163 related articles for article (PubMed ID: 18927126)
21. Impact of ancestry and common genetic variants on QT interval in African Americans.
Smith JG; Avery CL; Evans DS; Nalls MA; Meng YA; Smith EN; Palmer C; Tanaka T; Mehra R; Butler AM; Young T; Buxbaum SG; Kerr KF; Berenson GS; Schnabel RB; Li G; Ellinor PT; Magnani JW; Chen W; Bis JC; Curb JD; Hsueh WC; Rotter JI; Liu Y; Newman AB; Limacher MC; North KE; Reiner AP; Quibrera PM; Schork NJ; Singleton AB; Psaty BM; Soliman EZ; Solomon AJ; Srinivasan SR; Alonso A; Wallace R; Redline S; Zhang ZM; Post WS; Zonderman AB; Taylor HA; Murray SS; Ferrucci L; Arking DE; Evans MK; Fox ER; Sotoodehnia N; Heckbert SR; Whitsel EA; Newton-Cheh C;
Circ Cardiovasc Genet; 2012 Dec; 5(6):647-55. PubMed ID: 23166209
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. Relationship of common candidate gene variants to electrocardiographic T-wave peak to T-wave end interval and T-wave morphology parameters.
Porthan K; Marjamaa A; Viitasalo M; Väänänen H; Jula A; Toivonen L; Nieminen MS; Newton-Cheh C; Salomaa V; Kontula K; Oikarinen L
Heart Rhythm; 2010 Jul; 7(7):898-903. PubMed ID: 20215044
[TBL] [Abstract][Full Text] [Related]
25. Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome.
Earle N; Yeo Han D; Pilbrow A; Crawford J; Smith W; Shelling AN; Cameron V; Love DR; Skinner JR
Heart Rhythm; 2014 Jan; 11(1):76-82. PubMed ID: 24096169
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. 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]
29. Fine-mapping and initial characterization of QT interval loci in African Americans.
Avery CL; Sethupathy P; Buyske S; He Q; Lin DY; Arking DE; Carty CL; Duggan D; Fesinmeyer MD; Hindorff LA; Jeff JM; Klein L; Patton KK; Peters U; Shohet RV; Sotoodehnia N; Young AM; Kooperberg C; Haiman CA; Mohlke KL; Whitsel EA; North KE
PLoS Genet; 2012; 8(8):e1002870. PubMed ID: 22912591
[TBL] [Abstract][Full Text] [Related]
30. Inducible over-expression of cardiac Nos1ap causes short QT syndrome in transgenic mice.
Jänsch M; Lubomirov LT; Trum M; Williams T; Schmitt J; Schuh K; Qadri F; Maier LS; Bader M; Ritter O
FEBS Open Bio; 2023 Jan; 13(1):118-132. PubMed ID: 36352324
[TBL] [Abstract][Full Text] [Related]
31. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
Lahrouchi N; Tadros R; Crotti L; Mizusawa Y; Postema PG; Beekman L; Walsh R; Hasegawa K; Barc J; Ernsting M; Turkowski KL; Mazzanti A; Beckmann BM; Shimamoto K; Diamant UB; Wijeyeratne YD; Kucho Y; Robyns T; Ishikawa T; Arbelo E; Christiansen M; Winbo A; Jabbari R; Lubitz SA; Steinfurt J; Rudic B; Loeys B; Shoemaker MB; Weeke PE; Pfeiffer R; Davies B; Andorin A; Hofman N; Dagradi F; Pedrazzini M; Tester DJ; Bos JM; Sarquella-Brugada G; Campuzano Ó; Platonov PG; Stallmeyer B; Zumhagen S; Nannenberg EA; Veldink JH; van den Berg LH; Al-Chalabi A; Shaw CE; Shaw PJ; Morrison KE; Andersen PM; Müller-Nurasyid M; Cusi D; Barlassina C; Galan P; Lathrop M; Munter M; Werge T; Ribasés M; Aung T; Khor CC; Ozaki M; Lichtner P; Meitinger T; van Tintelen JP; Hoedemaekers Y; Denjoy I; Leenhardt A; Napolitano C; Shimizu W; Schott JJ; Gourraud JB; Makiyama T; Ohno S; Itoh H; Krahn AD; Antzelevitch C; Roden DM; Saenen J; Borggrefe M; Odening KE; Ellinor PT; Tfelt-Hansen J; Skinner JR; van den Berg MP; Olesen MS; Brugada J; Brugada R; Makita N; Breckpot J; Yoshinaga M; Behr ER; Rydberg A; Aiba T; Kääb S; Priori SG; Guicheney P; Tan HL; Newton-Cheh C; Ackerman MJ; Schwartz PJ; Schulze-Bahr E; Probst V; Horie M; Wilde AA; Tanck MWT; Bezzina CR
Circulation; 2020 Jul; 142(4):324-338. PubMed ID: 32429735
[TBL] [Abstract][Full Text] [Related]
32. Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populations.
Avery CL; Wassel CL; Richard MA; Highland HM; Bien S; Zubair N; Soliman EZ; Fornage M; Bielinski SJ; Tao R; Seyerle AA; Shah SJ; Lloyd-Jones DM; Buyske S; Rotter JI; Post WS; Rich SS; Hindorff LA; Jeff JM; Shohet RV; Sotoodehnia N; Lin DY; Whitsel EA; Peters U; Haiman CA; Crawford DC; Kooperberg C; North KE
Heart Rhythm; 2017 Apr; 14(4):572-580. PubMed ID: 27988371
[TBL] [Abstract][Full Text] [Related]
33. The genetic variation rs12143842 in NOS1AP increases idiopathic ventricular tachycardia risk in Chinese Han populations.
Zhang R; Chen F; Yu H; Gao L; Yin X; Dong Y; Yang Y; Xia Y
Sci Rep; 2017 Aug; 7(1):8356. PubMed ID: 28827735
[TBL] [Abstract][Full Text] [Related]
34. Evaluating Common NOS1AP Variants in Patients with Implantable Cardioverter Defibrillators for Secondary Prevention : Evaluating SNPs in NOS1AP.
Zang X; Zhang S; Li S; Wang X; Song W; Chen K; Ma J; Tu X; Xia Y; Zhao Y; Gao C
J Interv Card Electrophysiol; 2022 Sep; 64(3):793-800. PubMed ID: 35353321
[TBL] [Abstract][Full Text] [Related]
35. Genetic variants and effect modifiers of QT interval prolongation in patients with sickle cell disease.
Zhang M; Hillegass WB; Yu X; Majumdar S; Daryl Pollard J; Jackson E; Knudson J; Wolfe D; Kato GJ; Maher JF; Mei H
Gene; 2024 Jan; 890():147824. PubMed ID: 37741592
[TBL] [Abstract][Full Text] [Related]
36. Cardiac muscle-restricted partial loss of Nos1ap expression has limited but significant impact on electrocardiographic features.
Smith A; Auer D; Johnson M; Sanchez E; Ross H; Ward C; Chakravarti A; Kapoor A
G3 (Bethesda); 2023 Nov; 13(11):. PubMed ID: 37708408
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval.
Kim JW; Hong KW; Go MJ; Kim SS; Tabara Y; Kita Y; Tanigawa T; Cho YS; Han BG; Oh B
Am J Hum Genet; 2012 Jul; 91(1):180-4. PubMed ID: 22726844
[TBL] [Abstract][Full Text] [Related]
39. Association of common variants in NOS1AP gene with sudden unexplained nocturnal death syndrome in the southern Chinese Han population.
Huang L; Yu Y; Chen Y; Tester DJ; Tang S; Ackerman MJ; Yuan Z; Cheng J
Int J Legal Med; 2014 Nov; 128(6):933-8. PubMed ID: 24504561
[TBL] [Abstract][Full Text] [Related]
40. Association of a Common
Chang KC; Chen KW; Huang CL; Liao WL; Wu MY; Lin YK; Shiao YT; Chung WH; Lin YN; Lane HY
J Pers Med; 2022 May; 12(5):. PubMed ID: 35629257
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
