High frequency of long qt syndrome-associated genetic variants in patients with early-onset lone atrial fibrillation

被引：0
|
作者：
Nielsen, J. B. [1 ]
Refsgaard, L. [1 ]
Jabbari, J. [1 ]
Holst, A. G. [1 ]
Haunso, S. [1 ]
Svendsen, J. H. [1 ]
Olesen, M. S. [1 ]
机构：
[1] Copenhagen Univ Hosp, Ctr Heart, Dept Cardiol, Rigshosp, Copenhagen, Denmark
来源：
EUROPEAN HEART JOURNAL | 2013年 / 34卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：422 / 422
页数：1
相关论文
共 50 条
  • [41] Common Polymorphisms in KCNJ5 Are Associated with Early-Onset Lone Atrial Fibrillation in Caucasians (vol 118, pg 116, 2011)
    Jabbari, J.
    CARDIOLOGY, 2011, 119 (03) : 186 - 186
  • [42] Frequency of genetic variants in a population with early-onset obesity: a single center experience
    Umano, Giuseppina Rosaria
    Rondinelli, Giulia
    Di Sessa, Anna
    Cirillo, Grazia
    del Giudice, Emanuele Miraglia
    HORMONE RESEARCH IN PAEDIATRICS, 2024, 97 : 106 - 106
  • [43] Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation
    Ahlberg, Gustav
    Refsgaard, Lena
    Lundegaard, Pia R.
    Andreasen, Laura
    Ranthe, Mattis F.
    Linscheid, Nora
    Nielsen, Jonas B.
    Melbye, Mads
    Haunso, Stig
    Sajadieh, Ahmad
    Camp, Lu
    Olesen, Soren-Peter
    Rasmussen, Simon
    Lundby, Alicia
    Ellinor, Patrick T.
    Holst, Anders G.
    Svendsen, Jesper H.
    Olesen, Morten S.
    NATURE COMMUNICATIONS, 2018, 9
  • [44] Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation
    Gustav Ahlberg
    Lena Refsgaard
    Pia R. Lundegaard
    Laura Andreasen
    Mattis F. Ranthe
    Nora Linscheid
    Jonas B. Nielsen
    Mads Melbye
    Stig Haunsø
    Ahmad Sajadieh
    Lu Camp
    Søren-Peter Olesen
    Simon Rasmussen
    Alicia Lundby
    Patrick T. Ellinor
    Anders G. Holst
    Jesper H. Svendsen
    Morten S. Olesen
    Nature Communications, 9
  • [45] In search of the holy grail in the channelopathy field: Proving pathogenicity of long QT syndrome-associated variants?
    Wilde, Arthur A. M.
    Semsarian, Christopher
    HEART RHYTHM, 2017, 14 (08) : 1180 - 1181
  • [46] Frequency of Bardet-Biedl syndrome variants in a population with early-onset obesity
    Argente, Jesus
    Umano, Giuseppina Rosaria
    Yildiz, Melek
    Carmon, Lior
    Sleiman, Patrick
    Savoie, Charles
    Le Roux, Carel
    Goldstone, Anthony
    HORMONE RESEARCH IN PAEDIATRICS, 2024, 97 : 52 - 53
  • [47] A Genetic Basis Responsible for the Patients with Short-QT Syndrome and Atrial Fibrillation
    Hong, Kui
    CIRCULATION, 2010, 122 (02) : E120 - E120
  • [48] Unstable glycaemia in rare, early-onset Shwachman-Diamond syndrome-associated diabetes mellitus
    Navasardyan, Lusine
    Furlan, Ingrid
    Brandt, Stephanie
    Schulz, Ansgar
    Wabitsch, Martin
    Denzer, Christian
    HORMONE RESEARCH IN PAEDIATRICS, 2022, 95 (SUPPL 2): : 202 - 203
  • [49] A Spectrum of Functional Phenotypes Associated with LQT1 Mutations Identified in Patients with Early-Onset Atrial Fibrillation
    Bartos, Daniel C.
    Schmidt, Eric S.
    Burgess, Don E.
    Delisle, Brian P.
    BIOPHYSICAL JOURNAL, 2011, 100 (03) : 427 - 427
  • [50] A polymorphism associated with increased levels of YKL-40 and the risk of early onset of lone atrial fibrillation
    Henningsen, Kristoffer
    Olesen, Morten
    Sajadieh, Golnaz
    Haunsoe, Stig
    Svendsen, Jesper
    JOURNAL OF NEGATIVE RESULTS IN BIOMEDICINE, 2013, 12
12345