Sean J. Jurgens
Amsterdam, NH, Netherlands
Last Updated: 09/26/2026
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Found 84 publications
An Updated Evidence Assessment of the Genetic Causes of Dilated Cardiomyopathy.
Journal: Circulation
Published: September 08, 2026
Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.
Journal: medRxiv : the preprint server for health sciences
Published: July 17, 2026
Integrating multi-ancestry common and rare variant mapping accelerates therapeutic target discovery.
Integrating multi-ancestry common and rare variant mapping accelerates therapeutic target discovery.
Journal: medRxiv : the preprint server for health sciences
Published: July 17, 2026
A Common CD36 Variant and the Genetic Landscape of Dilated Cardiomyopathy in Individuals of African Ancestry.
Journal: medRxiv : the preprint server for health sciences
Published: June 05, 2026
Perspectives on phenotype in genetic testing for early-onset atrial fibrillation.
Journal: European journal of human genetics : EJHG
Published: June 02, 2026
Genetically Mediated Differences in LDL Cholesterol and Risk of Venous Thromboembolism.
Journal: Journal of the American College of Cardiology
Published: April 06, 2026
Patterns and Clinical Outcomes of Physical Activity and Sedentary Behavior Across 20 Million Days of Wearable Monitoring in U.S. Adults.
Journal: medRxiv : the preprint server for health sciences
Published: February 23, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies.
Journal: Research square
Published: February 06, 2026
Atrial Fibrillation and Primary Cilia-Associated Genes: The Role of CEP68.
Journal: International journal of molecular sciences
Published: January 11, 2026
Circulating Proteins Associated With Myocardial Interstitial Fibrosis.
Journal: Journal of the American Heart Association
Published: December 03, 2025
Last Updated: 09/26/2026