PubRank

Kunimasa Arima

Author PubWeight™ 58.93‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease. N Engl J Med 2009 1.96
2 The association between the Val158Met polymorphism of the catechol-O-methyl transferase gene and morphological abnormalities of the brain in chronic schizophrenia. Brain 2005 1.48
3 The prediction of rapid conversion to Alzheimer's disease in mild cognitive impairment using regional cerebral blood flow SPECT. Neuroimage 2005 1.47
4 Brain hydrogen sulfide is severely decreased in Alzheimer's disease. Biochem Biophys Res Commun 2002 1.32
5 An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies. Acta Neuropathol 2006 1.24
6 Tubulin seeds alpha-synuclein fibril formation. J Biol Chem 2001 1.18
7 Diffusion abnormalities of the uncinate fasciculus in Alzheimer's disease: diffusion tensor tract-specific analysis using a new method to measure the core of the tract. Neuroradiology 2008 1.17
8 Human astrocytes express aquaporin-1 and aquaporin-4 in vitro and in vivo. Neuropathology 2007 1.14
9 Hippocampal complexin proteins and cognitive dysfunction in schizophrenia. Arch Gen Psychiatry 2005 1.11
10 Cerebral small-vessel disease protein HTRA1 controls the amount of TGF-β1 via cleavage of proTGF-β1. Hum Mol Genet 2011 1.08
11 Arterial changes in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in relation to pathogenesis of diffuse myelin loss of cerebral white matter: examination of cerebral medullary arteries by reconstruction of serial sections of an autopsy case. Stroke 2002 1.08
12 TDP-43 dimerizes in human cells in culture. Cell Mol Neurobiol 2009 1.04
13 Nogo-A and nogo receptor expression in demyelinating lesions of multiple sclerosis. J Neuropathol Exp Neurol 2005 1.03
14 Molecular network analysis suggests aberrant CREB-mediated gene regulation in the Alzheimer disease hippocampus. Dis Markers 2009 1.03
15 Immunohistochemical characterization of microglia in Nasu-Hakola disease brains. Neuropathology 2010 0.98
16 Renal disease in Arima syndrome is nephronophthisis as in other Joubert-related Cerebello-oculo-renal syndromes. Am J Med Genet A 2004 0.96
17 Expression patterns of tau mRNA isoforms correlate with susceptible lesions in progressive supranuclear palsy and corticobasal degeneration. Brain Res Mol Brain Res 2002 0.96
18 Failure to confirm an association between the PLXNA2 gene and schizophrenia in a Japanese population. Prog Neuropsychopharmacol Biol Psychiatry 2007 0.92
19 Genetic variations of human neuropsin gene and psychiatric disorders: polymorphism screening and possible association with bipolar disorder and cognitive functions. Neuropsychopharmacology 2008 0.92
20 Increased cerebrospinal fluid interleukin-6 levels in patients with schizophrenia and those with major depressive disorder. J Psychiatr Res 2013 0.92
21 Criterion and construct validity of the CogState Schizophrenia Battery in Japanese patients with schizophrenia. PLoS One 2011 0.92
22 Extensive loss of arterial medial smooth muscle cells and mural extracellular matrix in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL). Neuropathology 2007 0.92
23 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy. Neurology 2002 0.92
24 Autotaxin expression is enhanced in frontal cortex of Alzheimer-type dementia patients. Neurosci Lett 2006 0.91
25 The effect of tau genotype on clinical features in FTDP-17. Parkinsonism Relat Disord 2005 0.91
26 Potential pathophysiological role of D-amino acid oxidase in schizophrenia: immunohistochemical and in situ hybridization study of the expression in human and rat brain. J Neural Transm (Vienna) 2009 0.91
27 Dystrophic neurites express C9orf72 in Alzheimer's disease brains. Alzheimers Res Ther 2012 0.90
28 Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy cases. Acta Neuropathol 2005 0.90
29 The 14-3-3 protein epsilon isoform expressed in reactive astrocytes in demyelinating lesions of multiple sclerosis binds to vimentin and glial fibrillary acidic protein in cultured human astrocytes. Am J Pathol 2004 0.90
30 Altered distribution of KCC2 in cortical dysplasia in patients with intractable epilepsy. Epilepsia 2007 0.88
31 Diffusion abnormality in the posterior cingulum and hippocampal volume: correlation with disease progression in Alzheimer's disease. Magn Reson Imaging 2008 0.87
32 Localization of CKII beta subunits in Lewy bodies of Parkinson's disease. J Neurol Sci 2007 0.87
33 Effects of the CACNA1C risk allele on neurocognition in patients with schizophrenia and healthy individuals. Sci Rep 2012 0.87
34 Diffusion abnormality in posterior cingulate fiber tracts in Alzheimer's disease: tract-specific analysis. Radiat Med 2008 0.86
35 Alterations in human tau transcripts correlate with those of neurofilament in sporadic tauopathies. Neurosci Lett 2004 0.86
36 Relationship between apathy and diffusion tensor imaging metrics of the brain in Alzheimer's disease. Int J Geriatr Psychiatry 2011 0.86
37 Possible association of the semaphorin 3D gene (SEMA3D) with schizophrenia. J Psychiatr Res 2010 0.86
38 Astrocytic deformity and globular structures are characteristic of the brains of patients with aceruloplasminemia. J Neuropathol Exp Neurol 2002 0.84
39 Association study of the vesicular monoamine transporter 1 (VMAT1) gene with schizophrenia in a Japanese population. Behav Brain Funct 2006 0.84
40 Negative correlation between cerebrospinal fluid oxytocin levels and negative symptoms of male patients with schizophrenia. Schizophr Res 2012 0.84
41 Human astrocytes express 14-3-3 sigma in response to oxidative and DNA-damaging stresses. Neurosci Res 2006 0.83
42 Aberrant neuronal migration in the brainstem of fukuyama-type congenital muscular dystrophy. J Neuropathol Exp Neurol 2003 0.83
43 Activation of microglia/macrophages expressing phosphorylated S6 ribosomal protein in a case of hemimegalencephaly with progressive calcification and atrophy. J Neurol Sci 2009 0.82
44 Expression of various glutamate receptors including N-methyl-D-aspartate receptor (NMDAR) in an ovarian teratoma removed from a young woman with anti-NMDAR encephalitis. Intern Med 2010 0.82
45 Neuromyelitis optica/Devic's disease: gene expression profiling of brain lesions. Neuropathology 2008 0.82
46 Triple immunofluorolabeling with two rabbit polyclonal antibodies and a mouse monoclonal antibody allowing three-dimensional analysis of cotton wool plaques in Alzheimer disease. J Histochem Cytochem 2003 0.82
47 Phosphorylated Syk expression is enhanced in Nasu-Hakola disease brains. Neuropathology 2011 0.81
48 LC3, an autophagosome marker, is expressed on oligodendrocytes in Nasu-Hakola disease brains. Orphanet J Rare Dis 2014 0.81
49 Expression of Ca²⁺-dependent activator protein for secretion 2 is increased in the brains of schizophrenic patients. Prog Neuropsychopharmacol Biol Psychiatry 2011 0.80
50 Close association of water channel AQP1 with amyloid-beta deposition in Alzheimer disease brains. Acta Neuropathol 2008 0.80
51 Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients. Acta Neuropathol 2008 0.79
52 Perceptual change in response to a bistable picture increases neuromagnetic beta-band activities. Neurosci Res 2008 0.79
53 Concordance between (99m)Tc-ECD SPECT and 18F-FDG PET interpretations in patients with cognitive disorders diagnosed according to NIA-AA criteria. Int J Geriatr Psychiatry 2014 0.79
54 Prion disease causes less severe lesions in human hippocampus than other parts of brain. Psychiatry Clin Neurosci 2008 0.78
55 Three-repeat Tau 69 is a major tau isoform in laser-microdissected Pick bodies. Amyloid 2006 0.76
56 The relationship between positive and negative automatic thought and activity in the prefrontal and temporal cortices: a multi-channel near-infrared spectroscopy (NIRS) study. J Affect Disord 2013 0.76
57 Protein microarray analysis identifies cyclic nucleotide phosphodiesterase as an interactor of Nogo-A. Neuropathology 2009 0.76
58 The 14-3-3 protein forms a molecular complex with heat shock protein Hsp60 and cellular prion protein. J Neuropathol Exp Neurol 2005 0.76
59 Misfolded SOD1 forms high-density molecular complexes with synaptic molecules in mutant SOD1-linked familial amyotrophic lateral sclerosis cases. J Neurol Sci 2011 0.76
60 Failure to confirm an association between Epsin 4 and schizophrenia in a Japanese population. J Neural Transm (Vienna) 2008 0.76
61 Simplification of the modified Gallyas method. Neuropathology 2014 0.76
62 Absence of small-vessel abnormalities in alternating hemiplegia of childhood. Brain Dev 2010 0.75
63 Haplotype-phenotype correlations in kindreds with the N279K mutation in the tau gene. Arch Neurol 2004 0.75
64 Autosomal dominant leukoencephalopathy with mild clinical symptoms due to cerebrovascular dysfunctions: a new disease entity? Brain Dev 2007 0.75
65 Pathological heterogeneity of the precentral gyrus in Pick's disease: a study of 16 autopsy cases. Acta Neuropathol 2006 0.75
66 Association of plasma IL-6 and soluble IL-6 receptor levels with the Asp358Ala polymorphism of the IL-6 receptor gene in schizophrenic patients. J Psychiatr Res 2011 0.75
67 Co-existence of nemaline and cytoplasmic bodies in muscle of an infant with nemaline myopathy. Neuropathology 2002 0.75
68 Coexistence of familial transthyretin amyloidosis ATTR Val30Met and spinocerebellar ataxia type 1 in a Japanese family--a follow-up autopsy report. Amyloid 2004 0.75
69 Postmortem findings in a patient with cerebral amyloid angiopathy actively treated with corticosteroid. Amyloid 2012 0.75