Human Genome Epidemiology Literature Finder
|
Records 1 - 15 (of 15 Records) |
| Query Trace: Syndrome and NOS1AP[original query] |
|---|
| Evidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate. Human heredity 2009 67 (3): 163-73. Kremeyer Barbara, García Jenny, Kymäläinen Hanna, Wratten Naomi, Restrepo Gabriel, Palacio Carlos, Miranda Ana Lucía, López Carlos, Restrepo Margarita, Bedoya Gabriel, Brzustowicz Linda M, Ospina-Duque Jorge, Arbeláez María Patricia, Ruiz-Linares Andr |
Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
Nature genetics 2009 Apr 41 (4): 4. Pfeufer A, Sanna S, Arking DE, Müller M, Gateva V, Fuchsberger C, Ehret GB, Orrú M, Pattaro C, Köttgen A, Perz S, Usala G, Barbalic M, Li M, Pütz B, Scuteri A, Prineas RJ, Sinner MF, Gieger C, Najjar SS, Kao WH, Mühleisen TW, Dei M, Happle C, Möhlenkamp S, Crisponi L, Erbel R, Jöckel KH, Naitza S, Steinbeck G, Marroni F, Hicks AA, Lakatta E, Müller-Myhsok B, Pramstaller PP, Wichmann HE, Schlessinger D, Boerwinkle E, Meitinger T, Uda M, Coresh J, Kääb S, Abecasis GR, Chakravarti A |
| 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 |
| 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 |
| Polymorphisms in the NOS1AP gene modulate QT interval duration and risk of arrhythmias in the long QT syndrome. Journal of the American College of Cardiology 2010 Jun 55 (24): 2745-52. Tomás Marta, Napolitano Carlo, De Giuli Luciana, Bloise Raffaella, Subirana Isaac, Malovini Alberto, Bellazzi Riccardo, Arking Dan E, Marban Eduardo, Chakravarti Aravinda, Spooner Peter M, Priori Silvia |
| 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 |
| Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia. Journal of the American College of Cardiology 2012 Aug 60 (9): 841-50. Jamshidi Yalda, Nolte Ilja M, Dalageorgou Chrysoula, Zheng Dongling, Johnson Toby, Bastiaenen Rachel, Ruddy Suzanne, Talbott Daniel, Norris Kris J, Snieder Harold, George Alfred L, Marshall Vanessa, Shakir Saad, Kannankeril Prince J, Munroe Patricia B, Camm A John, Jeffery Steve, Roden Dan M, Behr Elijah |
| 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 |
| 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 |
| 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 |
| Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis. BMC medical genetics 2017 07 18 (1): 74. Winbo Annika, Stattin Eva-Lena, Westin Ida Maria, Norberg Anna, Persson Johan, Jensen Steen M, Rydberg Anni |
| Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder population. Stem cell research 2019 8 39 101510. 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 |
| 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 |
| 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 |
- Page last reviewed:Feb 1, 2024
- Content source: