Human Genome Epidemiology Literature Finder
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Records 1 - 18 (of 18 Records) |
| Query Trace: Disease and NOS1AP[original query] |
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| SNP association and sequence analysis of the NOS1AP gene in SIDS. Legal medicine (Tokyo, Japan) 2009 Apr 11 Suppl 1 S307-8. Osawa Motoki, Kimura Ryousuke, Hasegawa Iwao, Mukasa Nahoko, Satoh Fumi |
| Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations. Circulation 2009 Feb 119 (7): 940-51. Kao W H Linda, Arking Dan E, Post Wendy, Rea Thomas D, Sotoodehnia Nona, Prineas Ronald J, Bishe Bryan, Doan Betty Q, Boerwinkle Eric, Psaty Bruce M, Tomaselli Gordon F, Coresh Josef, Siscovick David S, Marbán Eduardo, Spooner Peter M, Burke Gregory L, Chakravarti Aravin |
| 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 |
| 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 |
GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.
BMC cardiovascular disorders 2011 11 (1): 29. Aouizerat Bradley E, Vittinghoff Eric, Musone Stacy L, Pawlikowska Ludmila, Kwok Pui-Yan, Olgin Jeffrey E, Tseng Zian |
| Diabetes, lower extremity amputation, loss of protective sensation, and neuronal nitric oxide synthase associated protein in the chronic renal insufficiency cohort study. Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society 0 21 (1): 17-24. Margolis David J, Gupta Jayanta, Thom Stephen R, Townsend Raymond R, Kanetsky Peter A, Hoffstad Ole, Papdopoulos Maryte, Fischer Michael, Schelling Jeffrey R, Mitra Nandi |
| 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 |
| The genetic contribution of the NO system at the glutamatergic post-synapse to schizophrenia: further evidence and meta-analysis. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2014 Jan 24 (1): 65-85. Weber H, Klamer D, Freudenberg F, Kittel-Schneider S, Rivero O, Scholz C-J, Volkert J, Kopf J, Heupel J, Herterich S, Adolfsson R, Alttoa A, Post A, Grußendorf H, Kramer A, Gessner A, Schmidt B, Hempel S, Jacob C P, Sanjuán J, Moltó M D, Lesch K-P, Freitag C M, Kent L, Reif |
| 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 |
| Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults.
PloS one 2014 9 (8): e105062. Scannell Bryan Molly, Argos Maria, Pierce Brandon, Tong Lin, Rakibuz-Zaman Muhammad, Ahmed Alauddin, Rahman Mahfuzar, Islam Tariqul, Yunus Muhammad, Parvez Faruque, Roy Shantanu, Jasmine Farzana, Baron John A, Kibriya Muhammad G, Ahsan Habib |
| Association of NOS1AP variants and depression phenotypes in schizophrenia. Journal of affective disorders 2015 Sep 188 263-269. Cheah Sern-Yih, Lawford Bruce R, Young Ross McD, Morris C Phillip, Voisey Joan |
| 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 |
| Insights into the genetics of blood pressure in black South African individuals: the Birth to Twenty cohort.
BMC medical genomics 2018 Jan 11 (1): 2. Hendry Liesl M, Sahibdeen Venesa, Choudhury Ananyo, Norris Shane A, Ramsay Michèle, Lombard Zané, |
| 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 |
| 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 |
| Genetic variants and effect modifiers of QT interval prolongation in patients with sickle cell disease. Gene 2023 9 890 147824. Mengna Zhang, William B Hillegass, Xue Yu, Suvankar Majumdar, J Daryl Pollard, Erin Jackson, Jarrod Knudson, Douglas Wolfe, Gregory J Kato, Joseph F Maher, Hao M |
| PTPRD gene variant rs10739150: A potential game-changer in hypertension diagnosis. PloS one 2024 6 19 (6): e0304950. Laith Al-Eit |
- Page last reviewed:Feb 1, 2024
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