HuGE Literature Finder
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| Association of Circulating Cathepsin B Levels With Blood Pressure and Aortic Dilation. Frontiers in cardiovascular medicine 2022 4 9 762468. Chai Tianci, Tian Mengyue, Yang Xiaojie, Qiu Zhihuang, Lin Xinjian, Chen Liangw |
High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease.
Nature genetics 2022 6 54 (6): 772-782. Tcheandjieu Catherine, Xiao Ke, Tejeda Helio, Lynch Julie A, Ruotsalainen Sanni, Bellomo Tiffany, Palnati Madhuri, Judy Renae, Klarin Derek, Kember Rachel L, Verma Shefali, , , , Palotie Aarno, Daly Mark, Ritchie Marylyn, Rader Daniel J, Rivas Manuel A, Assimes Themistocles, Tsao Philip, Damrauer Scott, Priest James |
| Molecular characterization and clinical investigation of patients with heritable thoracic aortic aneurysm and dissection. The Journal of thoracic and cardiovascular surgery 2022 12 . Yang Hang, Shen Huayan, Zhu Guoyan, Shao Xinyang, Chen Qianlong, Yang Fangfang, Zhang Yinhui, Zhang Yujing, Zhao Kun, Luo Mingyao, Zhou Zhou, Shu Cha |
| Evaluating the monogenic contribution and genotype-phenotype correlation in patients with isolated thoracic aortic aneurysm. European journal of human genetics : EJHG 2021 Apr . Li Yang, Kong Yu, Duan Weixun, Yu Shiqiang, Zhou Xinmin, Hu Yerong, Ou Jing-Song, Yi Dinghua, Xie Jinsheng, Zhu Junming, Sun Lizhong, Li Yulin, Du J |
| A systematic study of mosaicism in heritable thoracic aortic aneurysm and dissection. Genomics 2021 12 114 (1): 196-201. Yang Hang, Zhu Guoyan, Zhou Weizhen, Luo Mingyao, Zhang Yujing, Zhang Yinhui, Shu Chang, Zhou Zh |
| Analysis of the contribution of 129 candidate genes to thoracic aortic aneurysm or dissection of a mixed cohort of sporadic and familial cases in South China. American journal of translational research 2021 6 13 (5): 4281-4295. Li Ying, Fang Miaoxian, Yang Jue, Yu Changjiang, Kuang Juntao, Sun Tucheng, Fan Ruix |
| 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 |
| Identification of novel genetic susceptibility loci for thoracic and abdominal aortic aneurysms via genome-wide association study using the UK Biobank Cohort.
PloS one 2021 9 16 (9): e0247287. Ashvetiya Tamara, Fan Sherry X, Chen Yi-Ju, Williams Charles H, O'Connell Jeffery R, Perry James A, Hong Charles |
| Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm.
American journal of human genetics 2021 7 108 (9): 1578-1589. Roychowdhury Tanmoy, Lu Haocheng, Hornsby Whitney E, Crone Bradley, Wang Gao T, Guo Dong-Chuan, Sendamarai Anoop K, Devineni Poornima, Lin Maoxuan, Zhou Wei, Graham Sarah E, Wolford Brooke N, Surakka Ida, Wang Zhenguo, Chang Lin, Zhang Jifeng, Mathis Michael, Brummett Chad M, Melendez Tori L, Shea Michael J, Kim Karen Meekyong, Deeb G Michael, Patel Himanshu J, Eliason Jonathan, Eagle Kim A, Yang Bo, Ganesh Santhi K, Brumpton Ben, Åsvold Bjørn Olav, Skogholt Anne Heidi, Hveem Kristian, , Pyarajan Saiju, Klarin Derek, Tsao Philip S, Damrauer Scott M, Leal Suzanne M, Milewicz Dianna M, Chen Y Eugene, Garcia-Barrio Minerva T, Willer Cristen |
| Acute Stanford type B aortic dissection-who benefits from genetic testing? Journal of thoracic disease 2020 12 12 (11): 6806-6812. Erhart Philipp, Gieldon Laura, Ante Marius, Körfer Daniel, Strom Tim, Grond-Ginsbach Caspar, Böckler Dittm |
| Increased frequency of FBN1 frameshift and nonsense mutations in Marfan syndrome patients with aortic dissection. Molecular genetics & genomic medicine 2019 12 8 (1): e1041. Xu Shijun, Li Lei, Fu Yuwei, Wang Xin, Sun Hairui, Wang Jianbin, Han Lu, Wu Zining, Liu Yongmin, Zhu Junming, Sun Lizhong, Lan Feng, He Yihua, Zhang Hongj |
| Association of modifiers and other genetic factors explain Marfan syndrome clinical variability.
European journal of human genetics : EJHG 2018 12 26 (12): 1759-1772. Aubart Melodie, Gazal Steven, Arnaud Pauline, Benarroch Louise, Gross Marie-Sylvie, Buratti Julien, Boland Anne, Meyer Vincent, Zouali Habib, Hanna Nadine, Milleron Olivier, Stheneur Chantal, Bourgeron Thomas, Desguerre Isabelle, Jacob Marie-Paule, Gouya Laurent, Génin Emmanuelle, Deleuze Jean-François, Jondeau Guillaume, Boileau Catheri |
| Targeted genetic analysis in a large cohort of familial and sporadic cases of aneurysm or dissection of the thoracic aorta. Genetics in medicine : official journal of the American College of Medical Genetics 2018 3 20 (11): 1414-1422. Weerakkody Ruwan, Ross David, Parry David A, Ziganshin Bulat, Vandrovcova Jana, Gampawar Piyush, Abdullah Abdulshakur, Biggs Jennifer, Dumfarth Julia, Ibrahim Yousef, , Bicknell Colin, Field Mark, Elefteriades John, Cheshire Nick, Aitman Timothy |
| Role of TGFBR1 and TGFBR2 genetic variants in Marfan syndrome. Journal of vascular surgery 2017 Aug . De Cario Rosina, Sticchi Elena, Lucarini Laura, Attanasio Monica, Nistri Stefano, Marcucci Rossella, Pepe Guglielmina, Giusti Bet |
| Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis. Frontiers in physiology 2017 8 612. Giusti Betti, Sticchi Elena, De Cario Rosina, Magi Alberto, Nistri Stefano, Pepe Guglielmi |
| Association between Fibrillin1 Polymorphisms (rs2118181, rs10519177) and Transforming Growth Factor ß1 Concentration in Human Plasma. Molecular medicine (Cambridge, Mass.) 2015 Aug . Sepetiene Ramune, Patamsyte Vaiva, Zukovas Giedrius, Jariene Giedre, Stanioniene Zita, Benetis Rimantas, Tamosiunas Abdonas, Lesauskaite Vai |
| First genetic analysis of aneurysm genes in familial and sporadic abdominal aortic aneurysm. Human genetics 2015 Aug 134 (8): 881-93. van de Luijtgaarden Koen M, Heijsman Daphne, Maugeri Alessandra, Weiss Marjan M, Verhagen Hence J M, IJpma Arne, Brüggenwirth Hennie T, Majoor-Krakauer Daniel |
| FBN1 polymorphisms in patients with the dilatative pathology of the ascending thoracic aorta. European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery 2015 Apr 47 (4): e124-30. Lesauskaite Vaiva, Sepetiene Ramune, Jariene Giedre, Patamsyte Vaiva, Zukovas Giedrius, Grabauskyte Ingrida, Stanioniene Zita, Sirmenis Raimondas, Benetis Rimant |
| Wide mutation spectrum and frequent variant Ala27Thr of FBN1 identified in a large cohort of Chinese patients with sporadic TAAD. Scientific reports 2015 5 13115. Guo Jun, Cai Lun, Jia Lixin, Li Xiaoyan, Xi Xin, Zheng Shuai, Liu Xuxia, Piao Chunmei, Liu Tingting, Sun Zhongsheng, Cai Tao, Du J |
| Mutation of ACTA2 gene as an important cause of familial and nonfamilial nonsyndromatic thoracic aortic aneurysm and/or dissection (TAAD). Human mutation 2009 Oct 30 (10): 1406-11. Morisaki Hiroko, Akutsu Koichi, Ogino Hitoshi, Kondo Norihiro, Yamanaka Itaru, Tsutsumi Yoshiaki, Yoshimuta Tsuyoshi, Okajima Toshiya, Matsuda Hitoshi, Minatoya Kenji, Sasaki Hiroaki, Tanaka Hiroshi, Ishibashi-Ueda Hatsue, Morisaki Takayu |
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