ESC Guidelines 1363 levels, once the guidelines have been endorsed by the ESC member
societies, and translated into the national language. Implementation programmes are …

Disease-associated genetic variants that lie in non-coding regions found by genome-wide
association studies are thought to alter the functionality of transcription regulatory elements …

Association testing of multiple correlated phenotypes offers better power than univariate
analysis of single traits. We analyzed 6,600 individuals from two population-based cohorts …

Objective: End‐stage coagulation and the structure/function of fibrin are implicated in the
pathogenesis of ischemic stroke. We explored whether genetic variants associated with end …

Stroke has been emerged as one of major health problems for women worldwide.
Increasing of knowledge in this field has provided new data in this area which contribute to …

Objectives: This study sought to identify nonredundant atrial fibrillation (AF) genetic
susceptibility signals and examine their cumulative relations with AF risk. Background: AF …

Atrial fibrillation (AF) and congestive heart failure (CHF) are among the most common
medical conditions and are associated with significant morbidity. These two conditions share …

Atrial fibrillation (AF), the most common sustained cardiac arrhythmia encountered in clinical
practice, is associated with increased morbidity and mortality. Electrophysiologically, it is …

Objectives: This study tested the hypothesis that response to antiarrhythmic drugs (AADs) is
modulated by 3 common loci associated with atrial fibrillation (AF). Background: Recent …

Background: Atrial fibrillation (AF) has a substantial genetic basis. Identification of
individuals at greatest AF risk could minimize the incidence of cardioembolic stroke …