PubRank

Patrick Vourc'h

Author PubWeight™ 37.18‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis. Arch Neurol 2008 1.39
2 What was the set of ubiquitin and ubiquitin-like conjugating enzymes in the eukaryote common ancestor? J Mol Evol 2009 1.30
3 1H-NMR-based metabolomic profiling of CSF in early amyotrophic lateral sclerosis. PLoS One 2010 1.12
4 Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level. Biol Psychiatry 2009 1.11
5 Deficit in BDNF does not increase vulnerability to stress but dampens antidepressant-like effects in the unpredictable chronic mild stress. Behav Brain Res 2009 1.08
6 Partial recovery of dopaminergic pathway after graft of adult mesenchymal stem cells in a rat model of Parkinson's disease. Neurochem Int 2008 1.05
7 Variable effects of chronic subcutaneous administration of rotenone on striatal histology. J Comp Neurol 2004 1.04
8 Neuronal differentiation of stem cells isolated from adult muscle. J Neurosci Res 2002 1.03
9 Fetal exposure to teratogens: evidence of genes involved in autism. Neurosci Biobehav Rev 2010 1.02
10 Behavior and serotonergic disorders in rats exposed prenatally to valproate: a model for autism. Neurosci Lett 2009 0.96
11 Influence of MMP-2 and MMP-9 promoter polymorphisms on gene expression and clinical outcome of non-small cell lung cancer. Lung Cancer 2007 0.95
12 Renal impairment and ischemic stroke risk assessment in patients with atrial fibrillation: the Loire Valley Atrial Fibrillation Project. J Am Coll Cardiol 2013 0.92
13 Adult reserve stem cells and their potential for tissue engineering. Cell Biochem Biophys 2004 0.88
14 Co-occurrence of progressive anarthria with an S393L TARDBP mutation and ALS within a family. Amyotroph Lateral Scler 2011 0.88
15 Hemin decreases cardiac oxidative stress and fibrosis in a rat model of systemic hypertension via PI3K/Akt signalling. Cardiovasc Res 2011 0.87
16 A deletion causing NF2 exon 9 skipping is associated with familial autosomal dominant intramedullary ependymoma. Neuro Oncol 2013 0.84
17 Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis. J Neurol Sci 2012 0.84
18 1H-13C NMR-based urine metabolic profiling in autism spectrum disorders. Talanta 2013 0.83
19 Homozygous SMN2 deletion is a protective factor in the Swedish ALS population. Eur J Hum Genet 2012 0.83
20 Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis. J Neurol Sci 2011 0.83
21 Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation. Hum Genet 2008 0.82
22 GC-MS-based urine metabolic profiling of autism spectrum disorders. Anal Bioanal Chem 2013 0.82
23 Effect of the oligodendrocyte myelin glycoprotein (OMgp) on the expansion and neuronal differentiation of rat neural stem cells. Brain Res 2009 0.82
24 Protein SUMOylation, an emerging pathway in amyotrophic lateral sclerosis. Int J Neurosci 2013 0.81
25 A rare motor neuron deleterious missense mutation in the DPYSL3 (CRMP4) gene is associated with ALS. Hum Mutat 2013 0.80
26 Transplantation of multipotent cells extracted from adult skeletal muscles into the subventricular zone of adult rats. J Comp Neurol 2005 0.79
27 The BDNF Val(66)Met polymorphism is associated with escitalopram response in depressed patients. Psychopharmacology (Berl) 2014 0.79
28 mRNA-selective translation induced by FSH in primary Sertoli cells. Mol Endocrinol 2012 0.78
29 A functional tetranucleotide (AAAT) polymorphism in an Alu element in the NF1 gene is associated with mental retardation. Neurosci Lett 2011 0.78
30 Urinary elimination of coproporphyrins is dependent on ABCC2 polymorphisms and represents a potential biomarker of MRP2 activity in humans. J Biomed Biotechnol 2011 0.78
31 Idiopathic Parkinson's disease phenotype related to C9ORF72 repeat expansions: contribution of the neuropsychological assessment. BMC Res Notes 2013 0.78
32 Mutation screening of the ubiquitin ligase gene RNF135 in French patients with autism. Psychiatr Genet 2015 0.77
33 Primary lateral sclerosis may occur within familial amyotrophic lateral sclerosis pedigrees. Amyotroph Lateral Scler 2010 0.77
34 Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband. Neurosci Res 2007 0.77
35 CADASIL and ALS: a link? Amyotroph Lateral Scler 2010 0.77
36 Novel SOD1 mutation p.V31A identified with a slowly progressive form of amyotrophic lateral sclerosis. Neurobiol Aging 2013 0.76
37 Serum influence on in-vitro gene delivery using microbubble-assisted ultrasound. J Drug Target 2014 0.76
38 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. Amyotroph Lateral Scler Frontotemporal Degener 2014 0.76
39 The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis. Amyotroph Lateral Scler 2010 0.76
40 Inhibition of Pathogenic Mutant SOD1 Aggregation in Cultured Motor Neuronal Cells by Prevention of Its SUMOylation on Lysine 75. Neurodegener Dis 2015 0.75
41 LIMK2d, a truncated isoform of Lim kinase 2 regulates neurite growth in absence of the LIM kinase domain. Biochem Biophys Res Commun 2012 0.75
42 Routine determination of GFR in renal transplant recipients by HPLC quantification of plasma iohexol concentrations and comparison with estimated GFR. J Clin Lab Anal 2012 0.75
43 Study of the serotonin transporter (SLC6A4) and BDNF genes in French patients with non syndromic mental deficiency. BMC Med Genet 2010 0.75
44 Association study of the ubiquitin conjugating enzyme gene UBE2H in sporadic ALS. Amyotroph Lateral Scler 2009 0.75
45 Exclusion of the coding sequence of the doublecortin gene as a susceptibility locus in autistic disorder. Am J Med Genet 2002 0.75
46 Benign lower limb amyotrophy due to TARDBP mutation or post-polio syndrome? Amyotroph Lateral Scler Frontotemporal Degener 2013 0.75
47 Could a citrus keep the haematologist away? Br J Haematol 2014 0.75
48 Total protein level in cerebrospinal fluid is stable in elderly adults. J Am Geriatr Soc 2013 0.75
49 Development of monoclonal antibodies to human kallikrein-related peptidase 6 (KLK6) and their use in an immunofluorometric assay for free KLK6. Biol Chem 2014 0.75