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Patrick Vourc'h

Research Profile

Chemicals & Drugs

Disorders

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Polymerase Chain Reaction

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Publications

TOP 3
Patrick Emond; Frédéric Laumonnier; Sylvie Mavel; Marc Merten; Frédéric Montigny; Lydie Nadal Desbarats; Pierre Sarda; Patrick Vourc'h; Nacima Aïdoud; Catherine Barthélémy; Hélène Blasco; Frédérique Bonnet-Brilhault; Christian R Andres
GC-MS-based urine metabolic profiling of autism spectrum disorders.
Audrey Dangoumau; Julien Praline; Charlotte Veyrat-Durebex; Christian R Andres; Hélène Blasco; Philippe Corcia; Patrick Vourc'h
Protein SUMOylation, an emerging pathway in amyotrophic lateral sclerosis.
Amitava Banerjee; Laurent Fauchier; Jean Michel Halimi; Sophie Taillandier; Patrick Vourc'h; Christian R Andres; Gregory Y H Lip
Renal impairment and ischemic stroke risk assessment in patients with atrial fibrillation: the loire valley atrial fibrillation project.

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All Publications

2013: Patrick Emond; Frédéric Laumonnier; Sylvie Mavel; Marc Merten; Frédéric Montigny; Lydie Nadal Desbarats; Pierre Sarda; Patrick Vourc'h; Nacima Aïdoud; Catherine Barthélémy; Hélène Blasco; Frédérique Bonnet-Brilhault; Christian R Andres
GC-MS-based urine metabolic profiling of autism spectrum disorders.
Analytical and bioanalytical chemistry 2013;405(15):5291-300.
2013: Audrey Dangoumau; Julien Praline; Charlotte Veyrat-Durebex; Christian R Andres; Hélène Blasco; Philippe Corcia; Patrick Vourc'h
Protein SUMOylation, an emerging pathway in amyotrophic lateral sclerosis.
The International journal of neuroscience 2013;123(6):366-74.
2013: Amitava Banerjee; Laurent Fauchier; Jean Michel Halimi; Sophie Taillandier; Patrick Vourc'h; Christian R Andres; Gregory Y H Lip
Renal impairment and ischemic stroke risk assessment in patients with atrial fibrillation: the loire valley atrial fibrillation project.
Journal of the American College of Cardiology 2013;61(20):2079-87.
2013: M Huc-Chabrolle; Frédéric Laumonnier; S Le Gallic; Martine Raynaud; E Sizaret; R A Thepault; A Toutain; G Tripi; Patrick Vourc'h; D Campion; C Charon; A Guilmatre; J Hager; Christian Andres; M A Barthez; Frédérique Bonnet-Brilhault
Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families.
Behavior genetics 2013;43(2):132-40.
2004: Patrick Vourc'h; Christian Andres
Oligodendrocyte myelin glycoprotein (OMgp): evolution, structure and function.
Brain research. Brain research reviews 2004;45(2):115-24.
2003: Patrick Vourc'h; Isabelle Martin; Frédérique Bonnet-Brilhault; Sylviane Marouillat; Catherine Barthélémy; Jean Pierre Müh; Christian Andres
Mutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder.
Psychiatric genetics 2003;13(4):221-5.
2003: Patrick Vourc'h; Sabine Dessay; Olivier Mbarek; Sylviane Marouillat Védrine; Jean-Pierre Müh; Christian Andres
The oligodendrocyte-myelin glycoprotein gene is highly expressed during the late stages of myelination in the rat central nervous system.
Brain research. Developmental brain research 2003;144(2):159-68.
2003: Patrick Vourc'h; Thierry Moreau; Flavie Arbion; Sylviane Marouillat-Védrine; Jean-Pierre Müh; Christian Andres
Oligodendrocyte myelin glycoprotein growth inhibition function requires its conserved leucine-rich repeat domain, not its glycosylphosphatidyl-inositol anchor.
Journal of neurochemistry 2003;85(4):889-97.
2003: Patrick Vourc'h; Isabelle Martin; Sylviane Marouillat; Jean-Louis Adrien; Catherine Barthélémy; Claude Moraine; Jean-Pierre Müh; Christian Andres
Molecular analysis of the oligodendrocyte myelin glycoprotein gene in autistic disorder.
Neuroscience letters 2003;338(2):115-8.
2002: Patrick Vourc'h; Elisabeth Petit; Jean-Pierre Müh; Christian Andres; Thierry Bienvenu; Cherif Beldjord; Jamel Chelly; Catherine Barthélémy
Exclusion of the coding sequence of the doublecortin gene as a susceptibility locus in autistic disorder.
American journal of medical genetics 2002;108(2):164-7.
2001: Patrick Vourc'h; T Bienvenu; Cherif Beldjord; Jamel Chelly; Catherine Barthélémy; Jean-Pierre Müh; Christian Andres
No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.
European journal of human genetics : EJHG 2001;9(7):556-8.