Pia K. Kuusisto

Thermo Scientific Molecular Biology Products, Thermo Fisher Scientific

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 14	2012

Other Publications

Article	Year
Insulin resistance syndrome predicts coronary heart disease events in elderly nondiabetic men. Circulation\| PubMed ID: 10402440	1999
Type-2 diabetes and cognitive function in a non-demented population. Acta neurologica Scandinavica\| PubMed ID: 10442450	1999
Bee and wasp sting reactions in current beekeepers. Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology\| PubMed ID: 8933782	1996
Epidemiological evidence for the association of hyperglycaemia and atherosclerotic vascular disease in non-insulin-dependent diabetes mellitus. Annals of medicine\| PubMed ID: 8949972	1996
Stability of age-associated memory impairment during a longitudinal population-based study. Journal of the American Geriatrics Society\| PubMed ID: 8994504	1997
The Ala54Thr polymorphism of the fatty acid binding protein 2 gene does not influence insulin sensitivity in Finnish nondiabetic and NIDDM subjects. Diabetes\| PubMed ID: 9075815	1997
Detection of Chlamydia pneumoniae in human nonrheumatic stenotic aortic valves. Journal of the American College of Cardiology\| PubMed ID: 9120159	1997
The importance of fluorescence distribution and kinetics of ALA-induced PpIX in the bladder in photodynamic therapy. Journal of photochemistry and photobiology. B, Biology\| PubMed ID: 9203390	1997
Protoporphyrin-IX distribution and photodynamic effect in rat oesophagus after aminolaevulinic acid administration. Scandinavian journal of gastroenterology\| PubMed ID: 9246700	1997
The Trp64Arg polymorphism of the beta 3-Adrenergic receptor gene. Lack of association with NIDDM and features of insulin resistance syndrome. Diabetes care\| PubMed ID: 9250462	1997
Association between features of the insulin resistance syndrome and Alzheimer's disease independently of apolipoprotein E4 phenotype: cross sectional population based study. BMJ (Clinical research ed.)\| PubMed ID: 9366728	1997
New variants in the glycogen synthase gene (Gln71His, Met416Val) in patients with NIDDM from eastern Finland. Diabetologia\| PubMed ID: 9389424	1997
Time-resolved fluorescence imaging in islet cell autoantibody quantitation. Journal of immunological methods\| PubMed ID: 9433472	1997
Cognitive function in an elderly population with persistent impaired glucose tolerance. Diabetes care\| PubMed ID: 9540022	1998
Comparison of the oral health status and salivary flow rate of asthmatic patients with those of nonasthmatic adults--results of a pilot study. Allergy\| PubMed ID: 9542614	1998
Randomised comparison of cost effectiveness of guided self management and traditional treatment of asthma in Finland. BMJ (Clinical research ed.)\| PubMed ID: 9552954	1998
Can degenerative aortic valve stenosis be related to persistent Chlamydia pneumoniae infection? Annals of internal medicine\| PubMed ID: 9556468	1998
Stimulated salivary flow rate and composition in asthmatic and non-asthmatic adults. Archives of oral biology\| PubMed ID: 9602294	1998
Lymphocyte subpopulations, cytokine release and specific immunoglobulin G in reactive and nonreactive beekeepers. Journal of investigational allergology & clinical immunology : official organ of the International Association of Asthmology (INTERASMA) and Sociedad Latinoamericana de Alergia e InmunologÃa\| PubMed ID: 9615305	1998
Glucokinase gene islet promoter region variant (G-->A) at nucleotide -30 is not associated with reduced insulin secretion in Finns. Diabetes care\| PubMed ID: 9653619	1998
A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity. Nature genetics\| PubMed ID: 9806549	1998
Expression of seizure-related PTZ-17 is induced by potassium deprivation in cerebellar granule cells. Biochemical and biophysical research communications\| PubMed ID: 9813137	1998
The cardiac beta-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population. Journal of the American College of Cardiology\| PubMed ID: 9822100	1998
Pogosta disease: clinical observations during an outbreak in the province of North Karelia, Finland. British journal of rheumatology\| PubMed ID: 9851265	1998
Exopolysaccharide-producing bacteria from sugar beets. Applied and environmental microbiology\| PubMed ID: 9925632	1999
Prandial glucose regulation and cardiovascular disease in type 2 diabetes. European journal of clinical investigation\| PubMed ID: 10383604	1999
Simultaneous hypertrophic cardiomyopathy and ventricular septal defect in children. The American journal of cardiology\| PubMed ID: 10468097	1999
LDL size and risk of coronary heart disease in elderly men and women. Arteriosclerosis, thrombosis, and vascular biology\| PubMed ID: 10559020	1999
Epidemiological study of nephropathia epidemica in Finland 1989-96. Scandinavian journal of infectious diseases\| PubMed ID: 10576121	1999
The cardiac troponin I gene is not associated with hypertrophic cardiomyopathy in patients from eastern Finland. Journal of molecular and cellular cardiology\| PubMed ID: 10591029	1999
A differential display protocol to identify differentially expressed mRNAs in potassium-deprived cerebellar granule cells. Brain research. Brain research protocols\| PubMed ID: 10775830	2000
Sulfonylurea receptor 1 gene variants are associated with gestational diabetes and type 2 diabetes but not with altered secretion of insulin. Diabetes care\| PubMed ID: 10857971	2000
[The pathogenesis of aortic valvular stenosis will soon be known]. Duodecim; lÃ¤Ã¤ketieteellinen aikakauskirja\| PubMed ID: 10892110	1997
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... Atherosclerosis\| PubMed ID: 10924736	2000
Historical trends in lake and river ice cover in the northern hemisphere Science (New York, N.Y.)\| PubMed ID: 10976066	2000
Gene encoding the catalytic subunit p110beta of human phosphatidylinositol 3-kinase: cloning, genomic structure, and screening for variants in patients with type 2 diabetes. Diabetes\| PubMed ID: 11016459	2000
Variants in the hepatocyte nuclear factor-1alpha and -4alpha genes in Finnish and Chinese subjects with late-onset type 2 diabetes. Diabetes care\| PubMed ID: 11023148	2000
Apolipoprotein E phenotype alone does not influence survival in Alzheimer's disease: a population-based longitudinal study. Neuroepidemiology\| PubMed ID: 11060507	2000
Prolonged arthritis associated with sindbis-related (Pogosta) virus infection. Rheumatology (Oxford, England)\| PubMed ID: 11085809	2000
Insulin-like growth factor binding protein 5 and type-1 insulin-like growth factor receptor are differentially regulated during apoptosis in cerebellar granule cells. Journal of neurochemistry\| PubMed ID: 11145973	2001
Ubiquitin-binding protein p62 expression is induced during apoptosis and proteasomal inhibition in neuronal cells. Biochemical and biophysical research communications\| PubMed ID: 11162503	2001
APOE-epsilon4 is associated with weight loss in women with AD: a population-based study. Neurology\| PubMed ID: 11245719	2001
Ubiquitin-binding protein p62 is present in neuronal and glial inclusions in human tauopathies and synucleinopathies. Neuroreport\| PubMed ID: 11447312	2001
New amino acid substitutions in the IRS-2 gene in Finnish and Chinese subjects with late-onset type 2 diabetes. Diabetes\| PubMed ID: 11473060	2001
Insulin resistance syndrome predicts coronary heart disease events in elderly type 2 diabetic men. Diabetes care\| PubMed ID: 11522711	2001
[Sarcomere gene mutations--a cause of hypertrophic cardiomyopathy]. Duodecim; lÃ¤Ã¤ketieteellinen aikakauskirja\| PubMed ID: 11877825	1999
Occurrence and destruction of PAHs, PCBs, CIPhs, CIBzs, and PCDD/Fs in ash from gasification of straw. Environmental science & technology\| PubMed ID: 12038829	2002
Early accumulation of p62 in neurofibrillary tangles in Alzheimer's disease: possible role in tangle formation. Neuropathology and applied neurobiology\| PubMed ID: 12060347	2002
No variants in the cardiac actin gene in Finnish patients with dilated or hypertrophic cardiomyopathy. American heart journal\| PubMed ID: 12075240	2002
Prolonged arthritis associated with Sindbis-related (Pogosta) virus infection. Rheumatology (Oxford, England)\| PubMed ID: 12096239	2002
Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland. Journal of molecular medicine (Berlin, Germany)\| PubMed ID: 12110947	2002
Epidemiology of Sindbis virus infections in Finland 1981-96: possible factors explaining a peculiar disease pattern. Epidemiology and infection\| PubMed ID: 12403109	2002
First-pass MR imaging in the assessment of perfusion impairment in patients with hypertrophic cardiomyopathy and the Asp175Asn mutation of the alpha-tropomyosin gene. Radiology\| PubMed ID: 12511681	2003
Cardiac adrenergic activity is associated with left ventricular hypertrophy in genetically homogeneous subjects with hypertrophic cardiomyopathy. Journal of nuclear medicine : official publication, Society of Nuclear Medicine\| PubMed ID: 12679389	2003
[Cases of oculopharyngeal muscular dystrophy even in Finland]. Duodecim; lÃ¤Ã¤ketieteellinen aikakauskirja\| PubMed ID: 12762202	2003
[Problematic fever]. Duodecim; lÃ¤Ã¤ketieteellinen aikakauskirja\| PubMed ID: 12806734	2003
[NARP syndrome--a less known mitochondrial disease]. Duodecim; lÃ¤Ã¤ketieteellinen aikakauskirja\| PubMed ID: 14535029	2003
A novel mutation, Arg71Thr, in the delta-sarcoglycan gene is associated with dilated cardiomyopathy. Journal of molecular medicine (Berlin, Germany)\| PubMed ID: 14564412	2003
A new technique for multiparameter imaging microscopy: use of long decay time photoluminescent labels enables multiple color immunocytochemistry with low channel-to-channel crosstalk. Microscopy research and technique\| PubMed ID: 14601145	2003
[Multiple sclerosis in a female patient]. Duodecim; lÃ¤Ã¤ketieteellinen aikakauskirja\| PubMed ID: 14655534	2003
Morphogenesis of Lewy bodies: dissimilar incorporation of alpha-synuclein, ubiquitin, and p62. Journal of neuropathology and experimental neurology\| PubMed ID: 14692700	2003
[What new about hypertrophic cardiomyopathy?]. Duodecim; lÃ¤Ã¤ketieteellinen aikakauskirja\| PubMed ID: 14702797	2003
Inducibility of life-threatening ventricular arrhythmias is related to maximum left ventricular thickness and clinical markers of sudden cardiac death in patients with hypertrophic cardiomyo... Journal of molecular and cellular cardiology\| PubMed ID: 14734051	2004
Genetics of hypertrophic cardiomyopathy in eastern Finland: few founder mutations with benign or intermediary phenotypes. Annals of medicine\| PubMed ID: 15000344	2004
Increase in CCR5 Delta32/Delta32 genotype in multiple sclerosis. Acta neurologica Scandinavica\| PubMed ID: 15080861	2004
A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy. European heart journal\| PubMed ID: 15140538	2004
The Val103Ile polymorphism of melanocortin-4 receptor regulates energy expenditure and weight gain. Obesity research\| PubMed ID: 15292469	2004
Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy. European journal of heart failure\| PubMed ID: 15556047	2004
Atherosclerosis-like lesions of the aortic valve are common in adults of all ages: a necropsy study. Heart (British Cardiac Society)\| PubMed ID: 15831636	2005
Cine MR imaging of myocardial contractile impairment in patients with hypertrophic cardiomyopathy attributable to Asp175Asn mutation in the alpha-tropomyosin gene. Radiology\| PubMed ID: 16014439	2005
Enteroviruses and the risk of MS in the Finnish Twin Cohort. European journal of neurology : the official journal of the European Federation of Neurological Societies\| PubMed ID: 16128872	2005
The efficacy of glatiramer acetate in beta-interferon-intolerant MS patients. Acta neurologica Scandinavica\| PubMed ID: 16146492	2005
Increased disability and MRI lesions after discontinuation of IFN-beta-1a in secondary progressive MS. Acta neurologica Scandinavica\| PubMed ID: 16146494	2005
Synthesis and structure-activity relationship of the first nonpeptidergic inverse agonists for the human cytomegalovirus encoded chemokine receptor US28. Journal of medicinal chemistry\| PubMed ID: 16190772	2005
Periodontal disease and bacterial vaginosis increase the risk for adverse pregnancy outcome. Infectious diseases in obstetrics and gynecology\| PubMed ID: 16338781	2005
Effect of high-dose methylprednisolone treatment on CCR5 expression on blood cells in MS exacerbation. Acta neurologica Scandinavica\| PubMed ID: 16441245	2006
Gene expression profiles in Finnish twins with multiple sclerosis. BMC medical genetics\| PubMed ID: 16504146	2006
Diastolic dysfunction without left ventricular hypertrophy is an early finding in children with hypertrophic cardiomyopathy-causing mutations in the beta-myosin heavy chain, alpha-tropomyosi... American heart journal\| PubMed ID: 16504640	2006
Novel mutations in the lamin A/C gene in heart transplant recipients with end stage dilated cardiomyopathy. Heart (British Cardiac Society)\| PubMed ID: 16537768	2006
Interleukin-6 promoter polymorphism and late-onset Alzheimer's disease in the Finnish population. Journal of neurogenetics\| PubMed ID: 16540406	2005
Common polymorphisms of calpain-10 are associated with abdominal obesity in subjects at high risk of type 2 diabetes. Diabetologia\| PubMed ID: 16752174	2006
[Not Available]. Duodecim; lÃ¤Ã¤ketieteellinen aikakauskirja\| PubMed ID: 16862763	2006
Myocardial late gadolinium enhancement is associated with raised serum amino-terminal propeptide of type III collagen concentrations in patients with hypertrophic cardiomyopathy attributable... Heart (British Cardiac Society)\| PubMed ID: 16908707	2006
Association of metabolic syndrome with Alzheimer disease: a population-based study. Neurology\| PubMed ID: 16966548	2006
NARP syndrome and adult-onset generalised seizures. Epileptic disorders : international epilepsy journal with videotape\| PubMed ID: 16987741	2006
Association analysis of peroxisome proliferator-activated receptor gamma polymorphisms and late onset Alzheimer's disease in the Finnish population. Dementia and geriatric cognitive disorders\| PubMed ID: 16988505	2006
Discovering inhibitors of human sirtuin type 2: novel structural scaffolds. Journal of medicinal chemistry\| PubMed ID: 17125277	2006
Time-resolved fluorescence imaging of islet cell autoantibodies. Annals of the New York Academy of Sciences\| PubMed ID: 17130559	2006
PCB contaminated dust on indoor surfaces--health risks and acceptable surface concentrations in residential and occupational settings. Chemosphere\| PubMed ID: 17166563	2007
N,N'-Bisbenzylidenebenzene-1,4-diamines and N,N'-Bisbenzylidenenaphthalene-1,4-diamines as Sirtuin Type 2 (SIRT2) Inhibitors. Journal of medicinal chemistry\| PubMed ID: 17181175	2006
The metabolic syndrome predicts cardiovascular mortality: a 13-year follow-up study in elderly non-diabetic Finns. European heart journal\| PubMed ID: 17303589	2007
N-(3-(4-Hydroxyphenyl)-propenoyl)-amino acid tryptamides as SIRT2 inhibitors. Bioorganic & medicinal chemistry letters\| PubMed ID: 17329104	2007
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... Diabetologia\| PubMed ID: 17437080	2007
Cytokines, interstitial collagen and ventricular remodelling in dilated cardiomyopathy. International journal of cardiology\| PubMed ID: 17442428	2008
Myocardial perfusion, oxidative metabolism, and free fatty acid uptake in patients with hypertrophic cardiomyopathy attributable to the Asp175Asn mutation in the alpha-tropomyosin gene: a po... Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology\| PubMed ID: 17556170	2007
Once-weekly 22microg subcutaneous IFN-beta-1a in secondary progressive MS: a 3-year follow-up study on brain MRI measurements and serum MMP-9 levels. Acta neurologica Scandinavica\| PubMed ID: 17587254	2007
The biarsenical dye Lumio exhibits a reduced ability to specifically detect tetracysteine-containing proteins within live cells. Journal of fluorescence\| PubMed ID: 17805945	2007
Metabolic syndrome and incident end-stage peripheral vascular disease: a 14-year follow-up study in elderly Finns. Diabetes care\| PubMed ID: 17848614	2007
Human herpes virus 6 and multiple sclerosis: a Finnish twin study. Multiple sclerosis (Houndmills, Basingstoke, England)\| PubMed ID: 17893113	2008
Use of p62/SQSTM1 antibodies for neuropathological diagnosis. Neuropathology and applied neurobiology\| PubMed ID: 17961133	2008
Atherosclerosis and cardiovascular risk reduction with PPAR agonists. Current atherosclerosis reports\| PubMed ID: 18173954	2007
Single nucleotide polymorphisms of the MCHR1 gene do not affect metabolism in humans. Obesity (Silver Spring, Md.)\| PubMed ID: 18198296	2007
Long-term retention rate of entacapone in the treatment of Parkinson's disease. European journal of neurology : the official journal of the European Federation of Neurological Societies\| PubMed ID: 18284429	2008
Single-nucleotide polymorphism rs7754840 of CDKAL1 is associated with impaired insulin secretion in nondiabetic offspring of type 2 diabetic subjects and in a large sample of men with normal... The Journal of clinical endocrinology and metabolism\| PubMed ID: 18285412	2008
The metabolic syndrome predicts incident stroke: a 14-year follow-up study in elderly people in Finland. Stroke; a journal of cerebral circulation\| PubMed ID: 18323501	2008
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nature genetics\| PubMed ID: 18372903	2008
Significance of plasma levels of N-terminal Pro-B-type natriuretic peptide on left ventricular remodeling in non-obstructive hypertrophic cardiomyopathy attributable to the Asp175Asn mutatio... The American journal of cardiology\| PubMed ID: 18394456	2008
Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. The Journal of clinical investigation\| PubMed ID: 18521185	2008
Clinical significance of troponin I efflux and troponin autoantibodies in patients with dilated cardiomyopathy. Journal of cardiac failure\| PubMed ID: 18672196	2008
WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels. American journal of human genetics\| PubMed ID: 18674750	2008
Characterization of the binding properties of SIRT2 inhibitors with a N-(3-phenylpropenoyl)-glycine tryptamide backbone. Bioorganic & medicinal chemistry\| PubMed ID: 18701307	2008
Concordance and heritability of multiple sclerosis in Finland: study on a nationwide series of twins. European journal of neurology : the official journal of the European Federation of Neurological Societies\| PubMed ID: 18727671	2008
Early familial dilated cardiomyopathy: identification with determination of disease state parameter from cine MR image data. Radiology\| PubMed ID: 18796670	2008
The C-terminus of apoptin represents a unique tumor cell-enhanced nuclear targeting module. International journal of cancer. Journal international du cancer\| PubMed ID: 18798550	2008
Association of sequence variations in the gene encoding insulin-like growth factor binding protein 5 with adiponectin. International journal of obesity (2005)\| PubMed ID: 18957933	2009
Apoptosis-related molecules in blood in multiple sclerosis. Journal of neuroimmunology\| PubMed ID: 18963025	2008
High-resolution signal-averaged analysis of atrial electromagnetic characteristics in patients with paroxysmal lone atrial fibrillation. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc\| PubMed ID: 18973495	2008
The genetic variation in the tenomodulin gene is associated with serum total and LDL cholesterol in a body size-dependent manner. International journal of obesity (2005)\| PubMed ID: 18982016	2008
Variance of the SGK1 gene is associated with insulin secretion in different European populations: results from the TUEF, EUGENE2, and METSIM studies. PloS one\| PubMed ID: 18985156	2008
Galanin preproprotein is associated with elevated plasma triglycerides. Arteriosclerosis, thrombosis, and vascular biology\| PubMed ID: 18988886	2009
Crosstalk between Hsp70 molecular chaperone, lysosomes and proteasomes in autophagy-mediated proteolysis in human retinal pigment epithelial cells. Journal of cellular and molecular medicine\| PubMed ID: 19017362	2009
Common variants at 30 loci contribute to polygenic dyslipidemia. Nature genetics\| PubMed ID: 19060906	2009
Variants in MTNR1B influence fasting glucose levels. Nature genetics\| PubMed ID: 19060907	2009
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion. Nature genetics\| PubMed ID: 19060908	2009
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nature genetics\| PubMed ID: 19079261	2009
A randomized, double-blind study comparing Clostridium difficile immune whey and metronidazole for recurrent Clostridium difficile-associated diarrhoea: efficacy and safety data of a prematu... Scandinavian journal of infectious diseases\| PubMed ID: 19086244	2008
Association of common genetic variation in the FOXO1 gene with beta-cell dysfunction, impaired glucose tolerance, and type 2 diabetes. The Journal of clinical endocrinology and metabolism\| PubMed ID: 19141580	2009
Therapeutic activities of intravenous immunoglobulins in multiple sclerosis involve modulation of chemokine expression. Journal of neuroimmunology\| PubMed ID: 19217671	2009
Changes in insulin sensitivity and insulin release in relation to glycemia and glucose tolerance in 6,414 Finnish men. Diabetes\| PubMed ID: 19223598	2009
The need for comprehensive cardiac and neurologic assessment of lamin A/C mutation carriers. Radiology\| PubMed ID: 19332860	2009
Long-term retention rate of pramipexole in the treatment of Parkinson's disease. European journal of clinical pharmacology\| PubMed ID: 19415250	2009
Genome-wide association study identifies eight loci associated with blood pressure. Nature genetics\| PubMed ID: 19430483	2009
Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men. Diabetes\| PubMed ID: 19502414	2009
Elevated cerebrospinal fluid adiponectin and adipsin levels in patients with multiple sclerosis: a Finnish co-twin study. European journal of neurology : the official journal of the European Federation of Neurological Societies\| PubMed ID: 19538214	2010
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. PLoS genetics\| PubMed ID: 19557161	2009
Experiences with the electronic nursing discharge summary. Studies in health technology and informatics\| PubMed ID: 19592839	2009
Underlying genetic models of inheritance in established type 2 diabetes associations. American journal of epidemiology\| PubMed ID: 19602701	2009
Cardiac sympathetic activity is associated with inflammation and neurohumoral activation in patients with idiopathic dilated cardiomyopathy. Clinical physiology and functional imaging\| PubMed ID: 19622106	2009
Identification of the UBP1 locus as a critical blood pressure determinant using a combination of mouse and human genetics. PLoS genetics\| PubMed ID: 19662162	2009
The ATF6-Met[67]Val substitution is associated with increased plasma cholesterol levels. Arteriosclerosis, thrombosis, and vascular biology\| PubMed ID: 19667116	2009
Common polymorphisms within the NR4A3 locus, encoding the orphan nuclear receptor Nor-1, are associated with enhanced beta-cell function in non-diabetic subjects. BMC medical genetics\| PubMed ID: 19682370	2009
Additive effects of genetic variation in GCK and G6PC2 on insulin secretion and fasting glucose. Diabetes\| PubMed ID: 19741163	2009
Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes. Human molecular genetics\| PubMed ID: 19933169	2010
The metabolic syndrome predicts incident congestive heart failure: a 20-year follow-up study of elderly Finns. Atherosclerosis\| PubMed ID: 19945701	2010
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Nature genetics\| PubMed ID: 20081857	2010
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nature genetics\| PubMed ID: 20081858	2010
Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans. Diabetes\| PubMed ID: 20185807	2010
Association of the FTO gene variant (rs9939609) with cardiovascular disease in men with abnormal glucose metabolism--the Finnish Diabetes Prevention Study. Nutrition, metabolism, and cardiovascular diseases : NMCD\| PubMed ID: 20400278	2011
Pregnancy and childbirth in carriers of the lamin A/C-gene mutation. European journal of heart failure\| PubMed ID: 20413395	2010
Insulin sensitivity regulates cholesterol metabolism to a greater extent than obesity: lessons from the METSIM Study. Journal of lipid research\| PubMed ID: 20436182	2010
Identification of undiagnosed type 2 diabetic individuals by the finnish diabetes risk score and biochemical and genetic markers: a population-based study of 7232 Finnish men. The Journal of clinical endocrinology and metabolism\| PubMed ID: 20463095	2010
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nature genetics\| PubMed ID: 20581827	2010
p62/sequestosome 1 as a regulator of proteasome inhibitor-induced autophagy in human retinal pigment epithelial cells. Molecular vision\| PubMed ID: 20680098	2010
Diverse associations of 25-hydroxyvitamin D and 1,25-dihydroxy-vitamin D with dyslipidaemias. Journal of internal medicine\| PubMed ID: 20831628	2010
Common variants at 10 genomic loci influence hemoglobin Aâ‚(C) levels via glycemic and nonglycemic pathways. Diabetes\| PubMed ID: 20858683	2010
A role for coding functional variants in HNF4A in type 2 diabetes susceptibility. Diabetologia\| PubMed ID: 20878384	2011
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nature genetics\| PubMed ID: 20935629	2010
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature genetics\| PubMed ID: 20935630	2010
A novel surrogate index for hepatic insulin resistance. Diabetologia\| PubMed ID: 21107521	2011
The D299G/T399I Toll-like receptor 4 variant associates with body and liver fat: results from the TULIP and METSIM Studies. PloS one\| PubMed ID: 21125016	2010
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. Diabetologia\| PubMed ID: 21153532	2011
A common variant in TFB1M is associated with reduced insulin secretion and increased future risk of type 2 diabetes. Cell metabolism\| PubMed ID: 21195351	2011
Glucose tolerance, insulin sensitivity and insulin release in European non-diabetic carriers of a polymorphism upstream of CDKN2A and CDKN2B. Diabetologia\| PubMed ID: 21234743	2011
Cardiac MRI assessed left ventricular hypertrophy in differentiating hypertensive heart disease from hypertrophic cardiomyopathy attributable to a sarcomeric gene mutation. European radiology\| PubMed ID: 21274714	2011
Hospital training program increases awareness of Good Clinical Practice (GCP). Contemporary clinical trials\| PubMed ID: 21278002	2011
Serum lipidomics meets cardiac magnetic resonance imaging: profiling of subjects at risk of dilated cardiomyopathy. PloS one\| PubMed ID: 21283746	2011
Intravenous immunoglobulins are a therapeutic option in the treatment of multiple sclerosis relapse. Clinical neuropharmacology\| PubMed ID: 21301327	2011
Usability of electronic nursing record systems: definition and results from an evaluation study in Finland. Studies in health technology and informatics\| PubMed ID: 21335733	2011
Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals. Breast cancer research : BCR\| PubMed ID: 21356067	2011
Evidence of how rs7575840 influences apolipoprotein B-containing lipid particles. Arteriosclerosis, thrombosis, and vascular biology\| PubMed ID: 21393584	2011
Effects of 34 risk loci for type 2 diabetes or hyperglycemia on lipoprotein subclasses and their composition in 6,580 nondiabetic Finnish men. Diabetes\| PubMed ID: 21421807	2011
Pre-treatment expectations in clients: impact on retention and effectiveness in outpatient substance abuse treatment. Behavioural and cognitive psychotherapy\| PubMed ID: 21489349	2011
Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy. Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance\| PubMed ID: 21689390	2011
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile. Nature genetics\| PubMed ID: 21706003	2011
Pleiotropic effects of GIP on islet function involve osteopontin. Diabetes\| PubMed ID: 21810601	2011
SIRT3 deficiency and mitochondrial protein hyperacetylation accelerate the development of the metabolic syndrome. Molecular cell\| PubMed ID: 21856199	2011
What is our role in promoting literacy for children who are "blind" or visually impaired? Optometry (St. Louis, Mo.)\| PubMed ID: 21871393	2011
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. Diabetes\| PubMed ID: 21873549	2011
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature\| PubMed ID: 21909115	2011
Glomerular filtration rate and parathyroid hormone are associated with 1,25-dihydroxyvitamin D in men without chronic kidney disease. Journal of internal medicine\| PubMed ID: 21995281	2012
Serum interleukin 1 receptor antagonist as an independent marker of non-alcoholic steatohepatitis in humans. Journal of hepatology\| PubMed ID: 22027586	2012
Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children. PLoS medicine\| PubMed ID: 22069379	2011
The birth weight lowering C-allele of rs900400 near LEKR1 and CCNL1 associates with elevated insulin release following an oral glucose challenge. PloS one\| PubMed ID: 22073261	2011
The interplay between lipoprotein phenotypes, adiponectin, and alcohol consumption. Annals of medicine\| PubMed ID: 22077217	2012
Global enhancement of nuclear localization-dependent nuclear transport in transformed cells. FASEB journal : official publication of the Federation of American Societies for Experimental Biology\| PubMed ID: 22155563	2012
A genome-wide association search for type 2 diabetes genes in African Americans. PloS one\| PubMed ID: 22238593	2012
Evaluation of the national nursing model and four nursing documentation systems in Finland - Lessons learned and directions for the future. International journal of medical informatics\| PubMed ID: 22386236	2012
Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits. Circulation. Cardiovascular genetics\| PubMed ID: 22399527	2012
No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels. Diabetes\| PubMed ID: 22415877	2012
Low-grade inflammation and the phenotypic expression of myocardial fibrosis in hypertrophic cardiomyopathy. Heart (British Cardiac Society)\| PubMed ID: 22447464	2012
Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population. Annals of medicine\| PubMed ID: 22462493	2012
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS genetics\| PubMed ID: 22479202	2012
Association between liver insulin resistance and cardiovascular risk factors. Journal of internal medicine\| PubMed ID: 22486802	2012
Hyperglycemia and a common variant of GCKR are associated with the levels of eight amino acids in 9,369 Finnish men. Diabetes\| PubMed ID: 22553379	2012
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nature genetics\| PubMed ID: 22581228	2012
Lipoprotein subclass profiles in individuals with varying degrees of glucose tolerance: a population-based study of 9399 Finnish men. Journal of internal medicine\| PubMed ID: 22650159	2012
Circulating TNF-Alpha and IL-6 Concentrations and TNF-Alpha -308 Gâ€‰>â€‰A Polymorphism in Children with Premature Adrenarche. Frontiers in endocrinology\| PubMed ID: 22654787	2010
Plasma levels of antibodies against oxidized LDL are inherited but not associated with HDL-cholesterol level in families with early coronary heart disease. Atherosclerosis\| PubMed ID: 22818623	2012
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nature genetics\| PubMed ID: 22885922	2012
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nature genetics\| PubMed ID: 22885924	2012
Retention rate of selegiline in early Parkinson's disease: a retrospective survey. International journal of clinical practice\| PubMed ID: 22994335	2012