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 *

231 related articles for article (PubMed ID: 32490690)

  • 1. Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry.
    Jimmy Juang JM; Liu YB; Julius Chen CY; Yu QY; Chattopadhyay A; Lin LY; Chen WJ; Yu CC; Huang HC; Ho LT; Lai LP; Hwang JJ; Lin TT; Liao MT; Chen JJ; Sherri Yeh SF; Chuang JY; Yang DH; Lin JL; Lu TP; Chuang EY; Ackerman MJ
    Circ Genom Precis Med; 2020 Aug; 13(4):e002797. PubMed ID: 32490690
    [TBL] [Abstract][Full Text] [Related]  

  • 2.
    Wijeyeratne YD; Tanck MW; Mizusawa Y; Batchvarov V; Barc J; Crotti L; Bos JM; Tester DJ; Muir A; Veltmann C; Ohno S; Page SP; Galvin J; Tadros R; Muggenthaler M; Raju H; Denjoy I; Schott JJ; Gourraud JB; Skoric-Milosavljevic D; Nannenberg EA; Redon R; Papadakis M; Kyndt F; Dagradi F; Castelletti S; Torchio M; Meitinger T; Lichtner P; Ishikawa T; Wilde AAM; Takahashi K; Sharma S; Roden DM; Borggrefe MM; McKeown PP; Shimizu W; Horie M; Makita N; Aiba T; Ackerman MJ; Schwartz PJ; Probst V; Bezzina CR; Behr ER
    Circ Genom Precis Med; 2020 Dec; 13(6):e002911. PubMed ID: 33164571
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan.
    Juang JM; Tsai CT; Lin LY; Liu YB; Yu CC; Hwang JJ; Chen JJ; Chiu FC; Chen WJ; Tseng CD; Chiang FT; Yeh HM; Sherri Yeh SF; Lai LP; Lin JL
    J Formos Med Assoc; 2015 Jul; 114(7):620-6. PubMed ID: 26154754
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype-Phenotype Correlation of
    Milman A; Behr ER; Gray B; Johnson DC; Andorin A; Hochstadt A; Gourraud JB; Maeda S; Takahashi Y; Jm Juang J; Kim SH; Kamakura T; Aiba T; Postema PG; Mizusawa Y; Denjoy I; Giustetto C; Conte G; Huang Z; Sarquella-Brugada G; Mazzanti A; Jespersen CH; Arbelo E; Brugada R; Calo L; Corrado D; Casado-Arroyo R; Allocca G; Takagi M; Delise P; Brugada J; Tfelt-Hansen J; Priori SG; Veltmann C; Yan GX; Brugada P; Gaita F; Leenhardt A; Wilde AAM; Kusano KF; Nam GB; Hirao K; Probst V; Belhassen B
    Circ Genom Precis Med; 2021 Oct; 14(5):e003222. PubMed ID: 34461752
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand.
    Makarawate P; Glinge C; Khongphatthanayothin A; Walsh R; Mauleekoonphairoj J; Amnueypol M; Prechawat S; Wongcharoen W; Krittayaphong R; Anannab A; Lichtner P; Meitinger T; Tjong FVY; Lieve KVV; Amin AS; Sahasatas D; Ngarmukos T; Wichadakul D; Payungporn S; Sutjaporn B; Wandee P; Poovorawan Y; Tfelt-Hansen J; Tanck MWT; Tadros R; Wilde AAM; Bezzina CR; Veerakul G; Nademanee K
    Heart Rhythm; 2020 Dec; 17(12):2145-2153. PubMed ID: 32619740
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
    Bezzina CR; Barc J; Mizusawa Y; Remme CA; Gourraud JB; Simonet F; Verkerk AO; Schwartz PJ; Crotti L; Dagradi F; Guicheney P; Fressart V; Leenhardt A; Antzelevitch C; Bartkowiak S; Borggrefe M; Schimpf R; Schulze-Bahr E; Zumhagen S; Behr ER; Bastiaenen R; Tfelt-Hansen J; Olesen MS; Kääb S; Beckmann BM; Weeke P; Watanabe H; Endo N; Minamino T; Horie M; Ohno S; Hasegawa K; Makita N; Nogami A; Shimizu W; Aiba T; Froguel P; Balkau B; Lantieri O; Torchio M; Wiese C; Weber D; Wolswinkel R; Coronel R; Boukens BJ; Bézieau S; Charpentier E; Chatel S; Despres A; Gros F; Kyndt F; Lecointe S; Lindenbaum P; Portero V; Violleau J; Gessler M; Tan HL; Roden DM; Christoffels VM; Le Marec H; Wilde AA; Probst V; Schott JJ; Dina C; Redon R
    Nat Genet; 2013 Sep; 45(9):1044-9. PubMed ID: 23872634
    [TBL] [Abstract][Full Text] [Related]  

  • 7. SCN5A mutation status increases the risk of major arrhythmic events in Asian populations with Brugada syndrome: systematic review and meta-analysis.
    Rattanawong P; Chenbhanich J; Mekraksakit P; Vutthikraivit W; Chongsathidkiet P; Limpruttidham N; Prasitlumkum N; Chung EH
    Ann Noninvasive Electrocardiol; 2019 Jan; 24(1):e12589. PubMed ID: 30126015
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Brugada syndrome: clinical presentation and genotype-correlation with magnetic resonance imaging parameters.
    Rudic B; Schimpf R; Veltmann C; Doesch C; Tülümen E; Schoenberg SO; Borggrefe M; Papavassiliu T
    Europace; 2016 Sep; 18(9):1411-9. PubMed ID: 26511399
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Common Variant Near HEY2 Has a Protective Effect on Ventricular Fibrillation Occurrence in Brugada Syndrome by Regulating the Repolarization Current.
    Nakano Y; Ochi H; Onohara Y; Toshishige M; Tokuyama T; Matsumura H; Kawazoe H; Tomomori S; Sairaku A; Watanabe Y; Ikenaga H; Motoda C; Suenari K; Hayashida Y; Miki D; Oda N; Kishimoto S; Oda N; Yoshida Y; Tashiro S; Chayama K; Kihara Y
    Circ Arrhythm Electrophysiol; 2016 Jan; 9(1):e003436. PubMed ID: 26729854
    [TBL] [Abstract][Full Text] [Related]  

  • 10. SCN5A gene variants and arrhythmic risk in Brugada syndrome: An updated systematic review and meta-analysis.
    Doundoulakis I; Pannone L; Chiotis S; Della Rocca DG; Sorgente A; Tsioufis P; Del Monte A; Vetta G; Piperis C; Overeinder I; Bala G; Almorad A; Ströker E; Sieira J; La Meir M; Brugada P; Tsiachris D; Sarkozy A; Chierchia GB; de Asmundis C
    Heart Rhythm; 2024 Oct; 21(10):1987-1997. PubMed ID: 38614189
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry.
    Chen CJ; Juang JJ; Lin LY; Liu YB; Ho LT; Yu CC; Huang HC; Lin TT; Liao MC; Chen JJ; Hwang JJ; Chen WJ; Yeh SS; Yang DH; Chiang FT; Lin JL; Lai LP; Horie M;
    QJM; 2019 May; 112(5):343-350. PubMed ID: 30690642
    [TBL] [Abstract][Full Text] [Related]  

  • 12. GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death.
    Juang JJ; Binda A; Lee SJ; Hwang JJ; Chen WJ; Liu YB; Lin LY; Yu CC; Ho LT; Huang HC; Chen CJ; Lu TP; Lai LC; Yeh SS; Lai LP; Chuang EY; Rivolta I; Antzelevitch C
    EBioMedicine; 2020 Jul; 57():102843. PubMed ID: 32645615
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
    Barc J; Tadros R; Glinge C; Chiang DY; Jouni M; Simonet F; Jurgens SJ; Baudic M; Nicastro M; Potet F; Offerhaus JA; Walsh R; Choi SH; Verkerk AO; Mizusawa Y; Anys S; Minois D; Arnaud M; Duchateau J; Wijeyeratne YD; Muir A; Papadakis M; Castelletti S; Torchio M; Ortuño CG; Lacunza J; Giachino DF; Cerrato N; Martins RP; Campuzano O; Van Dooren S; Thollet A; Kyndt F; Mazzanti A; Clémenty N; Bisson A; Corveleyn A; Stallmeyer B; Dittmann S; Saenen J; Noël A; Honarbakhsh S; Rudic B; Marzak H; Rowe MK; Federspiel C; Le Page S; Placide L; Milhem A; Barajas-Martinez H; Beckmann BM; Krapels IP; Steinfurt J; Winkel BG; Jabbari R; Shoemaker MB; Boukens BJ; Škorić-Milosavljević D; Bikker H; Manevy F; Lichtner P; Ribasés M; Meitinger T; Müller-Nurasyid M; ; Veldink JH; van den Berg LH; Van Damme P; Cusi D; Lanzani C; Rigade S; Charpentier E; Baron E; Bonnaud S; Lecointe S; Donnart A; Le Marec H; Chatel S; Karakachoff M; Bézieau S; London B; Tfelt-Hansen J; Roden D; Odening KE; Cerrone M; Chinitz LA; Volders PG; van de Berg MP; Laurent G; Faivre L; Antzelevitch C; Kääb S; Arnaout AA; Dupuis JM; Pasquie JL; Billon O; Roberts JD; Jesel L; Borggrefe M; Lambiase PD; Mansourati J; Loeys B; Leenhardt A; Guicheney P; Maury P; Schulze-Bahr E; Robyns T; Breckpot J; Babuty D; Priori SG; Napolitano C; ; de Asmundis C; Brugada P; Brugada R; Arbelo E; Brugada J; Mabo P; Behar N; Giustetto C; Molina MS; Gimeno JR; Hasdemir C; Schwartz PJ; Crotti L; McKeown PP; Sharma S; Behr ER; Haissaguerre M; Sacher F; Rooryck C; Tan HL; Remme CA; Postema PG; Delmar M; Ellinor PT; Lubitz SA; Gourraud JB; Tanck MW; George AL; MacRae CA; Burridge PW; Dina C; Probst V; Wilde AA; Schott JJ; Redon R; Bezzina CR
    Nat Genet; 2022 Mar; 54(3):232-239. PubMed ID: 35210625
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel microsatellite polymorphism of sodium channel beta1-subunit gene (SCN1B) may underlie abnormal cardiac excitation manifested by coved-type ST-elevation compatible with Brugada syndrome in Japanese.
    Ogawa R; Kishi R; Takagi A; Sakaue I; Takahashi H; Matsumoto N; Masuhara K; Nakazawa K; Kobayashi S; Miyake F; Echizen H
    Int J Clin Pharmacol Ther; 2010 Feb; 48(2):109-19. PubMed ID: 20137763
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Nonmodifiable Risk Factors Predict Outcomes in Brugada Syndrome.
    Kukavica D; Trancuccio A; Mazzanti A; Napolitano C; Morini M; Pili G; Memmi M; Gambelli P; Bloise R; Nastoli J; Colombi B; Guarracino A; Marino M; Ceriotti C; Galimberti P; Ottaviano L; Mantica M; Priori SG
    J Am Coll Cardiol; 2024 Nov; 84(21):2087-2098. PubMed ID: 39387761
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype-Phenotype Correlation of
    Yamagata K; Horie M; Aiba T; Ogawa S; Aizawa Y; Ohe T; Yamagishi M; Makita N; Sakurada H; Tanaka T; Shimizu A; Hagiwara N; Kishi R; Nakano Y; Takagi M; Makiyama T; Ohno S; Fukuda K; Watanabe H; Morita H; Hayashi K; Kusano K; Kamakura S; Yasuda S; Ogawa H; Miyamoto Y; Kapplinger JD; Ackerman MJ; Shimizu W
    Circulation; 2017 Jun; 135(23):2255-2270. PubMed ID: 28341781
    [TBL] [Abstract][Full Text] [Related]  

  • 17.
    Makarawate P; Chaosuwannakit N; Vannaprasaht S; Sahasthas D; Koo SH; Lee EJD; Tassaneeyakul W; Barajas-Martinez H; Hu D; Sawanyawisuth K
    J Am Heart Assoc; 2017 Jun; 6(6):. PubMed ID: 28584071
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Brugada syndrome risk loci seem protective against atrial fibrillation.
    Andreasen L; Nielsen JB; Darkner S; Christophersen IE; Jabbari J; Refsgaard L; Thiis JJ; Sajadieh A; Tveit A; Haunsø S; Svendsen JH; Schmitt N; Olesen MS
    Eur J Hum Genet; 2014 Dec; 22(12):1357-61. PubMed ID: 24667784
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation.
    Pambrun T; Mercier A; Chatelier A; Patri S; Schott JJ; Le Scouarnec S; Chahine M; Degand B; Bois P
    Heart Rhythm; 2014 Aug; 11(8):1393-400. PubMed ID: 24768612
    [TBL] [Abstract][Full Text] [Related]  

  • 20. H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promoters.
    Matsumura H; Nakano Y; Ochi H; Onohara Y; Sairaku A; Tokuyama T; Tomomori S; Motoda C; Amioka M; Hironobe N; Toshishige M; Takahashi S; Imai K; Sueda T; Chayama K; Kihara Y
    J Biomed Sci; 2017 Dec; 24(1):91. PubMed ID: 29202755
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.