Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Breast Neoplasms and NOTCH2[original query] |
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A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).
Nature genetics 2009 May 41 (5): 579-84. Thomas Gilles, Jacobs Kevin B, Kraft Peter, Yeager Meredith, Wacholder Sholom, Cox David G, Hankinson Susan E, Hutchinson Amy, Wang Zhaoming, Yu Kai, Chatterjee Nilanjan, Garcia-Closas Montserrat, Gonzalez-Bosquet Jesus, Prokunina-Olsson Ludmila, Orr Nick, Willett Walter C, Colditz Graham A, Ziegler Regina G, Berg Christine D, Buys Saundra S, McCarty Catherine A, Feigelson Heather Spencer, Calle Eugenia E, Thun Michael J, Diver Ryan, Prentice Ross, Jackson Rebecca, Kooperberg Charles, Chlebowski Rowan, Lissowska Jolanta, Peplonska Beata, Brinton Louise A, Sigurdson Alice, Doody Michele, Bhatti Parveen, Alexander Bruce H, Buring Julie, Lee I-Min, Vatten Lars J, Hveem Kristian, Kumle Merethe, Hayes Richard B, Tucker Margaret, Gerhard Daniela S, Fraumeni Joseph F, Hoover Robert N, Chanock Stephen J, Hunter David |
NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tumors without TP53 mutations. Molecular cancer 2010 9 (1): 113. Fu Yi-Ping, Edvardsen Hege, Kaushiva Alpana, Arhancet Juan P, Howe Tiffany M, Kohaar Indu, Porter-Gill Patricia, Shah Anushi, Landmark-Høyvik Hege, Fosså Sophie D, Ambs Stefan, Naume Bjørn, Børresen-Dale Anne-Lise, Kristensen Vessela N, Prokunina-Olsson Ludmi |
Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium. Journal of the National Cancer Institute 2011 Aug 103 (16): 1252-63. Campa Daniele, Kaaks Rudolf, Le Marchand Loïc, Haiman Christopher A, Travis Ruth C, Berg Christine D, Buring Julie E, Chanock Stephen J, Diver W Ryan, Dostal Lucie, Fournier Agnes, Hankinson Susan E, Henderson Brian E, Hoover Robert N, Isaacs Claudine, Johansson Mattias, Kolonel Laurence N, Kraft Peter, Lee I-Min, McCarty Catherine A, Overvad Kim, Panico Salvatore, Peeters Petra H M, Riboli Elio, Sanchez Maria José, Schumacher Fredrick R, Skeie Guri, Stram Daniel O, Thun Michael J, Trichopoulos Dimitrios, Zhang Shumin, Ziegler Regina G, Hunter David J, Lindström Sara, Canzian Federi |
Breast cancer susceptibility risk associations and heterogeneity by E-cadherin tumor tissue expression. Breast cancer research and treatment 2014 Jan 143 (1): 181-7. Horne Hisani N, Sherman Mark E, Garcia-Closas Montserrat, Pharoah Paul D, Blows Fiona M, Yang Xiaohong R, Hewitt Stephen M, Conway Catherine M, Lissowska Jolanta, Brinton Louise A, Prokunina-Olsson Ludmila, Dawson Sarah-Jane, Caldas Carlos, Easton Douglas F, Chanock Stephen J, Figueroa Jonine |
Notch1 single nucleotide polymorphism rs3124591 is associated with the risk of development of invasive ductal breast carcinoma in a Chinese population. International journal of clinical and experimental pathology 2014 7 (7): 4286-94. Cao Yu-Wen, Wan Guo-Xing, Zhao Chun-Xia, Hu Jian-Ming, Li Li, Liang Wei-Hua, Li Wen-Qin, Li Yu-Cong, Li Yi-Xiao, Du Xiao-Ming, Yu Shi-Ying, Li Fe |
PEST domain mutations in Notch receptors comprise an oncogenic driver segment in triple-negative breast cancer sensitive to a ?-secretase inhibitor. Clinical cancer research : an official journal of the American Association for Cancer Research 2015 1 21 (6): 1487-96. Wang Kai, Zhang Qin, Li Danan, Ching Keith, Zhang Cathy, Zheng Xianxian, Ozeck Mark, Shi Stephanie, Li Xiaorong, Wang Hui, Rejto Paul, Christensen James, Olson Pet |
Comprehensive DNA Methylation and Extensive Mutation Analyses of HER2-Positive Breast Cancer. Oncology 2015 88 (6): 377-84. Yamaguchi Takeshi, Mukai Hirofumi, Yamashita Satoshi, Fujii Satoshi, Ushijima Toshika |
Targeted next-generation sequencing identifies clinically relevant somatic mutations in a large cohort of inflammatory breast cancer. Breast cancer research : BCR 2018 Aug 20 (1): 88. Liang Xu, Vacher Sophie, Boulai Anais, Bernard Virginie, Baulande Sylvain, Bohec Mylene, Bièche Ivan, Lerebours Florence, Callens Céli |
Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer. Frontiers in genetics 2018 9 161. Torrezan Giovana T, de Almeida Fernanda G Dos Santos R, Figueiredo Márcia C P, Barros Bruna D de Figueiredo, de Paula Cláudia A A, Valieris Renan, de Souza Jorge E S, Ramalho Rodrigo F, da Silva Felipe C C, Ferreira Elisa N, de Nóbrega Amanda F, Felicio Paula S, Achatz Maria I, de Souza Sandro J, Palmero Edenir I, Carraro Dirce |
Design of a Targeted Sequencing Assay to Detect Rare Mutations in Circulating Tumor DNA. Genetic testing and molecular biomarkers 2019 4 23 (4): 264-269. Chen Jianxia, Chen Jun, He Fusheng, Huang Yiqiong, Lu Shan, Fan Haibo, Wang Mingbang, Xu Ruihu |
Association between tumor mutation profile and clinical outcomes among Hispanic Latina women with triple-negative breast cancer. PloS one 2020 9 15 (9): e0238262. Philipovskiy Alexander, Dwivedi Alok K, Gamez Roberto, McCallum Richard, Mukherjee Debabrata, Nahleh Zeina, Aguilera Renato J, Gaur Sum |
Genetic Variation in CCL5 Signaling Genes and Triple Negative Breast Cancer: Susceptibility and Prognosis Implications. Frontiers in oncology 2019 9 1328. Shan Jingxuan, Chouchane Aziz, Mokrab Younes, Saad Mohamad, Boujassoum Salha, Sayaman Rosalyn W, Ziv Elad, Bouaouina Noureddine, Remadi Yasmine, Gabbouj Sallouha, Roelands Jessica, Ma Xiaojing, Bedognetti Davide, Chouchane Lot |
Genomics of ERBB2-Positive Breast Cancer in Young Women Before and After Exposure to Chemotherapy Plus Trastuzumab. JCO precision oncology 2023 6 7 e2300076. Marla Lipsyc-Sharf, Esha Jain, Laura C Collins, Shoshana M Rosenberg, Kathryn J Ruddy, Rulla M Tamimi, Lidia Schapira, Steven E Come, Jeffrey M Peppercorn, Virginia F Borges, Ellen Warner, Craig Snow, Ian E Krop, Dewey Kim, Jakob Weiss, Jorge Gomez Tejeda Zanudo, Ann H Partridge, Nikhil Wagle, Adrienne G Wa |
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- Page last updated:May 06, 2024
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