Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 48 Records) |
| Query Trace: Neoplasms and WRN[original query] |
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| Analysis of DNA Repair Genes Polymorphisms in Breast Cancer. Pathology oncology research : POR 2016 Aug . Romanowicz Hanna, Pyziak ?ukasz, Jab?o?ski Filip, Bry? Magdalena, Forma Ewa, Smolarz Bea |
| Determining the frequency of pathogenic germline variants from exome sequencing in patients with castrate-resistant prostate cancer. BMJ open 2016 6 (4): e010332. Hart Steven N, Ellingson Marissa S, Schahl Kim, Vedell Peter T, Carlson Rachel E, Sinnwell Jason P, Barman Poulami, Sicotte Hugues, Eckel-Passow Jeanette E, Wang Liguo, Kalari Krishna R, Qin Rui, Kruisselbrink Teresa M, Jimenez Rafael E, Bryce Alan H, Tan Winston, Weinshilboum Richard, Wang Liewei, Kohli Mani |
| Association Between XRCC1 and WRN as Genetic Markers of Stability and Susceptibility to Cancer in Patients with HIV/AIDS and Cancer: a Cross-Sectional Study Asian Pacific journal of cancer prevention : APJCP 2017 03 18 (3): 615-620. Maldonado Gabriel de Carvalho, Terra Júnior Orlando Nascimento, Arnóbio Adriano, Alfradique Guilherme Rohem, Ornellas Maria Helena, da Silva Roberto Irineu, de Lima Dirce Bonf |
| Targeted exome sequencing of Korean triple-negative breast cancer reveals homozygous deletions associated with poor prognosis of adjuvant chemotherapy-treated patients. Oncotarget 2017 Sep 8 (37): 61538-61550. Jeong Hae Min, Kim Ryong Nam, Kwon Mi Jeong, Oh Ensel, Han Jinil, Lee Se Kyung, Choi Jong-Sun, Park Sara, Nam Seok Jin, Gong Gyung Yup, Nam Jin Wu, Choi Doo Ho, Lee Hannah, Nam Byung-Ho, Choi Yoon-La, Shin Young K |
| Mutation Spectrum of Cancer-Associated Genes in Patients With Early Onset of Colorectal Cancer. Frontiers in oncology 2019 8 9 673. Zhunussova Gulnur, Afonin Georgiy, Abdikerim Saltanat, Jumanov Abai, Perfilyeva Anastassiya, Kaidarova Dilyara, Djansugurova Ley |
| Recommendations for Preventive Care for Women with Rare Genetic Cause of Breast and Ovarian Cancer. Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti 2019 8 32 (Supplementum2): 6-13. Foretová Lenka, Navrátilová Marie, Svoboda Marek, Vaší?ková Petra, S?ahlová Eva Hrabincová, Házová Jana, Kleiblová Petra, Kleibl Zden?k, Machá?ková Eva, Palácová Markéta, Petráková Katarí |
| Germline Pathogenic Variants in Homologous Recombination and DNA Repair Genes in an Asian Cohort of Young-Onset Colorectal Cancer. JNCI cancer spectrum 2018 Oct 2 (4): pky054. Toh Ming Ren, Chiang Jian Bang, Chong Siao Ting, Chan Sock Hoai, Ishak Nur Diana Binte, Courtney Eliza, Lee Wei Hao, Syed Abdillah Al Syed Muhammad Fahmy Bin, Carson Allen John, Lim Kiat Hon, Davila Sonia, Tan Patrick, Lim Weng Khong, Tan Iain Bee Huat, Ngeow Joan |
| Associations of mRNA expression of DNA repair genes and genetic polymorphisms with cancer risk: a bioinformatics analysis and meta-analysis. Journal of Cancer 2019 10 (16): 3593-3607. Wu Huizhe, Li Shanqiong, Hu Xiaoyun, Qin Wenyan, Wang Yilin, Sun Tong, Wu Zhikun, Wang Xiufang, Lu Senxu, Xu Dongping, Li Yalun, Guan Shu, Zhao Haishan, Yao Weifan, Liu Mingyan, Wei Minj |
| Near-Comprehensive Resequencing of Cancer-Associated Genes in Surgically Resected Metastatic Liver Tumors of Gastric Cancer. The American journal of pathology 2019 Jan . Ikari Naoki, Serizawa Akiko, Mitani Shohei, Yamamoto Masakazu, Furukawa To |
| Identifying sequence variants contributing to hereditary breast and ovarian cancer in BRCA1 and BRCA2 negative breast and ovarian cancer patients. Scientific reports 2019 12 9 (1): 19986. Jarhelle Elisabeth, Riise Stensland Hilde Monica Frostad, Hansen Geir Åsmund Myge, Skarsfjord Siri, Jonsrud Christoffer, Ingebrigtsen Monica, Strømsvik Nina, Van Ghelue Marij |
| Polymorphisms in DNA repair pathway genes and ABCG2 gene in advanced colorectal cancer: correlation with tumor characteristics and clinical outcome in oxaliplatin-based chemotherapy. Cancer management and research 2019 11 285-297. Hu Xiaoyun, Qin Wenyan, Li Shanqiong, He Miao, Wang Yilin, Guan Shu, Zhao Haishan, Yao Weifan, Wei Minjie, Liu Mingyan, Wu Huiz |
| Werner Syndrome Protein Expression in Breast Cancer. Clinical breast cancer 2020 9 21 (1): 57-73.e7. Savva Constantinos, Sadiq Maaz, Sheikh Omar, Karim Syed, Trivedi Sachin, Green Andrew R, Rakha Emad A, Madhusudan Srinivasan, Arora Arvi |
| High-Throughput Sequencing of Gastric Cancer Patients: Unravelling Genetic Predispositions Towards an Early-Onset Subtype. Cancers 2020 7 12 (7): . Machlowska Julita, Kapusta Przemys?aw, Baj Jacek, Morsink Folkert H M, Wo?kow Pawe?, Maciejewski Ryszard, Offerhaus G Johan A, Sitarz Robe |
| WRN-Mutated Colorectal Cancer Is Characterized by a Distinct Genetic Phenotype. Cancers 2020 5 12 (5): . Zimmer Kai, Puccini Alberto, Xiu Joanne, Baca Yasmine, Spizzo Gilbert, Lenz Heinz-Josef, Battaglin Francesca, Goldberg Richard M, Grothey Axel, Shields Anthony F, Salem Mohamed E, Marshall John L, Korn W Michael, Wolf Dominik, Kocher Florian, Seeber Andre |
| Gene Panel Testing in Hereditary Breast Cancer. Archives of Iranian medicine 2020 Mar 23 (3): 155-162. Rostami Parvin, Zendehdel Kazem, Shirkoohi Reza, Ebrahimi Elmira, Ataei Mitra, Imanian Hashem, Najmabadi Hossein, Akbari Mohammad Reza, Sanati Mohammad Hosse |
| Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 Genes. Biomedicines 2020 Oct 8 (10): . Stolarova Lenka, Jelinkova Sandra, Storchova Radka, Machackova Eva, Zemankova Petra, Vocka Michal, Kodet Ondrej, Kral Jan, Cerna Marta, Volkova Zuzana, Janatova Marketa, Soukupova Jana, Stranecky Viktor, Dundr Pavel, Foretova Lenka, Macurek Libor, Kleiblova Petra, Kleibl Zden |
| Investigation of monogenic causes of familial breast cancer: data from the BEACCON case-control study. NPJ breast cancer 2021 Jun 7 (1): 76. Li Na, Lim Belle W X, Thompson Ella R, McInerny Simone, Zethoven Magnus, Cheasley Dane, Rowley Simone M, Wong-Brown Michelle W, Devereux Lisa, Gorringe Kylie L, Sloan Erica K, Trainer Alison, Scott Rodney J, James Paul A, Campbell Ian |
| Whole exome sequencing and deep sequencing of esophageal squamous cell carcinoma and adenocarcinoma in Japanese patients using the Japanese version of the Genome Atlas, JCGA. Esophagus : official journal of the Japan Esophageal Society 2021 Apr . Booka Eisuke, Tsubosa Yasuhiro, Yokota Tomoya, Mayanagi Shuhei, Ishii Kenjiro, Urakami Kenichi, Ohshima Keiichi, Ohnami Shumpei, Nagashima Takeshi, Yamaguchi K |
| DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population. DNA repair 2021 3 101 103079. Niazi Yasmeen, Thomsen Hauke, Smolkova Bozena, Vodickova Ludmila, Vodenkova So?a, Kroupa Michal, Vymetalkova Veronika, Kazimirova Alena, Barancokova Magdalena, Volkovova Katarina, Staruchova Marta, Hoffmann Per, Nöthen Markus M, Dusinska Maria, Musak Ludovit, Vodicka Pavel, Försti Asta, Hemminki Ka |
| Germline and Somatic Whole-Exome Sequencing Identifies New Candidate Genes Involved in Familial Predisposition to Serrated Polyposis Syndrome. Cancers 2021 3 13 (4): . Soares de Lima Yasmin, Arnau-Collell Coral, Díaz-Gay Marcos, Bonjoch Laia, Franch-Expósito Sebastià, Muñoz Jenifer, Moreira Leticia, Ocaña Teresa, Cuatrecasas Miriam, Herrera-Pariente Cristina, Carballal Sabela, Moreno Lorena, Díaz de Bustamante Aránzazu, Castells Antoni, Bujanda Luis, Cubiella Joaquín, Rodríguez-Alcalde Daniel, Balaguer Francesc, Castellví-Bel Ser |
| Cancer-Predisposition Genetic Analysis in Children with Brain Tumors Treated at a Single Institution in Japan. Oncology 2021 12 100 (3): 163-172. Fukushima Hiroko, Suzuki Ryoko, Yamaki Yuni, Hosaka Sho, Inaba Masako, Muroi Ai, Tsurubuchi Takao, Morii Wataru, Noguchi Emiko, Takada Hidetos |
| Untangling the clinicopathological significance of MRE11-RAD50-NBS1 complex in sporadic breast cancers. NPJ breast cancer 2021 Nov 7 (1): 143. Alblihy Adel, Shoqafi Ahmed, Toss Michael S, Algethami Mashael, Harris Anna E, Jeyapalan Jennie N, Abdel-Fatah Tarek, Servante Juliette, Chan Stephen Y T, Green Andrew, Mongan Nigel P, Rakha Emad A, Madhusudan Srinivas |
| Genomic Profiling Reveals the Molecular Landscape of Gastrointestinal Tract Cancers in Chinese Patients. Frontiers in genetics 2021 12 608742. Zhu Chunrong, Zhu Liangjun, Gu Yanhong, Liu Ping, Tong Xiaoling, Wu Guozhong, Zhu Wenyu, Shen Wenxiang, Bao Hua, Ma Xiangyuan, Yu Ruoying, Wu Xue, Zhu Dongqin, Shu Yongqian, Feng Jife |
| The impact of rare germline variants on human somatic mutation processes. Nature communications 2022 6 13 (1): 3724. Vali-Pour Mischan, Lehner Ben, Supek Fr |
| Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families. PloS one 2022 1 17 (1): e0262419. Fidalgo Felipe, Torrezan Giovana Tardin, Sá Bianca Costa Soares de, Barros Bruna Durães de Figueiredo, Moredo Luciana Facure, Valieris Renan, de Souza Sandro J, Duprat João Pereira, Krepischi Ana Cristina Victorino, Carraro Dirce Mar |
| Co-Occurrence of Germline Genomic Variants and Copy Number Variations in Hereditary Breast and Colorectal Cancer Patients. Genes 2023 8 14 (8): . Luiza Côrtes, Tatiane Ramos Basso, Rolando André Rios Villacis, Jeferson Dos Santos Souza, Mads Malik Aagaard Jørgensen, Maria Isabel Achatz, Silvia Regina Rogat |
| Next generation sequencing reveals a high prevalence of pathogenic mutations in homologous recombination DNA damage repair genes among patients with uterine sarcoma. Gynecologic oncology 2023 8 177 14-19. Dimitrios Nasioudis, Nawar A Latif, Emily M Ko, Lori Cory, Sarah H Kim, Lainie Martin, Fiona Simpkins, Robert Giunto |
| Lynch-like syndrome with germline WRN mutation in Bulgarian patient with synchronous endometrial and ovarian cancer. Hereditary cancer in clinical practice 2023 7 21 (1): 13. Zornitsa Bogomilova Kamburova, Polina Damyanova Dimitrova, Diana Strateva Dimitrova, Katya Stefanova Kovacheva, Savelina Lubenova Popovska, Slavena Enkova Nikolo |
| Polymorphisms in the non-homologous end-joining DNA repair pathway are associated with HPV integration in cervical dysplasia. Cancer prevention research (Philadelphia, Pa.) 2023 5 . Jennifer M Geris, E Susan Amirian, Deborah A Marquez-Do, Martial Guillaud, Laura M Dillon, Michele Follen, Michael E Scheur |
| Germline cancer gene expression quantitative trait loci are associated with local and global tumor mutations. Cancer research 2023 2 . Liu Yuxi, Gusev Alexander, Kraft Pet |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 18, 2023
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