Last Updated: 09/26/2026
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Found 16 publications
A sex-adjusted 7-biomarker clinical aging clock for translational preventative medicine.
Journal: Scientific reports
Published: December 25, 2024
Rare and Common Variants Uncover the Role of the Atria in Coarctation of the Aorta.
Journal: Genes
Published: February 18, 2022
Cardiac MRI e-prime predicts myocardial late gadolinium enhancement and diastolic dysfunction in hypertrophic cardiomyopathy.
Journal: European journal of radiology
Published: December 15, 2021
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.
Journal: HGG advances
Published: December 10, 2021
Hypertrophic Cardiomyopathy: What's a Few Millimeters Among Friends?
Journal: JACC. Asia
Published: September 21, 2021
Marked Up-Regulation of ACE2 in Hearts of Patients With Obstructive Hypertrophic Cardiomyopathy: Implications for SARS-CoV-2-Mediated COVID-19.
Journal: Mayo Clinic proceedings
Published: April 13, 2020
Hypertrophic Cardiomyopathy: An Overview of Genetics and Management.
Journal: Biomolecules
Published: November 12, 2019
Fabry Disease in Families With Hypertrophic Cardiomyopathy: Clinical Manifestations in the Classic and Later-Onset Phenotypes.
Journal: Circulation. Cardiovascular genetics
Published: October 07, 2016
Detection of Cell Proliferation Markers by Immunofluorescence Staining and Microscopy Imaging in Paraffin-Embedded Tissue Sections.
Journal: Current protocols in molecular biology
Published: July 02, 2016
Nationwide study on hypertrophic cardiomyopathy in Iceland: evidence of a MYBPC3 founder mutation.
Journal: Circulation
Published: August 01, 2014
5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy.
Journal: The Journal of clinical investigation
Published: March 25, 2013
Last Updated: 09/26/2026