P. Vourc'h

发表

What Was the Set of Ubiquitin and Ubiquitin-Like Conjugating Enzymes in the Eukaryote Common Ancestor?

C. Michelle, P. Vourc'h, L. Mignon, 2009, Journal of Molecular Evolution.

Serum influence on in-vitro gene delivery using microbubble-assisted ultrasound

A. Novell, J. Escoffre, P. Vourc'h, 2014, Journal of drug targeting.

Validation of amino-acids measurement in dried blood spot by FIA-MS/MS for PKU management.

D. Guilloteau, P. Vourc'h, C. Andres, 2016, Clinical biochemistry.

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

Annelot M. Dekker, Raymond D. Schellevis, P. Visscher, 2017 .

Further development of biomarkers in amyotrophic lateral sclerosis

P. Vourc'h, P. Corcia, P. Gordon, 2016, Expert review of molecular diagnostics.

Routine Determination of GFR in Renal Transplant Recipients by HPLC Quantification of Plasma Iohexol Concentrations and Comparison With Estimated GFR

P. Vourc'h, C. Andres, J. Halimi, 2012, Journal of clinical laboratory analysis.

The debated toxic role of aggregated TDP-43 in amyotrophic lateral sclerosis: a resolution in sight?

P. Vourc'h, C. Andres, P. Corcia, 2019, Brain : a journal of neurology.

A Rare Motor Neuron Deleterious Missense Mutation in the DPYSL3 (CRMP4) Gene is Associated with ALS

B. Pettmann, P. Andersen, V. Meininger, 2013, Human mutation.

Oligodendrocyte myelin glycoprotein (OMgp): evolution, structure and function

Christian Andres, P. Vourc'h, C. Andres, 2004, Brain Research Reviews.

A functional tetranucleotide (AAAT) polymorphism in an Alu element in the NF1 gene is associated with mental retardation

P. Vourc'h, L. Mignon, C. Andres, 2011, Neuroscience Letters.

Wildtype motoneurons, ALS‐Linked SOD1 mutation and glutamate profoundly modify astrocyte metabolism and lactate shuttling

P. Vourc'h, C. Andres, C. Raoul, 2017, Glia.

Disruption of TCA Cycle and Glutamate Metabolism Identified by Metabolomics in an In Vitro Model of Amyotrophic Lateral Sclerosis

D. Devos, P. Vourc'h, C. Andres, 2016, Molecular Neurobiology.

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis.

V. Meininger, P. Vourc'h, C. Andres, 2008, Archives of neurology.

Aβ1-42 and Tau as Potential Biomarkers for Diagnosis and Prognosis of Amyotrophic Lateral Sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2020, International journal of molecular sciences.

Metabo-lipidomics of Fibroblasts and Mitochondrial-Endoplasmic Reticulum Extracts from ALS Patients Shows Alterations in Purine, Pyrimidine, Energetic, and Phospholipid Metabolisms

C. Bris, G. Lenaers, P. Reynier, 2019, Molecular Neurobiology.

Inhibition of Pathogenic Mutant SOD1 Aggregation in Cultured Motor Neuronal Cells by Prevention of Its SUMOylation on Lysine 75

R. Uzbekov, P. Vourc'h, C. Andres, 2015, Neurodegenerative Diseases.

The Roles of NEDD4 Subfamily of HECT E3 Ubiquitin Ligases in Neurodevelopment and Neurodegeneration

P. Vourc'h, C. Andres, P. Corcia, 2022, International journal of molecular sciences.

GC-MS-based urine metabolic profiling of autism spectrum disorders

C. Barthélémy, P. Vourc'h, C. Andres, 2013, Analytical and Bioanalytical Chemistry.

Identification of metabolic pathway disturbances using multimodal metabolomics in autistic disorders in a Middle Eastern population

P. Vourc'h, C. Andres, L. Nadal-Desbarats, 2018, Journal of pharmaceutical and biomedical analysis.

Post hoc analysis of plasma amino acid profiles: towards a specific pattern in autism spectrum disorder and intellectual disability

P. Vourc'h, C. Andres, M. Raynaud, 2018, Annals of clinical biochemistry.

Advances in Cellular Models to Explore the Pathophysiology of Amyotrophic Lateral Sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2013, Molecular Neurobiology.

Development of monoclonal antibodies to human kallikrein-related peptidase 6 (KLK6) and their use in an immunofluorometric assay for free KLK6

P. Vourc'h, P. Corcia, C. Jolivet-Reynaud, 2014, Biological chemistry.

Influence of MMP-2 and MMP-9 promoter polymorphisms on gene expression and clinical outcome of non-small cell lung cancer.

P. Vourc'h, Y. Gruel, S. Iochmann, 2007, Lung cancer.

Benign lower limb amyotrophy due to TARDBP mutation or post-polio syndrome?

P. Vourc'h, C. Andres, P. Corcia, 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients

C. Barthélémy, P. Vourc'h, C. Andres, 2001, European Journal of Human Genetics.

Total Protein Level in Cerebrospinal Fluid is Stable in Elderly Adults

C. Hommet, K. Mondon, É. Beaufils, 2013, Journal of the American Geriatrics Society.

Behavior and serotonergic disorders in rats exposed prenatally to valproate: A model for autism

D. Guilloteau, C. Belzung, P. Vourc'h, 2010, Neuroscience Letters.

The specific metabolome profiling of patients infected by SARS-COV-2 supports the key role of tryptophan-nicotinamide pathway and cytosine metabolism

L. Plantier, P. Vourc'h, C. Andres, 2020, Scientific Reports.

Causative Genes in Amyotrophic Lateral Sclerosis and Protein Degradation Pathways: a Link to Neurodegeneration

P. Vourc'h, C. Andres, P. Corcia, 2018, Molecular Neurobiology.

[TBK1 gene stresses the major role of autophagy in ALS].

V. Meininger, P. Vourc'h, P. Corcia, 2015, Revue neurologique.

Iron Metabolism Disturbance in a French Cohort of ALS Patients

D. Devos, C. Moreau, P. Vourc'h, 2014, BioMed research international.

Autism and Nonsyndromic Mental Retardation Associated with a De Novo Mutation in the NLGN4X Gene Promoter Causing an Increased Expression Level

C. Barthélémy, P. Vourc'h, C. Andres, 2009, Biological Psychiatry.

Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesions

G. Lenaers, P. Reynier, V. Procaccio, 2018, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Panel of Oxidative Stress and Inflammatory Biomarkers in ALS: A Pilot Study

G. Garçon, D. Devos, P. Vourc'h, 2016, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Advances in disease-modifying pharmacotherapies for the treatment of amyotrophic lateral sclerosis

P. Vourc'h, P. Corcia, P. Couratier, 2020, Expert opinion on pharmacotherapy.

SMN1 gene, but not SMN2, is a risk factor for sporadic ALS

B. Giraudeau, P. Vourc'h, C. Andres, 2006, Neurology.

Some CSF Kynurenine Pathway Intermediates Associated with Disease Evolution in Amyotrophic Lateral Sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2021, Biomolecules.

Effect of the oligodendrocyte myelin glycoprotein (OMgp) on the expansion and neuronal differentiation of rat neural stem cells

C. Michelle, P. Vourc'h, C. Andres, 2009, Brain Research.

Metabolomics in amyotrophic lateral sclerosis: how far can it take us?

P. Vourc'h, P. Corcia, P. Gordon, 2016, European journal of neurology.

Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis

V. Meininger, P. Vourc'h, C. Andres, 2011, Journal of the Neurological Sciences.

Behavioral, Hormonal, Inflammatory, and Metabolic Effects Associated with FGF21-Pathway Activation in an ALS Mouse Model

P. Vourc'h, P. Corcia, C. Veyrat-Durebex, 2020, Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics.

Protein SUMOylation, an emerging pathway in amyotrophic lateral sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2013, The International journal of neuroscience.

Renal impairment and stroke risk assessment in patients with atrial fibrillation

A. Banerjee, L. Fauchier, P. Vourc'h, 2013 .

The Effect of SMN Gene Dosage on ALS Risk and Disease Severity

M. Eberle, A. Al-Chalabi, P. Andersen, 2021, Annals of neurology.

Homozygous SMN2 deletion is a protective factor in the Swedish ALS population

P. Andersen, P. Vourc'h, C. Andres, 2012, European Journal of Human Genetics.

LIMK2d, a truncated isoform of Lim kinase 2 regulates neurite growth in absence of the LIM kinase domain.

C. Michelle, P. Vourc'h, C. Andres, 2012, Biochemical and biophysical research communications.

Respiratory onset in an ALS family with L144F SOD1 mutation

P. Vourc'h, P. Corcia, P. Gordon, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

InFUSing antisense oligonucleotides for treating ALS.

P. Vourc'h, J. Cassereau, P. Codron, 2022, Trends in molecular medicine.

Exclusion of the coding sequence of the doublecortin gene as a susceptibility locus in autistic disorder.

C. Barthélémy, P. Vourc'h, C. Andres, 2002, American journal of medical genetics.

A role for SUMOylation in the Formation and Cellular Localization of TDP-43 Aggregates in Amyotrophic Lateral Sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2019, Molecular Neurobiology.

Deep sequencing is an appropriate tool for the selection of unique Hepatitis C virus (HCV) variants after single genomic amplification

A. Moreau, P. Vourc'h, C. Gaudy-Graffin, 2017, PloS one.

Association of a paraneoplastic motor neuron disease with anti-Ri antibodies and a novel SOD1 I18del mutation

C. Diard-Detoeuf, P. Vourc'h, C. Andres, 2014, Journal of the Neurological Sciences.

A novel SOD1 mutation p.V31A identified with a slowly progressive form of amyotrophic lateral sclerosis

J. Pouget, P. Vourc'h, C. Andres, 2014, Neurobiology of Aging.

Inflammatory mediators, lipoproteins and apolipoproteins in early diagnosis of Amyotrophic Lateral Sclerosis.

P. Vourc'h, C. Andres, P. Corcia, 2022, SLAS technology.

Phenotypic and genotypic studies of ALS cases in ALS-SMA families

V. Meininger, F. Salachas, F. Viader, 2018, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Lipidomics Reveals Cerebrospinal-Fluid Signatures of ALS

G. Lenaers, P. Reynier, P. Vourc'h, 2017, Scientific Reports.

A decrease in blood cholesterol after gastrostomy could impact survival in ALS

V. Meininger, P. Vourc'h, P. Corcia, 2017, European Journal of Clinical Nutrition.

Biological follow‐up in amyotrophic lateral sclerosis: decrease in creatinine levels and increase in ferritin levels predict poor prognosis

P. Vourc'h, P. Corcia, E. Piver, 2015, European journal of neurology.

The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

CADASIL and ALS: A link?

P. Vourc'h, C. Andres, P. Corcia, 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

The post-translational modification SUMO affects TDP-43 phase separation, compartmentalization, and aggregation in a zebrafish model

P. Vourc'h, C. Maurel, R. Chung, 2022, bioRxiv.

A novel mutation of the C-terminal amino acid of FUS (Y526C) strengthens FUS gene as the most frequent genetic factor in aggressive juvenile ALS

P. Vourc'h, C. Andres, P. Corcia, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Conditioned Medium from Cells Overexpressing TDP-43 Alters the Metabolome of Recipient Cells

P. Vourc'h, C. Andres, P. Corcia, 2020, Cells.

Absence of the OPTN mutation in a patient with ALS and familial primary open angle glaucoma

P. Vourc'h, P. Corcia, P. Gordon, 2011, Journal of the Neurological Sciences.

Pure cerebellar ataxia linked to large C9orf72 repeat expansion

V. Meininger, P. Vourc'h, C. Andres, 2016, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Co-occurrence of progressive anarthria with an S393L TARDBP mutation and ALS within a family

P. Vourc'h, P. Corcia, C. Veyrat-Durebex, 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Primary lateral sclerosis may occur within familial amyotrophic lateral sclerosis pedigrees

P. Vourc'h, P. Corcia, J. Praline, 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Taking Advantages of Blood–Brain or Spinal Cord Barrier Alterations or Restoring Them to Optimize Therapy in ALS?

J. Escoffre, P. Vourc'h, C. Andres, 2022, Journal of personalized medicine.

The combination of four analytical methods to explore skeletal muscle metabolomics: Better coverage of metabolic pathways or a marketing argument?

P. Reynier, F. Bonnier, P. Vourc'h, 2018, Journal of pharmaceutical and biomedical analysis.

Study of the serotonin transporter (SLC6A4) and BDNF genes in French patients with non syndromic mental deficiency

P. Vourc'h, L. Mignon, C. Andres, 2010, BMC Medical Genetics.

Typical bulbar ALS can be linked to GARS mutation

P. Vourc'h, P. Corcia, S. Marouillat, 2019, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Hemin decreases cardiac oxidative stress and fibrosis in a rat model of systemic hypertension via PI3K/Akt signalling.

V. Eder, P. Vourc'h, K. Belmokhtar, 2011, Cardiovascular research.

Mutations in the tail domain of the neurofilament heavy chain gene increase the risk of amyotrophic lateral sclerosis

A. Al-Chalabi, J. Glass, J. Landers, 2022, medRxiv.

Metabolic Profile and Pathological Alterations in the Muscle of Patients with Early-Stage Amyotrophic Lateral Sclerosis

P. Reynier, P. Vourc'h, C. Andres, 2022, Biomedicines.

Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival

Ashley R. Jones, G. Breen, A. Al-Chalabi, 2022, Frontiers in Cellular Neuroscience.

ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization

Annelot M. Dekker, A. Al-Chalabi, C. Shaw, 2020, Brain communications.

Search for RASA1 Variants in Capillary Malformations of the Legs in 113 Children: Results from the French National Paediatric Cohort CONAPE.

C. Chiaverini, P. Vourc'h, C. Andres, 2018, Acta dermato-venereologica.

The BDNF Val66Met polymorphism is associated with escitalopram response in depressed patients

V. Camus, C. Belzung, P. Vourc'h, 2015, Psychopharmacology.

Treatment of hereditary amyotrophic lateral sclerosis.

P. Vourc'h, H. Blasco, S. Beltran, 2022, Revue neurologique.

Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data

Ross P. Byrne, Ashley R. Jones, A. Al-Chalabi, 2022, Frontiers in Cellular Neuroscience.

Relation between pH alterations in cellular models of amyotrophic lateral sclerosis and TDP-43 protein aggregation

P. Vourc'h, S. Marouillat, H. Blasco, 2022, bioRxiv.

Comparison between PFN1 and SOD1 mutations in amyotrophic lateral sclerosis

V. Meininger, P. Vourc'h, H. Blasco, 2022, European journal of neurology.

Familial clustering of primary lateral sclerosis and amyotrophic lateral sclerosis: Supplementary evidence for a continuum

M. Carvalho, P. Vourc'h, S. Pinto, 2021, European Journal of Neurology.

Causative Genes in Amyotrophic Lateral Sclerosis and Protein Degradation Pathways: a Link to Neurodegeneration

P. Vourc'h, S. Marouillat, H. Blasco, 2018, Molecular Neurobiology.

Multiple capillary malformations of progressive onset: Capillary malformation-arteriovenous malformation syndrome (CM-AVM).

L. Misery, P. Vourc'h, K. L'herondelle, 2018, Annales de dermatologie et de venereologie.

Omics to Explore Amyotrophic Lateral Sclerosis Evolution: the Central Role of Arginine and Proline Metabolism

P. Vourc'h, C. Andres, P. Corcia, 2017, Molecular Neurobiology.

Partial recovery of dopaminergic pathway after graft of adult mesenchymal stem cells in a rat model of Parkinson's disease

D. Guilloteau, P. Vourc'h, L. Sensébé, 2008, Neurochemistry International.

mRNA-selective translation induced by FSH in primary Sertoli cells.

J. Morales, A. Poupon, P. Vourc'h, 2012, Molecular endocrinology.

Adult reserve stem cells and their potential for tissue engineering

Robert A. Bray, Louis Terracio, Haruchika Masuda, 2007, Cell Biochemistry and Biophysics.

Molecular analysis of the oligodendrocyte myelin glycoprotein gene in autistic disorder

C. Barthélémy, P. Vourc'h, C. Andres, 2003, Neuroscience Letters.

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Ewout J. N. Groen, Annelot M. Dekker, Ross P. Byrne, 2021, Nature Genetics.

Genome-wide study of DNA methylation in Amyotrophic Lateral Sclerosis identifies differentially methylated loci and implicates metabolic, inflammatory and cholesterol pathways

Annelot M. Dekker, Ahmad Al Khleifat, N. Wray, 2021, medRxiv.

Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS

Annelot M. Dekker, N. Wray, A. McRae, 2022, Science Translational Medicine.

Ductal adenocarcinoma of the prostate: Clinical and biological profiles

L. Salomon, Y. Allory, F. Bruyère, 2017, The Prostate.

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

Ross P. Byrne, Ashley R. Jones, A. Al-Chalabi, 2022, NPJ genomic medicine.

Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders

P. Vourc'h, C. Andres, S. Marouillat, 2019, Molecular genetics & genomic medicine.

Metabolomics: A Tool to Understand the Impact of Genetic Mutations in Amyotrophic Lateral Sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2020, Genes.

Genetics of amyotrophic lateral sclerosis.

V. Meininger, P. Vourc'h, C. Andres, 2017, Revue neurologique.

A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population

M. Palkovits, P. Vourc'h, C. Andres, 2015, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Advances in Cellular Models to Explore the Pathophysiology of Amyotrophic Lateral Sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2014, Molecular Neurobiology.

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

Denis C. Bauer, Annelot M. Dekker, Ashley R. Jones, 2017, Nature Communications.

A deletion causing NF2 exon 9 skipping is associated with familial autosomal dominant intramedullary ependymoma.

A. Kitzis, B. Parfait, P. Vourc'h, 2014, Neuro-oncology.

Isolation and characterization of cells with neurogenic potential from adult skeletal muscle.

M. Chesselet, P. Vourc'h, H. E. Young, 2004, Biochemical and biophysical research communications.

Neuronal differentiation of stem cells isolated from adult muscle

M. Chesselet, P. Vourc'h, H. E. Young, 2002, Journal of neuroscience research.

1H-NMR-Based Metabolomic Profiling of CSF in Early Amyotrophic Lateral Sclerosis

Patrick Emond, Caroline Moreau, David Devos, 2010, PloS one.

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Ewout J. N. Groen, Annelot M. Dekker, Ross P. Byrne, 2021, Nature Genetics.

Genes containing hexanucleotide repeats resembling C9ORF72 and expressed in the central nervous system are frequent in the human genome

P. Vourc'h, C. Andres, P. Corcia, 2020, Neurobiology of Aging.

Metabo-lipidomics of Fibroblasts and Mitochondrial-Endoplasmic Reticulum Extracts from ALS Patients Shows Alterations in Purine, Pyrimidine, Energetic, and Phospholipid Metabolisms

C. Bris, G. Lenaers, P. Reynier, 2019, Molecular Neurobiology.

Reply to the letter from Gazulla et al.

M. de Carvalho, P. Vourc'h, S. Pinto, 2021, European journal of neurology.

Impact of a frequent nearsplice SOD1 variant in amyotrophic lateral sclerosis: optimising SOD1 genetic screening for gene therapy opportunities

Y. Marie, V. Meininger, F. Salachas, 2021, Journal of Neurology, Neurosurgery, and Psychiatry.

The Relevancy of Data Regarding the Metabolism of Iron to Our Understanding of Deregulated Mechanisms in ALS; Hypotheses and Pitfalls

H. Puy, P. Vourc'h, C. Andres, 2019, Front. Neurosci..

Renal impairment and ischemic stroke risk assessment in patients with atrial fibrillation: the Loire Valley Atrial Fibrillation Project.

A. Banerjee, L. Fauchier, P. Vourc'h, 2013, Journal of the American College of Cardiology.

Xq27 FRAXA Locus is a Strong Candidate for Dyslexia: Evidence from a Genome-Wide Scan in French Families

D. Campion, C. Charon, A. Toutain, 2013, Behavior Genetics.

Dysregulations of Expression of Genes of the Ubiquitin/SUMO Pathways in an In Vitro Model of Amyotrophic Lateral Sclerosis Combining Oxidative Stress and SOD1 Gene Mutation

P. Vourc'h, C. Andres, P. Corcia, 2021, International journal of molecular sciences.

Mutation screening of the ubiquitin ligase gene RNF135 in French patients with autism

C. Barthélémy, A. Toutain, P. Vourc'h, 2015, Psychiatric genetics.

Rodent models for autism: A critical review

C. Belzung, P. Vourc'h, C. Andres, 2005 .

Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation

A. Rötig, P. Vourc'h, C. Andres, 2008, Human Genetics.

Mutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder

C. Barthélémy, P. Vourc'h, C. Andres, 2003, Psychiatric genetics.

Urinary Elimination of Coproporphyrins Is Dependent on ABCC2 Polymorphisms and Represents a Potential Biomarker of MRP2 Activity in Humans

J. Hulot, P. Vourc'h, C. Andres, 2011, Journal of biomedicine & biotechnology.

New Sampling Strategy Using a Bayesian Approach to Assess Iohexol Clearance in Kidney Transplant Recipients

P. Vourc'h, C. Andres, P. Gatault, 2012, Therapeutic drug monitoring.

The Metabolic Disturbances of Motoneurons Exposed to Glutamate

P. Vourc'h, C. Andres, C. Raoul, 2018, Molecular Neurobiology.

[Genetics of motor neuron disorders].

P. Vourc'h, P. Corcia, J. Praline, 2008, Revue neurologique.

Primary Lateral Sclerosis: Clinical, radiological and molecular features.

P. Vourc'h, P. Bede, J. Lope, 2021, Revue neurologique (Paris).

Fetal exposure to teratogens: Evidence of genes involved in autism

D. Guilloteau, P. Vourc'h, C. Andres, 2011, Neuroscience & Biobehavioral Reviews.

The oligodendrocyte-myelin glycoprotein gene is highly expressed during the late stages of myelination in the rat central nervous system.

P. Vourc'h, C. Andres, O. Mbarek, 2003, Brain research. Developmental brain research.

Xq27 FRAXA Locus is a Strong Candidate for Dyslexia: Evidence from a Genome-Wide Scan in French Families

D. Campion, C. Charon, A. Toutain, 2013, Behavior Genetics.

Roles of LIM kinases in central nervous system function and dysfunction

P. Vourc'h, B. Vallée, H. Bénédetti, 2015, FEBS letters.

Correction: 1H-NMR-Based Metabolomic Profiling of CSF in Early Amyotrophic Lateral Sclerosis

Patrick Emond, Caroline Moreau, David Devos, 2010, PLoS ONE.

1H-13C NMR-based urine metabolic profiling in autism spectrum disorders.

C. Barthélémy, P. Vourc'h, C. Andres, 2013, Talanta.

Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband

G. Rouleau, P. Vourc'h, C. Andres, 2007, Neuroscience Research.

C-reactive protein: A promising biomarker in ALS?

P. Vourc'h, P. Corcia, P. Couratier, 2017, Revue neurologique.

Low specificity of urinary 3-methoxytyramine in screening of dopamine-secreting pheochromocytomas and paragangliomas.

P. Vourc'h, C. Andres, H. Blasco, 2016, Clinical biochemistry.

Combined Metabolomics and Transcriptomics Approaches to Assess the IL-6 Blockade as a Therapeutic of ALS: Deleterious Alteration of Lipid Metabolism

P. Vourc'h, C. Andres, P. Corcia, 2016, Neurotherapeutics.

A prospective study of estimated glomerular filtration rate and outcomes in patients with atrial fibrillation: the Loire Valley Atrial Fibrillation Project.

A. Banerjee, L. Fauchier, P. Vourc'h, 2014, Chest.

A role for SUMOylation in the Formation and Cellular Localization of TDP-43 Aggregates in Amyotrophic Lateral Sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2019, Molecular Neurobiology.

Low IDL-B and high LDL-1 subfraction levels in serum of ALS patients

P. Vourc'h, C. Andres, P. Corcia, 2017, Journal of the Neurological Sciences.

A novel mutation in the cleavage site N291 of TDP-43 protein in a familial case of amyotrophic lateral sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2020, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Mutation in the RRM2 domain of TDP-43 in Amyotrophic Lateral Sclerosis with rapid progression associated with ubiquitin positive aggregates in cultured motor neurons

P. Vourc'h, C. Andres, P. Corcia, 2018, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on HECW1 Encoding the E3 Ligase NEDL1

P. Vourc'h, C. Andres, P. Corcia, 2023, International journal of molecular sciences.

APOE ε4 allele is associated with an increased risk of bulbar‐onset amyotrophic lateral sclerosis in men

P. Vourc'h, C. Andres, P. Corcia, 2011, European journal of neurology.

Effect of familial clustering in the genetic screening of 235 French ALS families

V. Meininger, F. Salachas, F. Viader, 2021, Journal of Neurology, Neurosurgery, and Psychiatry.

Variable effects of chronic subcutaneous administration of rotenone on striatal histology

M. Chesselet, P. Vourc'h, P. Fernagut, 2004, The Journal of comparative neurology.

TAR DNA-binding protein of 43 kDa (TDP-43) and amyotrophic lateral sclerosis (ALS): a promising therapeutic target

P. Vourc'h, P. Corcia, H. Blasco, 2022, Expert opinion on therapeutic targets.

Contribution of the dihydropyrimidinase-like proteins family in synaptic physiology and in neurodevelopmental disorders

P. Vourc'h, F. Laumonnier, M. Jeanne, 2023, Frontiers in Neuroscience.

Lipidomics Reveals Cerebrospinal-Fluid Signatures of ALS

G. Lenaers, P. Reynier, P. Vourc'h, 2017, Scientific Reports.

SOD1 mutation can mask C9orf72 abnormal expansion

P. Vourc'h, P. Corcia, P. Couratier, 2017, European Journal of Neurology.

Deficits in information transfer between hospital-based and primary-care physicians, the case of kidney disease: a cross-sectional study

B. Giraudeau, P. Vourc'h, J. Halimi, 2015, Journal of Nephrology.

NSC-34 Motor Neuron-Like Cells Are Unsuitable as Experimental Model for Glutamate-Mediated Excitotoxicity

P. Vourc'h, C. Andres, C. Raoul, 2016, Front. Cell. Neurosci..

TDP-43-Mediated Toxicity in HEK293T Cells: A Fast and Reproducible Protocol To Be Employed in the Search of New Therapeutic Options against Amyotrophic Lateral Sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2019, Cells.

LIMK2-1 is a Hominidae-Specific Isoform of LIMK2 Expressed in Central Nervous System and Associated with Intellectual Disability

A. Toutain, P. Vourc'h, C. Andres, 2019, Neuroscience.

Changes in glomerular filtration rate and outcomes in patients with atrial fibrillation

G. Lip, L. Fauchier, D. Babuty, 2017, American heart journal.

The Metabolic Disturbances of Motoneurons Exposed to Glutamate

P. Vourc'h, C. Andres, C. Raoul, 2018, Molecular Neurobiology.

Time for optimism in amyotrophic lateral sclerosis

P. Vourc'h, P. Corcia, P. Pradat, 2023 .

LIMK2-1, a new isoform of human LIMK2, regulates actin cytoskeleton remodeling via a different signaling pathway than that of its two homologs, LIMK2a and LIMK2b.

P. Vourc'h, C. Andres, D. Gosset, 2018, The Biochemical journal.

Pre-symptomatic diagnosis in ALS.

C. Cazeneuve, P. Vourc'h, P. Corcia, 2020, Revue neurologique.

Idiopathic Parkinson’s disease phenotype related to C9ORF72 repeat expansions: contribution of the neuropsychological assessment

C. Hommet, K. Mondon, É. Beaufils, 2013, BMC Research Notes.

Idiopathic Parkinson’s disease phenotype related to C9ORF72 repeat expansions: contribution of the neuropsychological assessment

C. Hommet, K. Mondon, É. Beaufils, 2013, BMC Research Notes.

TDP43 aggregates: the ‘Schrödinger’s cat’ in amyotrophic lateral sclerosis

P. Vourc'h, P. Corcia, H. Blasco, 2021, Nature Reviews Neuroscience.

Association study of the ubiquitin conjugating enzyme gene UBE2H in sporadic ALS

P. Vourc'h, C. Andres, P. Corcia, 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis

P. Vourc'h, C. Andres, W. Camu, 2012, Journal of the Neurological Sciences.

The future of ALS might move towards Genetic Therapy.

P. Vourc'h, P. Corcia, P. Couratier, 2021, Revue neurologique.

Deficit in BDNF does not increase vulnerability to stress but dampens antidepressant-like effects in the unpredictable chronic mild stress

C. Belzung, P. Vourc'h, C. Andres, 2009, Behavioural Brain Research.

Plasma creatinine and amyotrophic lateral sclerosis prognosis: a systematic review and meta-analysis

P. Vourc'h, C. Andres, H. Blasco, 2019, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Transplantation of multipotent cells extracted from adult skeletal muscles into the subventricular zone of adult rats

M. Chesselet, P. Vourc'h, L. Mignon, 2005, The Journal of comparative neurology.

A novel p.E121G SOD1 mutation in slowly progressive form of amyotrophic lateral sclerosis induces cytoplasmic aggregates in cultured motor neurons and reduces cell viability

B. Pettmann, P. Vourc'h, C. Andres, 2015, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Evaluation of arterial blood gas parameters as prognostic markers in amyotrophic lateral sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2023, European journal of neurology.

Unsupervised machine-learning identifies clinically distinct subtypes of ALS that reflect different genetic architectures and biological mechanisms

Ahmad Al Khleifat, A. Al-Chalabi, P. Andersen, 2023, medRxiv.

Oligodendrocyte myelin glycoprotein growth inhibition function requires its conserved leucine‐rich repeat domain, not its glycosylphosphatidyl‐inositol anchor

P. Vourc'h, C. Andres, T. Moreau, 2003, Journal of neurochemistry.

The BDNF Val66Met polymorphism is associated with escitalopram response in depressed patients

V. Camus, C. Belzung, P. Vourc'h, 2014, Psychopharmacology.

Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients

P. Vourc'h, C. Andres, P. Corcia, 2023, International journal of molecular sciences.

French National Protocol for genetic of amyotrophic lateral sclerosis.

P. Vourc'h, M. Soriani, K. Mouzat, 2023, Revue neurologique.

A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population

M. Palkovits, P. Vourc'h, C. Andres, 2015, Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration.

Protein SUMOylation, an emerging pathway in amyotrophic lateral sclerosis

P. Vourc'h, C. Andres, P. Corcia, 2013, The International journal of neuroscience.

Time for optimism in amyotrophic lateral sclerosis

P. Vourc'h, P. Corcia, P. Pradat, 2023, European journal of neurology.

Primary lateral sclerosis may occur within familial amyotrophic lateral sclerosis pedigrees

P. Vourc'h, P. Corcia, J. Praline, 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Impact of a frequent nearsplice SOD1 variant in Amyotrophic Lateral Sclerosis: optimizing SOD1 genetic screening for gene therapy opportunities

F. Salachas, M. Amador, C. Cazeneuve, 2022 .

Impact of a frequent nearsplice SOD1 variant in Amyotrophic Lateral Sclerosis: optimizing SOD1 genetic screening for gene therapy opportunities

F. Salachas, M. Amador, C. Cazeneuve, 2022 .

Genetic variability in sporadic amyotrophic lateral sclerosis

A. Al-Chalabi, P. Andersen, J. Glass, 2023, Brain : a journal of neurology.

Familial clustering of primary lateral sclerosis and amyotrophic lateral sclerosis: Supplementary evidence for a continuum

M. de Carvalho, P. Vourc'h, S. Pinto, 2021, European journal of neurology.

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

Annelot M. Dekker, Raymond D. Schellevis, Ashley R. Jones, 2016, Nature Genetics.

Could a citrus keep the haematologist away?

P. Vourc'h, P. Colombat, C. Dartigeas, 2014, British journal of haematology.