V
Virginie Pinchot
Publications - 3
Citations - 822
Virginie Pinchot is an academic researcher. The author has contributed to research in topics: Gene & Single-nucleotide polymorphism. The author has an hindex of 2, co-authored 3 publications receiving 806 citations.
Papers
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Journal ArticleDOI
Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia.
Ilya Chumakov,Marta Blumenfeld,Oxana Guerassimenko,Laurent Cavarec,Marta Palicio,Hadi Abderrahim,Lydie Bougueleret,C Barry,Hiroaki Tanaka,Philippe La Rosa,Anne Puech,Nadia Tahri,Annick Cohen-Akenine,Sylvain Delabrosse,Sébastien Lissarrague,Françoise-Pascaline Picard,Karelle Maurice,Laurent Essioux,Philippe Millasseau,Pascale Grel,Virginie Debailleul,Anne-Marie Simon,Dominique Caterina,Isabelle Dufaure,Kattayoun Malekzadeh,Maria Belova,Jian-Jian Luan,Michel Bouillot,Jean-Luc Sambucy,Gwenael Primas,Martial Saumier,Nadia Boubkiri,Sandrine Martin-Saumier,Myriam Nasroune,Hélène Peixoto,A Delaye,Virginie Pinchot,Mariam Bastucci,Sophie Guillou,Magali Chevillon,Ricardo Sainz-Fuertes,Said Meguenni,Joan Aurich-Costa,Dorra Cherif,Anne Gimalac,Cornelia M. van Duijn,Denis Gauvreau,Gail Ouelette,Isabel Fortier,John Realson,Tatiana Sherbatich,Nadejda Riazanskaia,Evgeny I. Rogaev,Peter Raeymaekers,Jeroen Aerssens,Frank Konings,Walter Luyten,Fabio Macciardi,Pak C. Sham,Richard E. Straub,Daniel R. Weinberger,Nadine Cohen,Daniel Cohen +62 more
TL;DR: A map of 191 single-nucleotide polymorphism (SNPs) was built across a 5-Mb segment from chromosome 13q34 that has been genetically linked to schizophrenia, pointing to the involvement of this N-methyl-d-aspartate receptor regulation pathway in schizophrenia.
Journal Article
Erratum: Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia (Proceedings of the National Academy of Sciences of the United States of America (October 15, 2002) 99:21 (13675-13680))
Ilya Chumakov,M Blumenfeld,O Guerassimenko,Laurent Cavarec,M Palicio,H Abderrahim,L Bougueleret,C Barry,Hiromasa Tanaka,P La Rosa,Anne Puech,N Tahri,A Cohen-Akenine,S Delabrosse,S Lissarrague,F P Picard,K Maurice,Laurent Essioux,P Millasseau,P Grel,V Debailleul,A M Simon,D Caterina,I Dufaure,K Malekzadeh,M Belova,J J Luan,M Bouillot,J L Sambucy,G Primas,M Saumier,N Boubkiri,S Martin-Saumier,M Nasroune,H Peixoto,A Delaye,Virginie Pinchot,M Bastucci,S Guillou,M Chevillon,Ricardo Sainz-Fuertes,S Meguenni,J Aurich-Costa,Dorra Cherif,Anne Gimalac,C M van Duijn,Denis Gauvreau,G Ouellette,Isabel Fortier,J Raelson,T Sherbatich,N Riazanskaia,Evgeny I. Rogaev,P Raeymaekers,Jeroen Aerssens,F Konings,Walter Luyten,Fabio Macciardi,Pak C. Sham,Richard E. Straub,Daniel R. Weinberger,Nadine Cohen,Daniel Cohen +62 more
Patent
Method for diagnosing propionibacterium bacteria infections
Julie Roge,Hélène Nuyttens,Karine Yvonne Gabrielle Mignon Godefroy,Damien Thomas,Virginie Pinchot +4 more
TL;DR: In this paper, an in vitro method for determining if an individual is infected by a bacterium of the Propionibacterium genus comprising: (i) detecting antibodies directed against at least one protein of sequence SEQ ID NO: 2, SEQID NO: 4, SEQLID No: 6 or SEQL ID No: 8, in a biological sample of the individual, and (ii) deducing therefrom that the individual is infection by a B.