Assistant Professor of Medicine, Brigham and Women's Hospital
Cardiology
Dr. Carolyn Y. Ho, MD
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Carolyn works in the field of Cardiology. She graduated from Harvard Medical School. Harvard Medical School is a top medical college. Harvard Medical School is ranked 1/12 in Research/PrimaryCare. Dr. Carolyn Y. Ho is a published doctor as well. She has 31 publications published. The latest was: Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity. Dr. Carolyn Y. Ho is registered with Medicare.
Publications
- Results of clinical genetic testing of 2,912 probands with hypertrophic Cardiomyopathy: expanded panels offer limited additional sensitivity.
- Diltiazem Treatment for Pre-Clinical Hypertrophic Cardiomyopathy Sarcomere Mutation Carriers: A Pilot Randomized Trial to Modify Disease Expression.
- Effects of losartan on left ventricular hypertrophy and fibrosis in patients with nonobstructive hypertrophic Cardiomyopathy.
- Multimodality non-invasive imaging of a Coronary cameral fistula.
- Erratum to: Hypertrophic Cardiomyopathy: Preclinical and Early Phenotype.
- Genetic testing for inherited Heart disease.
- T1 measurements identify extracellular volume expansion in hypertrophic Cardiomyopathy sarcomere mutation carriers with and without left ventricular hypertrophy.
- Genetic testing for dilated Cardiomyopathy in clinical practice.
- Electrocardiographic Features of Sarcomere Mutation Carriers With and Without Clinically Overt Hypertrophic Cardiomyopathy.
- New Paradigms in Hypertrophic Cardiomyopathy: Insights from Genetics.
- Genetics and clinical destiny: improving care in hypertrophic Cardiomyopathy.
- Profound left ventricular remodeling associated with LAMP2 Cardiomyopathy.
- Myocardial fibrosis as an early manifestation of hypertrophic Cardiomyopathy.
- Short communication: the cardiac myosin binding protein C Arg502Trp mutation: a common cause of hypertrophic Cardiomyopathy.
- A novel custom resequencing array for dilated Cardiomyopathy.
- Clinical features and outcome of hypertrophic Cardiomyopathy associated with triple sarcomere protein gene mutations.
- Hypertrophic Cardiomyopathy.
- Familial dilated Cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated Cardiomyopathy.
- Hypertrophic Cardiomyopathy: preclinical and early phenotype.
- Echocardiographic strain imaging to assess early and late consequences of sarcomere mutations in hypertrophic Cardiomyopathy.
- Defining the pathogenicity of DNA sequence variation.
- Clinical outcome and phenotypic expression in LAMP2 Cardiomyopathy.
- Hypertrophic Cardiomyopathy without hypertrophy: an emerging pre-clinical subgroup composed of genetically affected family members.
- Handheld echocardiography offers rapid assessment of clinical volume status.
- Heart failure and genomics.
- A contemporary approach to hypertrophic Cardiomyopathy.
- Novel locus for an inherited Cardiomyopathy maps to chromosome 7.
- A clinician's guide to tissue Doppler imaging.
- Gene mutations in apical hypertrophic Cardiomyopathy.
- Assessment of diastolic function with Doppler tissue imaging to predict genotype in preclinical hypertrophic Cardiomyopathy.
Schools
Harvard Medical School
Brigham and Women39s Hospital
Procedures Preformed
- Ablation for Treatment of Cardiac Arrhythmias
- Cardiac Catheterization (incl. Coronary Angiography)
- Cardiac Imaging
- Cardiac MRI (Magnetic Resonance Imaging) of Heart or Chest
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Conditions Treated
- Aneurysm and Dissection of Heart
- Angina and Acute Coronary Syndrome
- Aortic Aneurysm
- Aortic Dissection
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Doctors Specialties
- Cardiology
Accepted Insurances
Education
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Brigham and Women's Hospital -
Harvard Medical School
Hospital
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Brigham and Women's Hospital
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