Published in J Vasc Res on July 13, 2013
Genetic-based prediction of disease traits: prediction is very difficult, especially about the future. Front Genet (2014) 1.12
microRNA-221 and microRNA-18a identification in stool as potential biomarkers for the non-invasive diagnosis of colorectal carcinoma. Br J Cancer (2014) 1.07
microRNA expression in peripheral blood cells following acute ischemic stroke and their predicted gene targets. PLoS One (2014) 0.96
MicroRNAs involved in the lipid metabolism and their possible implications for atherosclerosis development and treatment. Mediators Inflamm (2014) 0.84
The diagnostic value of circulating microRNAs for middle-aged (40-60-year-old) coronary artery disease patients. Clinics (Sao Paulo) (2015) 0.80
Association of serum microRNA-21 levels with Visfatin, inflammation, and acute coronary syndromes. Heart Vessels (2016) 0.78
Characterization of Dysregulated miRNA in Peripheral Blood Mononuclear Cells from Ischemic Stroke Patients. Mol Neurobiol (2017) 0.76
Non-coding RNAs and neuroprotection after acute CNS injuries. Neurochem Int (2017) 0.76
Prospective and therapeutic screening value of non-coding RNA as biomarkers in cardiovascular disease. Ann Transl Med (2016) 0.76
Regulatory networks in retinal ischemia-reperfusion injury. BMC Genet (2015) 0.76
Long non-coding RNA MIAT acts as a biomarker in diabetic retinopathy by absorbing miR-29b and regulating cell apoptosis. Biosci Rep (2017) 0.76
Plasma MicroRNA-16 Is a Biomarker for Diagnosis, Stratification, and Prognosis of Hyperacute Cerebral Infarction. PLoS One (2016) 0.75
Increased Circulating Exosomal miRNA-223 Is Associated with Acute Ischemic Stroke. Front Neurol (2017) 0.75
miR-21 alters circulating Treg function in vascular disease-hope for restoring immunoregulatory responses in atherosclerosis? Ann Transl Med (2017) 0.75
MicroRNA-93 inhibits inflammatory responses and cell apoptosis after cerebral ischemia reperfusion by targeting interleukin-1 receptor-associated kinase 4. Exp Ther Med (2017) 0.75
MicroRNA Changes in Cerebrospinal Fluid After Subarachnoid Hemorrhage. Stroke (2017) 0.75
MicroRNA-15a/16-1 Antagomir Ameliorates Ischemic Brain Injury in Experimental Stroke. Stroke (2017) 0.75
Carotid Plaque Rupture Is Accompanied by an Increase in the Ratio of Serum circR-284 to miR-221 Levels. Circ Cardiovasc Genet (2017) 0.75
Elevation of brain-enriched miRNAs in cerebrospinal fluid of patients with acute ischemic stroke. Biomark Res (2017) 0.75
A genomewide screen of 345 families for autism-susceptibility loci. Am J Hum Genet (2003) 2.51
Role of interleukin-28B polymorphisms in the treatment of hepatitis C virus genotype 2 infection in Asian patients. Hepatology (2011) 1.68
Get With the Guidelines-Stroke performance indicators: surveillance of stroke care in the Taiwan Stroke Registry: Get With the Guidelines-Stroke in Taiwan. Circulation (2010) 1.64
Cytotoxic T-lymphocyte associated antigen 4 gene polymorphisms and autoimmune thyroid disease: a meta-analysis. J Clin Endocrinol Metab (2007) 1.57
A functional polymorphism of PON1 interferes with microRNA binding to increase the risk of ischemic stroke and carotid atherosclerosis. Atherosclerosis (2013) 1.56
OxLDL up-regulates microRNA-29b, leading to epigenetic modifications of MMP-2/MMP-9 genes: a novel mechanism for cardiovascular diseases. FASEB J (2011) 1.53
Psychometric comparisons of 4 measures for assessing upper-extremity function in people with stroke. Phys Ther (2009) 1.52
OxLDL causes both epigenetic modification and signaling regulation on the microRNA-29b gene: novel mechanisms for cardiovascular diseases. J Mol Cell Cardiol (2011) 1.49
Mechanisms of cough syncope as evaluated by valsalva maneuver. Kaohsiung J Med Sci (2007) 1.48
Profound week 4 interferon responsiveness is mandatory for hepatitis C genotype 1 patients with unfavorable IL-28B genotype. J Clin Virol (2013) 1.45
Genetic and environmental contributions to carotid intima-media thickness and obesity phenotypes in the Northern Manhattan Family Study. Stroke (2004) 1.42
Pain has a strong negative impact on the fluoxetine response in hospitalized patients with major depressive disorder. Clin J Pain (2011) 1.39
Impact of family history of high myopia on level and onset of myopia. Invest Ophthalmol Vis Sci (2004) 1.26
Design of a family study among high-risk Caribbean Hispanics: the Northern Manhattan Family Study. Ethn Dis (2007) 1.25
Heritability and linkage analysis for carotid intima-media thickness: the family study of stroke risk and carotid atherosclerosis. Stroke (2009) 1.24
ITPKC single nucleotide polymorphism associated with the Kawasaki disease in a Taiwanese population. PLoS One (2011) 1.21
CASP3 gene single-nucleotide polymorphism (rs72689236) and Kawasaki disease in Taiwanese children. J Hum Genet (2010) 1.19
Interleukin-28B genetic variants in identification of hepatitis C virus genotype 1 patients responding to 24 weeks peginterferon/ribavirin. J Hepatol (2011) 1.18
Computational analysis of mRNA expression profiles identifies microRNA-29a/c as predictor of colorectal cancer early recurrence. PLoS One (2012) 1.12
Clinical applications of susceptibility weighted imaging in patients with major stroke. J Neurol (2011) 1.08
Association of ORAI1 haplotypes with the risk of HLA-B27 positive ankylosing spondylitis. PLoS One (2011) 1.07
MicroRNA-93 inhibits tumor growth and early relapse of human colorectal cancer by affecting genes involved in the cell cycle. Carcinogenesis (2012) 1.05
A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes. Hum Genet (2001) 1.04
Systematic assessment of the tagging polymorphisms of the COL1A1 gene for high myopia. J Hum Genet (2007) 1.03
Localization of a novel melanoma susceptibility locus to 1p22. Am J Hum Genet (2003) 1.03
Association between polymorphisms in DNA base excision repair genes XRCC1, APE1, and ADPRT and differentiated thyroid carcinoma. Clin Cancer Res (2008) 1.02
Host interleukin-28B genetic variants versus viral kinetics in determining responses to standard-of-care for Asians with hepatitis C genotype 1. Antiviral Res (2011) 1.00
Sex-differential genetic effect of phosphodiesterase 4D (PDE4D) on carotid atherosclerosis. BMC Med Genet (2010) 1.00
ORAI1 genetic polymorphisms associated with the susceptibility of atopic dermatitis in Japanese and Taiwanese populations. PLoS One (2012) 0.99
MicroRNA-195 regulates vascular smooth muscle cell phenotype and prevents neointimal formation. Cardiovasc Res (2012) 0.98
A functional polymorphism at 3'UTR of the PAX6 gene may confer risk for extreme myopia in the Chinese. Invest Ophthalmol Vis Sci (2011) 0.97
Relationship between childhood physical maltreatment and migraine in adolescents. Headache (2010) 0.97
Circulating microRNAs have a sex-specific association with metabolic syndrome. J Biomed Sci (2013) 0.96
The role of event-related potentials in cognitive decline in Alzheimer's disease. Clin Neurophysiol (2009) 0.96
A polymorphism of the ORAI1 gene is associated with the risk and recurrence of calcium nephrolithiasis. J Urol (2011) 0.96
Genome-wide scanning for linkage in Finnish breast cancer families. Eur J Hum Genet (2004) 0.95
Negative feedback regulation between microRNA let-7g and the oxLDL receptor LOX-1. J Cell Sci (2011) 0.94
Heritability of carotid artery distensibility in Hispanics: the Northern Manhattan Family Study. Stroke (2005) 0.94
The impact of osteopontin promoter polymorphisms on the risk of calcium urolithiasis. Clin Chim Acta (2010) 0.94
PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort. PLoS One (2012) 0.94
MicroRNA-152 mediates DNMT1-regulated DNA methylation in the estrogen receptor α gene. PLoS One (2012) 0.93
Cerebral white matter hyperintensities predict functional stroke outcome. Cerebrovasc Dis (2009) 0.93
Heritability of left ventricular mass and other morphologic variables in Caribbean Hispanic subjects: the Northern Manhattan Family Study. J Am Coll Cardiol (2005) 0.93
The risk of the metabolic syndrome on carotid thickness and stiffness: sex and age specific effects. Atherosclerosis (2009) 0.92
Comparison of higher-order wavefront aberrations with 3 aberrometers. J Cataract Refract Surg (2005) 0.92
Sex differential genetic effect of chromosome 9p21 on subclinical atherosclerosis. PLoS One (2010) 0.91
Promoter polymorphism of the CD14 endotoxin receptor gene is associated with biliary atresia and idiopathic neonatal cholestasis. Pediatrics (2005) 0.91
The functional significance of microRNA-29c in patients with colorectal cancer: a potential circulating biomarker for predicting early relapse. PLoS One (2013) 0.91
Segment-specific genetic effects on carotid intima-media thickness: the Northern Manhattan study. Stroke (2008) 0.91
Eligibility for recombinant tissue plasminogen activator in acute ischemic stroke: way to endeavor. Cerebrovasc Dis (2006) 0.91
Arecoline, a major alkaloid of areca nut, inhibits p53, represses DNA repair, and triggers DNA damage response in human epithelial cells. Toxicology (2008) 0.89
Carotid intima-media thickness and stiffness are independent risk factors for atherosclerotic diseases. J Investig Med (2010) 0.89
Carotid intima-media thickness in late-onset major depressive disorder. Int J Geriatr Psychiatry (2006) 0.89
Homocysteine levels, MTHFR C677T genotype, and MRI Hyperintensities in late-onset major depressive disorder. Am J Geriatr Psychiatry (2005) 0.89
MicroRNA-328 may influence myopia development by mediating the PAX6 gene. Invest Ophthalmol Vis Sci (2012) 0.89
Chromosome 9p21 genetic variants are associated with myocardial infarction but not with ischemic stroke in a Taiwanese population. J Investig Med (2011) 0.89
Decreased microRNA-221 is associated with high levels of TNF-α in human adipose tissue-derived mesenchymal stem cells from obese woman. Cell Physiol Biochem (2013) 0.88
Additive effect of ANRIL and BRAP polymorphisms on ankle-brachial index in a Taiwanese population. Circ J (2011) 0.88
Histamine regulates cyclooxygenase 2 gene activation through Orai1-mediated NFκB activation in lung cancer cells. Cell Calcium (2011) 0.88
Comparison of measurements of refractive errors between the hand-held Retinomax and on-table autorefractors in cyclopleged and noncyclopleged children. Am J Ophthalmol (2003) 0.88
Headache disability among adolescents: a student population-based study. Headache (2009) 0.88
Anti-atherogenic effect of San-Huang-Xie-Xin-Tang, a traditional Chinese medicine, in cultured human aortic smooth muscle cells. J Ethnopharmacol (2010) 0.87
Vascular endothelial growth factor gene polymorphisms in thyroid cancer. J Endocrinol (2007) 0.86
Cytotoxic T lymphocyte-associated molecule-4 gene polymorphism and hyperthyroid Graves' disease relapse after antithyroid drug withdrawal: a follow-up study. J Clin Endocrinol Metab (2007) 0.86
Lack of association between ORAI1/CRACM1 gene polymorphisms and Kawasaki disease in the Taiwanese children. J Clin Immunol (2011) 0.86
Carotid plaque and candidate genes related to inflammation and endothelial function in Hispanics from northern Manhattan. Stroke (2011) 0.86
Revisiting the stopping rule for hepatitis C genotype 1 patients treated with peginterferon plus ribavirin. PLoS One (2012) 0.86
Association of the homeobox transcription factor gene ENGRAILED 2 with autistic disorder in Chinese children. Neuropsychobiology (2008) 0.85
Proton magnetic resonance spectroscopy of late-life major depressive disorder. Psychiatry Res (2009) 0.85
Reappraisal of heart rate variability in acute ischemic stroke. Kaohsiung J Med Sci (2011) 0.85