Publications by authors named "Mathilde Varret"

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Cardiometabolic risk in pseudohypertriglyceridemia resulting from hyperglycerolemia.
Boris Hansel, Philippe Couvert, Alain Carrié, Randa Bittar, Mathilde Varret

J Clin Lipidol· December 2025

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Dysfunction of COX-2/mPGES-1/PGE pathway and EP4 receptor in bronchi from COPD patients.
Salma Mani, Zhipeng Li, Hichem Badji, Gaelle Merheb, Sébastien Dupont, Mathilde Varret

Prostaglandins Leukot Essent Fatty Acids· October 2025

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The singular French PCSK9-p.Ser127Arg gain-of-function variant: A significant player in cholesterol levels from a 775-year-old common ancestor.
Yara Azar, Thomas E Ludwig, Hugo Le Bon, Thea Bismo Strøm, Olivier Bluteau, Mathilde Varret

Atherosclerosis· December 2024

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Integrated omics approach for the identification of HDL structure-function relationships in PCSK9-related familial hypercholesterolemia.
Maryam Darabi, Marie Lhomme, Maharajah Ponnaiah, Maja Pučić-Baković, Isabelle Guillas, Mathilde Varret

J Clin Lipidol· December 2023

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Corrigendum to "APOE gene variants in primary dyslipidemia" [Atherosclerosis (2021 Jul) 328 11-22].
Yara Abou Khalil, Jean-Pierre Rabès, Catherine Boileau, Mathilde Varret

Atherosclerosis· December 2023

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Additive Effect of Rare Variants on the Phenotype of Familial Hypercholesterolemia.
Oriane Marmontel, Yara Abou-Khalil, Olivier Bluteau, Bertrand Cariou, Valérie Carreau, Mathilde Varret

Arterioscler Thromb Vasc Biol· July 2023

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Low circulating PCSK9 levels in homozygous children with chylomicronemia syndrome in a syrian refugee family in Lebanon.
Carine Ayoub, Yara Azar, Dina Maddah, Youmna Ghaleb, Sandy Elbitar, Mathilde Varret

Front Genet· August 2022

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Molecular Spectrum in a French Cohort with Primary Dyslipidemia.
Yara Abou Khalil, Oriane Marmontel, Jean Ferrières, François Paillard, Cécile Yelnik, Mathilde Varret

Int J Mol Sci· May 2022

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Circulating PCSK9 Linked to Dyslipidemia in Lebanese Schoolchildren.
Yara Azar, Marie-Hélène Gannagé-Yared, Elie Naous, Carine Ayoub, Yara Abou Khalil, Mathilde Varret

Metabolites· May 2022

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Whole Exome/Genome Sequencing Joint Analysis of a Family with Oligogenic Familial Hypercholesterolemia.
Youmna Ghaleb, Sandy Elbitar, Anne Philippi, Petra El Khoury, Yara Azar, Mathilde Varret

Metabolites· March 2022

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Posttranscriptional Regulation of the Human LDL Receptor by the U2-Spliceosome.
Paolo Zanoni, Grigorios Panteloglou, Alaa Othman, Joel T Haas, Roger Meier, Mathilde Varret

Circ Res· January 2022

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Ephrin-B2 PB-mononuclear cells reduce early post-stroke deficit in diabetic mice but not long-term memory impairment.
Adrien Cogo, Gabrielle Mangin, Sarah Mouazan, Tatiana Merkulova-Rainon, Jean-Pierre Riveline, Mathilde Varret

Exp Neurol· December 2021

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Lipoprotein(a): Pathophysiology, measurement, indication and treatment in cardiovascular disease. A consensus statement from the Nouvelle Société Francophone d'Athérosclérose (NSFA).
Vincent Durlach, Dominique Bonnefont-Rousselot, Franck Boccara, Mathilde Varret, Mathilde Di-Filippo Charcosset

Arch Cardiovasc Dis· December 2021

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Identification of a Variant in Gene as a Major Cause of Hypobetalipoproteinemia in Lebanese Families.
Carine Ayoub, Yara Azar, Yara Abou-Khalil, Youmna Ghaleb, Sandy Elbitar, Mathilde Varret

Metabolites· August 2021

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APOE gene variants in primary dyslipidemia.
Yara Abou Khalil, Jean-Pierre Rabès, Catherine Boileau, Mathilde Varret

Atherosclerosis· July 2021

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Polymorphisms rs2745557 in PTGS2 and rs2075797 in PTGER2 are associated with the risk of chronic obstructive pulmonary disease development in a Tunisian cohort.
Salma Mani, Xavier Norel, Mathilde Varret, Sarra Bchir, Amel Ben Anes

Prostaglandins Leukot Essent Fatty Acids· March 2021

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Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm.
Sandy Elbitar, Marjolijn Renard, Pauline Arnaud, Nadine Hanna, Marie-Paule Jacob, Mathilde Varret

Genet Med· January 2021

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Postprandial lipid absorption in seven heterozygous carriers of deleterious variants of MTTP in two abetalipoproteinemic families.
Mathilde Di Filippo, Mathilde Varret, Vanessa Boehm, Jean-Pierre Rabès, Latifa Ferkdadji

J Clin Lipidol· May 2020

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Identification of the first Tangier disease patient in Lebanon carrying a new pathogenic variant in ABCA1.
Petra El Khoury, Philippe Couvert, Sandy Elbitar, Youmna Ghaleb, Yara Abou-Khalil, Mathilde Varret

J Clin Lipidol· October 2019

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High burden of recurrent cardiovascular events in heterozygous familial hypercholesterolemia: The French Familial Hypercholesterolemia Registry.
Sophie Béliard, Franck Boccara, Bertrand Cariou, Alain Carrié, Xavier Collet, Mathilde Varret

Atherosclerosis· October 2018

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Plasma proprotein-convertase-subtilisin/kexin type 9 (PCSK9) and cardiovascular events in type 2 diabetes.
Petra El Khoury, Ronan Roussel, Frederic Fumeron, Yara Abou-Khalil, Gilberto Velho, Mathilde Varret

Diabetes Obes Metab· April 2018

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Usefulness of the genetic risk score to identify phenocopies in families with familial hypercholesterolemia?
Youmna Ghaleb, Sandy Elbitar, Petra El Khoury, Eric Bruckert, Valérie Carreau, Mathilde Varret

Eur J Hum Genet· April 2018

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New Sequencing technologies help revealing unexpected mutations in Autosomal Dominant Hypercholesterolemia.
Sandy Elbitar, Delia Susan-Resiga, Youmna Ghaleb, Petra El Khoury, Gina Peloso, Mathilde Varret

Sci Rep· January 2018

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PCSK9 Mutations in Familial Hypercholesterolemia: from a Groundbreaking Discovery to Anti-PCSK9 Therapies.
Petra El Khoury, Sandy Elbitar, Youmna Ghaleb, Yara Abou Khalil, Mathilde Varret

Curr Atheroscler Rep· October 2017

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Proprotein convertase subtilisin / kexin 9 (PCSK9) inhibitors and the future of dyslipidemia therapy: an updated patent review (2011-2015).
Sandy Elbitar, Petra El Khoury, Youmna Ghaleb, Jean-Pierre Rabès, Mathilde Varret

Expert Opin Ther Pat· December 2016

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