PubRank

Chiung-Mei Chen

Author PubWeight™ 59.41‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Identification of a novel risk variant in the FUS gene in essential tremor. Neurology 2013 2.84
2 Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis. Hum Mol Genet 2003 1.96
3 Hirayama flexion myelopathy: neutral-position MR imaging findings--importance of loss of attachment. Radiology 2004 1.54
4 Glucocerebrosidase gene mutation is a risk factor for early onset of Parkinson disease among Taiwanese. J Neurol Neurosurg Psychiatry 2007 1.47
5 Dystonia as a presenting sign of spinocerebellar ataxia type 1. Mov Disord 2004 1.46
6 Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease. Am J Hum Genet 2006 1.32
7 A clinical study of Hirayama disease in Taiwan. Muscle Nerve 2008 1.22
8 Analysis of heat-shock protein 70 gene polymorphisms and the risk of Parkinson's disease. Hum Genet 2003 1.19
9 Modulation of energy deficiency in Huntington's disease via activation of the peroxisome proliferator-activated receptor gamma. Hum Mol Genet 2010 1.03
10 Electrophysiological features of Hirayama disease. Muscle Nerve 2011 0.97
11 Dysregulation of C/EBPalpha by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease. Hum Mol Genet 2007 0.97
12 A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan. BMC Neurol 2006 0.96
13 Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease. Mov Disord 2006 0.96
14 Pantothenate kinase-associated neurodegeneration in two Taiwanese siblings: identification of a novel PANK2 gene mutation. Mov Disord 2009 0.96
15 SCA8 mRNA expression suggests an antisense regulation of KLHL1 and correlates to SCA8 pathology. Brain Res 2008 0.95
16 Spontaneous intrapetrous internal carotid artery dissection: a case report and literature review. J Neurol Sci 2007 0.94
17 Intrahippocampal administration of A beta(1-40) impairs spatial learning and memory in hyperglycemic mice. Neurobiol Learn Mem 2007 0.93
18 Deleted 4977-bp mitochondrial DNA mutation is associated with sporadic amyotrophic lateral sclerosis: a hospital-based case-control study. Muscle Nerve 2003 0.93
19 Intractable epilepsy as the presentation of vitamin B deficiency in the absence of macrocytic anemia. Epilepsia 2005 0.92
20 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
21 Role of the CCAAT-binding protein NFY in SCA17 pathogenesis. PLoS One 2012 0.89
22 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
23 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
24 Clinical and radiological findings suggesting disorders other than tolosa-hunt syndrome among ophthalmoplegic patients: a retrospective analysis. Headache 2015 0.87
25 Genetic analysis of NFE2L2 promoter variation in Taiwanese Parkinson's disease. Parkinsonism Relat Disord 2012 0.87
26 The need for appropriate genotyping strategies for glucocerebrosidase mutations in cohorts with Parkinson disease. Arch Neurol 2008 0.86
27 Spinocerebellar ataxia type 8 larger triplet expansion alters histone modification and induces RNA foci. BMC Mol Biol 2009 0.86
28 Dysregulated brain creatine kinase is associated with hearing impairment in mouse models of Huntington disease. J Clin Invest 2011 0.86
29 Ubiquitin specific proteases USP24 and USP40 and ubiquitin thiolesterase UCHL1 polymorphisms have synergic effect on the risk of Parkinson's disease among Taiwanese. Clin Chim Acta 2010 0.86
30 Decreased intrathecal synthesis of prostaglandin D2 synthase in the cerebrospinal fluid of patients with acute inflammatory demyelinating polyneuropathy. J Neuroimmunol 2008 0.85
31 Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan. Neurosci Lett 2005 0.85
32 Altered expression of HSPA5, HSPA8 and PARK7 in spinocerebellar ataxia type 17 identified by 2-dimensional fluorescence difference in gel electrophoresis. Clin Chim Acta 2008 0.85
33 Association of TNF-alpha gene with spontaneous deep intracerebral hemorrhage in the Taiwan population: a case control study. BMC Neurol 2010 0.85
34 Neuroprotective effects of granulocyte-colony stimulating factor in a novel transgenic mouse model of SCA17. J Neurochem 2011 0.85
35 Analyses of transthyretin concentration in the cerebrospinal fluid of patients with Guillain-Barré syndrome and other neurological disorders. Clin Chim Acta 2009 0.84
36 Markedly asymmetrical parkinsonism as a leading feature of adult-onset Huntington's disease. Mov Disord 2004 0.83
37 Genetic variants ofLRRK2 in Taiwanese Parkinson's disease. PLoS One 2013 0.83
38 SLC1A2 variant is associated with essential tremor in Taiwanese population. PLoS One 2013 0.82
39 A comparison of benign and inflammatory manifestations of Tolosa-Hunt syndrome. Cephalalgia 2013 0.82
40 Validation of a Chinese version of disease specific quality of life scale (HFS-36) for hemifacial spasm in Taiwan. Health Qual Life Outcomes 2009 0.82
41 Phenotypic features and genetic findings in 2 chinese families with Miyoshi distal myopathy. Arch Neurol 2004 0.82
42 Elevated haptoglobin level of cerebrospinal fluid in Guillain-Barré syndrome revealed by proteomics analysis. Proteomics Clin Appl 2007 0.81
43 Genetic variations of GAK in two Chinese Parkinson's disease populations: a case-control study. PLoS One 2013 0.81
44 Increased prothrombin, apolipoprotein A-IV, and haptoglobin in the cerebrospinal fluid of patients with Huntington's disease. PLoS One 2011 0.81
45 The CAG repeat in SCA12 functions as a cis element to up-regulate PPP2R2B expression. Hum Genet 2010 0.80
46 Analyses of haptoglobin level in the cerebrospinal fluid and serum of patients with neuromyelitis optica and multiple sclerosis. Clin Chim Acta 2012 0.80
47 Aqueous Extract of Paeonia lactiflora and Paeoniflorin as Aggregation Reducers Targeting Chaperones in Cell Models of Spinocerebellar Ataxia 3. Evid Based Complement Alternat Med 2013 0.79
48 Basal Ganglia-thalamic hemorrhage in young adults: a hospital-based study. Cerebrovasc Dis 2006 0.79
49 Analyses of interaction effect between apolipoprotein E polymorphism and alcohol use as well as cholesterol concentrations on spontaneous deep intracerebral hemorrhage in the Taiwan population. Clin Chim Acta 2009 0.78
50 Oxidative markers in spontaneous intracerebral hemorrhage: leukocyte 8-hydroxy-2'-deoxyguanosine as an independent predictor of the 30-day outcome. J Neurosurg 2011 0.78
51 Downregulation of genes involved in metabolism and oxidative stress in the peripheral leukocytes of Huntington's disease patients. PLoS One 2012 0.78
52 Association between PARK16 and Parkinson's disease in the Han Chinese population: a meta-analysis. Neurobiol Aging 2013 0.77
53 LINGO-2 polymorphism and the risk of Parkinson's disease in Taiwan. Parkinsonism Relat Disord 2011 0.77
54 Risk factors of respiratory failure in children with Guillain-Barré syndrome. Pediatr Neonatol 2012 0.77
55 Downregulation of proteins involved in the endoplasmic reticulum stress response and Nrf2-ARE signaling in lymphoblastoid cells of spinocerebellar ataxia type 17. J Neural Transm (Vienna) 2014 0.77
56 SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications. Hum Genet 2009 0.77
57 Association between GRN rs5848 polymorphism and Parkinson's disease in Taiwanese population. PLoS One 2013 0.77
58 Genetic analysis of "leucine-rich repeat (LRR) and immunoglobulin (Ig) domain-containing, Nogo receptor-interacting protein-1 (LINGO1)" in two independent Chinese parkinson's disease populations. Am J Med Genet B Neuropsychiatr Genet 2010 0.76
59 STK39, But Not BST1, HLA-DQB1, and SPPL2B Polymorphism, Is Associated With Han-Chinese Parkinson's Disease in Taiwan. Medicine (Baltimore) 2015 0.76
60 Coexistence of pernicious anemia and myasthenia gravis--a rare combination of autoimmune diseases in Taiwan. J Formos Med Assoc 2006 0.76
61 Interleukin-1alpha and -1beta promoter polymorphisms in Taiwanese patients with dementia. Dement Geriatr Cogn Disord 2007 0.76
62 Identification of gene networks and pathways associated with Guillain-Barré syndrome. PLoS One 2012 0.76
63 Internal ribosome entry segment activity of ATXN8 opposite strand RNA. PLoS One 2013 0.76
64 Comparison between the cranial magnetic resonance imaging features of neuromyelitis optica spectrum disorder versus multiple sclerosis in Taiwanese patients. BMC Neurol 2014 0.75
65 Associations of Matrix Metalloproteinase-9 and Tissue Inhibitory Factor-1 Polymorphisms With Parkinson Disease in Taiwan. Medicine (Baltimore) 2016 0.75
66 The potential of indole and a synthetic derivative for polyQ aggregation reduction by enhancement of the chaperone and autophagy systems. ACS Chem Neurosci 2014 0.75
67 Protein kinase Cη polymorphism and the susceptibilities to intracerebral hemorrhage in the Taiwan population. Neurosci Lett 2012 0.75
68 Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese. Clin Neurol Neurosurg 2008 0.75
69 Mutations of proline-rich transmembrane protein-2 and paroxysmal kinesigenic dyskinesia in Taiwan. Mov Disord 2013 0.75
70 Clinical characteristics of corticobasal syndrome amongst Chinese in Taiwan. Parkinsonism Relat Disord 2006 0.75
71 Novel Lactulose and Melibiose Targeting Autophagy to Reduce PolyQ Aggregation in Cell Models of Spinocerebellar Ataxia 3. CNS Neurol Disord Drug Targets 2016 0.75
72 Sensory neuropathy as the initial manifestation of multiple system atrophy. J Formos Med Assoc 2004 0.75
73 Study of a Taiwanese family with oculopharyngeal muscular dystrophy. J Neurol Sci 2008 0.75