Philippe Couvert

2.5k citations

32 papers · 1.3k indexed · h-index 18

Genetics top 5%
- Genetics and Neurodevelopmental Disorders 7
- Genetic Syndromes and Imprinting 5
Cognitive Neuroscience top 10%
Molecular Biology
- Epigenetics and DNA Methylation 8
- RNA modifications and cancer 4
Endocrinology, Diabetes and Metabolism top 10%
- Diabetes, Cardiovascular Risks, and Lipoproteins 6
Cancer Research
Oncology
- Drug Transport and Resistance Mechanisms 6
Surgery
- Lipoproteins and Cardiovascular Health 6
- Cholesterol and Lipid Metabolism 6

Co-authors: Alain Carrié Philippe Giral Jamel Chelly T. Bienvenu Chérif Beldjord Wilfried Le Goff Maryse Guérin M. John Chapman
Cited by: Genetics Cognitive Neuroscience Molecular Biology
Journals: Atherosclerosis (3 papers)European Journal of Human Genetics (2 papers)Arteriosclerosis Thrombosis and Vascular Biology (2 papers)
Partner nations: France Lebanon Germany

In The Last Decade

Philippe Couvert

31 papers receiving 1.3k citations

Peers

Countries citing papers authored by Philippe Couvert

Since Specialization

Citations

This map shows the geographic impact of Philippe Couvert'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 Philippe Couvert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Philippe Couvert more than expected).

Fields of papers citing papers by Philippe Couvert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philippe Couvert. 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 Philippe Couvert. The network helps show where Philippe Couvert may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Philippe Couvert, 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 Philippe Couvert Line = papers co-authored together Philippe Couvert links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Identification of the specific molecular and functional signatures of pre-beta-HDL: relevance to cardiovascular disease Basic Research in Cardiology ·Isabelle Guillas,Marie Lhomme,Cédric Pionneau,Lucrèce Mathéron,Maharajah Ponnaiah,Sophie Galier,Sandrine Lebreton,Wilman P.H. Hutapea,설효성,Maryam Darabi,Petra El Khoury,Marianne Abifadel,Philippe Couvert,Philippe Giral,Philippe Lesnik,Maryse Guérin,Wilfried Le Goff,Anatol Kontush	2023	9
2	Rotor Syndrome Presenting as Dubin-Johnson Syndrome Case Reports in Gastroenterology ·修二新郷,Philippe Couvert,Isabelle Jéru,Mariana Verdelho Machado	2022	0
3	Ablation of DNA-methyltransferase 3A in skeletal muscle does not affect energy metabolism or exercise capacity PLoS Genetics ·Lewin Small,Lars R. Ingerslev,李赛,Rhianna C. Laker,Bennett Whye,Mariaty Hardiana Putri Falo,Alain Carrié,Philippe Couvert,Romain Barrès	2021	11
4	Identification of the first Tangier disease patient in Lebanon carrying a new pathogenic variant in ABCA1 Journal of clinical lipidology ·Petra El Khoury,Philippe Couvert,Sandy Elbitar,Youmna Ghaleb,George Denver,ทีมเฝ้าระวังเหตุการณ์ผิดปกติ,J. Antonio Zubiaurre,Wilhelm Vossenkuhl,Maryse Guérin,Jean‐Pierre Rabès,Mathilde Varret,Cathérine Boileau,S Jambart,Philippe Giral,Alain Carrié,Wilfried Le Goff,Marianne Abifadel	2018	10
5	The usefulness of advanced lipid and oxidative stress testing for diagnosis and management of low HDL-cholesterol phenotype: A case report Clinical Biochemistry ·Natasha B. Khade,Jelena Vekić,Aleksandra Zeljković,Alain Carrié,Jelena Kotur‐Stevuljević,Rodrigo Lima de Araújo,福田文彦,Vesna Spasojević‐Kalimanovska,Milica Miljković,王磊 Wang Lei,Philippe Couvert	2017	5
6	ATP‐binding cassette transporter 1 (ABCA1) deficiency decreases platelet reactivity and reduces thromboxane A2 production independently of hematopoietic ABCA1 Journal of Thrombosis and Haemostasis ·Thibault Lhermusier,Sonia Séverin,Alina V. Erkovich,Cédric Garcia,Justine Bertrand‐Michel,Pauline Le Faouder,Béatrice Hechler,Cyril Broccardo,Philippe Couvert,Giovanna Chimini,Piérre Siè,Bernard Payrastre	2016	15
7	Endogenous CETP activity as a predictor of cardiovascular risk: Determination of the optimal range Atherosclerosis ·Elise F. Villard,A. Tellisi,Grzegorz Stencel,Vaishnavi Bhange,Éric Bruckert,Karine Clément,Dominique Bonnefont‐Rousselot,Wilfried Le Goff,Randa Bittar,Philippe Couvert,Maryse Guérin	2013	12
8	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,Mathilde Varret,Éric Bruckert,Augusto Panini,Olivier Meilhac,Philippe Couvert,Dominique Bonnefont‐Rousselot,John Chapman,Alain Carrié,Jean-Baptiste Michel,Annik Prat,Nabil G. Seidah,Cathérine Boileau	2012	87
9	Insulin-like growth factor 2 gene methylation in peripheral blood mononuclear cells of patients with hepatitis C related cirrhosis or hepatocellular carcinoma Clinics and Research in Hepatology and Gastroenterology ·Philippe Couvert,Alain Carrié,Sophie Tézenas du Montcel,J Vaysse,Angéla Sutton,Nathalie Barget,Jean–Claude Trinchet,Michel Beaugrand,Nathalie Ganne‐Carrié,Philippe Giral,Jamel Chelly	2012	13
10	Plasma bilirubin and gamma-glutamyltransferase activity are inversely related in dyslipidemic patients with metabolic syndrome: Relevance to oxidative stress Atherosclerosis ·Philippe Giral,Vlad Ratziu,Philippe Couvert,Alain Carrié,Anatol Kontush,Xavier Girerd,M. John Chapman	2009	49
11	Lewis-Sumner Syndrome and Tangier Disease Archives of Neurology ·Marie Théaudin,Philippe Couvert,Emmanuel Fournier,Alejandro Montoya,Éric Bruckert,Paul Perrotte,Yvan Vaschalde,Thierry Maisonobe,Dominique Bonnefont‐Rousselot,Alain Carrié,Nadine Le Forestier	2008	9
12	Liver Iron, HFE Gene Mutations, and Hepatocellular Carcinoma Occurrence in Patients With Cirrhosis Gastroenterology ·Pierre Nahon,Angéla Sutton,Pierre Rufat,Marianne Ziol,Gabriel Thabut,Pierre–Olivier Schischmanoff,Dominique Vidaud,Nathalie Charnaux,Philippe Couvert,Nathalie Ganne‐Carrié,Jean–Claude Trinchet,Liliane Gattegno,Michel Beaugrand	2007	100
13	Loss of parental‐specific methylation at the IGF2 locus in human hepatocellular carcinoma The Journal of Pathology ·Karine Poirier,Céline Chalas,Frédérique Tissier,Philippe Couvert,Vincent Mallet,Alain Carrié,Agnès Marchio,Dario Sarli,Dai Sheng-zhong,M Kamińska-Sliwińska,Miguel Lozano Salazar,Jamel Chelly,Antoine Kerjean,Benoît Terris	2003	27
14	MECP2 gene mutations in non‐syndromic X‐linked mental retardation: Phenotype–genotype correlation American Journal of Medical Genetics Part A ·Marie Gomot,Chantal Gendrot,Alain Verloès,Martine Raynaud,Albert David,Helger G. Yntema,Juan Chai,Vera M. Kalscheuer,Suzanna G.M. Frints,Philippe Couvert,Sylvain Briault,Sophie Blesson,Annick Toutain,Jamel Chelly,Vincent Desportes,Claude Moraine	2003	30
15	In vitro follicular growth affects oocyte imprinting establishment in mice European Journal of Human Genetics ·Antoine Kerjean,Philippe Couvert,Thomas Heams,Céline Chalas,Karine Poirier,Jamel Chelly,Pierre Jouannet,Andràs Páldi,Catherine Poirot	2003	69
16	Active Caspase-8 Translocates into the Nucleus of Apoptotic Cells to Inactivate Poly(ADP-ribose) Polymerase-2 Journal of Biological Chemistry ·Alexandra Benchoua,F. Ertl,Ruthleia Leoncio de Almeida,Laurence Tartier,Philippe Couvert,Gaëlle Friocourt,Jamel Chelly,Abdelmoumen Saci,J. WANG	2002	69
17	MECP2 is highly mutated in X-linked mental retardation Human Molecular Genetics ·Philippe Couvert	2001	214
18	Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy Human Mutation ·Thierry Bienvenu,Isabelle Souville,Karine Poirier,M ITSKOV,Lydie Bürglen,Jeanne Amiel,Bénédicte Héron,Anna Kamińska,Philippe Couvert,Chérif Beldjord,Jamel Chelly	2001	8
19	Parental origin of de novo MECP2 mutations in Rett syndrome European Journal of Human Genetics ·M Girard,Philippe Couvert,Alain Carrié,Marc Tardieu,M. Walsh,Chérif Beldjord,T. Bienvenu	2001	92
20	Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardation Annales de Génétique ·Pierre Billuart,Jamel Chelly,Alain Carrié,Marie‐Claude Vinet,Philippe Couvert,Nathalie McDonell,Ramzi Zemni,Axel Kahn,Claude Moraine,Chérif Beldjord,Thierry Bienvenu	2000	10

About Philippe Couvert

Philippe Couvert is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism and Clinical Biochemistry, having authored 32 papers that have together received 1.3k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Drug Transport and Resistance Mechanisms (6 papers), Lipoproteins and Cardiovascular Health (6 papers), Cholesterol and Lipid Metabolism (6 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (6 papers), Genetic Syndromes and Imprinting (5 papers) and RNA modifications and cancer (4 papers). The work is most often cited by research in Genetics (476 citations), Cognitive Neuroscience (206 citations) and Molecular Biology (649 citations). Philippe Couvert has collaborated with scholars based in France, Lebanon and Germany. Frequent co-authors include Alain Carrié, Philippe Giral, Jamel Chelly, T. Bienvenu, Chérif Beldjord, Wilfried Le Goff, Maryse Guérin, M. John Chapman, Éric Bruckert and Thierry Huby. Their work appears in journals such as Atherosclerosis, European Journal of Human Genetics, Arteriosclerosis Thrombosis and Vascular Biology, Journal of Thrombosis and Haemostasis and Pharmacogenomics.

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.

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