 (3): 238-241. Pan Jie, Zhu Fangchao, Pan Da, Zhang Hui, Ye Qiong, Xu Peiso |
| Germline mutational profile of Chinese patients under 70 years old with colorectal cancer. Cancer communications (London, England) 2020 Sep . Jiang Teng-Jia, Wang Fang, Wang Ying-Nan, Hu Jia-Jia, Ding Pei-Rong, Lin Jun-Zhong, Pan Zhi-Zhong, Chen Gong, Shao Jian-Yong, Xu Rui-Hua, Zhao Qi, Wang Fe |
| Genetic Variants Detected Using Cell-Free DNA from Blood and Tumor Samples in Patients with Inflammatory Breast Cancer. International journal of molecular sciences 2020 Feb 21 (4): . Winn Jennifer S, Hasse Zachary, Slifker Michael, Pei Jianming, Arisi-Fernandez Sebastian M, Talarchek Jacqueline N, Obeid Elias, Baldwin Donald A, Gong Yulan, Ross Eric, Cristofanilli Massimo, Alpaugh R Katherine, Fernandez Sandra |
| Clinical Characterization of Mismatch Repair Gene-Deficient Metastatic Castration-Resistant Prostate Cancer. Frontiers in oncology 2020 10 10 533282. Ye Senlin, Wang Haohui, He Kancheng, Peng Mou, Wang Yinhuai, Li Yuanwei, Jiang Shusuan, Li Jin, Yi Lu, Cui Rongro |
| Analysis of 11 candidate genes in 849 adult patients with suspected hereditary cancer predisposition. Genes, chromosomes & cancer 2020 Oct . Cavaillé Mathias, Uhrhammer Nancy, Privat Maud, Ponelle-Chachuat Flora, Gay-Bellile Mathilde, Lepage Mathis, Molnar Ioana, Viala Sandrine, Bidet Yannick, Bignon Yves-Je |
| Somatic mutations in benign breast disease tissues and association with breast cancer risk. BMC medical genomics 2021 7 14 (1): 185. Winham Stacey J, Wang Chen, Heinzen Ethan P, Bhagwate Aditya, Liu Yuanhang, McDonough Samantha J, Stallings-Mann Melody L, Frost Marlene H, Vierkant Robert A, Denison Lori A, Carter Jodi M, Sherman Mark E, Radisky Derek C, Degnim Amy C, Cunningham Julie |
| Application of Multigene Panel Testing in Patients With High Risk for Hereditary Colorectal Cancer: A Descriptive Report Focused on Genotype-Phenotype Correlation. Diseases of the colon and rectum 2021 12 65 (6): 793-803. Park Ji Soo, Park Jung Won, Shin Saeam, Lee Seung-Tae, Shin Sang Joon, Min Byung Soh, Park Soo Jung, Park Jae Jun, Cheon Jae Hee, Kim Won Ho, Kim Tae |
| Comparison of whole exome sequencing in circulating tumor cells of primitive and metastatic nasopharyngeal carcinoma. Translational cancer research 2022 2 9 (7): 4080-4092. Si Jinyuan, Huang Bo, Lan Guiping, Zhang Benjian, Wei Jiazhang, Deng Zhuoxia, Li Yiliang, Qin Ying, Li Bing, Lu Yan, Si Yongfe |
| Prevalence and Spectrum of Predisposition Genes With Germline Mutations Among Chinese Patients With Bowel Cancer. Frontiers in genetics 2022 2 12 755629. Xie Zhengyong, Ke Yongli, Chen Junyong, Li Zehang, Wang Changzheng, Chen Yuhong, Ding Hongliang, Cheng Liya |
| A unique case of rectal cancer with coexistence of multiple pathways of carcinogenesis. World journal of surgical oncology 2023 9 21 (1): 275. Nisha Rateria, Ritu Ojha, Mridula Shukla, Manoj Pand |
| 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 |
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