Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: FANCE[original query] |
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Evaluation of Fanconi Anemia genes in familial breast cancer predisposition. Cancer research 2003 12 63 (24): 8596-9. Seal Sheila, Barfoot Rita, Jayatilake Hiran, Smith Paula, Renwick Anthony, Bascombe Linda, McGuffog Lesley, Evans D Gareth, Eccles Diana, Easton Douglas F, Stratton Michael R, Rahman Nazneen, |
Genetic variants in DNA repair pathway genes and risk of esophageal squamous cell carcinoma and gastric adenocarcinoma in a Chinese population. Carcinogenesis 2013 Jul 34 (7): 1536-42. Li Wen-Qing, Hu Nan, Hyland Paula L, Gao Ying, Wang Zhao-Ming, Yu Kai, Su Hua, Wang Chao-Yu, Wang Le-Min, Chanock Stephen J, Burdett Laurie, Ding Ti, Qiao You-Lin, Fan Jin-Hu, Wang Yuan, Xu Yi, Shi Jian-Xin, Gu Fangyi, Wheeler William, Xiong Xiao-Qin, Giffen Carol, Tucker Margaret A, Dawsey Sanford M, Freedman Neal D, Abnet Christian C, Goldstein Alisa M, Taylor Philip |
The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer. European journal of human genetics : EJHG 2016 May . Esteban-Jurado Clara, Franch-Expósito Sebastià, Muñoz Jenifer, Ocaña Teresa, Carballal Sabela, López-Cerón Maria, Cuatrecasas Miriam, Vila-Casadesús Maria, Lozano Juan José, Serra Enric, Beltran Sergi, Brea-Fernández Alejandro, Ruiz-Ponte Clara, Castells Antoni, Bujanda Luis, Garre Pilar, Caldés Trinidad, Cubiella Joaquín, Balaguer Francesc, Castellví-Bel Ser |
Germline Mutations in Cancer Predisposition Genes are Frequent in Sporadic Sarcomas. Scientific reports 2017 9 7 (1): 10660. Chan Sock Hoai, Lim Weng Khong, Ishak Nur Diana Binte, Li Shao-Tzu, Goh Wei Lin, Tan Gek San, Lim Kiat Hon, Teo Melissa, Young Cedric Ng Chuan, Malik Simeen, Tan Mann Hong, Teh Jonathan Yi Hui, Chin Francis Kuok Choon, Kesavan Sittampalam, Selvarajan Sathiyamoorthy, Tan Patrick, Teh Bin Tean, Soo Khee Chee, Farid Mohamad, Quek Richard, Ngeow Joan |
Assessing the spectrum of germline variation in Fanconi anemia genes among patients with head and neck carcinoma before age 50. Cancer 2017 Jul . Chandrasekharappa Settara C, Chinn Steven B, Donovan Frank X, Chowdhury Naweed I, Kamat Aparna, Adeyemo Adebowale A, Thomas James W, Vemulapalli Meghana, Hussey Caroline S, Reid Holly H, Mullikin James C, Wei Qingyi, Sturgis Erich |
Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings. Journal of cancer research and clinical oncology 2018 10 144 (12): 2495-2513. Bonache Sandra, Esteban Irene, Moles-Fernández Alejandro, Tenés Anna, Duran-Lozano Laura, Montalban Gemma, Bach Vanessa, Carrasco Estela, Gadea Neus, López-Fernández Adrià, Torres-Esquius Sara, Mancuso Francesco, Caratú Ginevra, Vivancos Ana, Tuset Noemí, Balmaña Judith, Gutiérrez-Enríquez Sara, Diez Orla |
Clinical and Molecular Correlates of Tumor Mutation Burden in Non-Small Cell Lung Cancer. Lung cancer (Amsterdam, Netherlands) 2020 6 146 36-41. Sharpnack Michael F, Cho Ju Hwan, Johnson Travis S, Otterson Gregory A, Shields Peter G, Huang Kun, Carbone David P, He K |
Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients. Cancers 2020 4 12 (4): . Del Valle Jesús, Rofes Paula, Moreno-Cabrera José Marcos, López-Dóriga Adriana, Belhadj Sami, Vargas-Parra Gardenia, Teulé Àlex, Cuesta Raquel, Muñoz Xavier, Campos Olga, Salinas Mónica, de Cid Rafael, Brunet Joan, González Sara, Capellá Gabriel, Pineda Marta, Feliubadaló Lídia, Lázaro Con |
A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects. Human mutation 2021 Sep . George Merin, Solanki Avani, Chavan Niranjan, Rajendran Aruna, Raj Revathi, Mohan Sheila, Nemani Sandeep, Kanvinde Shailesh, Munirathnam Deendayalan, Rao Sudha, Radhakrishnan Nita, Lashkari Harsha Prasada, Ghildhiyal Radha Gulati, Manglani Mamta, Shanmukhaiah Chandrakala, Bhat Sunil, Ramesh Sowmyashree, Cherian Anchu, Junagade Pritesh, Vundinti Babu R |
Case report: identification of EGFR R776H and FANCE R381H germline mutations in a patient with multiple pulmonary nodules. Journal of cancer research and clinical oncology 2022 9 149 (2): 921-927. Wu Zhenzhen, Wang Yanli, Jin Linling, Wei Juan, Han Li, Su Junyan, Cao Shuliang, Liu Siyao, Duan Xiaohong, Zhao X |
Germline Variants Associated with Nasopharyngeal Carcinoma Predisposition Identified through Whole-Exome Sequencing. Cancers 2022 Jul 14 (15): . Lee Ning-Yuan, Hum Melissa, Ong Pei-Yi, Myint Matthew Khine, Ong Enya H W, Low Kar-Perng, Li Zheng, Goh Boon-Cher, Tay Joshua K, Loh Kwok-Seng, Chua Melvin L K, Lee Soo-Chin, Khor Chiea-Chuen, Lee Ann S |
Germline Variants in Cancer Genes from Young Breast Cancer Mexican Patients. Cancers 2022 4 14 (7): . Gómez-Flores-Ramos Liliana, Barraza-Arellano Angélica Leticia, Mohar Alejandro, Trujillo-Martínez Miguel, Grimaldo Lizbeth, Ortiz-Lopez Rocío, Treviño Víct |
Association of variations in the Fanconi anemia complementation group and prognosis in Non-small cell lung cancer patients with Platinum-based chemotherapy. Gene 2022 3 825 146398. Mo Jun-Luan, Liu Jia-Si, Xiao Qi, Hong Wen-Xu, Yin Ji-Ye, Chen Juan, Liu Zhao-Qi |
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 |
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- Page last updated:Apr 22, 2024
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