Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Disease and TBX3[original query] |
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Genome-wide association study of blood pressure and hypertension.
Nature genetics 2009 Jun 41 (6): 677-87. Levy Daniel, Ehret Georg B, Rice Kenneth, Verwoert Germaine C, Launer Lenore J, Dehghan Abbas, Glazer Nicole L, Morrison Alanna C, Johnson Andrew D, Aspelund Thor, Aulchenko Yurii, Lumley Thomas, Köttgen Anna, Vasan Ramachandran S, Rivadeneira Fernando, Eiriksdottir Gudny, Guo Xiuqing, Arking Dan E, Mitchell Gary F, Mattace-Raso Francesco U S, Smith Albert V, Taylor Kent, Scharpf Robert B, Hwang Shih-Jen, Sijbrands Eric J G, Bis Joshua, Harris Tamara B, Ganesh Santhi K, O'Donnell Christopher J, Hofman Albert, Rotter Jerome I, Coresh Josef, Benjamin Emelia J, Uitterlinden André G, Heiss Gerardo, Fox Caroline S, Witteman Jacqueline C M, Boerwinkle Eric, Wang Thomas J, Gudnason Vilmundur, Larson Martin G, Chakravarti Aravinda, Psaty Bruce M, van Duijn Cornelia |
| Genetic analysis of the TBX3 gene promoter in ventricular septal defects. Gene 2013 Jan 512 (2): 185-8. Chen Dongfeng, Qiao Yanli, Meng Haihong, Pang Shuchao, Huang Wenhui, Zhang Hongyu, Yan |
| Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.
Human molecular genetics 2015 Feb 24 (3): 865-74. Lu Xiangfeng, Wang Laiyuan, Lin Xu, Huang Jianfeng, Charles Gu C, He Meian, Shen Hongbing, He Jiang, Zhu Jingwen, Li Huaixing, Hixson James E, Wu Tangchun, Dai Juncheng, Lu Ling, Shen Chong, Chen Shufeng, He Lin, Mo Zengnan, Hao Yongchen, Mo Xingbo, Yang Xueli, Li Jianxin, Cao Jie, Chen Jichun, Fan Zhongjie, Li Ying, Zhao Liancheng, Li Hongfan, Lu Fanghong, Yao Cailiang, Yu Lin, Xu Lihua, Mu Jianjun, Wu Xianping, Deng Ying, Hu Dongsheng, Zhang Weidong, Ji Xu, Guo Dongshuang, Guo Zhirong, Zhou Zhengyuan, Yang Zili, Wang Renping, Yang Jun, Zhou Xiaoyang, Yan Weili, Sun Ningling, Gao Pingjin, Gu Dongfe |
| Association analysis identifies new risk loci for congenital heart disease in Chinese populations. Nature communications 2015 6 8082. Lin Yuan, Guo Xuejiang, Zhao Bijun, Liu Juanjuan, Da Min, Wen Yang, Hu Yuanli, Ni Bixian, Zhang Kai, Yang Shiwei, Xu Jing, Dai Juncheng, Wang Xiaowei, Xia Yankai, Ma Hongxia, Jin Guangfu, Yu Shiqiang, Liu Jiayin, Keavney Bernard D, Goodship Judith A, Cordell Heather J, Wang Xinru, Shen Hongbing, Sha Jiahao, Zhou Zuomin, Chen Yijiang, Mo Xuming, Luo Lingfei, Hu Zhib |
| Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation.
Nature communications 2015 6 8658. Artigas María Soler, Wain Louise V, Miller Suzanne, Kheirallah Abdul Kader, Huffman Jennifer E, Ntalla Ioanna, Shrine Nick, Obeidat Ma'en, Trochet Holly, McArdle Wendy L, Alves Alexessander Couto, Hui Jennie, Zhao Jing Hua, Joshi Peter K, Teumer Alexander, Albrecht Eva, Imboden Medea, Rawal Rajesh, Lopez Lorna M, Marten Jonathan, Enroth Stefan, Surakka Ida, Polasek Ozren, Lyytikäinen Leo-Pekka, Granell Raquel, Hysi Pirro G, Flexeder Claudia, Mahajan Anubha, Beilby John, Bossé Yohan, Brandsma Corry-Anke, Campbell Harry, Gieger Christian, Gläser Sven, González Juan R, Grallert Harald, Hammond Chris J, Harris Sarah E, Hartikainen Anna-Liisa, Heliövaara Markku, Henderson John, Hocking Lynne, Horikoshi Momoko, Hutri-Kähönen Nina, Ingelsson Erik, Johansson Åsa, Kemp John P, Kolcic Ivana, Kumar Ashish, Lind Lars, Melén Erik, Musk Arthur W, Navarro Pau, Nickle David C, Padmanabhan Sandosh, Raitakari Olli T, Ried Janina S, Ripatti Samuli, Schulz Holger, Scott Robert A, Sin Don D, Starr John M, , Viñuela Ana, Völzke Henry, Wild Sarah H, Wright Alan F, Zemunik Tatijana, Jarvis Deborah L, Spector Tim D, Evans David M, Lehtimäki Terho, Vitart Veronique, Kähönen Mika, Gyllensten Ulf, Rudan Igor, Deary Ian J, Karrasch Stefan, Probst-Hensch Nicole M, Heinrich Joachim, Stubbe Beate, Wilson James F, Wareham Nicholas J, James Alan L, Morris Andrew P, Jarvelin Marjo-Riitta, Hayward Caroline, Sayers Ian, Strachan David P, Hall Ian P, Tobin Martin |
| Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population. BMC cancer 2016 16 (1): 165. Marouf Chaymaa, Göhler Stella, Filho Miguel Inacio Da Silva, Hajji Omar, Hemminki Kari, Nadifi Sellama, Försti As |
| Copy number variation underlies complex phenotypes in domestic dog breeds and other canids. Genome research 2021 4 31 (5): 762-774. Serres-Armero Aitor, Davis Brian W, Povolotskaya Inna S, Morcillo-Suarez Carlos, Plassais Jocelyn, Juan David, Ostrander Elaine A, Marques-Bonet Tom |
| High prevalence of somatic PIK3CA and TP53 pathogenic variants in the normal mammary gland tissue of sporadic breast cancer patients revealed by duplex sequencing. NPJ breast cancer 2022 6 8 (1): 76. Kostecka Anna, Nowikiewicz Tomasz, Olszewski Pawe?, Koczkowska Magdalena, Horbacz Monika, Heinzl Monika, Andreou Maria, Salazar Renato, Mair Theresa, Madanecki Piotr, Gucwa Magdalena, Davies Hanna, Skokowski Jaros?aw, Buckley Patrick G, P?ksa Rafa?, ?rutek Ewa, Szylberg ?ukasz, Hartman Johan, Jankowski Micha?, Zegarski Wojciech, Tiemann-Boege Irene, Dumanski Jan P, Piotrowski Arkadiu |
| Identification of key variants correlated with susceptibility of primary osteoporosis in the Chinese Han group. Annals of human genetics 2022 Dec . Li Yanjiao, Liu Qi, Ma Qiuye, Ma Zhaoxia, Chen Juan, Yu An, Ma Changguo, Qiu Lihua, Shi Hong, Liang Hongsuo, Hu M |
| Association of Germline Variation in Driver Genes with Breast Cancer Risk in Chilean Population. International journal of molecular sciences 2023 11 24 (22): . Sebastián Morales-Pison, Julio C Tapia, Sarai Morales-González, Edio Maldonado, Mónica Acuña, Gloria M Calaf, Lilian Ja |
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