Mathilde Varret

8.2k citations

83 papers · 6.6k · 3 hit papers · h-index 29

Impact in

Surgery top 0.5%
- Lipoproteins and Cardiovascular Health
- Cholesterol and Lipid Metabolism
Genetics top 2%
- Connective tissue disorders research
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases

Papers in

Surgery 62
- Lipoproteins and Cardiovascular Health 61
- Cholesterol and Lipid Metabolism 6
Genetics 11
- Connective tissue disorders research 4
- Genomics and Rare Diseases 4
- Genetic Associations and Epidemiology 3

Co-authors: Cathérine Boileau (51 shared papers)Jean‐Pierre Rabès (40 shared papers)Marianne Abifadel (35 shared papers)Claudine Junien (12 shared papers)Martine Devillers (7 shared papers)Delphine Allard (5 shared papers)Arnold Münnich (5 shared papers)Daniele Erlich (5 shared papers)
Journals: Atherosclerosis (11 papers)Human Mutation (8 papers)Clinica Chimica Acta (4 papers)Journal of clinical lipidology (4 papers)Nature Genetics (3 papers)
Partner nations: France Lebanon Tunisia

In The Last Decade

Mathilde Varret

79 papers receiving 6.4k citations

Mathilde Varret's Hit Papers

align trajectories log scale

APOE gene variants in primary dyslipidemia 2021 · 118 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2021 Atherosclerosis
2004 Journal of Biological Chemistry
2003 Nature Genetics

Peers

Countries citing papers authored by Mathilde Varret

Since Specialization

Citations

This map shows the geographic impact of Mathilde Varret's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mathilde Varret with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mathilde Varret more than expected).

Fields of papers citing papers by Mathilde Varret

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mathilde Varret. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mathilde Varret. The network helps show where Mathilde Varret may publish in the future.

Co-authors

The 25 scholars most cited alongside Mathilde Varret, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mathilde Varret Line = papers co-authored together Mathilde Varret links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 83 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in PCSK9 cause autosomal dominant hypercholesterolemia Nature Genetics ·Marianne Abifadel, Mathilde Varret, Jean‐Pierre Rabès, Delphine Allard, Khadija Ouguerram, Martine Devillers, Corinne Cruaud, Suzanne Benjannet Hit paper breakdown →	2003	2446
2	NARC-1/PCSK9 and Its Natural Mutants Journal of Biological Chemistry ·Suzanne Benjannet, David Rhainds, Rachid Essalmani, Janice Mayne, Weijun Jin, Josée Hamelin, Mathilde Varret, Delphine Allard Hit paper breakdown →	2004	559
3	Heterozygous TGFBR2 mutations in Marfan syndrome Nature Genetics ·Takeshi Mizuguchi, Gwenaëlle Collod‐Béroud, Takushi Akiyama, Marianne Abifadel, Naoki Harada, Takayuki Morisaki, Delphine Allard, Mathilde Varret	2004	502
4	TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome Nature Genetics ·Cathérine Boileau, Dong Guo, Nadine Hanna, Ellen S. Regalado, Delphine Détaint, Limin Gong, Mathilde Varret, Siddharth K. Prakash	2012	302
5	Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease Human Mutation ·Marianne Abifadel, Jean‐Pierre Rabès, Martine Devillers, Arnold Münnich, Daniele Erlich, Claudine Junien, Mathilde Varret, Cathérine Boileau	2009	215
6	Novel mutations of thePCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia Human Mutation ·Delphine Allard, Sabine Amsellem, Marianne Abifadel, Mélanie Trillard, Martine Devillers, Gérald Luc, Michel Krempf, Yves Reznik	2005	174
7	Genetic heterogeneity of autosomal dominant hypercholesterolemia Clinical Genetics ·Mathilde Varret, Marianne Abifadel, Jean‐Pierre Rabès, Cathérine Boileau	2007	161
8	Apolipoprotein B100 Metabolism in Autosomal-Dominant Hypercholesterolemia Related to Mutations inPCSK9 Arteriosclerosis Thrombosis and Vascular Biology ·Khadija Ouguerram, Maud Chétiveaux, Yassine Zaïr, Philippe Costet, Marianne Abifadel, Mathilde Varret, Cathérine Boileau, Thierry Magot	2004	159
9	Molecular analysis and intestinal expression of SAR1 genes and proteins in Anderson's disease (Chylomicron retention disease) Orphanet Journal of Rare Diseases ·Amandine Georges, Dominique Bonnefont‐Rousselot, Jacqueline Champigneulle, Jean‐Pierre Rabès, Marianne Abifadel, Thomas Aparicio, Jean C Guenedet, Éric Bruckert	2011	145
10	A Third Major Locus for Autosomal Dominant Hypercholesterolemia Maps to 1p34.1-p32 The American Journal of Human Genetics ·Mathilde Varret, Jean‐Pierre Rabès, Bruno Saint-Jore, Ana Cenarro, Jean‐Christophe Marinoni, Fernando Civeira, Martine Devillers, Michel Krempf	1999	139
11	APOE gene variants in primary dyslipidemia Atherosclerosis ·Yara Abou Khalil, Jean‐Pierre Rabès, Cathérine Boileau, Mathilde Varret Hit paper breakdown →	2021	118
12	Description of a Large Family with Autosomal Dominant Hypercholesterolemia Associated with theAPOEp.Leu167del Mutation Human Mutation ·Marie Marduel, Khadija Ouguerram, Valérie Serre, Dominique Bonnefont‐Rousselot, Alice Marques-Pinheiro, Knut Erik Berge, Martine Devillers, Gérald Luc	2012	117
13	MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections The American Journal of Human Genetics ·Mathieu Barbier, Marie‐Sylvie Gross, Mélodie Aubart, Nadine Hanna, Ketty Kessler, Laurent Tosolini, Benoît Ho‐Tin‐Noé, Ellen S. Regalado	2014	108
14	Molecular Spectrum of Autosomal Dominant Hypercholesterolemia in France Human Mutation ·Marie Marduel, Alain Carrié, Agnès Sassolas, Martine Devillers, Valérie Carreau, Mathilde Di Filippo, Daniele Erlich, Marianne Abifadel	2010	96
15	Identification and characterization of new gain-of-function mutations in the PCSK9 gene responsible for autosomal dominant hypercholesterolemia Atherosclerosis ·Marianne Abifadel, Maryse Guérin, Suzanne Benjannet, Jean‐Pierre Rabès, Wilfried Le Goff, Zélie Julia, Josée Hamelin, Valérie Carreau	2012	95
16	The UMD-LDLR database: additions to the software and 490 new entries to the database Human Mutation ·Ludovic Villéger, Marianne Abifadel, Delphine Allard, Jean‐Pierre Rabès, Rochelle Thiart, Maritha J. Kotze, Christophe Béroud, Claudine Junien	2002	87
17	Living the PCSK9 Adventure: from the Identification of a New Gene in Familial Hypercholesterolemia Towards a Potential New Class of Anticholesterol Drugs Current Atherosclerosis Reports ·Marianne Abifadel, Sandy Elbitar, Petra El Khoury, Youmna Ghaleb, Melody Chemaly, Marie-Line Moussalli, Jean‐Pierre Rabès, Mathilde Varret	2014	87
18	The molecular basis of familial hypercholesterolemia in Lebanon: Spectrum ofLDLRmutations and role ofPCSK9as a modifier gene Human Mutation ·Marianne Abifadel, Jean‐Pierre Rabès, S Jambart, Georges Halaby, Marie‐Hélène Gannagé‐Yared, Antoine Sarkis, Ghada Beaino, Mathilde Varret	2009	84
19	LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis Nucleic Acids Research ·Mathilde Varret	1998	80
20	Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis Human Mutation ·Christine P. Diggle, Clare V. Logan, Paul Laissue, Carolina Rivera, Carlos Martín Restrepo, Dora Janeth Fonseca, Joanne Morgan, Yannick Allanore	2012	76

About Mathilde Varret

Mathilde Varret is a scholar working on Surgery, Genetics, Cardiology and Cardiovascular Medicine, Immunology and Orthopedics and Sports Medicine, having authored 83 papers that have together received 6.6k indexed citations. Recurring topics across this work include Lipoproteins and Cardiovascular Health (61 papers), Lipid metabolism and disorders (8 papers), Cholesterol and Lipid Metabolism (6 papers), Connective tissue disorders research (4 papers), Genomics and Rare Diseases (4 papers), Genetic Associations and Epidemiology (3 papers), Atherosclerosis and Cardiovascular Diseases (3 papers) and Systemic Sclerosis and Related Diseases (2 papers). The work is most often cited by research in Surgery (4.1k citations), Genetics (1.3k citations), Cardiology and Cardiovascular Medicine (511 citations), Cancer Research (154 citations) and Immunology (208 citations). Mathilde Varret has collaborated with scholars based in France, Lebanon and Tunisia. Frequent co-authors include Cathérine Boileau, Jean‐Pierre Rabès, Marianne Abifadel, Claudine Junien, Martine Devillers, Delphine Allard, Arnold Münnich, Daniele Erlich, Michel Krempf and Nabil Georges Seidah. Their work appears in journals such as Atherosclerosis, Human Mutation, Clinica Chimica Acta, Journal of clinical lipidology and Nature Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Mathilde Varret

Impact in

Papers in i

In The Last Decade

Mathilde Varret

Mathilde Varret's Hit Papers

Peers

Countries citing papers authored by Mathilde Varret

Fields of papers citing papers by Mathilde Varret

All Works

About Mathilde Varret

Explore authors with similar magnitude of impact

Papers in