|
1
|
Mapping human genetic diversity in Asia.
|
Science
|
2009
|
7.40
|
|
2
|
Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping.
|
Am J Hum Genet
|
2003
|
4.58
|
|
3
|
High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastoma.
|
Cancer Biol Ther
|
2009
|
1.47
|
|
4
|
The contributions of oxytocin and vasopressin pathway genes to human behavior.
|
Horm Behav
|
2011
|
1.40
|
|
5
|
Spinal muscular atrophy: from gene discovery to clinical trials.
|
Ann Hum Genet
|
2013
|
1.15
|
|
6
|
Dynamics of co-transcriptional pre-mRNA folding influences the induction of dystrophin exon skipping by antisense oligonucleotides.
|
PLoS One
|
2008
|
1.09
|
|
7
|
U-shaped relation between plasma oxytocin levels and behavior in the trust game.
|
PLoS One
|
2012
|
0.88
|
|
8
|
Dopaminergic polymorphisms associated with time-on-task declines and fatigue in the Psychomotor Vigilance Test.
|
PLoS One
|
2012
|
0.87
|
|
9
|
A prospective study in the rational design of efficient antisense oligonucleotides for exon skipping in the DMD gene.
|
Hum Gene Ther
|
2012
|
0.86
|
|
10
|
Identification and characterisation of human dysferlin transcript variants: implications for dysferlin mutational screening and isoforms.
|
Hum Genet
|
2009
|
0.84
|
|
11
|
Paramyotonia congenita: from clinical diagnosis to in silico protein modeling analysis.
|
Pediatr Int
|
2012
|
0.81
|
|
12
|
Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes.
|
BMC Genet
|
2009
|
0.81
|
|
13
|
Identification and characterization of a novel human dysferlin transcript: dysferlin_v1.
|
Hum Genet
|
2006
|
0.80
|
|
14
|
Dimeric gold nanoparticle assembly for detection and discrimination of single nucleotide mutation in Duchenne muscular dystrophy.
|
Biosens Bioelectron
|
2010
|
0.79
|
|
15
|
Molecular diagnosis of neurogenetic disorders involving trinucleotide repeat expansions.
|
Expert Rev Mol Diagn
|
2005
|
0.77
|
|
16
|
Diagnostic strategy for the detection of dystrophin gene mutations in asian patients and carriers using immortalized cell lines.
|
J Child Neurol
|
2006
|
0.75
|
|
17
|
Efficient mining of haplotype patterns for linkage disequilibrium mapping.
|
J Bioinform Comput Biol
|
2010
|
0.75
|
|
18
|
IL-10 synergistically enhances GM-CSF-induced CCR1 expression in myelomonocytic cells.
|
Biochem Biophys Res Commun
|
2003
|
0.75
|