BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 18927126)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Common candidate gene variants are associated with QT interval duration in the general population.
    Marjamaa A; Newton-Cheh C; Porthan K; Reunanen A; Lahermo P; Väänänen H; Jula A; Karanko H; Swan H; Toivonen L; Nieminen MS; Viitasalo M; Peltonen L; Oikarinen L; Palotie A; Kontula K; Salomaa V
    J Intern Med; 2009 Apr; 265(4):448-58. PubMed ID: 19019189
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A NOS1AP gene variant is associated with a paradoxical increase of the QT-interval shortening effect of digoxin.
    Soroush N; Aarnoudse AJ; Kavousi M; Kors JA; Ikram MA; Newton-Cheh C; Ahmadizar F; Stricker BH
    Pharmacogenomics J; 2022 Feb; 22(1):55-61. PubMed ID: 34616002
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Associations between NOS1AP single nucleotide polymorphisms (SNPs) and QT interval duration in four racial/ethnic groups in the Multi-Ethnic Study of Atherosclerosis (MESA).
    Shah SA; Herrington DM; Howard TD; Divers J; Arnett DK; Burke GL; Kao WH; Guo X; Siscovick DS; Chakravarti A; Lima JA; Psaty BM; Tomaselli GF; Rich SS; Bowden DW; Post W
    Ann Noninvasive Electrocardiol; 2013 Jan; 18(1):29-40. PubMed ID: 23347024
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population.
    Arking DE; Khera A; Xing C; Kao WH; Post W; Boerwinkle E; Chakravarti A
    PLoS One; 2009; 4(1):e4333. PubMed ID: 19180230
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Effect of Sex and Underlying Disease on the Genetic Association of QT Interval and Sudden Cardiac Death.
    Mitchell RN; Ashar FN; Jarvelin MR; Froguel P; Sotoodehnia N; Brody JA; Sebert S; Huikuri H; Rioux J; Goyette P; Newcomb CE; Junttila MJ; Arking DE
    J Am Heart Assoc; 2019 Dec; 8(23):e013751. PubMed ID: 31747862
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish.
    Post W; Shen H; Damcott C; Arking DE; Kao WH; Sack PA; Ryan KA; Chakravarti A; Mitchell BD; Shuldiner AR
    Hum Hered; 2007; 64(4):214-9. PubMed ID: 17565224
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia.
    Jamshidi Y; Nolte IM; Dalageorgou C; Zheng D; Johnson T; Bastiaenen R; Ruddy S; Talbott D; Norris KJ; Snieder H; George AL; Marshall V; Shakir S; Kannankeril PJ; Munroe PB; Camm AJ; Jeffery S; Roden DM; Behr ER
    J Am Coll Cardiol; 2012 Aug; 60(9):841-50. PubMed ID: 22682551
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.
    Marroni F; Pfeufer A; Aulchenko YS; Franklin CS; Isaacs A; Pichler I; Wild SH; Oostra BA; Wright AF; Campbell H; Witteman JC; Kääb S; Hicks AA; Gyllensten U; Rudan I; Meitinger T; Pattaro C; van Duijn CM; Wilson JF; Pramstaller PP;
    Circ Cardiovasc Genet; 2009 Aug; 2(4):322-8. PubMed ID: 20031603
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.