HuGE Literature Finder
Records
1
-
30
| Association of a Common NOS1AP Variant with Attenuation of QTc Prolongation in Men with Heroin Dependence Undergoing Methadone Treatment. Journal of personalized medicine 2022 5 12 (5): . Chang Kuan-Cheng, Chen Ke-Wei, Huang Chieh-Liang, Liao Wen-Ling, Wu Mei-Yao, Lin Yu-Kai, Shiao Yi-Tzone, Chung Wei-Hsin, Lin Yen-Nien, Lane Hsien-Yu |
| Evaluating Common NOS1AP Variants in Patients with Implantable Cardioverter Defibrillators for Secondary Prevention : Evaluating SNPs in NOS1AP. Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing 2022 3 64 (3): 793-800. Zang Xiaobiao, Zhang Shulong, Li Sisi, Wang Xianqing, Song Weifeng, Chen Ke, Ma Jifang, Tu Xin, Xia Yunlong, Zhao Yonghui, Gao Chuan |
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
Circulation 2020 Jul 142 (4): 324-338. Lahrouchi Najim, Tadros Rafik, Crotti Lia, Mizusawa Yuka, Postema Pieter G, Beekman Leander, Walsh Roddy, Hasegawa Kanae, Barc Julien, Ernsting Marko, Turkowski Kari L, Mazzanti Andrea, Beckmann Britt M, Shimamoto Keiko, Diamant Ulla-Britt, Wijeyeratne Yanushi D, Kucho Yu, Robyns Tomas, Ishikawa Taisuke, Arbelo Elena, Christiansen Michael, Winbo Annika, Jabbari Reza, Lubitz Steven A, Steinfurt Johannes, Rudic Boris, Loeys Bart, Shoemaker M Ben, Weeke Peter E, Pfeiffer Ryan, Davies Brianna, Andorin Antoine, Hofman Nynke, Dagradi Federica, Pedrazzini Matteo, Tester David J, Bos J Martijn, Sarquella-Brugada Georgia, Campuzano Óscar, Platonov Pyotr G, Stallmeyer Birgit, Zumhagen Sven, Nannenberg Eline A, Veldink Jan H, van den Berg Leonard H, Al-Chalabi Ammar, Shaw Christopher E, Shaw Pamela J, Morrison Karen E, Andersen Peter M, Müller-Nurasyid Martina, Cusi Daniele, Barlassina Cristina, Galan Pilar, Lathrop Mark, Munter Markus, Werge Thomas, Ribasés Marta, Aung Tin, Khor Chiea C, Ozaki Mineo, Lichtner Peter, Meitinger Thomas, van Tintelen J Peter, Hoedemaekers Yvonne, Denjoy Isabelle, Leenhardt Antoine, Napolitano Carlo, Shimizu Wataru, Schott Jean-Jacques, Gourraud Jean-Baptiste, Makiyama Takeru, Ohno Seiko, Itoh Hideki, Krahn Andrew D, Antzelevitch Charles, Roden Dan M, Saenen Johan, Borggrefe Martin, Odening Katja E, Ellinor Patrick T, Tfelt-Hansen Jacob, Skinner Jonathan R, van den Berg Maarten P, Olesen Morten Salling, Brugada Josep, Brugada Ramón, Makita Naomasa, Breckpot Jeroen, Yoshinaga Masao, Behr Elijah R, Rydberg Annika, Aiba Takeshi, Kääb Stefan, Priori Silvia G, Guicheney Pascale, Tan Hanno L, Newton-Cheh Christopher, Ackerman Michael J, Schwartz Peter J, Schulze-Bahr Eric, Probst Vincent, Horie Minoru, Wilde Arthur A, Tanck Michael W T, Bezzina Connie |
| NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis. Cardiovascular research 2020 2 117 (2): 472-483. Ronchi Carlotta, Bernardi Joyce, Mura Manuela, Stefanello Manuela, Badone Beatrice, Rocchetti Marcella, Crotti Lia, Brink Paul, Schwartz Peter J, Gnecchi Massimiliano, Zaza Anton |
| Effect of Sex and Underlying Disease on the Genetic Association of QT Interval and Sudden Cardiac Death. Journal of the American Heart Association 2019 Dec 8 (23): e013751. Mitchell Rebecca N, Ashar Foram N, Jarvelin Marjo-Riitta, Froguel Philippe, Sotoodehnia Nona, Brody Jennifer A, Sebert Sylvain, Huikuri Heikki, Rioux John, Goyette Philippe, Newcomb Charles E, Junttila M Juhani, Arking Dan |
| Systematic Meta-Analysis of the Association Between a Common NOS1AP Genetic Polymorphism, the QTc Interval, and Sudden Death. International heart journal 2019 Aug . Zang Xiaobiao, Li Sisi, Zhao Yonghui, Chen Ke, Wang Xianqing, Song Weifeng, Ma Jifang, Tu Xin, Xia Yunlong, Zhang Shulong, Gao Chuan |
| Corrected QT Interval Prolongation in Psychopharmacological Treatment and Its Modulation by Genetic Variation. Neuropsychobiology 2019 77 (2): 67-72. Corponi Filippo, Fabbri Chiara, Boriani Giuseppe, Diemberger Igor, Albani Diego, Forloni Gianluigi, Serretti Alessand |
| Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene. Stem cell research 2019 3 36 101416. Mura Manuela, Pisano Federica, Stefanello Manuela, Ginevrino Monia, Boni Marina, Calabrò Federica, Crotti Lia, Valente Enza Maria, Schwartz Peter J, Brink Paul A, Gnecchi Massimilia |
| QT length during methadone maintenance treatment: gene × dose interaction. Fundamental & clinical pharmacology 2018 Aug . Zerdazi El-Hadi, Vorspan Florence, Marees Andries T, Naccache François, Lepine Jean-Pierre, Laplanche Jean-Louis, Prince Nathalie, Marie-Claire Cynthia, Bellivier Frank, Mouly Stéphane, Bloch Vanes |
| GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals.
Scientific reports 2017 Dec 7 (1): 17075. Méndez-Giráldez Raúl, Gogarten Stephanie M, Below Jennifer E, Yao Jie, Seyerle Amanda A, Highland Heather M, Kooperberg Charles, Soliman Elsayed Z, Rotter Jerome I, Kerr Kathleen F, Ryckman Kelli K, Taylor Kent D, Petty Lauren E, Shah Sanjiv J, Conomos Matthew P, Sotoodehnia Nona, Cheng Susan, Heckbert Susan R, Sofer Tamar, Guo Xiuqing, Whitsel Eric A, Lin Henry J, Hanis Craig L, Laurie Cathy C, Avery Christy |
| Ethnic Differences in Genetic Ion Channelopathies Associated with Sudden Cardiac Death: A Systematic Review and Meta-Analysis. Annals of clinical and laboratory science 2017 Aug 47 (4): 481-490. Kong Tim, Feulefack Joseph, Ruether Kim, Shen Fan, Zheng Wang, Chen Xing-Zhen, Sergi Consola |
| The role of known variants of KCNQ1, KCNH2, KCNE1, SCN5A, and NOS1AP in water-related deaths. International journal of legal medicine 2016 Jul . Tzimas Iliana, Zingraf Jana-Christin, Bajanowski Thomas, Poetsch Micae |
| NOS1AP Polymorphisms Modify QTc Interval Duration But Not Cardiac Arrest Risk in Hypertrophic Cardiomyopathy. Journal of cardiovascular electrophysiology 2015 Sep . Earle Nikki, Ingles Jodie, Bagnall Richard D, Gray Belinda, Crawford Jackie, Smith Warren, Shelling Andrew N, Love Donald R, Semsarian Chris, Skinner Jonathan |
| Genetic markers of repolarization and arrhythmic events after acute coronary syndromes. American heart journal 2015 Apr 169 (4): 579-86.e3. Earle N J, Poppe K K, Pilbrow A P, Cameron V A, Troughton R W, Skinner J R, Love D R, Shelling A N, Whalley G A, Ellis C J, Richards A M, Doughty R |
| Genetic variants in KCNE1, KCNQ1, and NOS1AP in sudden unexplained death during daily activities in Chinese Han population. Journal of forensic sciences 2015 Mar 60 (2): 351-6. Huang Jinglu, Wang Xiaoguang, Hao Bo, Chen Yijiu, Liu Hong, Quan Li, Tang Dawei, Sheng Lihui, Li Ming, Huang Erwen, Liu Chao, Luo B |
| Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome. PloS one 2015 10 (7): e0133037. Allegue Catarina, Coll Mònica, Mates Jesus, Campuzano Oscar, Iglesias Anna, Sobrino Beatriz, Brion Maria, Amigo Jorge, Carracedo Angel, Brugada Pedro, Brugada Josep, Brugada Ram |
| Association of common variants in NOS1AP gene with sudden unexplained nocturnal death syndrome in the southern Chinese Han population. International journal of legal medicine 2014 Nov 128 (6): 933-8. Huang Lei, Yu Yangeng, Chen Yili, Tester David J, Tang Shuangbo, Ackerman Michael J, Yuan Zichuang, Cheng Jiandi |
| [Correlation of NOS1AP gene polymorphisms with sudden unexpected death in Chinese Han population]. Fa yi xue za zhi 2014 Feb 30 (1): 27-30, 35. Huang Jing-Lu, Hao Bo, Wang Xiao-Guang, Liu Hong, Li Ming, Quan Li, Sheng Li-Hui, Liu Chao, Luo B |
| Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome. Heart rhythm : the official journal of the Heart Rhythm Society 2014 Jan 11 (1): 76-82. Earle Nikki, Yeo Han Dug, Pilbrow Anna, Crawford Jackie, Smith Warren, Shelling Andrew N, Cameron Vicky, Love Donald R, Skinner Jonathan |
| Associations between NOS1AP single nucleotide polymorphisms (SNPs) and QT interval duration in four racial/ethnic groups in the Multi-Ethnic Study of Atherosclerosis (MESA). Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2013 Jan 18 (1): 1. Shah SA, Herrington DM, Howard TD, Divers J, Arnett DK, Burke GL, Hong Kao W, Guo X, Siscovick DS, Chakravarti A, Lima JA, Psaty BM, Tomaselli GF, Rich SS, Bowden DW, Post W |
| Positive association between rs10918859 of the NOS1AP gene and coronary heart disease in male Han Chinese. Genetic testing and molecular biomarkers 2013 Jan 17 (1): 25-9. Huang Yi, Lian Jiangfang, Huang R Stephanie, Wang Feiming, Xu Limin, Le Yanping, Yang Xi, Xu Weifeng, Huang Xiaoyan, Ye Meng, Zhou Jianqing, Duan Shiw |
| Impact of ancestry and common genetic variants on QT interval in African Americans.
Circulation. Cardiovascular genetics 2012 Dec 5 (6): 647-55. Smith J Gustav, Avery Christy L, Evans Daniel S, Nalls Michael A, Meng Yan A, Smith Erin N, Palmer Cameron, Tanaka Toshiko, Mehra Reena, Butler Anne M, Young Taylor, Buxbaum Sarah G, Kerr Kathleen F, Berenson Gerald S, Schnabel Renate B, Li Guo, Ellinor Patrick T, Magnani Jared W, Chen Wei, Bis Joshua C, Curb J David, Hsueh Wen-Chi, Rotter Jerome I, Liu Yongmei, Newman Anne B, Limacher Marian C, North Kari E, Reiner Alexander P, Quibrera P Miguel, Schork Nicholas J, Singleton Andrew B, Psaty Bruce M, Soliman Elsayed Z, Solomon Allen J, Srinivasan Sathanur R, Alonso Alvaro, Wallace Robert, Redline Susan, Zhang Zhu-Ming, Post Wendy S, Zonderman Alan B, Taylor Herman A, Murray Sarah S, Ferrucci Luigi, Arking Dan E, Evans Michele K, Fox Ervin R, Sotoodehnia Nona, Heckbert Susan R, Whitsel Eric A, Newton-Cheh Christopher, |
| Integration of genetics into a systems model of electrocardiographic traits using HumanCVD BeadChip. Circulation. Cardiovascular genetics 2012 Dec 5 (6): 630-8. Gaunt Tom R, Shah Sonia, Nelson Christopher P, Drenos Fotios, Braund Peter S, Adeniran Ismail, Folkersen Lasse, Lawlor Debbie A, Casas Juan-Pablo, Amuzu Antoinette, Kivimaki Mika, Whittaker John, Eriksson Per, Zhang Henggui, Hancox Jules C, Tomaszewski Maciej, Burton Paul R, Tobin Martin D, Humphries Steve E, Talmud Philippa J, Macfarlane Peter W, Hingorani Aroon D, Samani Nilesh J, Kumari Meena, Day Ian N |
| A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval.
American journal of human genetics 2012 Jul 91 (1): 180-4. Kim Jong Wook, Hong Kyung-Won, Go Min Jin, Kim Sung Soo, Tabara Yasuharu, Kita Yoshikuni, Tanigawa Takeshi, Cho Yoon Shin, Han Bok-Ghee, Oh Bermse |
| Association of rs10918594 polymorphisms of nitric oxide synthase 1 adaptor protein (NOS1AP) with QTc interval prolongation during kidney transplantation. Transplantation proceedings 2011 Oct 43 (8): 2964-6. Kaczmarczyk M, Biernawska J, Zukowski M, Kotfis K, Zegan-Bara?ska M, Bi?czak-Kuleta A, Ciechanowicz A, Brykczy?ski M, Bohatyrewicz |
| Common variants in CASQ2, GPD1L, and NOS1AP are significantly associated with risk of sudden death in patients with coronary artery disease. Circulation. Cardiovascular genetics 2011 Aug 4 (4): 397-402. Westaway Shawn K, Reinier Kyndaron, Huertas-Vazquez Adriana, Evanado Audrey, Teodorescu Carmen, Navarro Jo, Sinner Moritz F, Gunson Karen, Jui Jonathan, Spooner Peter, Kaab Stefan, Chugh Sumeet |
| A common variant of NOS1AP is associated with QT interval duration in a Chinese population with Type 2 diabetes. Diabetic medicine : a journal of the British Diabetic Association 2010 Sep 27 (9): 1074-9. Lu J, Hu C, Hu W, Zhang R, Wang C, Qin W, Yu W, Xiang K, , Jia |
| Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study. Human molecular genetics 2009 Nov 18 (21): 4213-8. Eijgelsheim Mark, Newton-Cheh Christopher, Aarnoudse Adrianus L H J, van Noord Charlotte, Witteman Jacqueline C M, Hofman Albert, Uitterlinden André G, Stricker Bruno H |
| NOS1AP is a genetic modifier of the long-QT syndrome. Circulation 2009 Oct 120 (17): 1657-63. Crotti Lia, Monti Maria Cristina, Insolia Roberto, Peljto Anna, Goosen Althea, Brink Paul A, Greenberg David A, Schwartz Peter J, George Alfred |
| Association of the rs10918594 of nitric oxide synthase 1 adaptor protein (NOS1AP) polymorphisms with the graft function after kidney transplantation. Annals of transplantation : quarterly of the Polish Transplantation Society 0 16 (3): 72-6. Zukowski Maciej, Kotfis Katarzyna, Biernawska Jowita, Zegan-Baranska Malgorzata, Blaszczyk Wojciech, Kaczmarczyk Mariusz, Ciechanowicz Andrzej, Binczak-Kuleta Agnieszka, Brykczynski Miroslaw, Zietek Zbigniew, Bohatyrewicz Romua |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 31, 2023
- Content source: