C Nobile

Author PubWeight™ 26.36‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature 1986 4.13
2 Sleep habits and sleep disturbance in elementary school-aged children. J Dev Behav Pediatr 2000 2.49
3 Television-viewing habits and sleep disturbance in school children. Pediatrics 1999 1.77
4 cDNA sequences of human glucose 6-phosphate dehydrogenase cloned in pBR322. Nature 1981 1.69
5 Parental and self-report of sleep in children with attention-deficit/hyperactivity disorder. Arch Pediatr Adolesc Med 2000 1.63
6 Sleep and daytime behavior in children with obstructive sleep apnea and behavioral sleep disorders. Pediatrics 1998 1.38
7 Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases. Brain 2004 1.22
8 A 2.4-megabase physical map spanning the CYP2C gene cluster on chromosome 10q24. Genomics 1995 1.12
9 Adolescent motor vehicle crashes: the relationship between behavioral factors and self-reported injury. J Adolesc Health 2000 1.03
10 Nucleosome phasing on a DNA fragment from the replication origin of simian virus 40 and rephasing upon cruciform formation of the DNA. Mol Cell Biol 1986 0.97
11 Stable stem-loop and cruciform DNA structures: isolation of mutants with rearrangements of the palindromic sequence at the simian virus 40 replication origin. Intervirology 1986 0.96
12 Autosomal dominant partial epilepsy with auditory features: description of a new family. Epilepsia 2000 0.94
13 An integrated physical and genetic map spanning chromosome band 10q24. Genomics 1997 0.94
14 Incidence of parasomnias in children with obstructive sleep apnea. Sleep 1997 0.89
15 Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation. Neurology 2011 0.85
16 Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1. Neurology 2007 0.84
17 Increased expression of LGI1 gene triggers growth inhibition and apoptosis of neuroblastoma cells. J Cell Physiol 2006 0.83
18 A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures. Neurology 2007 0.83
19 Infantile acrodermatitis of Gianotti-Crosti and Lyme borreliosis. Acta Derm Venereol 1996 0.83
20 LGI1 microdeletion in autosomal dominant lateral temporal epilepsy. Neurology 2012 0.81
21 Concurrent mapping of an adenovirus 5/SV40 integration site and the U1 snRNA cluster (RNU1) within 400 kb of the chromosome region 1p36.1. Cytogenet Cell Genet 1994 0.78
22 X-linked muscular dystrophies: studies through functional assay and DNA polymorphisms. Adv Neurol 1988 0.75
23 Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy. Epilepsy Res 2006 0.75
24 [Sex education in the context of school health education]. Minerva Med 1967 0.75
25 [Combined hypnosis and logotherapy in 3 severe neurotics]. Minerva Med 1967 0.75
26 Molecular analysis of the Rett syndrome using cDNA synapsin I as a probe. Brain Dev 1990 0.75
27 Detailed physical analysis of a 1.5-megabase YAC contig containing the MXI1 and ADRA2A genes. Genomics 1997 0.75
28 [A case of absolute somnambulistic "succubance"]. Minerva Med 1968 0.75