Human Genome Epidemiology Literature Finder
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Records 1 - 18 (of 18 Records) |
| Query Trace: Disease and ERCC4[original query] |
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| Polymorphisms of DNA repair genes and risk of non-small cell lung cancer. Carcinogenesis 2006 Mar 27 (3): 560-7. Zienolddiny Shanbeh, Campa Daniele, Lind Helge, Ryberg David, Skaug Vidar, Stangeland Lodve, Phillips David H, Canzian Federico, Haugen Aa |
| Polymorphisms in the DNA repair genes XPD (ERCC2) and XPF (ERCC4) are not associated with sporadic late-onset Alzheimer's disease. Neuroscience letters 2006 Sep 404 (3): 258-61. Dogru-Abbasoglu Semra, Inceoglu Muzeyyen, Parildar-Karpuzoglu Hande, Hanagasi Hasmet A, Karadag Berrin, Gurvit Hakan, Emre Murat, Aykac-Toker Gulcin, Uysal Mujd |
| DNA repair gene variants associated with benign breast disease in high cancer risk women. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009 Jan 18 (1): 346-50. Jorgensen Timothy J, Helzlsouer Kathy J, Clipp Sandra C, Bolton Judy Hoffman, Crum Rosa M, Visvanathan Ka |
| Genetic variants in DNA repair predicts the survival of patients with esophageal cancer. Annals of surgery 2011 May 253 (5): 918-27. Lee Jang-Ming, Yang Pei-Wen, Yang Shi-Yi, Chuang Tzu-Hsuen, Tung En-Chi, Chen Jin-Shing, Huang Pei-Ming, Lee Yung-Ch |
| Validation of genetic sequence variants as prognostic factors in early-stage head and neck squamous cell cancer survival. Clinical cancer research : an official journal of the American Association for Cancer Research 2012 Jan 18 (1): 196-206. Azad Abul Kalam, Bairati Isabelle, Samson Elodie, Cheng Dangxiao, Mirshams Maryam, Qiu Xin, Savas Sevtap, Waldron John, Wang Changshu, Goldstein David, Xu Wei, Meyer Francois, Liu Geoffr |
| Single nucleotide polymorphisms in nucleotide excision repair genes, cancer treatment, and head and neck cancer survival. Cancer causes & control : CCC 2014 Apr 25 (4): 437-50. Wyss Annah B, Weissler Mark C, Avery Christy L, Herring Amy H, Bensen Jeannette T, Barnholtz-Sloan Jill S, Funkhouser William K, Olshan Andrew |
| Mutation analysis of the ERCC4/FANCQ gene in hereditary breast cancer. PloS one 2014 9 (1): e85334. Kohlhase Sandra, Bogdanova Natalia V, Schürmann Peter, Bermisheva Marina, Khusnutdinova Elza, Antonenkova Natalia, Park-Simon Tjoung-Won, Hillemanns Peter, Meyer Andreas, Christiansen Hans, Schindler Detlev, Dörk Thi |
| Germline mutations in young non-smoking women with lung adenocarcinoma. Lung cancer (Amsterdam, Netherlands) 2018 7 122 76-82. Donner Iikki, Katainen Riku, Sipilä Lauri J, Aavikko Mervi, Pukkala Eero, Aaltonen Lauri |
| Use of Big Data to Estimate Prevalence of Defective DNA Repair Variants in the US Population. JAMA dermatology 2019 Jan 155 (1): 72-78. Pugh Jennifer, Khan Sikandar G, Tamura Deborah, Goldstein Alisa M, Landi Maria Teresa, DiGiovanna John J, Kraemer Kenneth |
| Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting. American journal of human genetics 2019 1 104 (2): 275-286. Wright Caroline F, West Ben, Tuke Marcus, Jones Samuel E, Patel Kashyap, Laver Thomas W, Beaumont Robin N, Tyrrell Jessica, Wood Andrew R, Frayling Timothy M, Hattersley Andrew T, Weedon Michael |
| Germline Genetic Findings Which May Impact Therapeutic Decisions in Families with a Presumed Predisposition for Hereditary Breast and Ovarian Cancer. Cancers 2020 8 12 (8): . Velázquez Carolina, K De Leeneer, Esteban-Cardeñosa Eva M, Avila Cobos Francisco, Lastra Enrique, Abella Luis E, de la Cruz Virginia, Lobatón Carmen D, Claes Kathleen B, Durán Mercedes, Infante M |
| Loci associated with genomic damage levels in chronic kidney disease patients and controls. Mutation research 2020 04 852 503167. Corredor Zuray, da Silva Filho Miguel Inácio, Rodríguez-Ribera Lara, Catalano Calogerina, Hemminki Kari, Coll Elisabeth, Silva Irene, Diaz Juan Manuel, Ballarin José Aurelio, Henández Alba, Försti Asta, Marcos Ricard, Pastor Susa |
| Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population. Scientific reports 2020 Jan 10 (1): 144. Corredor Zuray, Filho Miguel Inácio da Silva, Rodríguez-Ribera Lara, Velázquez Antonia, Hernández Alba, Catalano Calogerina, Hemminki Kari, Coll Elisabeth, Silva Irene, Diaz Juan Manuel, Ballarin José, Vallés Prats Martí, Calabia Martínez Jordi, Försti Asta, Marcos Ricard, Pastor Susa |
| Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study. JNCI cancer spectrum 2021 7 5 (2): . Kim Jung, Gianferante Matthew, Karyadi Danielle M, Hartley Stephen W, Frone Megan N, Luo Wen, Robison Leslie L, Armstrong Gregory T, Bhatia Smita, Dean Michael, Yeager Meredith, Zhu Bin, Song Lei, Sampson Joshua N, Yasui Yutaka, Leisenring Wendy M, Brodie Seth A, de Andrade Kelvin C, Fortes Fernanda P, Goldstein Alisa M, Khincha Payal P, Machiela Mitchell J, McMaster Mary L, Nickerson Michael L, Oba Leatrisse, Pemov Alexander, Pinheiro Maisa, Rotunno Melissa, Santiago Karina, Wegman-Ostrosky Talia, Diver W Ryan, Teras Lauren, Freedman Neal D, Hicks Belynda D, Zhu Bin, Wang Mingyi, Jones Kristine, Hutchinson Amy A, Dagnall Casey, Savage Sharon A, Tucker Margaret A, Chanock Stephen J, Morton Lindsay M, Stewart Douglas R, Mirabello Li |
| The link of ERCC2 rs13181 and ERCC4 rs2276466 polymorphisms with breast cancer in the Bangladeshi population. Molecular biology reports 2021 Nov . Sahaba Shaid All, Rashid Mohammad Abdur, Islam Md Saiful, Nahid Noor Ahmed, Apu Mohd Nazmul Hasan, Sultana Taposhi Nahid, Chaity Nusrat Islam, Hasan Md Mehedi, Islam Mohammad Safiq |
| Association of nonsynonymous SNPs of nucleotide excision repair genes ERCC4 rs1800067 (G/A) and ERCC5 rs17655 (G/C) as predisposing risk factors for gallbladder cancer. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2022 Jun . Anjali Kumari, Kumar Tarun, Kumar Puneet, Narayan Gopeshwar, Singh Suni |
| Identification of novel candidate predisposing genes in familial nonmedullary thyroid carcinoma implicating DNA damage repair pathways. International journal of cancer 2024 9 . Carolina Pires, Inês J Marques, Ana Saramago, Margarida M Moura, Marta Pojo, Rafael Cabrera, Catarina Santos, Francisco Rosário, Diana Lousa, João B Vicente, Tiago M Bandeiras, Manuel R Teixeira, Valeriano Leite, Branca M Cava |
| Prevalence of germline variants in Brazilian pancreatic carcinoma patients. Scientific reports 2024 9 14 (1): 21083. Lívia Munhoz Rodrigues, Simone Maistro, Maria Lucia Hirata Katayama, Vinícius Marques Rocha, Rossana Veronica Mendoza Lopez, Edia Filomena di Tullio Lopes, Fernanda Toledo Gonçalves, Cintia Fridman, Pedro Adolpho de Menezes Pacheco Serio, Luciana Rodrigues Carvalho Barros, Luiz Antonio Senna Leite, Vanderlei Segatelli, Maria Del Pilar Estevez-Diz, Rodrigo Santa Cruz Guindalini, Ulysses Ribeiro Junior, Maria Aparecida Azevedo Koike Folguei |
- Page last reviewed:Feb 1, 2024
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