PubRank
Search
About
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