C. Scrimali

Diagnosis of familial hypercholesterolemia in a large cohort of Italian genotyped hypercholesterolemic patients.

C. Barbagallo, D. Noto, R. Spina, 2022, Atherosclerosis.

Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred.

C. Barbagallo, D. Noto, R. Monastero, 2017, Journal of clinical lipidology.

rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography.

G. I. Altieri, D. Girelli, O. Olivieri, 2021, Nutrition, metabolism, and cardiovascular diseases : NMCD.

Comparison of two polygenic risk score to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects.

C. Barbagallo, D. Noto, M. L. Simone, 2022, Journal of clinical lipidology.

TGF-β/VEGF-A Genetic Variants Interplay in Genetic Susceptibility to Non-Melanocytic Skin Cancer

D. Lio, G. Accardi, G. Candore, 2022, Genes.

Automated untargeted stable isotope assisted lipidomics of liver cells on high glucose shows alteration of sphingolipid kinetics.

D. Noto, R. Spina, M. Averna, 2020, Biochimica et biophysica acta. Molecular and cell biology of lipids.

PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study.

G. I. Altieri, C. Barbagallo, D. Noto, 2020, Atherosclerosis.

Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing.

G. I. Altieri, C. Barbagallo, D. Noto, 2017, Journal of clinical lipidology.