Published in Stroke on April 10, 2003
The epidemiology of silent brain infarction: a systematic review of population-based cohorts. BMC Med (2014) 1.14
Early cerebral small vessel disease and brain volume, cognition, and gait. Ann Neurol (2015) 0.96
Age-related white matter changes. J Aging Res (2011) 0.93
Hearing impairment risk and interaction of folate metabolism related gene polymorphisms in an aging study. BMC Med Genet (2011) 0.89
Common folate gene variant, MTHFR C677T, is associated with brain structure in two independent cohorts of people with mild cognitive impairment. Neuroimage Clin (2012) 0.88
Postoperative neurological complications and risk factors for pre-existing silent brain infarction in elderly patients undergoing coronary artery bypass grafting. J Anesth (2012) 0.88
MTHFR 677C>T effects on anterior cingulate structure and function during response monitoring in schizophrenia: a preliminary study. Brain Imaging Behav (2011) 0.86
Association of methylenetetrahydrofolate reductase (MTHFR 677C>T and 1298A>C) polymorphisms and haplotypes with silent brain infarction and homocysteine levels in a Korean population. Yonsei Med J (2010) 0.85
Heritability and genetic association analysis of neuroimaging measures in the Diabetes Heart Study. Neurobiol Aging (2014) 0.83
Candidate-gene analysis of white matter hyperintensities on neuroimaging. J Neurol Neurosurg Psychiatry (2015) 0.83
Genetics of stroke. Acta Pharmacol Sin (2010) 0.81
Influence of the MTHFR C677T polymorphism on magnetic resonance imaging hyperintensity volume and cognition in geriatric depression. Am J Geriatr Psychiatry (2009) 0.81
Analysis of genetic polymorphisms associated with leukoaraiosis in the southern Chinese population: A case-control study. Medicine (Baltimore) (2016) 0.79
Investigating silent strokes in hypertensives: a magnetic resonance imaging study (ISSYS): rationale and protocol design. BMC Neurol (2013) 0.79
Association of CVD candidate gene polymorphisms with ischemic stroke and cerebral hemorrhage in Chinese individuals. PLoS One (2014) 0.78
Vascular incontinence: incontinence in the elderly due to ischemic white matter changes. Neurol Int (2012) 0.77
Plasma total homocysteine level is associated with the pulsatility index of cerebral arteries in lacunar infarction. Yonsei Med J (2013) 0.77
White Matter Lesion Progression: Genome-Wide Search for Genetic Influences. Stroke (2015) 0.76
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature (2011) 13.25
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. Nat Genet (2011) 4.04
Mitochondrial genome variation in eastern Asia and the peopling of Japan. Genome Res (2004) 3.34
Meta-analysis identifies common variants associated with body mass index in east Asians. Nat Genet (2012) 2.70
Deep cerebral microbleeds are negatively associated with HDL-C in elderly first-time ischemic stroke patients. J Neurol Sci (2013) 1.97
An association between decreased estimated glomerular filtration rate and arterial stiffness. Intern Med (2008) 1.75
Identification of hypertension-susceptibility genes and pathways by a systemic multiple candidate gene approach: the millennium genome project for hypertension. Hypertens Res (2008) 1.72
Association of central systolic blood pressure with intracerebral small vessel disease in Japanese. Am J Hypertens (2010) 1.59
Effect of acute and long-term aerobic exercise on arterial stiffness in the elderly. Hypertens Res (2007) 1.55
The DYRK1A gene, encoded in chromosome 21 Down syndrome critical region, bridges between beta-amyloid production and tau phosphorylation in Alzheimer disease. Hum Mol Genet (2006) 1.50
Cross-sectional characterization of all classes of antihypertensives in terms of central blood pressure in Japanese hypertensive patients. Am J Hypertens (2009) 1.50
Postprandial hypotension as a risk marker for asymptomatic lacunar infarction. J Hypertens (2014) 1.50
Association of polymorphisms of the androgen receptor and klotho genes with bone mineral density in Japanese women. J Mol Med (Berl) (2004) 1.50
Prevalence of hyperesthesia detected by current perception threshold test in subjects with glucose metabolic impairments in a community. Intern Med (2002) 1.48
Accumulation of common polymorphisms is associated with development of hypertension: a 12-year follow-up from the Ohasama study. Hypertens Res (2009) 1.47
High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project. Hum Mol Genet (2007) 1.44
Fifteen-item geriatric depression scale predicts 8-year mortality in older Japanese. J Am Geriatr Soc (2011) 1.41
Correlation of systolic blood pressure with age and body mass index in native Papuan populations. Hypertens Res (2012) 1.38
Angiotensin-converting enzyme inhibitors as a new therapy for atrial fibrillation? Controversy. Am Heart J (2005) 1.37
Plasma resistin, associated with single nucleotide polymorphism -420, is correlated with insulin resistance, lower HDL cholesterol, and high-sensitivity C-reactive protein in the Japanese general population. Diabetes Care (2007) 1.34
Replication study of candidate genes associated with type 2 diabetes based on genome-wide screening. Diabetes (2008) 1.33
Arterial stiffness is associated with low thigh muscle mass in middle-aged to elderly men. Atherosclerosis (2010) 1.31
Common variants in the ATP2B1 gene are associated with susceptibility to hypertension: the Japanese Millennium Genome Project. Hypertension (2010) 1.26
The clock drawing test as a valid screening method for mild cognitive impairment. Dement Geriatr Cogn Disord (2004) 1.20
Mitochondrial ALDH2 deficiency as an oxidative stress. Ann N Y Acad Sci (2004) 1.12
Prevention of gastroesophageal reflux using an application of half-solid nutrients in patients with percutaneous endoscopic gastrostomy feeding. J Am Geriatr Soc (2004) 1.12
Radial augmentation index: a useful and easily obtainable parameter for vascular aging. Am J Hypertens (2005) 1.12
Effects of cognitive function on functional decline among community-dwelling non-disabled older Japanese. Arch Gerontol Geriatr (2005) 1.11
A genome-wide association study of hypertension-related phenotypes in a Japanese population. Circ J (2010) 1.10
A randomized controlled trial of multicomponent exercise in older adults with mild cognitive impairment. PLoS One (2013) 1.10
Refractive errors and factors associated with myopia in an adult Japanese population. Jpn J Ophthalmol (2003) 1.08
Diagnostic criteria for Werner syndrome based on Japanese nationwide epidemiological survey. Geriatr Gerontol Int (2012) 1.08
The GCKR rs780094 polymorphism is associated with susceptibility of type 2 diabetes, reduced fasting plasma glucose levels, increased triglycerides levels and lower HOMA-IR in Japanese population. J Hum Genet (2010) 1.08
The relationship between age and intraocular pressure in a Japanese population: the influence of central corneal thickness. Curr Eye Res (2002) 1.07
Resistin SNP-420 determines its monocyte mRNA and serum levels inducing type 2 diabetes. Biochem Biophys Res Commun (2005) 1.07
Effect of genetic polymorphism of OATP-C (SLCO1B1) on lipid-lowering response to HMG-CoA reductase inhibitors. Drug Metab Pharmacokinet (2004) 1.07
Is there a relevant effect of noise and smoking on hearing? A population-based aging study. Int J Audiol (2005) 1.05
Dietary magnesium intake and the future risk of coronary heart disease (the Honolulu Heart Program). Am J Cardiol (2003) 1.04
Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure loci. Hypertension (2013) 1.03
Genetic basis of inter-individual variability in the effects of exercise on the alleviation of lifestyle-related diseases. J Physiol (2009) 1.02
Abdominal fat, adipose-derived hormones and mild cognitive impairment: the J-SHIPP study. Dement Geriatr Cogn Disord (2010) 1.02
TRIC-A channels in vascular smooth muscle contribute to blood pressure maintenance. Cell Metab (2011) 1.02
High-sensitivity C-reactive protein and gamma-glutamyl transferase levels are synergistically associated with metabolic syndrome in community-dwelling persons. Cardiovasc Diabetol (2010) 1.02
An intronic variable number of tandem repeat polymorphisms of the cold-induced autoinflammatory syndrome 1 (CIAS1) gene modifies gene expression and is associated with essential hypertension. Eur J Hum Genet (2006) 1.02
Association of endothelin-1 gene variant with hypertension. Hypertension (2003) 1.02
No association between rs7566605 variant and being overweight in Japanese. Obesity (Silver Spring) (2007) 1.01
No association between INSIG2 Gene rs7566605 polymorphism and being overweight in Japanese population. Obesity (Silver Spring) (2008) 1.01
Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis. J Neurol Sci (2009) 1.01
High prevalence of sarcopenia and reduced leg muscle mass in Japanese patients immediately after a hip fracture. Geriatr Gerontol Int (2012) 0.98
Glutathione peroxidase 1 Pro198Leu variant contributes to the metabolic syndrome in men in a large Japanese cohort. Am J Clin Nutr (2008) 0.98
Mice lacking hypertension candidate gene ATP2B1 in vascular smooth muscle cells show significant blood pressure elevation. Hypertension (2012) 0.98
Association of polymorphisms of the osteoprotegerin gene with bone mineral density in Japanese women but not men. Mol Genet Metab (2003) 0.96
Association of candidate gene polymorphisms with bone mineral density in community-dwelling Japanese women and men. Int J Mol Med (2007) 0.96
Prevalence of knee pain, lumbar pain and its coexistence in Japanese men and women: The Longitudinal Cohorts of Motor System Organ (LOCOMO) study. J Bone Miner Metab (2013) 0.95
Silent cerebral microbleeds associated with arterial stiffness in an apparently healthy subject. Hypertens Res (2009) 0.95
The relationship between intraocular pressure and refractive error adjusting for age and central corneal thickness. Ophthalmic Physiol Opt (2004) 0.94