Tiinamaija Tuomi

Q: What Schools Are Affiliated With Tiinamaija Tuomi

Tiinamaija Tuomi is affiliated with the following schools: Lund University, Massachusetts General Hospital, Monash University, Harvard University, University of Helsinki

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Tiinamaija Tuomi

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Tiinamaija Tuomi's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Cardiovascular morbidity and mortality associated with the metabolic syndrome. (2001) (4830)
Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels (2007) (2888)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) (1882)
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) (1839)
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) (1801)
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (2009) (1735)
Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
Novel subgroups of adult-onset diabetes and their association with outcomes: a data-driven cluster analysis of six variables. (2018) (1169)
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes (2000) (1150)
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
The genetic architecture of type 2 diabetes (2016) (927)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes. (2007) (787)
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. (2000) (763)
Variants in MTNR1B influence fasting glucose levels (2009) (742)
Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus (2008) (739)
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion (2009) (698)
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge (2010) (648)
Antibodies to Glutamic Acid Decarboxylase Reveal Latent Autoimmune Diabetes Mellitus in Adults With a Non—Insulin-Dependent Onset of Disease (1993) (615)
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) (547)
Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (516)
The many faces of diabetes: a disease with increasing heterogeneity (2014) (515)
Clinical and genetic characteristics of type 2 diabetes with and without GAD antibodies. (1999) (514)
Clinical risk factors, DNA variants, and the development of type 2 diabetes. (2008) (503)
Latent Autoimmune Diabetes Mellitus in Adults (LADA): the Role of Antibodies to Glutamic Acid Decarboxylase in Diagnosis and Prediction of Insulin Dependency (1994) (435)
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes (2014) (405)
Common Single Nucleotide Polymorphisms in TCF7L2 Are Reproducibly Associated With Type 2 Diabetes and Reduce the Insulin Response to Glucose in Nondiabetic Individuals (2006) (395)
Predictors of and longitudinal changes in insulin sensitivity and secretion preceding onset of type 2 diabetes. (2005) (356)
Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci (2015) (349)
Insulin secretion and insulin sensitivity in relation to glucose tolerance: lessons from the Botnia Study. (2000) (349)
Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region. (2004) (322)
Early Metabolic Markers of the Development of Dysglycemia and Type 2 Diabetes and Their Physiological Significance (2013) (295)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) (294)
Common Missense Variant in the Glucokinase Regulatory Protein Gene Is Associated With Increased Plasma Triglyceride and C-Reactive Protein but Lower Fasting Glucose Concentrations (2008) (272)
The genetic abnormality in the beta cell determines the response to an oral glucose load (2002) (264)
Detailed Physiologic Characterization Reveals Diverse Mechanisms for Novel Genetic Loci Regulating Glucose and Insulin Metabolism in Humans (2010) (262)
The metabolic syndrome influences the risk of chronic complications in patients with Type II diabetes (2001) (256)
GAD Antibody Negative NIDDM in Adult Black Subjects with Diabetic Ketoacidosis and Increased Frequency of Human Leukocyte Antigen DR3 and DR4: Flatbush Diabetes (1994) (248)
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension (2016) (234)
Rheumatoid factors antedating clinical rheumatoid arthritis. (1991) (231)
Prevalence and clinical associations of 10 defined autoantibodies in autoimmune polyendocrine syndrome type I. (2004) (230)
Fasting Versus Postload Plasma Glucose Concentration and the Risk for Future Type 2 Diabetes (2009) (226)
Genetic Similarities Between Latent Autoimmune Diabetes in Adults, Type 1 Diabetes, and Type 2 Diabetes (2008) (221)
Evaluation of Common Variants in the Six Known Maturity-Onset Diabetes of the Young (MODY) Genes for Association With Type 2 Diabetes (2007) (217)
Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect. (1997) (213)
Heritability and familiality of type 2 diabetes and related quantitative traits in the Botnia Study (2011) (209)
The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis (2013) (199)
Genetic evidence of assortative mating in humans (2017) (199)
Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes (2011) (197)
Blood-based biomarkers of age-associated epigenetic changes in human islets associate with insulin secretion and diabetes (2016) (187)
Increased Melatonin Signaling Is a Risk Factor for Type 2 Diabetes. (2016) (186)
Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers (2020) (182)
GAD Antibodies in NIDDM: Ten-year follow-up from the diagnosis (1995) (180)
Age influences DNA methylation and gene expression of COX7A1 in human skeletal muscle (2008) (177)
Contribution of insulin-stimulated glucose uptake and basal hepatic insulin sensitivity to surrogate measures of insulin sensitivity. (2004) (166)
Genetic Prediction of Future Type 2 Diabetes (2005) (163)
The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts (2007) (163)
A Central Role for GRB10 in Regulation of Islet Function in Man (2014) (159)
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls (2019) (153)
High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes (1999) (150)
The SLC6A14 gene shows evidence of association with obesity. (2003) (150)
Smoking, lung function, and rheumatoid factors. (1990) (148)
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study. (2002) (139)
Antibodies to glutamic acid decarboxylase and insulin-dependent diabetes in patients with autoimmune polyendocrine syndrome type I. (1996) (136)
Autoantibodies against aromatic L-amino acid decarboxylase in autoimmune polyendocrine syndrome type I. (1997) (132)
DNA methylation of loci within ABCG1 and PHOSPHO1 in blood DNA is associated with future type 2 diabetes risk (2016) (131)
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes (2012) (129)
Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants (2011) (128)
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes (2013) (128)
Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms (2014) (120)
The shape of plasma glucose concentration curve during OGTT predicts future risk of type 2 diabetes (2010) (119)
Serum and follicular fluid leptin during in vitro fertilization: relationship among leptin increase, body fat mass, and reduced ovarian response. (1999) (119)
Modelling of OGTT curve identifies 1 h plasma glucose level as a strong predictor of incident type 2 diabetes: results from two prospective cohorts (2014) (109)
Type 1 and type 2 diabetes: what do they have in common? (2005) (107)
Chronic complications in patients with slowly progressing autoimmune type 1 diabetes (LADA). (1999) (106)
A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes (2011) (105)
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes (2018) (105)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
Mutation in the HNF-4alpha gene affects insulin secretion and triglyceride metabolism. (1999) (102)
Insulin and glucagon secretion in patients with slowly progressing autoimmune diabetes (LADA). (2000) (101)
Stressful Life Events and the Metabolic Syndrome (2009) (101)
Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus (2015) (98)
A Variant in the KCNQ1 Gene Predicts Future Type 2 Diabetes and Mediates Impaired Insulin Secretion (2009) (96)
Genetic architecture of human plasma lipidome and its link to cardiovascular disease (2019) (96)
Non-insulin-dependent diabetes mellitus--a collision between thrifty genes and an affluent society. (1997) (91)
Effects of Common Genetic Variants Associated With Type 2 Diabetes and Glycemic Traits on α- and β-Cell Function and Insulin Action in Humans (2013) (90)
Common Variants in Maturity-Onset Diabetes of the Young Genes and Future Risk of Type 2 Diabetes (2008) (89)
Pleiotropic Effects of GIP on Islet Function Involve Osteopontin (2011) (88)
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes (2018) (87)
Management of Latent Autoimmune Diabetes in Adults: A Consensus Statement From an International Expert Panel (2020) (86)
A family history of diabetes is associated with reduced physical fitness in the Prevalence, Prediction and Prevention of Diabetes (PPP)–Botnia study (2010) (86)
Classifying diabetes according to the new WHO clinical stages (2004) (85)
ss-cell autoantibodies, human leukocyte antigen II alleles, and type 1 diabetes in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. (2000) (85)
Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes. (2004) (83)
Common Variants in the ENPP1 Gene Are Not Reproducibly Associated With Diabetes or Obesity (2006) (83)
Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people. (2005) (82)
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes. (2003) (82)
Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study (2018) (82)
Latent Autoimmune Diabetes in Adults Differs Genetically From Classical Type 1 Diabetes Diagnosed After the Age of 35 Years (2010) (81)
Early metabolic markers identify potential targets for the prevention of type 2 diabetes (2017) (81)
Link Between GIP and Osteopontin in Adipose Tissue and Insulin Resistance (2013) (80)
Insulin secretion and insulin sensitivity in diabetic subgroups: studies in the prediabetic and diabetic state (2000) (79)
Consequences of a family history of type 1 and type 2 diabetes on the phenotype of patients with type 2 diabetes. (2000) (79)
Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance (2017) (79)
Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes. (2005) (78)
Loss of ZnT8 function protects against diabetes by enhanced insulin secretion (2018) (78)
Improved prandial glucose control with lower risk of hypoglycemia with nateglinide than with glibenclamide in patients with maturity-onset diabetes of the young type 3. (2006) (77)
Pilot study on obesity in caries prediction. (1989) (75)
Autoimmunity to CD38 and GAD in Type I and Type II diabetes: CD38 and HLA genotypes and clinical phenotypes (2002) (73)
Importance of obtaining independent measures of insulin secretion and insulin sensitivity during the same test: results with the Botnia clamp. (2003) (72)
A genome-wide scan in families with maturity-onset diabetes of the young: evidence for further genetic heterogeneity. (2003) (71)
Associations of autozygosity with a broad range of human phenotypes (2019) (68)
Possible human leukocyte antigen-mediated genetic interaction between type 1 and type 2 Diabetes. (2001) (68)
A saturated map of common genetic variants associated with human height (2022) (65)
The human L-type calcium channel Cav1.3 regulates insulin release and polymorphisms in CACNA1D associate with type 2 diabetes (2013) (64)
Overweight, obesity and the risk of LADA: results from a Swedish case–control study and the Norwegian HUNT Study (2018) (62)
Common variants in HNF-1 α and risk of type 2 diabetes (2006) (62)
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection (2021) (61)
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2020) (58)
Latent autoimmune diabetes in adults (LADA)—more than a name (2006) (55)
Complex Relationship Between Blood Pressure and Mortality in Type 2 Diabetic Patients: A Follow-Up of the Botnia Study (2006) (54)
The role of polygenic risk and susceptibility genes in breast cancer over the course of life (2020) (53)
The role of polygenic risk and susceptibility genes in breast cancer over the course of life (2020) (53)
Stressful Life Events and the Metabolic Syndrome - The Prevalence, Prediction and Prevention of Diabetes (PPP)-Botnia Study (2010) (53)
Type 2 diabetes susceptibility gene variants predispose to adult-onset autoimmune diabetes (2014) (53)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (53)
GAD Antibody Positivity Predicts Type 2 Diabetes in an Adult Population (2009) (52)
Autoantigenic properties of native and denatured glutamic acid decarboxylase: evidence for a conformational epitope. (1994) (52)
Clinical Heterogeneity in Monogenic Diabetes Caused by Mutations in the Glucokinase Gene (GCK-MODY) (2009) (51)
Antibodies to Glutamic Acid Decarboxylase in Australian Children with Insulin-Dependent Diabetes Mellitus and Their First-Degree Relatives (1993) (51)
Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people. (2005) (50)
New Blood Pressure–Associated Loci Identified in Meta-Analyses of 475 000 Individuals (2017) (50)
Minimal Contribution of Fasting Hyperglycemia to the Incidence of Type 2 Diabetes in Subjects With Normal 2-h Plasma Glucose (2009) (49)
Obstructive sleep apnoea and the risk for coronary heart disease and type 2 diabetes: a longitudinal population-based study in Finland (2018) (48)
Association between depressive symptoms and metabolic syndrome is not explained by antidepressant medication: Results from the PPP-Botnia Study (2012) (48)
Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health (2020) (47)
Association Studies of BMI and Type 2 Diabetes in the Neuropeptide Y Pathway (2007) (47)
Differing frequency of autoantibodies to glutamic acid decarboxylase among Koreans, Thais, and Australians with diabetes mellitus. (1995) (47)
Interference of immunoglobulin G (IgG) antibodies in IgA antibody determinations of Chlamydia pneumoniae by microimmunofluorescence test (1994) (47)
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk (2017) (43)
Sleep duration and insulin resistance in individuals without type 2 diabetes: The PPP-Botnia Study (2014) (42)
Metabolite Profiling Reveals Normal Metabolic Control in Carriers of Mutations in the Glucokinase Gene (MODY2) (2013) (42)
Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes (2021) (41)
Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (39)
HLA-DQ genotypes are associated with autoimmunity to glutamic acid decarboxylase in insulin-dependent diabetes mellitus patients. (1993) (38)
Common variants in HNF-1 alpha and risk of type 2 diabetes. (2006) (37)
High-density haplotype structure and association testing of the insulin-degrading enzyme (IDE) gene with type 2 diabetes in 4,206 people. (2006) (37)
Sweetened beverage intake and risk of latent autoimmune diabetes in adults (LADA) and type 2 diabetes. (2016) (37)
1-Hour Post-OGTT Glucose Improves the Early Prediction of Type 2 Diabetes by Clinical and Metabolic Markers (2018) (36)
Polymorphisms in the gene encoding the voltage-dependent Ca2+ channel CaV2.3 (CACNA1E) are associated with type 2 diabetes and impaired insulin secretion (2007) (36)
A combination of human leukocyte antigen DQB1*02 and the tumor necrosis factor alpha promoter G308A polymorphism predisposes to an insulin-deficient phenotype in patients with type 2 diabetes. (2003) (35)
Prediction of silent celiac disease at diagnosis of childhood type 1 diabetes by tissue transglutaminase autoantibodies and HLA (2001) (35)
Autoantibodies to Glutamic Acid Decarboxylase and Insulin in Islet Cell Antibody Positive Presymptomatic Type 1 Diabetes Mellitus: Frequency and Segregation by Age and Gender (1994) (35)
Genetic determinants of circulating GIP and GLP-1 concentrations. (2017) (34)
The Distribution of Class‐Specific Rheumatoid Factors Is Similar in Rheumatoid and Pre‐Illness Sera (1986) (33)
An investigation of serum concentration of apoM as a potential MODY3 marker using a novel ELISA (2010) (33)
Two-Step Approach for the Prediction of Future Type 2 Diabetes Risk (2011) (32)
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity. (2002) (32)
Family history of type 1 and type 2 diabetes and risk of latent autoimmune diabetes in adults (LADA). (2017) (31)
A common variant upstream of the PAX6 gene influences islet function in man (2011) (31)
Genetic Variation in ATP5O Is Associated with Skeletal Muscle ATP50 mRNA Expression and Glucose Uptake in Young Twins (2009) (31)
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes (2020) (29)
Depressive Symptoms, Antidepressant Medication Use, and Insulin Resistance (2011) (29)
How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study (2022) (28)
Diabetes and Prediabetes Classification Using Glycemic Variability Indices From Continuous Glucose Monitoring Data (2018) (27)
Codon 72 polymorphism (rs1042522) of TP53 is associated with changes in diastolic blood pressure over time (2011) (26)
The genetic variant of lactase persistence C (−13910) T as a risk factor for type I and II diabetes in the Finnish population (2004) (26)
A male-specific quantitative trait locus on 1p21 controlling human stature (2005) (26)
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2017) (25)
Smoking and the Risk of LADA: Results From a Swedish Population-Based Case-Control Study (2016) (25)
40th EASD Annual Meeting of the European Association for the Study of Diabetes (2004) (25)
Autoimmunity to glutamic acid decarboxylase in patients with autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy (APECED) (2000) (24)
Influence of Familial Renal Glycosuria Due to Mutations in the SLC5A2 Gene on Changes in Glucose Tolerance over Time (2016) (24)
Subjective Sleep Complaints Are Associated With Insulin Resistance in Individuals Without Diabetes (2012) (24)
Familiality of metabolic abnormalities is dependent on age at onset and phenotype of the type 2 diabetic proband. (2003) (23)
Zinc transporter type 8 autoantibodies (ZnT8A): prevalence and phenotypic associations in latent autoimmune diabetes patients and patients with adult onset type 1 diabetes (2013) (23)
Haplotype structures and large-scale association testing of the 5 ' AMP-activated protein kinase genes PRK4A2, PRKAB1, and PRK4B1 with type 2 diabetes (2006) (22)
Glutamic acid decarboxylase antibody positivity is associated with an impaired insulin response to glucose and arginine in nondiabetic patients with autoimmune thyroiditis. (2002) (22)
FinnGen provides genetic insights from a well-phenotyped isolated population (2023) (22)
Islet Gene View—a tool to facilitate islet research (2018) (21)
Fatty fish consumption and risk of latent autoimmune diabetes in adults (2014) (21)
Coffee consumption and the risk of latent autoimmune diabetes in adults—results from a Swedish case–control study (2014) (21)
Nonsuppressed Glucagon After Glucose Challenge as a Potential Predictor for Glucose Tolerance (2016) (21)
Measuring rheumatoid factor in nonrheumatoid subjects: immunoturbidimetric assay, latex slide test, and enzyme-linked immunosorbent assay compared. (1991) (21)
Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC (2019) (20)
Subgroups of patients with young-onset type 2 diabetes in India reveal insulin deficiency as a major driver (2021) (20)
Atypical Forms of Diabetes (2015) (20)
Clusters provide a better holistic view of type 2 diabetes than simple clinical features. (2019) (20)
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)) (2010) (20)
Low birthweight is associated with an increased risk of LADA and type 2 diabetes: results from a Swedish case–control study (2015) (19)
Lack of autoimmune serological reactions in rodent models of insulin dependent diabetes mellitus. (1996) (19)
Rheumatoid factors and rheumatoid arthritis. (1988) (19)
Is seropositive rheumatoid arthritis becoming less severe? (1989) (18)
Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes (2022) (18)
Rare variants identified in the HNF-4α β-cell-specific promoter and alternative exon 1 lack biological significance in maturity onset diabetes of the young and young onset Type II diabetes (2002) (18)
The Krüppel-Like Factor 11 (KLF11) Q62R Polymorphism Is Not Associated With Type 2 Diabetes in 8,676 People (2006) (17)
Urinary extracellular vesicles: Assessment of pre‐analytical variables and development of a quality control with focus on transcriptomic biomarker research (2021) (17)
Use of Swedish smokeless tobacco (snus) and the risk of Type 2 diabetes and latent autoimmune diabetes of adulthood (LADA) (2017) (17)
Biliary Anomalies in Patients With HNF1B Diabetes (2017) (16)
Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes (2016) (16)
HAPT2D: high accuracy of prediction of T2D with a model combining basic and advanced data depending on availability. (2018) (16)
Identification and Functional Characterization of G 6 PC 2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G 6 PC 2-ABCB 11 Locus (2015) (16)
Communicating polygenic and non-genetic risk for atherosclerotic cardiovascular disease - An observational follow-up study (2020) (16)
Accuracy of 1-Hour Plasma Glucose During the Oral Glucose Tolerance Test in Diagnosis of Type 2 Diabetes in Adults: A Meta-analysis (2021) (15)
Effect of a common variant of the PCSK2 gene on reduced insulin secretion (2012) (15)
Interaction between overweight and genotypes of HLA, TCF7L2, and FTO in relation to the risk of Latent Autoimmune Diabetes in Adults and type 2 diabetes. (2019) (15)
Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2011) (15)
Association testing of common variants in the insulin receptor substrate-1 gene (IRS1) with type 2 diabetes (2007) (14)
Diabetic sera react with the glutamic acid decarboxylase molecule in a dimeric‐oligomeric form (1996) (13)
Coffee consumption, genetic susceptibility and risk of latent autoimmune diabetes in adults: A population-based case-control study. (2018) (13)
Glucose-dependent insulinotropic peptide and risk of cardiovascular events and mortality: a prospective study (2020) (12)
Significance of rheumatoid factors in an eight-year longitudinal study on arthritis (2004) (12)
Subjective Sleep Complaints Are AssociatedWith Insulin Resistance in IndividualsWithout Diabetes The PPP-Botnia Study (2012) (12)
Cosegregation of MIDD and MODY in a pedigree: functional and clinical consequences. (2004) (12)
Fasting Versus Post-Load Plasma Glucose Concentration and the Risk for Future Type 2 Diabetes : Results From The Botnia Study Running Title : Fasting versus Post-Load Glucose & Diabetes Risk (2008) (12)
Clustering of adult-onset diabetes into novel subgroups guides therapy and improves prediction of outcome (2017) (12)
Genotypes of HLA, TCF7L2, and FTO as potential modifiers of the association between sweetened beverage consumption and risk of LADA and type 2 diabetes (2019) (12)
35th Annual meeting of the European Association for the Study of Diabetes. Brussels, Belgium, 28 September-2 October, 1999. Abstracts. (1999) (11)
Islet cell and glutamic acid decarboxylase antibodies and heat-shock protein 65 responses in children with newly diagnosed insulin-dependent diabetes mellitus. (1996) (10)
Haplotype structures and large-scale association testing of the 5' AMP-activated protein kinase genes PRKAA2, PRKAB1, and PRKAB2 [corrected] with type 2 diabetes. (2006) (10)
Human physiology of genetic defects causing beta-cell dysfunction. (2020) (10)
Independent measures of insulin secretion and insulin sensitivity during the same test: the glucagon–insulin tolerance test (2008) (9)
The timing of rheumatoid factor seroconversions. (1987) (9)
Persisting antibodies to glutamic acid decarboxylase in Type 1 (insulin-dependent) diabetes mellitus are not associated with neuropathy (1993) (9)
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes (2021) (9)
Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation (2019) (9)
Association of variants in HLA-DQA1-DQB1, PTPN22, INS, and CTLA4 with GAD autoantibodies and insulin secretion in nondiabetic adults of the Botnia Prospective Study. (2012) (9)
Family history of Type 1 diabetes affects insulin secretion in patients with ‘Type 2’ diabetes (2013) (9)
Oral Glucose Tolerance Test should Be Performed after Stroke and Transient Ischemic Attack (2011) (8)
Serious life events and the risk of latent autoimmune diabetes in adults (LADA) and Type 2 diabetes (2017) (8)
Glucose-Dependent Insulinotropic Peptide in the High-Normal Range Is Associated With Increased Carotid Intima-Media Thickness. (2020) (8)
Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes (2020) (8)
Genetic testing for maturity onset diabetes of the young: uptake, attitudes and comparison with hereditary non-polyposis colorectal cancer (2005) (8)
Consumption of red meat, genetic susceptibility, and risk of LADA and type 2 diabetes (2020) (7)
Genetic prediction of the metabolic syndrome (2008) (7)
EPMA-World Congress 2015 (2016) (7)
A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use—The P5 Study (2021) (7)
Aetiological differences between novel subtypes of diabetes derived from genetic associations (2020) (7)
Physical Activity, Genetic Susceptibility, and the Risk of Latent Autoimmune Diabetes in Adults and Type 2 Diabetes (2020) (6)
Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries (2018) (6)
The associations of daylight and melatonin receptor 1B gene rs10830963 variant with glycemic traits: the prospective PPP-Botnia study (2019) (6)
Onset of glucose intolerance in MODY3 Pro291fsInsC mutation carrierscoincides with pubertal years - a prospective follow-up study (2002) (5)
GENETIC SIMILARITIES BETWEEN LADA, TYPE 1 AND TYPE 2 DIABETES (2008) (5)
Rheumatoid factor isotypes in patients with rheumatoid arthritis and in subjects with "false-positive" reactions. (1988) (5)
Combined lifestyle factors and the risk of LADA and type 2 diabetes - Results from a Swedish population-based case-control study. (2021) (5)
A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY (2021) (5)
Novel diabetes subgroups - Authors' reply. (2018) (4)
Metabolite Pro fi ling Reveals Normal Metabolic Control in Carriers of Mutations in the Glucokinase Gene ( MODY 2 ) (2012) (4)
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2018) (4)
Influence of Familial Renal Glycosuria Due to Mutations in the SLC 5 A 2 Gene on Changes in Glucose Tolerance over Time Ottosson-Laakso , Emilia 2016-01-06 (4)
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells (2020) (4)
Melatonin receptor 1B gene rs10830963 polymorphism, depressive symptoms and glycaemic traits (2018) (4)
An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease (2020) (3)
One-Hour Post-OGTT Glucose Improves the Early Prediction of Type 2 Diabetes beyond Metabolic Markers (2018) (3)
Effect of Common Genetic Variants Associated with Type 2 Diabetes and Glycemic Traits on α-and β-cell Function and Insulin Action in Man (2013) (3)
Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers (2020) (2)
Smoking, use of smokeless tobacco, HLA genotypes and incidence of latent autoimmune diabetes in adults (2022) (2)
Birthweight, BMI in adulthood and latent autoimmune diabetes in adults: a Mendelian randomisation study (2022) (2)
[Update on current care guideline: diabetes]. (2013) (2)
Seronegative rheumatoid arthritis in an eight-year longitudinal study. (1987) (2)
O-039. Significant rise in serum leptin concentration during ovarian stimulation for IVF (1997) (2)
Heterozygous RFX6 protein truncating variants are associated with Maturity-Onset Diabetes of the Young (MODY) with reduced penetrance (2017) (2)
The Botnia study – on the trail of type 2 diabetes (2008) (2)
Low-cost exercise interventions improve long-term cardiometabolic health independently of a family history of type 2 diabetes: a randomized parallel group trial (2020) (2)
Identification of monogenic variants in more than ten per cent of children without type 1 diabetes-related autoantibodies at diagnosis in the Finnish Pediatric Diabetes Register (2022) (2)
Correction to: A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY (2022) (1)
Metabolic effects of novel type 2 diabetes genes in a population aged 18-75 years (2008) (1)
CART is a novel glucose-dependent peptide with antidiabetic actions in humans (2015) (1)
A genome scan reveals heterogeneity among European families with maturity onset diabetes of the young (2001) (1)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (1)
Sodium intake and the risk of type 2 diabetes and Latent Autoimmune Diabetes in Adults (LADA) (2017) (1)
Loci for insulin processing and secretion provide insight into type 2 diabetes risk. (2023) (1)
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population (2023) (1)
The role of adiposity in cardiometabolic traits (2013) (1)
Overweight, obesity, genetic susceptibility and the risk of LADA : Latent Autoimmune Diabetes in Adults (2017) (1)
Intrauterine hyperglycemia modifying the development of (monogenic) diabetes? (2003) (1)
Large scale trans-ethnic meta-analyses identify novel rare and common variants associated with blood pressure and hypertension (2016) (1)
An insulin hypersecretion phenotype precedes pancreatic β cell failure in MODY3 patient-specific cells. (2022) (1)
Subgroups of young type 2 diabetes in India reveal insulin deficiency as a major driver (2021) (1)
Genetic analyses implicate complex links between adult testosterone levels and health and disease (2023) (1)
Genetic analyses implicate complex links between adult testosterone levels and health and disease (2023) (1)
Rapid Publication Characterization of the MODY 3 Phenotype Early-Onset Diabetes Caused by an Insulin Secretion Defect (2018) (1)
Genetic analyses on the health impacts of testosterone highlights effects on female-specific diseases and sex differences (2021) (1)
[MODY diabetes--a monogenic developmental and functional disturbance of pancreatic beta cells]. (2012) (1)
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2021) (1)
Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases (2023) (0)
Research: Epidemiology Coffee consumption and the risk of latent autoimmune diabetes in adults—results from a Swedish case-control study (2014) (0)
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications (2023) (0)
Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata (2023) (0)
Monogenic variants in the Finnish Pediatric Diabetes Register (2021) (0)
Erratum. Accuracy of 1-Hour Plasma Glucose During the Oral Glucose Tolerance Test in Diagnosis of Type 2 Diabetes in Adults: A Meta-analysis. Diabetes Care 2021;44:1062–1069 (2021) (0)
Clustering of diabetes into novel subgroups provides improved prediction of outcome (2017) (0)
University of Southern Denmark Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC Mishra, (2020) (0)
1453-P: Adaption of the ACMG/AMP Variant Interpretation Guidelines for GCK, HNF1A, HNF4A-MODY: Recommendations from the ClinGen Monogenic Diabetes Expert Panel (2020) (0)
Edinburgh Research Explorer Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes (2018) (0)
[Diabetes of adult type is a polymorphic disease]. (2001) (0)
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls (2019) (0)
Genome-Wide Association Identi ﬁ es Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes (2011) (0)
Abstract of the Fast Tracked Online Articles (2013) (0)
42 HAPLOTYPE STRUCTURE AND ASSOCIATION OF COMMON VARIANTS IN THE GENE ENCODING THE ISLET ATP-SENSITIVE POTASSIUM CHANNEL WITH TYPE 2 DIABETES. (2004) (0)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2018) (0)
CGM-based glycemic variability indices allow accurate classification of IGT and T2D subjects (2017) (0)
[Not Available]. (2007) (0)
Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance (2017) (0)
Loss of ZnT8 function protects against diabetes by enhanced insulin secretion (2019) (0)
[Why is that the response to treatment of type 1 diabetes is not improving?]. (2005) (0)
Genetic factors affect the susceptibility to bacterial infections in diabetes (2021) (0)
[Long-acting insulin analog, glargine, in the treatment of type 1 diabetes]. (2004) (0)
Evidence for enhanced de novo lipogenesis and uncoupling of obesity from type 2 diabetes risk in the low-expression variant carriers of fatty acid-binding protein 4 (2016) (0)
Facilitation of information exhange between genetic research, primary health care and decision makers using a regional diabetes register DIREVA (Diabetes Register Vaasa) (2011) (0)
IX Eular Workshop for Rheumatology Research (1989) (0)
Genome-wide mRNA profiling in urinary extracellular vesicles reveals stress gene signature for diabetic kidney disease (2023) (0)
[Diabetic with hallucination]. (2005) (0)
Utilizing pre-existing imaging and data lake technology in the search of clinically neglected non-alcoholic fatty liver disease (NAFLD) (2020) (0)
A common variant in the PAX6 gene influences islet function in man (2010) (0)
GADA positivity predicts non-insulin dependent diabetes in an adult population Running title: GADA positivity predicts diabetes in adults (2009) (0)
Support vector machine fed by CGM-based glycemic variability indices can distinguish between IGT and T2D subjects (2017) (0)
Is the common variant rs10830963 in the melatonin receptor 1B gene influencing the associations between depressive symptoms and glycemic traits (2017) (0)
Correction to: Subgroups of patients with young-onset type 2 diabetes in India reveal insulin deficiency as a major driver (2021) (0)
Effect of variants in the RORA gene on risk of type 2 diabetes (2010) (0)
Table 2. [DRUG- INDUCED DIABETES]. (2015) (0)
IGT and T2D subjects automatically classified using a selection of CGM-based glycemic variability indices (2018) (0)
Consumer's Experiences on Crowdsourcing Campaign : “It’s nice that the company is interested in my opinion” (2015) (0)
EPMA-World Congress 2015 (2016) (0)
Abstracts 2007 (2007) (0)
Influence of novel genetic loci affecting glucose and insulin levels during OGTT on islet function in man (2010) (0)
Good accuracy of CGM-based glucose variability indices for IGT and T2D classification (2016) (0)
Incidence of LADA and Type 2 Diabetes in Relation to Tobacco Use and Genetic Susceptibility to Type 2 Diabetes and Related Traits: Findings From a Swedish Case-Control Study and the Norwegian HUNT Study (2023) (0)
[Table, Autosomal Dominant Disease]. (2015) (0)
Birth weight, BMI in adulthood and latent autoimmune diabetes in adults: A Mendelian randomization study (2021) (0)
Family history of type 1 and type 2 diabetes and the risk of LADA-results from a population-based study of incident cases (2014) (0)
Diabetes: definition, differential diagnosis and classification (2000) (0)
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2021) (0)
All-Cause Mortality, Cardiovascular and Microvascular Diseases in Latent Autoimmune Diabetes in Adults (2022) (0)
IgM-rheumatoid factors measured by ELISA in non-rheumatoid sera: comparison of human and rabbit Fc fragments as antigens. (1992) (0)
Genetic dissection of serum vaspin highlights its causal role in lipid metabolism (2023) (0)
The family-based assessment of HNF1A-MODY (2020) (0)
Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes (2022) (0)
Type 1 Diabetes in Autoimmune Syndromes (2003) (0)
Urine extracellular vesicles capture kidney transcriptome and hyperglycemia linked mRNA signatures for type 1 diabetic kidney disease (2021) (0)
[Persistent asthma and hypokalemia]. (2005) (0)
Assessing the likely function of HNF1A missense variants using CRP and allele frequency data (2016) (0)
[From the rickets in children to the osteomalacia in adults]. (2001) (0)
Increased risk of diabetes and hyperglycaemia associated with treatment with statins, beta-blockers and diuretics: the PPP-Botnia study (2017) (0)
[Update on Current Care Guideline. Diabetes]. (2016) (0)
Lipid-Associated Variants near ANGPTL3 and LPL Show Parent-of-Origin Specific Effects on Blood Lipid Levels and Obesity (2021) (0)
Increased Melatonin Signa ling Is a Risk Factor for Type 2 Diabetes Graphical (2016) (0)
[What are the responsibilities for a doctor-scientist?]. (2006) (0)
AUTOANTIBODIES IN NEW ONSET CHILDHOOD IDDM (1993) (0)
[Cystic kidney disease and diabetes--an underdiagnosed monogenic developmental disorder]. (2012) (0)

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