Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: NUMA1[original query] |
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A common coding variant in CASP8 is associated with breast cancer risk. Nature genetics 2007 Mar 39 (3): 352-8. Cox Angela, Dunning Alison M, Garcia-Closas Montserrat, Balasubramanian Sabapathy, Reed Malcolm W R, Pooley Karen A, Scollen Serena, Baynes Caroline, Ponder Bruce A J, Chanock Stephen, Lissowska Jolanta, Brinton Louise, Peplonska Beata, Southey Melissa C, Hopper John L, McCredie Margaret R E, Giles Graham G, Fletcher Olivia, Johnson Nichola, dos Santos Silva Isabel, Gibson Lorna, Bojesen Stig E, Nordestgaard Børge G, Axelsson Christen K, Torres Diana, Hamann Ute, Justenhoven Christina, Brauch Hiltrud, Chang-Claude Jenny, Kropp Silke, Risch Angela, Wang-Gohrke Shan, Schürmann Peter, Bogdanova Natalia, Dörk Thilo, Fagerholm Rainer, Aaltonen Kirsimari, Blomqvist Carl, Nevanlinna Heli, Seal Sheila, Renwick Anthony, Stratton Michael R, Rahman Nazneen, Sangrajrang Suleeporn, Hughes David, Odefrey Fabrice, Brennan Paul, Spurdle Amanda B, Chenevix-Trench Georgia, , Beesley Jonathan, Mannermaa Arto, Hartikainen Jaana, Kataja Vesa, Kosma Veli-Matti, Couch Fergus J, Olson Janet E, Goode Ellen L, Broeks Annegien, Schmidt Marjanka K, Hogervorst Frans B L, Van't Veer Laura J, Kang Daehee, Yoo Keun-Young, Noh Dong-Young, Ahn Sei-Hyun, Wedrén Sara, Hall Per, Low Yen-Ling, Liu Jianjun, Milne Roger L, Ribas Gloria, Gonzalez-Neira Anna, Benitez Javier, Sigurdson Alice J, Stredrick Denise L, Alexander Bruce H, Struewing Jeffery P, Pharoah Paul D P, Easton Douglas F, |
Genome-wide response to antihypertensive medication using home blood pressure measurements: a pilot study nested within the HOMED-BP study. Pharmacogenomics 2013 Nov 14 (14): 1709-21. Kamide Kei, Asayama Kei, Katsuya Tomohiro, Ohkubo Takayoshi, Hirose Takuo, Inoue Ryusuke, Metoki Hirohito, Kikuya Masahiro, Obara Taku, Hanada Hironori, Thijs Lutgarde, Kuznetsova Tatiana, Noguchi Yuichi, Sugimoto Ken, Ohishi Mitsuru, Morimoto Shigeto, Nakahashi Takeshi, Takiuchi Shin, Ishimitsu Toshihiko, Tsuchihashi Takuya, Soma Masayoshi, Higaki Jitsuo, Matsuura Hideo, Shinagawa Tatsuo, Sasaguri Toshiyuki, Miki Tetsuro, Takeda Kazuo, Shimamoto Kazuaki, Ueno Michio, Hosomi Naohisa, Kato Jyouji, Komai Norio, Kojima Shunichi, Sase Kazuhiro, Miyata Toshiyuki, Tomoike Hitonobu, Kawano Yuhei, Ogihara Toshio, Rakugi Hiromi, Staessen Jan A, Imai Yutaka, , |
Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency. BioMed research international 2016 3 2015 862039. Sandgren Johanna, Holm Stefan, Marino Ana Maria, Asmundsson Jurate, Grillner Pernilla, Nistér Monica, Díaz de Ståhl Teresi |
Targeted next-generation sequencing for molecular diagnosis of endometriosis-associated ovarian cancer. Journal of molecular medicine (Berlin, Germany) 2016 Feb . Er Tze-Kiong, Su Yu-Fa, Wu Chun-Chieh, Chen Chih-Chieh, Wang Jing, Hsieh Tsung-Hua, Herreros-Villanueva Marta, Chen Wan-Tzu, Chen Yi-Ting, Liu Ta-Chih, Chen Hung-Sheng, Tsai Eing-M |
A Genomic and Protein-Protein Interaction Analyses of Nonsyndromic Hearing Impairment in Cameroon Using Targeted Genomic Enrichment and Massively Parallel Sequencing. Omics : a journal of integrative biology 2017 1 21 (2): 90-99. Lebeko Kamogelo, Manyisa Noluthando, Chimusa Emile R, Mulder Nicola, Dandara Collet, Wonkam Ambroi |
Targeted exome sequencing for the identification of common mutational signatures and potential driver mutations for brain metastases and prognosis. Oncology letters 2021 2 21 (3): 179. Zhang Dainan, Wang Xi, Ma Shunchang, Li Peiliang, Xue Fei, Mao Beibei, Guan Xiudong, Zhou Wenjianlong, Peng Jiayi, Su Kun, Zhang Chuanbao, Jia Wa |
De novo 11q13.3q13.4 deletion in a patient with Fanconi renotubular syndrome and intellectual disability: Case report and review of literature. Frontiers in pediatrics 2023 5 11 1097062. Yingxiao Shen, Xiaoqin Xu, Jiansong Chen, Jingjing Wang, Guanping Dong, Ke Huang, Junfen Fu, Dingwen Wu, Wei |
Genetic variants of cancer?associated genes analyzed using next?generation sequencing in small sporadic vestibular schwannomas. Oncology letters 2023 2 25 (3): 121. Fujita Takeshi, Sakai Kazuko, Uehara Natsumi, Hoshi Yujiro, Mori Anjin, Koyama Hajime, Sato Mitsuo, Saito Kazuya, Osaki Yasuhiro, Nishio Kazuto, Doi Katsu |
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