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Antonietta Coppola
Author PubWeight™ 35.39
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Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
N Engl J Med
2008
10.88
2
Characterization of a recurrent 15q24 microdeletion syndrome.
Hum Mol Genet
2007
3.54
3
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.
Arch Neurol
2011
1.61
4
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.
J Neurol
2007
1.54
5
A pulse rapamycin therapy for infantile spasms and associated cognitive decline.
Neurobiol Dis
2011
1.26
6
Levetiracetam for cerebellar tremor in multiple sclerosis: an open-label pilot tolerability and efficacy study.
J Neurol
2006
1.20
7
Dramatic response to levetiracetam in post-ischaemic Holmes' tremor.
J Neurol Neurosurg Psychiatry
2007
1.13
8
Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases.
Am J Med Genet A
2006
0.95
9
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.
Epilepsia
2012
0.94
10
The syndrome gelastic seizures-hypothalamic hamartoma: severe, potentially reversible encephalopathy.
Epilepsia
2009
0.88
11
Effect of VDR polymorphisms on growth and bone mineral density in homozygous beta thalassaemia.
Br J Haematol
2002
0.87
12
Modeling new therapies for infantile spasms.
Epilepsia
2010
0.87
13
Epileptic myoclonus as ciprofloxacin-associated adverse effect.
Mov Disord
2007
0.86
14
Beneficial effects of VEGF secreted from stromal cells in supporting endothelial cell functions: therapeutic implications for critical limb ischemia.
Cell Transplant
2010
0.85
15
Reflex seizures and reflex epilepsies: old models for understanding mechanisms of epileptogenesis.
Epilepsy Res
2012
0.85
16
Inherited neuromyotonia: a clinical and genetic study of a family.
Neuromuscul Disord
2006
0.84
17
Dramatic response to levetiracetam in post-ischaemic Holmes' tremor.
BMJ Case Rep
2009
0.83
18
Evidence for mTOR pathway activation in a spectrum of epilepsy-associated pathologies.
Acta Neuropathol Commun
2014
0.80
19
Life-threatening status epilepticus following gabapentin administration in a patient with benign adult familial myoclonic epilepsy.
Epilepsia
2007
0.79
20
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome).
Epilepsia
2008
0.78
21
Progress from genome-wide association studies and copy number variant studies in epilepsy.
Curr Opin Neurol
2016
0.78
22
A pilot open-label trial of zonisamide in Unverricht-Lundborg disease.
Mov Disord
2010
0.77
23
A clinical and genetic study of 33 new cases with early-onset absence epilepsy.
Epilepsy Res
2011
0.77
24
Neuropsychological findings in patients with Unverricht-Lundborg disease.
Epilepsy Behav
2009
0.77
25
SIRT1 inhibition affects angiogenic properties of human MSCs.
Biomed Res Int
2014
0.77
26
From Cannabis to Cannabidiol to Treat Epilepsy, Where Are We?
Curr Pharm Des
2016
0.77
27
Antiepileptic Drugs Under Investigation for Treatment of Focal Epilepsy.
Clin Neuropharmacol
2016
0.75
28
Severe epilepsy in an adult with partial trisomy 18q.
Am J Med Genet A
2014
0.75