Expert in Cardiogenetics & Precision Medicine

Advancing personalized care and innovative research for patients with inherited heart diseases.

Clinical Excellence

Managed over 5,000 patient cases in the fields of cardiogenetics and oncogenetics

Affiliated Institutions and Collaborations

Assistance Publique - Hôpitaux de Paris Sapienza Università di Roma Université Paris Cité Università degli Studi di Perugia Harvard Medical School Qatar University

About Dr. Mohamed El Hachmi

Dr. Mohamed El Hachmi is a Cardiogeneticist specializing in Precision Medicine, with dual PhDs from Sapienza University of Rome and Paris Cité University. His research focuses on rare inherited heart diseases, with particular expertise in Hypertrophic Cardiomyopathy (HCM), Vascular Ehlers-Danlos Syndrome (vEDS), and Cardiac Amyloidosis (ATTR).

Dual PhD

Sapienza University of Rome & Paris Cité University

Executive Board Member

European Board of Medical Genetics (EBMG)

Former Cardiogeneticist

Hôpital Européen Georges Pompidou, Paris

Research Focus Areas

Hypertrophic Cardiomyopathy

HCM

Leading the GEREMY Registry for genetic profiling and precision treatment eligibility in HCM patients. Developing risk stratification models based on genetic variants.

For Patients

HCM causes the heart muscle to thicken, making it harder to pump blood. We're studying genetic factors to improve treatment options and predict who may develop symptoms.

Vascular Ehlers-Danlos Syndrome

vEDS

Principal investigator for the ARCADE trial, demonstrating efficacy of combination therapy with irbesartan and celiprolol in reducing major vascular events by over 50%.

For Patients

vEDS is a rare genetic disorder affecting collagen that can lead to fragile blood vessels. Our research is testing medications that may help strengthen blood vessels.

Cardiac Amyloidosis

ATTR

Researching TTR genetic mutations and their role in amyloid deposition in the heart. Developing novel diagnostic approaches for earlier detection.

For Patients

In cardiac amyloidosis, abnormal proteins build up in the heart. We're working on better ways to diagnose this condition earlier and develop targeted treatments.

Latest Publications

2025

Irbesartan and celiprolol combination therapy for vascular Ehlers-Danlos syndrome

Circulation

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2024

French Hypertrophic Cardiomyopathy Genetic Registry: 5-year outcomes and risk stratification

International Journal of Cardiology

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2024

Genetic Testing Score for Arrhythmogenic Left Ventricular Cardiomyopathy

Circulation: Genomic and Precision Medicine

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Seeking Collaborative Research Opportunities

Dr. El Hachmi is actively looking for research partners in multicenter studies, cohort data sharing, and genetic screening programs for inherited cardiac disorders.