These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 35389749)

  • 1. Monogenic and Polygenic Contributions to QTc Prolongation in the Population.
    Nauffal V; Morrill VN; Jurgens SJ; Choi SH; Hall AW; Weng LC; Halford JL; Austin-Tse C; Haggerty CM; Harris SL; Wong EK; Alonso A; Arking DE; Benjamin EJ; Boerwinkle E; Min YI; Correa A; Fornwalt BK; Heckbert SR; ; Kooperberg C; Lin HJ; J F Loos R; Rice KM; Gupta N; Blackwell TW; Mitchell BD; Morrison AC; Psaty BM; Post WS; Redline S; Rehm HL; Rich SS; Rotter JI; Soliman EZ; Sotoodehnia N; Lunetta KL; Ellinor PT; Lubitz SA;
    Circulation; 2022 May; 145(20):1524-1533. PubMed ID: 35389749
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Corrected QT Interval-Polygenic Risk Score and Its Contribution to Type 1, Type 2, and Type 3 Long-QT Syndrome in Probands and Genotype-Positive Family Members.
    Turkowski KL; Dotzler SM; Tester DJ; Giudicessi JR; Bos JM; Speziale AD; Vollenweider JM; Ackerman MJ
    Circ Genom Precis Med; 2020 Aug; 13(4):e002922. PubMed ID: 32469608
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.
    Choi SH; Jurgens SJ; Haggerty CM; Hall AW; Halford JL; Morrill VN; Weng LC; Lagerman B; Mirshahi T; Pettinger M; Guo X; Lin HJ; Alonso A; Soliman EZ; Kornej J; Lin H; Moscati A; Nadkarni GN; Brody JA; Wiggins KL; Cade BE; Lee J; Austin-Tse C; Blackwell T; Chaffin MD; Lee CJ; Rehm HL; Roselli C; ; Redline S; Mitchell BD; Sotoodehnia N; Psaty BM; Heckbert SR; Loos RJF; Vasan RS; Benjamin EJ; Correa A; Boerwinkle E; Arking DE; Rotter JI; Rich SS; Whitsel EA; Perez M; Kooperberg C; Fornwalt BK; Lunetta KL; Ellinor PT; Lubitz SA;
    Circ Genom Precis Med; 2021 Aug; 14(4):e003300. PubMed ID: 34319147
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland.
    Sveinbjornsson G; Benediktsdottir BD; Sigfusson G; Norland K; Davidsson OB; Thorolfsdottir RB; Tragante V; Arnadottir GA; Jensson BO; Katrinardottir H; Fridriksdottir R; Gudmundsdottir H; Aegisdottir HM; Fridriksson B; Thorgeirsson G; Magnusson V; Oddsson A; Sulem P; Gudbjartsson DF; Holm H; Arnar DO; Stefansson K
    J Am Heart Assoc; 2023 Jul; 12(14):e029845. PubMed ID: 37449562
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval.
    Ghouse J; Have CT; Weeke P; Bille Nielsen J; Ahlberg G; Balslev-Harder M; Appel EV; Skaaby T; Olesen SP; Grarup N; Linneberg A; Pedersen O; Haunsø S; Hastrup Svendsen J; Hansen T; Kanters JK; Salling Olesen M
    Eur Heart J; 2015 Oct; 36(37):2523-9. PubMed ID: 26159999
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Long QT syndrome type 5-Lite: Defining the clinical phenotype associated with the potentially proarrhythmic p.Asp85Asn-KCNE1 common genetic variant.
    Lane CM; Giudicessi JR; Ye D; Tester DJ; Rohatgi RK; Bos JM; Ackerman MJ
    Heart Rhythm; 2018 Aug; 15(8):1223-1230. PubMed ID: 29625280
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic QT Score and Sleep Apnea as Predictors of Sudden Cardiac Death in the UK Biobank.
    Arora A; Zareba W; Woosley RL; Klimentidis YC; Patel IY; Quan SF; Wendel C; Shamoun F; Guerra S; Parthasarathy S; Patel SI
    medRxiv; 2023 Nov; ():. PubMed ID: 37986981
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Antipsychotics in routine treatment are minor contributors to QT prolongation compared to genetics and age.
    Hommers L; Scherf-Clavel M; Stempel R; Roth J; Falter M; Deckert J; Mattheisen M; Unterecker S; Gawlik M
    J Psychopharmacol; 2021 Sep; 35(9):1127-1133. PubMed ID: 33779379
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 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. The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome.
    Vincent GM; Timothy KW; Leppert M; Keating M
    N Engl J Med; 1992 Sep; 327(12):846-52. PubMed ID: 1508244
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A.
    Seo SH; Kim SY; Cho SI; Park H; Lee S; Choi JM; Kim MJ; Lee JS; Ahn KJ; Song MK; Bae EJ; Park SS; Seong MW
    Ann Lab Med; 2018 Jan; 38(1):54-58. PubMed ID: 29071820
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-Wide Polygenic Score Predicts Large Number of High Risk Individuals in Monogenic Undiagnosed Young Onset Parkinson's Disease Patients from India.
    Kukkle PL; Geetha TS; Chaudhary R; Sathirapongsasuti JF; Goyal V; Kandadai RM; Kumar H; Borgohain R; Mukherjee A; Oliver M; Sunil M; Mootor MFE; Kapil S; Mandloi N; Wadia PM; Yadav R; Desai S; Kumar N; Biswas A; Pal PK; Muthane UB; Das SK; Sakthivel Murugan SM; Peterson AS; Stawiski EW; Seshagiri S; Gupta R; Ramprasad VL; Prai PRAOI
    Adv Biol (Weinh); 2022 Nov; 6(11):e2101326. PubMed ID: 35810474
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes.
    Huerta-Chagoya A; Schroeder P; Mandla R; Deutsch AJ; Zhu W; Petty L; Yi X; Cole JB; Udler MS; Dornbos P; Porneala B; DiCorpo D; Liu CT; Li JH; Szczerbiński L; Kaur V; Kim J; Lu Y; Martin A; Eizirik DL; Marchetti P; Marselli L; Chen L; Srinivasan S; Todd J; Flannick J; Gubitosi-Klug R; Levitsky L; Shah R; Kelsey M; Burke B; Dabelea DM; Divers J; Marcovina S; Stalbow L; Loos RJF; Darst BF; Kooperberg C; Raffield LM; Haiman C; Sun Q; McCormick JB; Fisher-Hoch SP; Ordoñez ML; Meigs J; Baier LJ; González-Villalpando C; González-Villalpando ME; Orozco L; García-García L; Moreno-Estrada A; ; Aguilar-Salinas CA; Tusié T; Dupuis J; Ng MCY; Manning A; Highland HM; Cnop M; Hanson R; Below J; Florez JC; Leong A; Mercader JM
    Diabetologia; 2023 Jul; 66(7):1273-1288. PubMed ID: 37148359
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Determinants of prolonged QT interval and their contribution to sudden death risk in coronary artery disease: the Oregon Sudden Unexpected Death Study.
    Chugh SS; Reinier K; Singh T; Uy-Evanado A; Socoteanu C; Peters D; Mariani R; Gunson K; Jui J
    Circulation; 2009 Feb; 119(5):663-70. PubMed ID: 19171855
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results From a National Biobank.
    Choi SH; Jurgens SJ; Weng LC; Pirruccello JP; Roselli C; Chaffin M; Lee CJ; Hall AW; Khera AV; Lunetta KL; Lubitz SA; Ellinor PT
    Circ Res; 2020 Jan; 126(2):200-209. PubMed ID: 31691645
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Incidence, Diagnosis, and Management of QT Prolongation Induced by Cancer Therapies: A Systematic Review.
    Porta-Sánchez A; Gilbert C; Spears D; Amir E; Chan J; Nanthakumar K; Thavendiranathan P
    J Am Heart Assoc; 2017 Dec; 6(12):. PubMed ID: 29217664
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Validation of Polygenic Scores for QT Interval in Clinical Populations.
    Rosenberg MA; Lubitz SA; Lin H; Kosova G; Castro VM; Huang P; Ellinor PT; Perlis RH; Newton-Cheh C
    Circ Cardiovasc Genet; 2017 Oct; 10(5):. PubMed ID: 28986454
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.