CarolynYungHoMD
Cardiology • Boston, MAEchocardiography, Cardiovascular Disease Genetics
Associate Professor of Medicine, Brigham and Women's Hospital
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Office
75 Francis St
Pbb 3
Boston, MA 02115Phone+1 617-732-7317
Education & Training
Brigham and Women's HospitalFellowship, Cardiovascular Disease, 1998 - 2001
Harvard Medical SchoolClass of 1995
Certifications & Licensure
MA State Medical License 2000 - 2026- American Board of Internal Medicine Cardiovascular Disease
Clinical Trials
- Treatment of Preclinical Hypertrophic Cardiomyopathy With Diltiazem Start of enrollment: 2006 Jan 01
- Valsartan for Attenuating Disease Evolution In Early Sarcomeric HCM Start of enrollment: 2014 Mar 01
- HCMR - Novel Markers of Prognosis in Hypertrophic Cardiomyopathy Start of enrollment: 2014 Apr 01
Publications & Presentations
PubMed
- 32 citationsLeft Atrial structure and function in hypertrophic cardiomyopathy sarcomere mutation carriers with and without left ventricular hypertrophyHoshang Farhad, Sara B. Seidelmann, Davis M. Vigneault, Siddique Abbasi, Eunice Yang
Journal of Cardiovascular Magnetic Resonance. 2017-12-28 - 94 citationsGenetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, Daniel P Judge, Paul F Kantor
Genetics in Medicine. 2018-09-01 - 35 citationsCare in Specialized Centers and Data Sharing Increase Agreement in Hypertrophic Cardiomyopathy Genetic Test InterpretationAisha Furqan, Patricia Arscott, Francesca Girolami, Allison L. Cirino, Michelle Michels
Circulation. Cardiovascular Genetics. 2017-10-01
Lectures
- Circulating microRNAs as a Biomarker of Pediatric Hypertrophic Cardiomyopathy2019 ACC Scientific Session & Expo, New Orleans - 3/17/2019
- The Future of HCM: new Diagnostic Tools and New Therapies2019 ACC Scientific Session & Expo, New Orleans - 3/16/2019
- Evaluation of Mavacamten in Symptomatic Patients with Nonobstructive Hypertrophic CardiomyopathyHarvard Medical School ,Department Of Continuing Education, Boston, Massachusetts - 10/13/2012
Authored Content
- Evaluation of Mavacamten in Symptomatic Patients with Nonobstructive Hypertrophic CardiomyopathyJune 2020
- Evaluation of Mavacamten in Symptomatic Patients with Nonobstructive Hypertrophic CardiomyopathyJune 2020
- Evaluation of Mavacamten in Symptomatic Patients with Nonobstructive Hypertrophic CardiomyopathyJune 2020
Press Mentions
Is Heart Disease Genetic?January 15th, 2021
MAVERICK-HCM: Mavacamten Well Tolerated in Patients with Nonobstructive HCMMarch 30th, 2020
MyoKardia Announces Mavacamten Treatment Well Tolerated and Significantly Reduced Biomarkers of Cardiac Injury and Wall Stress in Non-Obstructive Hypertrophic Cardiomyopathy PatientsMarch 30th, 2020- Join now to see all
Grant Support
- Using Genetics For Early Phenotyping &Prevention Of Hypertrophic CardiomyopathyNational Heart, Lung, And Blood Institute2010–2011
- Diagnostic And Treatment Strategies For Preclinical HCMNational Heart, Lung, And Blood Institute2005–2009
- Diastolic Function In Hypertrophic CardiomyopathyNational Heart, Lung, And Blood Institute2002–2003
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