Petra El Khoury

Paris, France

Last Updated: 09/26/2026

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Found 21 publications

PCSK9 expression in human atherosclerotic lesions and vascular smooth muscle cells.

PCSK9 expression in human atherosclerotic lesions and vascular smooth muscle cells.

Journal: Atherosclerosis
Published: July 18, 2025

Regulation of HDL dysfunctionality by phosphatidylethanolamine links poly-unsaturated fatty acids with atherosclerotic cardiovascular diseases.

Regulation of HDL dysfunctionality by phosphatidylethanolamine links poly-unsaturated fatty acids with atherosclerotic cardiovascular diseases.

Journal: Molecular metabolism
Published: June 10, 2025

Corrigendum to "Phospholipid transfer to high-density lipoprotein (HDL) upon triglyceride lipolysis is directly correlated with HDL-cholesterol levels and is not associated with cardiovascular risk" [Atherosclerosis 324C (2021) 1-8].

Corrigendum to "Phospholipid transfer to high-density lipoprotein (HDL) upon triglyceride lipolysis is directly correlated with HDL-cholesterol levels and is not associated with cardiovascular risk" [Atherosclerosis 324C (2021) 1-8].

Journal: Atherosclerosis
Published: April 05, 2023

Low circulating PCSK9 levels in LPL homozygous children with chylomicronemia syndrome in a syrian refugee family in Lebanon.

Low circulating PCSK9 levels in LPL homozygous children with chylomicronemia syndrome in a syrian refugee family in Lebanon.

Journal: Frontiers in genetics
Published: June 03, 2022

Circulating PCSK9 Linked to Dyslipidemia in Lebanese Schoolchildren.

Circulating PCSK9 Linked to Dyslipidemia in Lebanese Schoolchildren.

Journal: Metabolites
Published: April 26, 2022

Whole Exome/Genome Sequencing Joint Analysis of a Family with Oligogenic Familial Hypercholesterolemia.

Whole Exome/Genome Sequencing Joint Analysis of a Family with Oligogenic Familial Hypercholesterolemia.

Journal: Metabolites
Published: January 21, 2022

Identification of a Variant in APOB Gene as a Major Cause of Hypobetalipoproteinemia in Lebanese Families.

Identification of a Variant in APOB Gene as a Major Cause of Hypobetalipoproteinemia in Lebanese Families.

Journal: Metabolites
Published: July 24, 2021

Phospholipid transfer to high-density lipoprotein (HDL) upon triglyceride lipolysis is directly correlated with HDL-cholesterol levels and is not associated with cardiovascular risk.

Phospholipid transfer to high-density lipoprotein (HDL) upon triglyceride lipolysis is directly correlated with HDL-cholesterol levels and is not associated with cardiovascular risk.

Journal: Atherosclerosis
Published: July 07, 2020

Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm.

Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 03, 2020

Identification of the first Tangier disease patient in Lebanon carrying a new pathogenic variant in ABCA1.

Identification of the first Tangier disease patient in Lebanon carrying a new pathogenic variant in ABCA1.

Journal: Journal of clinical lipidology
Published: May 17, 2018

PCSK9 Mutations in Familial Hypercholesterolemia: from a Groundbreaking Discovery to Anti-PCSK9 Therapies.

PCSK9 Mutations in Familial Hypercholesterolemia: from a Groundbreaking Discovery to Anti-PCSK9 Therapies.

Journal: Current atherosclerosis reports
Published: October 18, 2017

New Sequencing technologies help revealing unexpected mutations in Autosomal Dominant Hypercholesterolemia.

New Sequencing technologies help revealing unexpected mutations in Autosomal Dominant Hypercholesterolemia.

Journal: Scientific reports
Published: October 18, 2017
Showing 1-12 of 21

Last Updated: 09/26/2026