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Marianne Abifadel | Researchclopedia

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Marianne Abifadel

101

Works

8,569

Citations

34

h-index

52

i10-index

Research Topics

Lipoproteins and Cardiovascular Health Cancer, Lipids, and Metabolism Diabetes, Cardiovascular Risks, and Lipoproteins

Affiliations

Université Claude Bernard Lyon 12010–2023

Délégation Paris 52009–2010

Hôpital Necker-Enfants Malades2002–2011

Inserm2002–2026

Délégation Paris 72012–2016

Top Works

Mutations in PCSK9 cause autosomal dominant hypercholesterolemia

Marianne Abifadel,Mathilde Varret,et al.

20032,978 citations

Lipid metabolism and disorders

Cholesterol and Lipid Metabolism

NARC-1/PCSK9 and Its Natural Mutants

Suzanne Benjannet,David Rhainds,et al.

2004620 citations

Heterozygous TGFBR2 mutations in Marfan syndrome

Takeshi Mizuguchi,Gwenaëlle Collod‐Béroud,et al.

2004613 citations

TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome

Cathérine Boileau,Dong Guo,et al.

2012374 citations

Global perspective of familial hypercholesterolaemia: a cross-sectional study from the EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC)

Antonio J. Vallejo‐Vaz,Christophe Stevens,et al.

2021288 citations

Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (<i>PCSK9</i>) gene in cholesterol metabolism and disease

Marianne Abifadel,Jean‐Pierre Rabès,et al.

2009248 citations

Overview of the current status of familial hypercholesterolaemia care in over 60 countries - The EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC)

Antonio J. Vallejo‐Vaz,Martina De Marco,et al.

2018233 citations

Genetic heterogeneity of autosomal dominant hypercholesterolemia

Mathilde Varret,Marianne Abifadel,et al.

2007201 citations

Novel mutations of thePCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia

Delphine Allard,Sabine Amsellem,et al.

2005184 citations