Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Death and FBN1[original query] |
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Observational cohort study of ventricular arrhythmia in adults with Marfan syndrome caused by FBN1 mutations. PloS one 2013 8 (12): e81281. Aydin Ali, Adsay Baran A, Sheikhzadeh Sara, Keyser Britta, Rybczynski Meike, Sondermann Claudia, Detter Christian, Steven Daniel, Robinson Peter N, Berger Jürgen, Schmidtke Jörg, Blankenberg Stefan, Willems Stephan, von Kodolitsch Yskert, Hoffmann Boris |
Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections. American journal of human genetics 2016 Sep 99 (3): 762-9. Guo Dong-Chuan, Grove Megan L, Prakash Siddharth K, Eriksson Per, Hostetler Ellen M, LeMaire Scott A, Body Simon C, Shalhub Sherene, Estrera Anthony L, Safi Hazim J, Regalado Ellen S, Zhou Wei, Mathis Michael R, , , Eagle Kim A, Yang Bo, Willer Cristen J, Boerwinkle Eric, Milewicz Dianna |
Impact of Pathogenic FBN1 Variant Types on the Progression of Aortic Disease in Patients With Marfan Syndrome. Circulation. Genomic and precision medicine 2018 Jun 11 (6): e002058. Takeda Norifumi, Inuzuka Ryo, Maemura Sonoko, Morita Hiroyuki, Nawata Kan, Fujita Daishi, Taniguchi Yuki, Yamauchi Haruo, Yagi Hiroki, Kato Masayoshi, Nishimura Hiroshi, Hirata Yoichiro, Ikeda Yuichi, Kumagai Hidetoshi, Amiya Eisuke, Hara Hironori, Fujiwara Takayuki, Akazawa Hiroshi, Suzuki Jun-Ichi, Imai Yasushi, Nagai Ryozo, Takamoto Shinichi, Hirata Yasunobu, Ono Minoru, Komuro Iss |
Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection.
JAMA cardiology 2020 May . Turley Tamiel N, O'Byrne Megan M, Kosel Matthew L, de Andrade Mariza, Gulati Rajiv, Hayes Sharonne N, Tweet Marysia S, Olson Timothy |
Genetic testing and clinical relevance of patients with thoracic aortic aneurysm and dissection in northwestern China. Molecular genetics & genomic medicine 2021 9 9 (10): e1800. Li Jinjie, Yang Liu, Diao Yanjun, Zhou Lei, Xin Yijuan, Jiang Liqing, Li Rui, Wang Juan, Duan Weixun, Liu Jiay |
Genetic variants in Chinese patients with sporadic Stanford type A aortic dissection. Journal of thoracic disease 2021 Jul 13 (7): 4008-4022. Chen Zhao-Ran, Bao Ming-Hui, Wang Xing-Yu, Yang Yan-Min, Huang Bi, Han Zhong-Li, Cai Jun, Fan Xiao-H |
Fibrillin-1 Gene Polymorphisms (rs145233125, rs11070646, rs201170905) Are Associated With the Susceptibility and Clinical Prognosis of DeBakey Type III Aortic Dissection in Chinese Han Population. Journal of cardiovascular pharmacology 2022 Apr . Sun Ling, Chang Yafei, Jiang Peipei, Wang Baozhu, Ma Yitong, Yuan Qinghua, Ma Xia |
Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility. American journal of medical genetics. Part A 2022 Jan . Murad Andrea M, Hill Hannah L, Wang Yu, Ghannam Michael, Yang Min-Lee, Pugh Norma L, Asch Federico M, Hornsby Whitney, Driscoll Anisa, McNamara Jennifer, Willer Cristen J, Regalado Ellen S, , , Milewicz Dianna M, Eagle Kim A, Ganesh Santhi |
Genetic architecture of thoracic aortic dissection in the female population. Gene 2023 8 887 147727. Yanghui Chen, Linlin Wang, Xin Xu, Ke Li, Yang Sun, Yan Wang, Dao Wen Wa |
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- Page last updated:Apr 22, 2024
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