Advancing personalized care and innovative research for patients with inherited heart diseases.
Managed over 5,000 patient cases in the fields of cardiogenetics and oncogenetics
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).
Sapienza University of Rome & Paris Cité University
European Board of Medical Genetics (EBMG)
Hôpital Européen Georges Pompidou, Paris
Leading the GEREMY Registry for genetic profiling and precision treatment eligibility in HCM patients. Developing risk stratification models based on genetic variants.
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.
Principal investigator for the ARCADE trial, demonstrating efficacy of combination therapy with irbesartan and celiprolol in reducing major vascular events by over 50%.
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.
Researching TTR genetic mutations and their role in amyloid deposition in the heart. Developing novel diagnostic approaches for earlier detection.
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.
Circulation
Read more →International Journal of Cardiology
Read more →Circulation: Genomic and Precision Medicine
Read more →Dr. El Hachmi is actively looking for research partners in multicenter studies, cohort data sharing, and genetic screening programs for inherited cardiac disorders.