Stéphanie Forté: Gene Therapy in Sickle Cell Disease from Molecular Advances to Clinical Care
Stéphanie Forté, Principal Researcher at the Innovation Hub at the CHUM Research Center (CRCHUM), shared a post on LinkedIn about a recent article she and her colleagues co-authored, adding:
“Very excited to share our new review on gene therapies in sickle cell disease, published in Cells:
The Journey of Gene Therapy in Sickle Cell Disease: How Molecular Advances Meet Clinical Care
Advances in gene therapy are ushering in a new era of hope for people living with sickle cell disease.
Our hope now is that these innovations become more equitably accessible worldwide.
The RED Network (Erythrocytes and Sickle Cell Network) continues to pursue this goal by strengthening international collaborations, patient registries, andclinical research in order to accelerate meaningful global progress for patients.”
Title: The Journey of Gene Therapy in Sickle Cell Disease: How Molecular Advances Meet Clinical Care
Authors: Magalie Tardif, Manon Saby, Stéphanie Forté, Thomas Pincez
Stay updated on all scientific advances with Hemostasis Today.
-
Aug 21, 2026, 14:32Kenneth Nollet: Building the Future of Transfusion Laboratory Science
-
Aug 21, 2026, 14:14Tareq Abadl: A Positive Antibody Screen is Not The Diagnosis
-
Aug 21, 2026, 14:08Katrina Snow։ Transfusion Trends and Quality Improvement in Sickle Cell Disease
-
Aug 21, 2026, 14:00Rucha Patil: The Power of Point-of-Care Testing in Hemostasis
-
Aug 21, 2026, 13:56Sarah Kowalski։ Supporting the Next Generation of Transfusion Laboratory Scientists
-
Aug 21, 2026, 13:51Join EHC 2026 Annual Conference
-
Aug 21, 2026, 12:57David McIntosh: Why Do Blood Supplies Still Fall Short?
-
Aug 21, 2026, 12:48Joshua Penrod: 35 Years of Progress in Plasma Safety
-
Aug 21, 2026, 12:42Moustafa Abdou: Diagnosis and Management of Pyruvate Kinase Deficiency