PubRank

Claudio Zucca

Author PubWeight™ 15.72‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome. PLoS Genet 2011 1.60
2 A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation. J Neurol Neurosurg Psychiatry 2010 1.04
3 Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletions. Eur J Hum Genet 2010 1.00
4 Pediatric biobanking: a pilot qualitative survey of practices, rules, and researcher opinions in ten European countries. Biopreserv Biobank 2011 0.94
5 Inter-rater reliability of the EEG reading in patients with childhood idiopathic epilepsy. Epilepsy Res 2005 0.90
6 Multimodal analysis of a sustained attention protocol: continuous performance test assessed with near infrared spectroscopy and EEG. Conf Proc IEEE Eng Med Biol Soc 2006 0.87
7 Complex segmental duplications mediate a recurrent dup(X)(p11.22-p11.23) associated with mental retardation, speech delay, and EEG anomalies in males and females. Am J Hum Genet 2009 0.85
8 Study of attentional processes in children with idiopathic epilepsy by Conners' Continuous Performance Test. J Child Neurol 2004 0.85
9 Analysis of the dynamical behaviour of the EEG rhythms during a test of sustained attention. Conf Proc IEEE Eng Med Biol Soc 2007 0.83
10 A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy. Epilepsia 2011 0.83
11 Ring chromosome 20 syndrome: a link between epilepsy onset and neuropsychological impairment in three children. Epilepsia 2009 0.82
12 Subtelomeric trisomy 21q: a new benign chromosomal variant. Eur J Med Genet 2006 0.80
13 Neuropsychological and behavioural aspects in children and adolescents with idiopathic epilepsy at diagnosis and after 12 months of treatment. Seizure 2010 0.80
14 Epilepsy and neuropsychologic deficit in a child with cerebellar astrocytoma. J Child Neurol 2006 0.78
15 Combined behavioral and EEG power analysis in DAI improve accuracy in the assessment of sustained attention deficit. Ann Biomed Eng 2008 0.78
16 Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature. Epilepsia 2012 0.77
17 Definition of the neurological phenotype associated with dup (X)(p11.22-p11.23). Epileptic Disord 2011 0.77
18 A novel mutation in STXBP1 gene in a child with epileptic encephalopathy and an atypical electroclinical pattern. J Child Neurol 2013 0.76
19 EEG-based index for engagement level monitoring during sustained attention. Conf Proc IEEE Eng Med Biol Soc 2015 0.75
20 International Classification of Functioning, Disability and Health in subjects with alternating hemiplegia of childhood. Disabil Rehabil 2009 0.75
21 Clinical experience with topiramate dosing and serum levels in patients with epilepsy. Seizure 2006 0.75