Olivier Bluteau
Paris, 75013, France
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 26 publications
ZMAT3 alleviates cell death in Fanconi anemia via adaptation of sphingolipid metabolism.
Journal: Science advances
Published: July 31, 2026
ABCG1 orchestrates adipose tissue macrophage plasticity and insulin resistance in obesity by rewiring saturated fatty acid pools.
Journal: Science translational medicine
Published: December 11, 2024
Clinical Expression of Familial Hypercholesterolemia in Patients from France and French Canada Carrying Identical-by-Descent Pathogenic LDLR Gene Variants: A Proof-of-Concept Study.
Journal: Journal of clinical medicine
Published: August 26, 2024
MDM4 overexpression alleviates developmental and hematopoietic defects in Fancg deficient mice.
Journal: Leukemia
Published: July 29, 2024
The singular French PCSK9-p.Ser127Arg gain-of-function variant: A significant player in cholesterol levels from a 775-year-old common ancestor.
Journal: Atherosclerosis
Published: May 22, 2024
Additive Effect of APOE Rare Variants on the Phenotype of Familial Hypercholesterolemia.
Journal: Arteriosclerosis, thrombosis, and vascular biology
Published: May 02, 2023
APOE Molecular Spectrum in a French Cohort with Primary Dyslipidemia.
Journal: International journal of molecular sciences
Published: April 24, 2022
Different impact of calreticulin mutations on human hematopoiesis in myeloproliferative neoplasms.
Journal: Oncogene
Published: December 11, 2019
Germline NPM1 mutations lead to altered rRNA 2'-O-methylation and cause dyskeratosis congenita.
Journal: Nature genetics
Published: January 23, 2019
Rare type 1-like and type 2-like calreticulin mutants induce similar myeloproliferative neoplasms as prevalent type 1 and 2 mutants in mice.
Journal: Oncogene
Published: February 26, 2018
Last Updated: 09/26/2026