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Frédérique René
Author PubWeight™ 13.60
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Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
Evidence for defective energy homeostasis in amyotrophic lateral sclerosis: benefit of a high-energy diet in a transgenic mouse model.
Proc Natl Acad Sci U S A
2004
2.26
2
Sodium valproate exerts neuroprotective effects in vivo through CREB-binding protein-dependent mechanisms but does not improve survival in an amyotrophic lateral sclerosis mouse model.
J Neurosci
2007
1.52
3
Increased peripheral lipid clearance in an animal model of amyotrophic lateral sclerosis.
J Lipid Res
2007
1.09
4
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons.
Hum Mol Genet
2010
1.09
5
Amyotrophic lateral sclerosis: all roads lead to Rome.
J Neurochem
2007
0.99
6
Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age.
Neurobiol Dis
2013
0.96
7
Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis.
Hum Mol Genet
2013
0.89
8
Evidence of a dosage effect and a physiological endplate acetylcholinesterase deficiency in the first mouse models mimicking Schwartz-Jampel syndrome neuromyotonia.
Hum Mol Genet
2008
0.89
9
Degeneration of serotonergic neurons in amyotrophic lateral sclerosis: a link to spasticity.
Brain
2012
0.82
10
A mouse model of Schwartz-Jampel syndrome reveals myelinating Schwann cell dysfunction with persistent axonal depolarization in vitro and distal peripheral nerve hyperexcitability when perlecan is lacking.
Am J Pathol
2012
0.82
11
The Onecut transcription factor HNF-6 regulates in motor neurons the formation of the neuromuscular junctions.
PLoS One
2012
0.80
12
Neuroendocrinology of neurodegenerative diseases. Insights from transgenic mouse models.
Neuroendocrinology
2003
0.78
13
Evaluating Behavior in Mouse Models of the Behavioral Variant of Frontotemporal Dementia: Which Test for Which Symptom?
Neurodegener Dis
2015
0.77