Publications

Publicly attributable research for Babken Asatryan. Attribution is conservative and still being expanded.

2020
An Evidence-based Assessment of Genes in Dilated Cardiomyopathy
2020
Identifying coronary artery disease patients at risk for sudden and/or arrhythmic death: remaining limitations of the electrocardiogram
2020
Enhancing Risk Stratification for Life-Threatening Ventricular Arrhythmias in Dilated Cardiomyopathy: The Peril and Promise of Precision Medicine
2020
Automated electrocardiographic quantification of myocardial scar in patients undergoing primary prevention implantable cardioverter-defibrillator implantation: Association with mortality and subsequent appropriate and inappropriate therapies
2020
Man vs machine: Performance of manual vs automated electrocardiogram analysis for predicting the chamber of origin of idiopathic ventricular arrhythmia
2020
The Ever-Expanding Landscape of Cardiomyopathies
2020
State of the Art Review on Genetics and Precision Medicine in Arrhythmogenic Cardiomyopathy
2020
Welche Bedeutung hat die Genetik in der Rhythmologie?
2019
Emerging Implications of Genetic Testing in Inherited Primary Arrhythmia Syndromes
first authorRCR 0.4611 citesPMID 29528859
2019
Revisiting the Approach to Diagnosis of Arrhythmogenic Cardiomyopathy: Stick to the Arrhythmia Criterion!
RCR 0.082 citesPMID 31542941
2019
Morphological and immunohystochemical characteristics of aspirated thrombi in patients with ST-elevation myocardial infarction,Морфологическая и иммуногистохимическая характеристика аспирированных из сосудов тромбов у больных инфарктом миокарда с подъемом ST сегмента
2019
Cardiac Sodium Channel Dysfunction and Dilated Cardiomyopathy: A Contemporary Reappraisal of Pathophysiological Concepts
2019
Electrocardiographic Diagnosis of Life-Threatening STEMI Equivalents
2019
Molecular and genetic insights into progressive cardiac conduction disease
2019
Usefulness of Genetic Testing in Sudden Cardiac Arrest Survivors With or Without Previous Clinical Evidence of Heart Disease
2018
Phenotypic Spectrum of HCN4 Mutations: A Clinical Case.
RCR 0.8421 citesPMID 29440115
2018
Recommendations for genetic testing and counselling after sudden cardiac death: practical aspects for Swiss practice.
RCR 0.6213 citesPMID 30044475
2018
Unexplained cardiac arrest: a tale of conflicting interpretations of KCNQ1 genetic test results.
RCR 0.246 citesPMID 29582136
2018
Late-onset severe long QT syndrome
first authorRCR 0.113 citesPMID 29194874
2018
Unexplained Cardiac Arrest in an Apparently Healthy Young Woman: What Is the Underlying Substrate of the Arrhythmia?
RCR 0.081 citesPMID 29685934

Compiled from PubMed, OpenAlex, and ORCID with field-normalized impact from NIH iCite RCR.