1
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A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity.
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Nat Genet
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1998
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8.02
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2
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Characterization of the early lesion of 'degenerative' valvular aortic stenosis. Histological and immunohistochemical studies.
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Circulation
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1994
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4.32
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3
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Osteopontin is expressed in human aortic valvular lesions.
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Circulation
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1995
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4.16
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4
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Apolipoproteins B, (a), and E accumulate in the morphologically early lesion of 'degenerative' valvular aortic stenosis.
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Arterioscler Thromb Vasc Biol
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1996
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2.60
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5
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Variants of transcription factor 7-like 2 (TCF7L2) gene predict conversion to type 2 diabetes in the Finnish Diabetes Prevention Study and are associated with impaired glucose regulation and impaired insulin secretion.
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Diabetologia
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2007
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1.97
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6
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Insulin resistance syndrome predicts coronary heart disease events in elderly nondiabetic men.
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Circulation
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1999
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1.64
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7
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Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes.
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Diabetologia
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2012
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1.55
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8
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Association of metabolic syndrome with Alzheimer disease: a population-based study.
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Neurology
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2006
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1.45
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9
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Glomerular filtration rate and parathyroid hormone are associated with 1,25-dihydroxyvitamin D in men without chronic kidney disease.
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J Intern Med
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2011
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1.43
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10
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Cognitive function in an elderly population with persistent impaired glucose tolerance.
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Diabetes Care
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1998
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1.39
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11
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Cardiovascular disease risk factors as predictors of type 2 (non-insulin-dependent) diabetes mellitus in elderly subjects.
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Diabetologia
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1993
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1.26
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12
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Serum proinsulin levels are disproportionately increased in elderly prediabetic subjects.
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Diabetologia
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1995
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1.13
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13
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Novel mutations in the lamin A/C gene in heart transplant recipients with end stage dilated cardiomyopathy.
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Heart
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2006
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1.12
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14
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The cardiac beta-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population.
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J Am Coll Cardiol
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1998
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1.12
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15
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Insulin receptor substrate-1 variants in non-insulin-dependent diabetes.
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J Clin Invest
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1994
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1.09
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16
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Memory functions in human subjects with different apolipoprotein E phenotypes during a 3-year population-based follow-up study.
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Neurosci Lett
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1996
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1.05
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17
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Microalbuminuria precedes the development of NIDDM.
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Diabetes
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1994
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1.04
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18
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Diverse associations of 25-hydroxyvitamin D and 1,25-dihydroxy-vitamin D with dyslipidaemias.
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J Intern Med
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2010
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1.01
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19
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Association of the FTO gene variant (rs9939609) with cardiovascular disease in men with abnormal glucose metabolism--the Finnish Diabetes Prevention Study.
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Nutr Metab Cardiovasc Dis
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2010
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1.01
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20
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Sulfonylurea receptor 1 gene variants are associated with gestational diabetes and type 2 diabetes but not with altered secretion of insulin.
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Diabetes Care
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2000
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1.00
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21
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Apolipoprotein E phenotype alone does not influence survival in Alzheimer's disease: a population-based longitudinal study.
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Neuroepidemiology
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2000
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0.98
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22
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Detection of Chlamydia pneumoniae in human nonrheumatic stenotic aortic valves.
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J Am Coll Cardiol
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1997
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0.96
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23
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Retroperitoneal fibrosis with antineutrophil cytoplasmic antibodies.
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J Rheumatol
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1996
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0.94
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24
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Lipoprotein subclass profiles in individuals with varying degrees of glucose tolerance: a population-based study of 9399 Finnish men.
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J Intern Med
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0.93
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25
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A role for coding functional variants in HNF4A in type 2 diabetes susceptibility.
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Diabetologia
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0.93
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26
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Increased risk of non-insulin-dependent diabetes mellitus in elderly hypertensive subjects.
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J Hypertens
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1994
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0.93
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27
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LDL size and risk of coronary heart disease in elderly men and women.
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Arterioscler Thromb Vasc Biol
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1999
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0.91
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28
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Association of indices of liver and adipocyte insulin resistance with 19 confirmed susceptibility loci for type 2 diabetes in 6,733 non-diabetic Finnish men.
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Diabetologia
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2010
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0.91
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29
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New amino acid substitutions in the IRS-2 gene in Finnish and Chinese subjects with late-onset type 2 diabetes.
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Diabetes
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2001
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0.91
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30
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A novel surrogate index for hepatic insulin resistance.
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Diabetologia
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2010
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0.90
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31
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Type-2 diabetes and cognitive function in a non-demented population.
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Acta Neurol Scand
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1999
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0.88
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32
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Prospective study of small LDLs as a risk factor for non-insulin dependent diabetes mellitus in elderly men and women.
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Circulation
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1995
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0.87
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33
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The Ala54Thr polymorphism of the fatty acid binding protein 2 gene does not influence insulin sensitivity in Finnish nondiabetic and NIDDM subjects.
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Diabetes
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0.86
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34
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Exopolysaccharide-producing bacteria from sugar beets.
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Appl Environ Microbiol
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1999
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0.86
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35
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The Pro12A1a substitution in the peroxisome proliferator activated receptor gamma 2 is associated with an insulin-sensitive phenotype in families with familial combined hyperlipidemia and in nondiabetic elderly subjects with dyslipidemia.
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Atherosclerosis
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0.86
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36
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Family history of type 2 diabetes increases the risk of both obesity and its complications: is type 2 diabetes a disease of inappropriate lipid storage?
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J Intern Med
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0.86
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APOE-epsilon4 is associated with weight loss in women with AD: a population-based study.
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Neurology
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0.85
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38
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Epidemiological evidence for the association of hyperglycaemia and atherosclerotic vascular disease in non-insulin-dependent diabetes mellitus.
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Ann Med
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0.85
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39
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The association of apolipoprotein E polymorphism with memory: a population based study.
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Neurosci Lett
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1995
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0.84
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40
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Inducibility of life-threatening ventricular arrhythmias is related to maximum left ventricular thickness and clinical markers of sudden cardiac death in patients with hypertrophic cardiomyopathy attributable to the Asp175Asn mutation in the alpha-tropomyosin gene.
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J Mol Cell Cardiol
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2004
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0.84
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41
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Association between liver insulin resistance and cardiovascular risk factors.
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42
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Can degenerative aortic valve stenosis be related to persistent Chlamydia pneumoniae infection?
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Ann Intern Med
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0.81
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43
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Myocardial late gadolinium enhancement is associated with raised serum amino-terminal propeptide of type III collagen concentrations in patients with hypertrophic cardiomyopathy attributable to the Asp175Asn mutation in the alpha tropomyosin gene: magnetic resonance imaging study.
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Heart
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0.81
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44
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Variants in the hepatocyte nuclear factor-1alpha and -4alpha genes in Finnish and Chinese subjects with late-onset type 2 diabetes.
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Diabetes Care
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0.81
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45
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Simultaneous hypertrophic cardiomyopathy and ventricular septal defect in children.
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Am J Cardiol
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1999
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0.80
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46
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Glucose tolerance, insulin sensitivity and insulin release in European non-diabetic carriers of a polymorphism upstream of CDKN2A and CDKN2B.
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Diabetologia
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2011
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0.80
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47
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Gender differences in left ventricular function at rest and with exercise in asymptomatic aortic stenosis.
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Am Heart J
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0.80
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48
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Association of sequence variations in the gene encoding insulin-like growth factor binding protein 5 with adiponectin.
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Int J Obes (Lond)
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0.79
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49
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Polymorphisms of the human hexokinase II gene: lack of association with NIDDM and insulin resistance.
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Diabetologia
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1995
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0.79
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50
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Glucokinase gene islet promoter region variant (G-->A) at nucleotide -30 is not associated with reduced insulin secretion in Finns.
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Diabetes Care
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1998
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0.79
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51
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Common polymorphisms of calpain-10 are associated with abdominal obesity in subjects at high risk of type 2 diabetes.
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Diabetologia
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2006
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0.79
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52
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The genetic variation in the tenomodulin gene is associated with serum total and LDL cholesterol in a body size-dependent manner.
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Int J Obes (Lond)
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2008
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0.78
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53
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The Trp64Arg polymorphism of the beta 3-Adrenergic receptor gene. Lack of association with NIDDM and features of insulin resistance syndrome.
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Diabetes Care
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1997
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0.78
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54
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Glucokinase gene variants in subjects with late-onset NIDDM and impaired glucose tolerance.
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Diabetes Care
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1995
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0.77
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55
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New variants in the glycogen synthase gene (Gln71His, Met416Val) in patients with NIDDM from eastern Finland.
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Diabetologia
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1997
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0.77
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56
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Stability of age-associated memory impairment during a longitudinal population-based study.
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J Am Geriatr Soc
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0.75
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57
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[Sarcomere gene mutations--a cause of hypertrophic cardiomyopathy].
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Duodecim
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0.75
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58
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Improvement of metabolic control does not normalize auditory brainstem latencies in subjects with insulin-dependent diabetes mellitus.
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Am J Otolaryngol
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0.75
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59
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[The pathogenesis of aortic valvular stenosis will soon be known].
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Gene encoding the catalytic subunit p110beta of human phosphatidylinositol 3-kinase: cloning, genomic structure, and screening for variants in patients with type 2 diabetes.
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61
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The cardiac troponin I gene is not associated with hypertrophic cardiomyopathy in patients from eastern Finland.
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J Mol Cell Cardiol
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1999
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0.75
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62
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Hyperinsulinemia predicts multiple atherogenic changes in lipoproteins in elderly subjects.
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0.75
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