Published in J Child Neurol on February 01, 2006
Mapping human genetic diversity in Asia. Science (2009) 7.40
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
High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastoma. Cancer Biol Ther (2009) 1.47
The contributions of oxytocin and vasopressin pathway genes to human behavior. Horm Behav (2011) 1.40
Spinal muscular atrophy: from gene discovery to clinical trials. Ann Hum Genet (2013) 1.15
Dynamics of co-transcriptional pre-mRNA folding influences the induction of dystrophin exon skipping by antisense oligonucleotides. PLoS One (2008) 1.09
Discovery of (2E)-3-{2-butyl-1-[2-(diethylamino)ethyl]-1H-benzimidazol-5-yl}-N-hydroxyacrylamide (SB939), an orally active histone deacetylase inhibitor with a superior preclinical profile. J Med Chem (2011) 0.89
U-shaped relation between plasma oxytocin levels and behavior in the trust game. PLoS One (2012) 0.88
Dopaminergic polymorphisms associated with time-on-task declines and fatigue in the Psychomotor Vigilance Test. PLoS One (2012) 0.87
A prospective study in the rational design of efficient antisense oligonucleotides for exon skipping in the DMD gene. Hum Gene Ther (2012) 0.86
Identification and characterisation of human dysferlin transcript variants: implications for dysferlin mutational screening and isoforms. Hum Genet (2009) 0.84
Acylurea connected straight chain hydroxamates as novel histone deacetylase inhibitors: Synthesis, SAR, and in vivo antitumor activity. Bioorg Med Chem Lett (2010) 0.82
Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes. BMC Genet (2009) 0.81
Paramyotonia congenita: from clinical diagnosis to in silico protein modeling analysis. Pediatr Int (2012) 0.81
Interpreting parents' concerns about their children's development with the Parents Evaluation of Developmental Status: culture matters. J Dev Behav Pediatr (2012) 0.80
Identification and characterization of a novel human dysferlin transcript: dysferlin_v1. Hum Genet (2006) 0.80
Dimeric gold nanoparticle assembly for detection and discrimination of single nucleotide mutation in Duchenne muscular dystrophy. Biosens Bioelectron (2010) 0.79
Factors predictive of outcome in childhood stroke in an Asian population. Ann Acad Med Singapore (2009) 0.78
Molecular diagnosis of neurogenetic disorders involving trinucleotide repeat expansions. Expert Rev Mol Diagn (2005) 0.77
N-Hydroxy-1,2-disubstituted-1H-benzimidazol-5-yl acrylamides as novel histone deacetylase inhibitors: design, synthesis, SAR studies, and in vivo antitumor activity. Bioorg Med Chem Lett (2009) 0.75
Efficient mining of haplotype patterns for linkage disequilibrium mapping. J Bioinform Comput Biol (2010) 0.75
IL-10 synergistically enhances GM-CSF-induced CCR1 expression in myelomonocytic cells. Biochem Biophys Res Commun (2003) 0.75
Should non-expert clinician examiners be used in objective structured assessment of communication skills among final year medical undergraduates? Med Teach (2007) 0.75