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Philippe Couvert

Research Profile

Chemicals & Drugs

Disorders

Physiology

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Anatomy

X Chromosome

Procedures

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Amino Acid Sequences

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Publications

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Elise F Villard; Wilfried Le Goff; Randa Bittar; Dominique Bonnefont-Rousselot; Eric Bruckert; Corinne Cherfils; Karine Clement; Philippe Couvert; MC Federspiel; Valérie Fesel-Fouquier; Maryse Guerin
Endogenous CETP activity as a predictor of cardiovascular risk: determination of the optimal range.
Julien Lagarde; Deepa Pothalil; Emmanuel Roze; Frédéric Sedel; Marie Vidailhet; Emmanuelle Apartis; Philippe Couvert; Bertrand Degos
Myoclonus and dystonia in cerebrotendinous xanthomatosis.
Philippe Couvert; Nathalie Ganne; Philippe Giral; Angela SUTTON; Sophie Tezenas du Montcel; Jean-Claude Trinchet; Jenny Vaysse; Nathalie Barget; Michel Beaugrand; Alain Carrié; Jamel Chelly
Insulin-like growth factor 2 gene methylation in peripheral blood mononuclear cells of patients with hepatitis C related cirrhosis or hepatocellular carcinoma.

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All Publications

2013: Elise F Villard; Wilfried Le Goff; Randa Bittar; Dominique Bonnefont-Rousselot; Eric Bruckert; Corinne Cherfils; Karine Clement; Philippe Couvert; MC Federspiel; Valérie Fesel-Fouquier; Maryse Guerin
Endogenous CETP activity as a predictor of cardiovascular risk: determination of the optimal range.
Atherosclerosis 2013;227(1):165-71.
2012: Julien Lagarde; Deepa Pothalil; Emmanuel Roze; Frédéric Sedel; Marie Vidailhet; Emmanuelle Apartis; Philippe Couvert; Bertrand Degos
Myoclonus and dystonia in cerebrotendinous xanthomatosis.
Movement disorders : official journal of the Movement Disorder Society 2012;27(14):1805-10.
2012: Philippe Couvert; Nathalie Ganne; Philippe Giral; Angela SUTTON; Sophie Tezenas du Montcel; Jean-Claude Trinchet; Jenny Vaysse; Nathalie Barget; Michel Beaugrand; Alain Carrié; Jamel Chelly
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 2012;36(4):345-51.
2012: Marianne Abifadel; Suzanne Benjannet; Dominique Bonnefont-Rousselot; Eric Bruckert; Valérie Carreau; Alain Carrié; John Chapman; Philippe Couvert; Maryse Guerin; Josée Hamelin; Zélie Julia; Wilfried Le Goff; Olivier Meilhac; Jean-Baptiste Michel; Annik Prat; Jean-Pierre Rabès; Nabil G Seidah; Laurent Tosolini; Mathilde Varret; catherine boileau
Identification and characterization of new gain-of-function mutations in the PCSK9 gene responsible for autosomal dominant hypercholesterolemia.
Atherosclerosis 2012;223(2):394-400.
2012: Julie Zyss; Christophe Vial; Anthony Béhin; Françoise Bouhour; Alain Carrié; Philippe Couvert; Violaine Denys; Ivan Kolev; A Lacour; Agnès Sassolas; Tanya Stojkovic
Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease.
Journal of neurology 2012;259(6):1222-6.
2012: Géraldine Androdias; Odile Boespflug-Tanguy; Alain Carrie; Christian Confavreux; Philippe Couvert; Laurence Gignoux; Sandra Vukusic; Marie-Thérèse Zabot; Cécile Acquaviva; Pierre Labauge
Leukodystrophy with a cerebellar cystic aspect and intracranial atherosclerosis: an atypical presentation of cerebrotendinous xanthomatosis.
Journal of neurology 2012;259(2):364-6.
2011: Philippe Couvert; M John Chapman; Alain Carrié
Impact of genetic variation in the SLCO1B1 gene on statin efficacy in low-density lipoprotein cholesterol-lowering therapy.
Pharmacogenomics 2011;12(2):137-9.
2010: Philippe Giral; Vlad Ratziu; Philippe Couvert; Alain Carrié; Anatol Kontush; Xavier Girerd; M John Chapman
Plasma bilirubin and gamma-glutamyltransferase activity are inversely related in dyslipidemic patients with metabolic syndrome: relevance to oxidative stress.
Atherosclerosis 2010;210(2):607-13.
2010: P Pichit; M Quillard; Philippe Couvert; J Sénant; A Carrié; R Bittar; D Hannequin; L Guyant-Maréchal
Tangier disease phenotype diversity in dizygous twin sisters.
Revue neurologique 2010;166(5):534-7.
2009: Sandra Larrede; Carmel M Quinn; Wendy Jessup; Eric Frisdal; Maryline Olivier; Victar Hsieh; Mi-Jurng Kim; Miranda Van Eck; Philippe Couvert; Alain Carrie; Philippe Giral; M John Chapman; Maryse Guerin; Wilfried Le Goff
Stimulation of cholesterol efflux by LXR agonists in cholesterol-loaded human macrophages is ABCA1-dependent but ABCG1-independent.
Arteriosclerosis, thrombosis, and vascular biology 2009;29(11):1930-6.
2008: Philippe Couvert; Alain Carrié; Jacques Pariès; Jenny Vaysse; Audrey Miroglio; Antoine Kerjean; Pierre Nahon; Jamel Chelly; Jean-Claude Trinchet; Michel Beaugrand; Nathalie Ganne-Carrié
Liver insulin-like growth factor 2 methylation in hepatitis C virus cirrhosis and further occurrence of hepatocellular carcinoma.
World journal of gastroenterology : WJG 2008;14(35):5419-27.
2008: Philippe Couvert; Philippe Giral; Sylvie Dejager; Jessie Gu; Thierry Huby; M John Chapman; Eric Bruckert; Alain Carrié
Association between a frequent allele of the gene encoding OATP1B1 and enhanced LDL-lowering response to fluvastatin therapy.
Pharmacogenomics 2008;9(9):1217-27.
2008: Marie Théaudin; Philippe Couvert; Emmanuel Fournier; Daniel Bouige; Eric Bruckert; Paul Perrotte; Yvan Vaschalde; Thierry Maisonobe; Dominique Bonnefont-Rousselot; Alain Carrié; Nadine Le Forestier
Lewis-Sumner syndrome and Tangier disease.
Archives of neurology 2008;65(7):968-70.
2008: Pierre Nahon; Angela SUTTON; Pierre Rufat; Marianne Ziol; Gabriel Thabut; Pierre-Olivier Schischmanoff; Dominique Vidaud; Nathalie Charnaux; Philippe Couvert; Nathalie Ganne-Carrie; Jean-Claude Trinchet; Liliane Gattegno; Michel Beaugrand
Liver iron, HFE gene mutations, and hepatocellular carcinoma occurrence in patients with cirrhosis.
Gastroenterology 2008;134(1):102-10.
2003: Marie Gomot; Chantal Gendrot; Alain Verloes; Martine Raynaud; Albert David; Helger G Yntema; Sabine Dessay; Vera Kalscheuer; Suzanna G M Frints; Philippe Couvert; Sylvain Briault; Sophie Blesson; Annick Toutain; Jamel Chelly; Vincent Desportes; Claude Moraine
MECP2 gene mutations in non-syndromic X-linked mental retardation: phenotype-genotype correlation.
American journal of medical genetics. Part A 2003;123A(2):129-39.
2003: Karine Poirier; Céline Chalas; Frédérique Tissier; Philippe Couvert; Vincent Mallet; Alain Carrié; Agnès Marchio; Dario Sarli; Christine Gicquel; Stanislas Chaussade; Cherif Beljord; Jamel Chelly; Antoine Kerjean; Benoît Terris
Loss of parental-specific methylation at the IGF2 locus in human hepatocellular carcinoma.
The Journal of pathology 2003;201(3):473-9.
2003: Antoine Kerjean; Philippe Couvert; Thomas Heams; Céline Chalas; Karine Poirier; Jamel Chelly; Pierre Jouannet; Andras Paldi; Catherine Poirot
In vitro follicular growth affects oocyte imprinting establishment in mice.
European journal of human genetics : EJHG 2003;11(7):493-6.
2003: Philippe Couvert; Karine Poirier; Alain Carrié; Céline Chalas; Pierre Jouannet; Cherif Beldjord; Thierry Bienvenu; Jamel Chelly; Antoine Kerjean
DHPLC-based method for DNA methylation analysis of differential methylated regions from imprinted genes.
BioTechniques 2003;34(2):356-62.
2002: Alexandra Benchoua; Cécile Couriaud; Christelle Guégan; Laurence Tartier; Philippe Couvert; Gaëlle Friocourt; Jamel Chelly; Josiane Ménissier-de Murcia; Brigitte Onténiente
Active caspase-8 translocates into the nucleus of apoptotic cells to inactivate poly(ADP-ribose) polymerase-2.
The Journal of biological chemistry 2002;277(37):34217-22.
2002: Thierry Bienvenu; Karine Poirier; Gaëlle Friocourt; Nadia Bahi; Delphine Beaumont; Fabien Fauchereau; Lamia Ben Jeema; Ramzi Zemni; Marie-Claude Vinet; Fiona Francis; Philippe Couvert; Marie Gomot; Claude Moraine; Hans van Bokhoven; Vera Kalscheuer; Suzanna G M Frints; Jozef Gecz; Kanae Ohzaki; Habiba Chaabouni; Jean-Pierre Fryns; Vincent Desportes; Cherif Beldjord; Jamel Chelly
ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation.
Human molecular genetics 2002;11(8):981-91.
2002: David Cohen; Gabriela Lazar; Philippe Couvert; Vincent Desportes; Didier Lippe; Philippe Mazet; Delphine Héron
MECP2 mutation in a boy with language disorder and schizophrenia.
The American journal of psychiatry 2002;159(1):148-9.
2001: Thierry Bienvenu; Isabelle Souville; Karine Poirier; C Aquaviva; L Burglen; J Amiel; Bénédicte Héron; A Kaminska; Philippe Couvert; Cherif Beldjord; Jamel Chelly
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 2001;18(3):251-2.
2001: Philippe Couvert; Thierry Bienvenu; C Aquaviva; Karine Poirier; Claude Moraine; Chantal Gendrot; Alain Verloes; C Andrès; A C Le Fevre; Isabelle Souville; J Steffann; Vincent des Portes; Hans-Hilger Ropers; Helger G Yntema; J P Fryns; Sylvain Briault; Jamel Chelly; B Cherif
MECP2 is highly mutated in X-linked mental retardation.
Human molecular genetics 2001;10(9):941-6.
2001: M Girard; Philippe Couvert; Alain Carrié; Marc Tardieu; Jamel Chelly; Cherif Beldjord; Thierry Bienvenu
Parental origin of de novo MECP2 mutations in Rett syndrome.
European journal of human genetics : EJHG 2001;9(3):231-6.
2000: Thierry Bienvenu; Vincent des Portes; N McDonell; Alain Carrié; Ramzi Zemni; Philippe Couvert; Hans-Hilger Ropers; Claude Moraine; Hans van Bokhoven; Jean-Pierre Fryns; K Allen; Christopher Walsh; J Boué; Axel Kahn; Jamel Chelly; Cherif Beldjord
Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation.
American journal of medical genetics 2000;93(4):294-8.
2000: Thierry Bienvenu; Alain Carrié; Nicolas De Roux; Marie-Claude Vinet; Philippe Jonveaux; Philippe Couvert; Laurent Villard; A Arzimanoglou; Cherif Beldjord; Michel Fontes; Marc Tardieu; Jamel Chelly
MECP2 mutations account for most cases of typical forms of Rett syndrome.
Human molecular genetics 2000;9(9):1377-84.
2000: Ramzi Zemni; Thierry Bienvenu; Marie-Claude Vinet; abdelaziz sefiani; Alain Carrié; Pierre Billuart; N McDonell; Philippe Couvert; Fiona Francis; Philippe Chafey; Fabien Fauchereau; Gaëlle Friocourt; Vincent des Portes; A Cardona; Suzanna G M Frints; Alfons Meindl; Oliver Brandau; Nathalie Ronce; Claude Moraine; Hans van Bokhoven; Hans-Hilger Ropers; Ralf Sudbrak; Axel Kahn; Jean-Pierre Fryns; Cherif Beldjord; Jamel Chelly
A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation.
Nature genetics 2000;24(2):167-70.
2000: Pierre Billuart; Jamel Chelly; Alain Carrié; Marie-Claude Vinet; Philippe Couvert; N McDonell; Ramzi Zemni; Axel Kahn; Claude Moraine; Cherif Beldjord; Thierry Bienvenu
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 2000;43(1):5-9.
1999: Alain Carrié; Lin Jun; Thierry Bienvenu; Marie-Claude Vinet; N McDonell; Philippe Couvert; Ramzi Zemni; A Cardona; Griet Van Buggenhout; Suzanna G M Frints; Ben Hamel; Claude Moraine; Hans-Hilger Ropers; T Strom; G R Howell; A Whittaker; Mark T Ross; Axel Kahn; Jean-Pierre Fryns; Cherif Beldjord; Peter Marynen; Jamel Chelly
A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation.
Nature genetics 1999;23(1):25-31.
1998: Thierry Bienvenu; Vincent des Portes; A Saint Martin; N McDonell; Pierre Billuart; Alain Carrié; Marie-Claude Vinet; Philippe Couvert; D Toniolo; Hans-Hilger Ropers; Claude Moraine; Hans van Bokhoven; Jean-Pierre Fryns; Axel Kahn; Cherif Beldjord; Jamel Chelly
Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitor.
Human molecular genetics 1998;7(8):1311-5.