Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Efficiency and ATM[original query] |
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Description and validation of high-throughput simultaneous genotyping and mutation scanning by high-resolution melting curve analysis. Human mutation 2009 Jun 30 (6): 884-90. Nguyen-Dumont Tú, Calvez-Kelm Florence Le, Forey Nathalie, McKay-Chopin Sandrine, Garritano Sonia, Gioia-Patricola Lydie, De Silva Deepika, Weigel Ron, Sangrajrang Suleeporn, Lesueur Fabienne, Tavtigian Sean V, , |
RAD51 and breast cancer susceptibility: no evidence for rare variant association in the Breast Cancer Family Registry study. PloS one 2012 7 (12): e52374. Le Calvez-Kelm Florence, Oliver Javier, Damiola Francesca, Forey Nathalie, Robinot Nivonirina, Durand Geoffroy, Voegele Catherine, Vallée Maxime P, Byrnes Graham, Registry Breast Cancer Family, Hopper John L, Southey Melissa C, Andrulis Irene L, John Esther M, Tavtigian Sean V, Lesueur Fabien |
Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes. European journal of human genetics : EJHG 2014 Nov 22 (11): 1305-13. Castéra Laurent, Krieger Sophie, Rousselin Antoine, Legros Angélina, Baumann Jean-Jacques, Bruet Olivia, Brault Baptiste, Fouillet Robin, Goardon Nicolas, Letac Olivier, Baert-Desurmont Stéphanie, Tinat Julie, Bera Odile, Dugast Catherine, Berthet Pascaline, Polycarpe Florence, Layet Valérie, Hardouin Agnes, Frébourg Thierry, Vaur Dominiq |
Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity. Breast cancer research and treatment 2016 Aug . Pinto Pedro, Paulo Paula, Santos Catarina, Rocha Patrícia, Pinto Carla, Veiga Isabel, Pinheiro Manuela, Peixoto Ana, Teixeira Manuel |
Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility.
Nature genetics 2017 May 49 (5): 674-679. Wright Daniel J, Day Felix R, Kerrison Nicola D, Zink Florian, Cardona Alexia, Sulem Patrick, Thompson Deborah J, Sigurjonsdottir Svanhvit, Gudbjartsson Daniel F, Helgason Agnar, Chapman J Ross, Jackson Steve P, Langenberg Claudia, Wareham Nicholas J, Scott Robert A, Thorsteindottir Unnur, Ong Ken K, Stefansson Kari, Perry John R |
Optimizing the identification of risk-relevant mutations by multigene panel testing in selected hereditary breast/ovarian cancer families. Cancer medicine 2018 01 7 (1): 46-55. Coppa Anna, Nicolussi Arianna, D'Inzeo Sonia, Capalbo Carlo, Belardinilli Francesca, Colicchia Valeria, Petroni Marialaura, Zani Massimo, Ferraro Sergio, Rinaldi Christian, Buffone Amelia, Bartolazzi Armando, Screpanti Isabella, Ottini Laura, Giannini Giusep |
Discovery of a Pathogenic Variant rs139379666 (p. P2974L) in ATM for Breast Cancer Risk in Chinese Populations. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2019 Jun . Guo Xingyi, Lin Weiqiang, Bai Mengqiu, Li Hongzhi, Wen Wanqing, Zeng Chenjie, Chen Zhishan, He Jing, Chen Jianghua, Cai Qiuyin, Long Jirong, Jia Wei-Hua, Shu Xiao-Ou, Zheng W |
Polymorphisms and rare variants identified by next-generation sequencing confer risk for lung cancer in han Chinese population. Pathology, research and practice 2020 Feb 152873. Li Xiaoqi, Liu Jinsheng, Wang Ke, Zhou Juan, Zhang Hang, Zhang Mancang, Shi Yongyo |
Genetic Profiling of Advanced Melanoma: Candidate Mutations for Predicting Sensitivity and Resistance to Targeted Therapy. Targeted oncology 2020 1 15 (1): 101-113. Olbryt Magdalena, Pig?owski Wojciech, Rajczykowski Marcin, Pfeifer Aleksandra, Student Sebastian, Fiszer-Kierzkowska An |
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