Published in Clin Chim Acta on March 17, 2010
Convergence of miRNA expression profiling, α-synuclein interacton and GWAS in Parkinson's disease. PLoS One (2011) 1.19
Lysine 92 amino acid residue of USP46, a gene associated with 'behavioral despair' in mice, influences the deubiquitinating enzyme activity. PLoS One (2011) 0.84
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Identification of candidate genes for familial early-onset essential tremor. Eur J Hum Genet (2015) 0.75
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Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals. Hum Mol Genet (2006) 5.50
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Evolutionary toggling of the MAPT 17q21.31 inversion region. Nat Genet (2008) 3.42
A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. Lancet Neurol (2007) 2.99
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease. Ann Neurol (2008) 2.95
Identification of a novel risk variant in the FUS gene in essential tremor. Neurology (2013) 2.84
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans. PLoS Genet (2007) 2.09
Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis. Hum Mol Genet (2003) 1.96
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Hum Mol Genet (2009) 1.93
Cerenkov radiation imaging as a method for quantitative measurements of beta particles in a microfluidic chip. Phys Med Biol (2009) 1.78
Hirayama flexion myelopathy: neutral-position MR imaging findings--importance of loss of attachment. Radiology (2004) 1.54
Genomewide SNP assay reveals mutations underlying Parkinson disease. Hum Mutat (2008) 1.49
Glucocerebrosidase gene mutation is a risk factor for early onset of Parkinson disease among Taiwanese. J Neurol Neurosurg Psychiatry (2007) 1.47
Dystonia as a presenting sign of spinocerebellar ataxia type 1. Mov Disord (2004) 1.46
Effect of statin treatment on adrenomyeloneuropathy with cerebral inflammation: a revisit. Clin Neurol Neurosurg (2012) 1.38
Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease. Am J Hum Genet (2006) 1.32
Untangling the tau gene association with neurodegenerative disorders. Hum Mol Genet (2006) 1.27
A clinical study of Hirayama disease in Taiwan. Muscle Nerve (2008) 1.22
Analysis of heat-shock protein 70 gene polymorphisms and the risk of Parkinson's disease. Hum Genet (2003) 1.19
Nanoscale control of phase variants in strain-engineered BiFeO₃. Nano Lett (2011) 1.16
Biomonitoring of bisphenol A concentrations in maternal and umbilical cord blood in regard to birth outcomes and adipokine expression: a birth cohort study in Taiwan. Environ Health (2011) 1.12
A rapid pathway toward a superb gene delivery system: programming structural and functional diversity into a supramolecular nanoparticle library. ACS Nano (2010) 1.10
Zinc oxide nanoparticles interfere with zinc ion homeostasis to cause cytotoxicity. Toxicol Sci (2011) 1.06
Whole blood-derived microRNA signatures in mice exposed to lipopolysaccharides. J Biomed Sci (2012) 1.06
Nanofiber optic sensor based on the excitation of surface plasmon wave near fiber tip. J Biomed Opt (2006) 1.04
Modulation of energy deficiency in Huntington's disease via activation of the peroxisome proliferator-activated receptor gamma. Hum Mol Genet (2010) 1.03
Maternal return to work and breastfeeding: a population-based cohort study. Int J Nurs Stud (2009) 1.02
Association of biometric factors with anterior chamber angle widening and intraocular pressure reduction after uneventful phacoemulsification for cataract. J Cataract Refract Surg (2011) 1.01
Local conduction at the BiFeO(3)-CoFe(2)O(4) tubular oxide interface. Adv Mater (2012) 1.00
SCA17 repeat expansion: mildly expanded CAG/CAA repeat alleles in neurological disorders and the functional implications. Clin Chim Acta (2009) 1.00
Profiling circulating microRNA expression in experimental sepsis using cecal ligation and puncture. PLoS One (2013) 0.99
Profiling muscle-specific microRNA expression after peripheral denervation and reinnervation in a rat model. J Neurotrauma (2009) 0.98
Histone H2B C-terminal helix mediates trans-histone H3K4 methylation independent of H2B ubiquitination. Mol Cell Biol (2010) 0.97
Electrophysiological features of Hirayama disease. Muscle Nerve (2011) 0.97
Dysregulation of C/EBPalpha by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease. Hum Mol Genet (2007) 0.97
A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan. BMC Neurol (2006) 0.96
Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease. Mov Disord (2006) 0.96
Atomic-scale evolution of local electronic structure across multiferroic domain walls. Adv Mater (2011) 0.96
The JmjN domain of Jhd2 is important for its protein stability, and the plant homeodomain (PHD) finger mediates its chromatin association independent of H3K4 methylation. J Biol Chem (2010) 0.96
Pantothenate kinase-associated neurodegeneration in two Taiwanese siblings: identification of a novel PANK2 gene mutation. Mov Disord (2009) 0.96
SCA8 mRNA expression suggests an antisense regulation of KLHL1 and correlates to SCA8 pathology. Brain Res (2008) 0.95
Spontaneous intrapetrous internal carotid artery dissection: a case report and literature review. J Neurol Sci (2007) 0.94
Detection of Hunter syndrome (mucopolysaccharidosis type II) in Taiwanese: biochemical and linkage studies of the iduronate-2-sulfatase gene defects in MPS II patients and carriers. Clin Chim Acta (2006) 0.94
Tuning the competition between ferromagnetism and antiferromagnetism in a half-doped manganite through magnetoelectric coupling. Phys Rev Lett (2013) 0.93
Differences in iris thickness among African Americans, Caucasian Americans, Hispanic Americans, Chinese Americans, and Filipino-Americans. J Glaucoma (2013) 0.93
Distribution of micromotion in implants and alveolar bone with different thread profiles in immediate loading: a finite element study. Int J Oral Maxillofac Implants (2012) 0.93
Structural genomic variation in ischemic stroke. Neurogenetics (2008) 0.93
Intrahippocampal administration of A beta(1-40) impairs spatial learning and memory in hyperglycemic mice. Neurobiol Learn Mem (2007) 0.93
Epitaxial photostriction-magnetostriction coupled self-assembled nanostructures. ACS Nano (2012) 0.93
Deleted 4977-bp mitochondrial DNA mutation is associated with sporadic amyotrophic lateral sclerosis: a hospital-based case-control study. Muscle Nerve (2003) 0.93
Intractable epilepsy as the presentation of vitamin B deficiency in the absence of macrocytic anemia. Epilepsia (2005) 0.92
Microfluidic-based 18F-labeling of biomolecules for immuno-positron emission tomography. Mol Imaging (2011) 0.92
Characterization of cortical neuron outgrowth in two- and three-dimensional culture systems. J Biomed Mater Res B Appl Biomater (2005) 0.92
Cellular site and molecular mode of synapsin action in associative learning. Learn Mem (2011) 0.91
Mitochondrial dysfunction and oxidative stress contribute to the pathogenesis of spinocerebellar ataxia type 12 (SCA12). J Biol Chem (2011) 0.91
Bilateral common carotid artery occlusion--a case report and literature review. J Neurol Sci (2005) 0.91
Surgical outcomes and prognostic factors of oral cancer associated with betel quid chewing and tobacco smoking in Taiwan. Oral Oncol (2010) 0.91
Concomitant spinal cord and vertebral body infarction is highly associated with aortic pathology: a clinical and magnetic resonance imaging study. J Neurol (2009) 0.90
Entrapment neuropathy results in different microRNA expression patterns from denervation injury in rats. BMC Musculoskelet Disord (2010) 0.90
Novel 2-step synthetic indole compound 1,1,3-tri(3-indolyl)cyclohexane inhibits cancer cell growth in lung cancer cells and xenograft models. Cancer (2008) 0.90
Role of the CCAAT-binding protein NFY in SCA17 pathogenesis. PLoS One (2012) 0.89
Assessing replication and beta cell function in adenovirally-transduced isolated rodent islets. J Vis Exp (2012) 0.89
Increased oxidative damage in peripheral blood correlates with severity of Parkinson's disease. Neurobiol Dis (2008) 0.89
The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairment. Parkinsonism Relat Disord (2006) 0.88
The A2A adenosine receptor rescues the urea cycle deficiency of Huntington's disease by enhancing the activity of the ubiquitin-proteasome system. Hum Mol Genet (2009) 0.88
Eradication of Helicobacter pylori infection by the probiotic strains Lactobacillus johnsonii MH-68 and L. salivarius ssp. salicinius AP-32. Helicobacter (2012) 0.88
Preparation of amino-acid-type selective isotope labeling of protein expressed in Pichia pastoris. Proteins (2006) 0.88
Sumoylation-promoted enterovirus 71 3C degradation correlates with a reduction in viral replication and cell apoptosis. J Biol Chem (2011) 0.88
Tumor necrosis factor-alpha promoter polymorphism is associated with the risk of Parkinson's disease. Am J Med Genet B Neuropsychiatr Genet (2007) 0.88
Circulating microRNA signatures in mice exposed to lipoteichoic acid. J Biomed Sci (2013) 0.88
The short-term effects of air pollution on adolescent lung function in Taiwan. Chemosphere (2011) 0.87
Exendin-4 protected against cognitive dysfunction in hyperglycemic mice receiving an intrahippocampal lipopolysaccharide injection. PLoS One (2012) 0.87
Serum ferritin and risk of the metabolic syndrome: a population-based study. Asia Pac J Clin Nutr (2013) 0.87
Clinical and radiological findings suggesting disorders other than tolosa-hunt syndrome among ophthalmoplegic patients: a retrospective analysis. Headache (2015) 0.87
Genetic analysis of NFE2L2 promoter variation in Taiwanese Parkinson's disease. Parkinsonism Relat Disord (2012) 0.87
Spinocerebellar ataxia type 8 larger triplet expansion alters histone modification and induces RNA foci. BMC Mol Biol (2009) 0.86
Dysregulated brain creatine kinase is associated with hearing impairment in mouse models of Huntington disease. J Clin Invest (2011) 0.86
Exploring topological defects in epitaxial BiFeO3 thin films. ACS Nano (2011) 0.86
The need for appropriate genotyping strategies for glucocerebrosidase mutations in cohorts with Parkinson disease. Arch Neurol (2008) 0.86