Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Disease and NCOR2[original query] |
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| Screening and association testing of common coding variation in steroid hormone receptor co-activator and co-repressor genes in relation to breast cancer risk: the Multiethnic Cohort. BMC cancer 2009 9 (1): 43. Haiman Christopher A, Garcia Rachel R, Hsu Chris, Xia Lucy, Ha Helen, Sheng Xin, Le Marchand Loic, Kolonel Laurence N, Henderson Brian E, Stallcup Michael R, Greene Geoffrey L, Press Michael |
| Nuclear receptor coregulator SNP discovery and impact on breast cancer risk. BMC cancer 2009 9 (1): 438. Hartmaier Ryan J, Tchatchou Sandrine, Richter Alexandra S, Wang Jay, McGuire Sean E, Skaar Todd C, Rae Jimmy M, Hemminki Kari, Sutter Christian, Ditsch Nina, Bugert Peter, Weber Bernhard H F, Niederacher Dieter, Arnold Norbert, Varon-Mateeva Raymonda, Wappenschmidt Barbara, Schmutzler Rita K, Meindl Alfons, Bartram Claus R, Burwinkel Barbara, Oesterreich Stef |
| Mutation detection in formalin-fixed prostate cancer biopsies taken at the time of diagnosis using next-generation DNA sequencing. Journal of clinical pathology 2015 Mar 68 (3): 212-7. Manson-Bahr David, Ball Richard, Gundem Gunes, Sethia Krishna, Mills Robert, Rochester Mark, Goody Victoria, Anderson Elizabeth, O'Meara Sarah, Flather Marcus, Keeling Matthew, Yazbek-Hanna Marcelino, Hurst Rachel, Curley Helen, Clark Jeremy, Brewer Daniel S, McDermott Ultan, Cooper Col |
| Whole Exome Sequencing of Ulcerative Colitis-associated Colorectal Cancer Based on Novel Somatic Mutations Identified in Chinese Patients. Inflammatory bowel diseases 2019 2 25 (8): 1293-1301. Yan Pengguang, Wang Yanan, Meng Xiangchen, Yang Hong, Liu Zhanju, Qian Jiaming, Zhou Weixun, Li Jingn |
| Acquired mutations and transcriptional remodeling in long-term estrogen-deprived locoregional breast cancer recurrences. Breast cancer research : BCR 2021 1 23 (1): 1. Priedigkeit Nolan, Ding Kai, Horne William, Kolls Jay K, Du Tian, Lucas Peter C, Blohmer Jens-Uwe, Denkert Carsten, Machleidt Anna, Ingold-Heppner Barbara, Oesterreich Steffi, Lee Adrian |
| Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencing. Human genomics 2022 09 16 (1): 36. Chen Shasha, Jin Qinchun, Hou Shiqiang, Li Mingfei, Zhang Yuan, Guan Lihua, Pan Wenzhi, Ge Junbo, Zhou Dax |
| Whole-genome sequencing reveals novel ethnicity-specific rare variants associated with Alzheimer's disease. Molecular psychiatry 2022 3 27 (5): 2554-2562. Shigemizu Daichi, Asanomi Yuya, Akiyama Shintaro, Mitsumori Risa, Niida Shumpei, Ozaki Kouic |
| Diffuse large B-cell lymphoma and red cell autoimmunity: clinical role and pathogenesis. Pathology 2022 11 55 (1): 104-112. Coombes Caitlin, Horikawa Keisuke, Jain Sanjiv, Jiang Simon, Lim Jun Hee, Saxena Kartik, Shadbolt Bruce, Smyth Lillian, Tobin Joshua, Talaulikar Dip |
Case-case genome-wide association analysis identifying genetic loci with divergent effects on Crohn's disease and ulcerative colitis.
Human molecular genetics 2022 9 32 (4): 677-684. Jung Seulgi, Kim Yongjae, Park Dohoon, Lee Yoonho, Park Sojung, Baek Jiwon, Hwang Sung Wook, Park Sang Hyoung, Yang Suk-Kyun, Ye Byong Duk, Han Buhm, Song Kyuyoung, Lee Ho- |
| Integrated Genomic Analysis of Primary Prostate Tumor Foci and Corresponding Lymph Node Metastases Identifies Mutations and Pathways Associated with Metastasis. Cancers 2023 12 15 (23): . Carlos S Moreno, Cynthia L Winham, Mehrdad Alemozaffar, Emma R Klein, Ismaheel O Lawal, Olayinka A Abiodun-Ojo, Dattatraya Patil, Benjamin G Barwick, Yijian Huang, David M Schuster, Martin G Sanda, Adeboye O Osunko |
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