81 related articles for article (PubMed ID: 18071084)
1. Letter by Herring and Paterson regarding article, "Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study".
Herring N; Paterson DJ
Circulation; 2007 Dec; 116(24):e564; author reply e565. PubMed ID: 18071084
[No Abstract] [Full Text] [Related]
2. Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study.
Aarnoudse AJ; Newton-Cheh C; de Bakker PI; Straus SM; Kors JA; Hofman A; Uitterlinden AG; Witteman JC; Stricker BH
Circulation; 2007 Jul; 116(1):10-6. PubMed ID: 17576865
[TBL] [Abstract][Full Text] [Related]
3. Calcium channel blockers, NOS1AP, and heart-rate-corrected QT prolongation.
van Noord C; Aarnoudse AJ; Eijgelsheim M; Sturkenboom MC; Straus SM; Hofman A; Kors JA; Newton-Cheh C; Witteman JC; Stricker BH
Pharmacogenet Genomics; 2009 Apr; 19(4):260-6. PubMed ID: 19247217
[TBL] [Abstract][Full Text] [Related]
4. Association of rs10918594 polymorphisms of nitric oxide synthase 1 adaptor protein (NOS1AP) with QTc interval prolongation during kidney transplantation.
Kaczmarczyk M; Biernawska J; Zukowski M; Kotfis K; Zegan-Barańska M; Bińczak-Kuleta A; Ciechanowicz A; Brykczyński M; Bohatyrewicz R
Transplant Proc; 2011 Oct; 43(8):2964-6. PubMed ID: 21996201
[TBL] [Abstract][Full Text] [Related]
5. A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.
Arking DE; Pfeufer A; Post W; Kao WH; Newton-Cheh C; Ikeda M; West K; Kashuk C; Akyol M; Perz S; Jalilzadeh S; Illig T; Gieger C; Guo CY; Larson MG; Wichmann HE; Marbán E; O'Donnell CJ; Hirschhorn JN; Kääb S; Spooner PM; Meitinger T; Chakravarti A
Nat Genet; 2006 Jun; 38(6):644-51. PubMed ID: 16648850
[TBL] [Abstract][Full Text] [Related]
6. Common variation in NOS1AP and KCNH2 genes and QT interval duration in young adults. The Cardiovascular Risk in Young Finns Study.
Raitakari OT; Blom-Nyholm J; Koskinen TA; Kähönen M; Viikari JS; Lehtimäki T
Ann Med; 2009; 41(2):144-51. PubMed ID: 18785031
[TBL] [Abstract][Full Text] [Related]
7. A common variant of NOS1AP is associated with QT interval duration in a Chinese population with Type 2 diabetes.
Lu J; Hu C; Hu W; Zhang R; Wang C; Qin W; Yu W; Xiang K; ; Jia W
Diabet Med; 2010 Sep; 27(9):1074-9. PubMed ID: 20722683
[TBL] [Abstract][Full Text] [Related]
8. Systematic Meta-Analysis of the Association Between a Common NOS1AP Genetic Polymorphism, the QTc Interval, and Sudden Death.
Zang X; Li S; Zhao Y; Chen K; Wang X; Song W; Ma J; Tu X; Xia Y; Zhang S; Gao C
Int Heart J; 2019 Sep; 60(5):1083-1090. PubMed ID: 31447468
[TBL] [Abstract][Full Text] [Related]
9. Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2.
Kolder ICRM; Tanck MWT; Postema PG; Barc J; Sinner MF; Zumhagen S; Husemann A; Stallmeyer B; Koopmann TT; Hofman N; Pfeufer A; Lichtner P; Meitinger T; Beckmann BM; Myerburg RJ; Bishopric NH; Roden DM; Kääb S; Wilde AAM; Schott JJ; Schulze-Bahr E; Bezzina CR
Circ Cardiovasc Genet; 2015 Jun; 8(3):447-456. PubMed ID: 25737393
[TBL] [Abstract][Full Text] [Related]
10. Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study.
Eijgelsheim M; Newton-Cheh C; Aarnoudse AL; van Noord C; Witteman JC; Hofman A; Uitterlinden AG; Stricker BH
Hum Mol Genet; 2009 Nov; 18(21):4213-8. PubMed ID: 19643915
[TBL] [Abstract][Full Text] [Related]
11. SNP association and sequence analysis of the NOS1AP gene in SIDS.
Osawa M; Kimura R; Hasegawa I; Mukasa N; Satoh F
Leg Med (Tokyo); 2009 Apr; 11 Suppl 1():S307-8. PubMed ID: 19289301
[TBL] [Abstract][Full Text] [Related]
12. 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.
Winbo A; Stattin EL; Westin IM; Norberg A; Persson J; Jensen SM; Rydberg A
BMC Med Genet; 2017 Jul; 18(1):74. PubMed ID: 28720088
[TBL] [Abstract][Full Text] [Related]
13. Association of NOS1AP genetic variants with QT interval duration in families from the Diabetes Heart Study.
Lehtinen AB; Newton-Cheh C; Ziegler JT; Langefeld CD; Freedman BI; Daniel KR; Herrington DM; Bowden DW
Diabetes; 2008 Apr; 57(4):1108-14. PubMed ID: 18235038
[TBL] [Abstract][Full Text] [Related]
14. Common variation in the NOS1AP gene is associated with reduced glucose-lowering effect and with increased mortality in users of sulfonylurea.
Becker ML; Aarnoudse AJ; Newton-Cheh C; Hofman A; Witteman JC; Uitterlinden AG; Visser LE; Stricker BH
Pharmacogenet Genomics; 2008 Jul; 18(7):591-7. PubMed ID: 18551039
[TBL] [Abstract][Full Text] [Related]
15. NOS1AP is a genetic modifier of the long-QT syndrome.
Crotti L; Monti MC; Insolia R; Peljto A; Goosen A; Brink PA; Greenberg DA; Schwartz PJ; George AL
Circulation; 2009 Oct; 120(17):1657-63. PubMed ID: 19822806
[TBL] [Abstract][Full Text] [Related]
16. Gender and effects of a common genetic variant in the NOS1 regulator NOS1AP on cardiac repolarization in 3761 individuals from two independent populations.
Tobin MD; Kähönen M; Braund P; Nieminen T; Hajat C; Tomaszewski M; Viik J; Lehtinen R; Ng GA; Macfarlane PW; Burton PR; Lehtimäki T; Samani NJ
Int J Epidemiol; 2008 Oct; 37(5):1132-41. PubMed ID: 18511491
[TBL] [Abstract][Full Text] [Related]
17. An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval.
Kapoor A; Sekar RB; Hansen NF; Fox-Talbot K; Morley M; Pihur V; Chatterjee S; Brandimarto J; Moravec CS; Pulit SL; ; Pfeufer A; Mullikin J; Ross M; Green ED; Bentley D; Newton-Cheh C; Boerwinkle E; Tomaselli GF; Cappola TP; Arking DE; Halushka MK; Chakravarti A
Am J Hum Genet; 2014 Jun; 94(6):854-69. PubMed ID: 24857694
[TBL] [Abstract][Full Text] [Related]
18. Identification of a common variant at the NOS1AP locus strongly associated to QT-interval duration.
Eijgelsheim M; Aarnoudse AL; Rivadeneira F; Kors JA; Witteman JC; Hofman A; van Duijn CM; Uitterlinden AG; Stricker BH
Hum Mol Genet; 2009 Jan; 18(2):347-57. PubMed ID: 18927126
[TBL] [Abstract][Full Text] [Related]
19. Influence of NOS1AP Risk Variants on the Corrected QT (QTc) Interval in the Pharmacotherapy of Schizophrenia.
Esen-Sehir D; Kopf J; Hägele S; Plichta MM; Reif A; Freudenberg F
Pharmacopsychiatry; 2022 Sep; 55(5):266-273. PubMed ID: 35732169
[TBL] [Abstract][Full Text] [Related]
20. Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations.
Kao WH; Arking DE; Post W; Rea TD; Sotoodehnia N; Prineas RJ; Bishe B; Doan BQ; Boerwinkle E; Psaty BM; Tomaselli GF; Coresh J; Siscovick DS; Marbán E; Spooner PM; Burke GL; Chakravarti A
Circulation; 2009 Feb; 119(7):940-51. PubMed ID: 19204306
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
