293 related articles for article (PubMed ID: 25737393)
1. 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]
2. 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]
3. Polymorphisms in the NOS1AP gene modulate QT interval duration and risk of arrhythmias in the long QT syndrome.
Tomás M; Napolitano C; De Giuli L; Bloise R; Subirana I; Malovini A; Bellazzi R; Arking DE; Marban E; Chakravarti A; Spooner PM; Priori SG
J Am Coll Cardiol; 2010 Jun; 55(24):2745-52. PubMed ID: 20538168
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. NOS1AP Polymorphisms Modify QTc Interval Duration But Not Cardiac Arrest Risk in Hypertrophic Cardiomyopathy.
Earle N; Ingles J; Bagnall RD; Gray B; Crawford J; Smith W; Shelling AN; Love DR; Semsarian C; Skinner JR
J Cardiovasc Electrophysiol; 2015 Dec; 26(12):1346-51. PubMed ID: 26332198
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. Electromechanical window negativity in genotyped long-QT syndrome patients: relation to arrhythmia risk.
ter Bekke RM; Haugaa KH; van den Wijngaard A; Bos JM; Ackerman MJ; Edvardsen T; Volders PG
Eur Heart J; 2015 Jan; 36(3):179-86. PubMed ID: 25205533
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Long QT syndrome in adults.
Sauer AJ; Moss AJ; McNitt S; Peterson DR; Zareba W; Robinson JL; Qi M; Goldenberg I; Hobbs JB; Ackerman MJ; Benhorin J; Hall WJ; Kaufman ES; Locati EH; Napolitano C; Priori SG; Schwartz PJ; Towbin JA; Vincent GM; Zhang L
J Am Coll Cardiol; 2007 Jan; 49(3):329-37. PubMed ID: 17239714
[TBL] [Abstract][Full Text] [Related]
16. Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients : Koponen et al. Follow-up of adult LQTS patients.
Koponen M; Havulinna AS; Marjamaa A; Tuiskula AM; Salomaa V; Laitinen-Forsblom PJ; Piippo K; Toivonen L; Kontula K; Viitasalo M; Swan H
BMC Med Genet; 2018 Apr; 19(1):56. PubMed ID: 29622001
[TBL] [Abstract][Full Text] [Related]
17. Relationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart Study.
Lehtinen AB; Daniel KR; Shah SA; Nelson MR; Ziegler JT; Freedman BI; Carr JJ; Herrington DM; Langefeld CD; Bowden DW
Ann Noninvasive Electrocardiol; 2009 Jan; 14(1):72-9. PubMed ID: 19149796
[TBL] [Abstract][Full Text] [Related]
18. Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome.
Duchatelet S; Crotti L; Peat RA; Denjoy I; Itoh H; Berthet M; Ohno S; Fressart V; Monti MC; Crocamo C; Pedrazzini M; Dagradi F; Vicentini A; Klug D; Brink PA; Goosen A; Swan H; Toivonen L; Lahtinen AM; Kontula K; Shimizu W; Horie M; George AL; Trégouët DA; Guicheney P; Schwartz PJ
Circ Cardiovasc Genet; 2013 Aug; 6(4):354-61. PubMed ID: 23856471
[TBL] [Abstract][Full Text] [Related]
19. "QT clock" to improve detection of QT prolongation in long QT syndrome patients.
Page A; Aktas MK; Soyata T; Zareba W; Couderc JP
Heart Rhythm; 2016 Jan; 13(1):190-8. PubMed ID: 26334569
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
