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175 PR articles • 33,181 PR citations • Sorted by year • Download PDF (PDF by citations)
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1Clinical use of polygenic scores in type 2 diabetes: challenges and possibilities
Diabetologia, 2025, 68, 1361-1374
7.62Citations (PDF)
2Effects of parental autoimmune diseases on type 1 diabetes in offspring can be partially explained by HLA and non-HLA polymorphisms
Cell Genomics, 2025, 5, 100854
6.81Citations (PDF)
3Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty
Nature Aging, 2025, 5, 1589-1600
14.51Citations (PDF)
4Precision stratification of prognostic risk factors associated with outcomes in gestational diabetes mellitus: a systematic review
Communications Medicine, 2024, 4,
4.515Citations (PDF)
5High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases
Laboratory Investigation, 2024, 104, 100325
3.24Citations (PDF)
6Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
Nature, 2024, 627, 347-357
37.9383Citations (PDF)
7Applying a genetic risk score model to enhance prediction of future multiple sclerosis diagnosis at first presentation with optic neuritis
Nature Communications, 2024, 15,
13.79Citations (PDF)
8Metabolic profiling of smoking, associations with type 2 diabetes and interaction with genetic susceptibility
European Journal of Epidemiology, 2024, 39, 667-678
5.314Citations (PDF)
9Islet autoantibodies as precision diagnostic tools to characterize heterogeneity in type 1 diabetes: a systematic review
Communications Medicine, 2024, 4,
4.532Citations (PDF)
10RFX6 haploinsufficiency predisposes to diabetes through impaired beta cell function
Diabetologia, 2024, 67, 1642-1662
7.612Citations (PDF)
11Precision treatment of beta-cell monogenic diabetes: a systematic review
Communications Medicine, 2024, 4,
4.512Citations (PDF)
12Genetic architecture of oral glucose-stimulated insulin release provides biological insights into type 2 diabetes aetiology
Nature Metabolism, 2024, 6, 1897-1912
17.18Citations (PDF)
13Exposure to antibiotics and risk of latent autoimmune diabetes in adults and type 2 diabetes: results from a Swedish case–control study (ESTRID) and the Norwegian HUNT study
Diabetologia, 2024, 68, 69-81
7.60Citations (PDF)
14Autoimmune diseases and the risk and prognosis of latent autoimmune diabetes in adults
Diabetologia, 2024, 68, 331-341
7.69Citations (PDF)
15An insulin hypersecretion phenotype precedes pancreatic β cell failure in MODY3 patient-specific cells
Cell Stem Cell, 2023, 30, 38-51.e8
16.421Citations (PDF)
16Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases
Nature Medicine, 2023, 29, 209-218
33.032Citations (PDF)
17FinnGen provides genetic insights from a well-phenotyped isolated population
Nature, 2023, 613, 508-518
37.93,207Citations (PDF)
18Genetic analyses implicate complex links between adult testosterone levels and health and disease
Communications Medicine, 2023, 3,
4.533Citations (PDF)
19Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata
Nature Communications, 2023, 14,
13.716Citations (PDF)
20Loci for insulin processing and secretion provide insight into type 2 diabetes risk
American Journal of Human Genetics, 2023, 110, 284-299
6.535Citations (PDF)
21Incidence 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
Diabetes Care, 2023, 46, 1028-1036
6.26Citations (PDF)
22Genome-wide mRNA profiling in urinary extracellular vesicles reveals stress gene signature for diabetic kidney disease
IScience, 2023, 26, 106686
3.628Citations (PDF)
23Antioxidant Nutrients and Risk of Latent Autoimmune Diabetes in Adults and Type 2 Diabetes: A Swedish Case-Control Study and Mendelian Randomization Analysis
Nutrients, 2023, 15, 2546
4.56Citations (PDF)
24Residual insulin secretion in individuals with type 1 diabetes in Finland: longitudinal and cross-sectional analyses
Lancet Diabetes and Endocrinology,the, 2023, 11, 465-473
21.825Citations (PDF)
25The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections
EBioMedicine, 2023, 93, 104630
9.713Citations (PDF)
26Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
Nature Genetics, 2023, 55, 973-983
25.261Citations (PDF)
27Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
Nature Communications, 2023, 14,
13.749Citations (PDF)
28Capturing the Kidney Transcriptome by Urinary Extracellular Vesicles—From Pre-Analytical Obstacles to Biomarker Research
Genes, 2023, 14, 1415
2.58Citations (PDF)
29All-Cause Mortality and Cardiovascular and Microvascular Diseases in Latent Autoimmune Diabetes in Adults
Diabetes Care, 2023, 46, 1857-1865
6.216Citations (PDF)
30Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine
Nature Medicine, 2023, 29, 2438-2457
33.0164Citations (PDF)
31Precision subclassification of type 2 diabetes: a systematic review
Communications Medicine, 2023, 3,
4.567Citations (PDF)
32The use of precision diagnostics for monogenic diabetes: a systematic review and expert opinion
Communications Medicine, 2023, 3,
4.529Citations (PDF)
33Impact of individual and environmental factors on dietary or lifestyle interventions to prevent type 2 diabetes development: a systematic review
Communications Medicine, 2023, 3,
4.519Citations (PDF)
34NTHL1 is a recessive cancer susceptibility gene
Scientific Reports, 2023, 13,
3.45Citations (PDF)
35Inferring compound heterozygosity from large-scale exome sequencing data
Nature Genetics, 2023, 56, 152-161
25.227Citations (PDF)
36An atlas of genetic determinants of forearm fracture
Nature Genetics, 2023, 55, 1820-1830
25.214Citations (PDF)
37A genomic mutational constraint map using variation in 76,156 human genomes
Nature, 2023, 625, 92-100
37.91,024Citations (PDF)
38Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
American Journal of Human Genetics, 2022, 109, 81-96
6.533Citations (PDF)
39How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study
Circulation Genomic and Precision Medicine, 2022, 15,
2.9102Citations (PDF)
40Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes
Communications Biology, 2022, 5,
4.436Citations (PDF)
41Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes
Human Molecular Genetics, 2022, 31, 3377-3391
2.9104Citations (PDF)
42New insights into the genetic etiology of Alzheimer’s disease and related dementias
Nature Genetics, 2022, 54, 412-436
25.22,005Citations (PDF)
43Lipid-Associated Variants near ANGPTL3 and LPL Show Parent-of-Origin Specific Effects on Blood Lipid Levels and Obesity
Genes, 2022, 13, 91
2.53Citations (PDF)
44Birthweight, BMI in adulthood and latent autoimmune diabetes in adults: a Mendelian randomisation study
Diabetologia, 2022, 65, 1510-1518
7.612Citations (PDF)
45Smoking, use of smokeless tobacco, HLA genotypes and incidence of latent autoimmune diabetes in adults
Diabetologia, 2022, 66, 70-81
7.612Citations (PDF)
46Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis
Communications Biology, 2022, 5,
4.415Citations (PDF)
47Islet Gene View—a tool to facilitate islet research
Life Science Alliance, 2022, 5, e202201376
2.640Citations (PDF)
48A saturated map of common genetic variants associated with human height
Nature, 2022, 610, 704-712
37.9687Citations (PDF)
49Identification 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
Diabetologia, 2022, 66, 438-449
7.622Citations (PDF)
50Glucose-Dependent Insulinotropic Peptide in the High-Normal Range Is Associated With Increased Carotid Intima-Media Thickness
Diabetes Care, 2021, 44, 224-230
6.228Citations (PDF)
51Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health
European Respiratory Journal, 2021, 57, 2003091
8.7161Citations (PDF)
52Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Nature Communications, 2021, 12,
13.7132Citations (PDF)
53Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Nature Communications, 2021, 12,
13.7365Citations (PDF)
54Accuracy 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
6.252Citations (PDF)
55Combined lifestyle factors and the risk of LADA and type 2 diabetes – Results from a Swedish population-based case-control study
Diabetes Research and Clinical Practice, 2021, 174, 108760
5.915Citations (PDF)
56Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
Nature Communications, 2021, 12,
13.724Citations (PDF)
57Genetic factors affect the susceptibility to bacterial infections in diabetes
Scientific Reports, 2021, 11,
3.44Citations (PDF)
58Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
Nature Communications, 2021, 12,
13.795Citations (PDF)
59Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection
Nature Medicine, 2021, 27, 1012-1024
33.0170Citations (PDF)
60Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
JAMA Ophthalmology, 2021, 139, 762
6.19Citations (PDF)
61Subgroups of patients with young-onset type 2 diabetes in India reveal insulin deficiency as a major driver
Diabetologia, 2021, 65, 65-78
7.668Citations (PDF)
62Urinary extracellular vesicles: Assessment of pre‐analytical variables and development of a quality control with focus on transcriptomic biomarker research
Journal of Extracellular Vesicles, 2021, 10,
12.648Citations (PDF)
63A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use—The P5 Study
Frontiers in Genetics, 2021, 12,
2.317Citations (PDF)
64Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes
Nature Genetics, 2021, 53, 1534-1542
25.2152Citations (PDF)
65A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY
Diabetologia, 2021, 65, 632-643
7.620Citations (PDF)
66Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC
Diabetes Care, 2020, 43, 418-425
6.232Citations (PDF)
67Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
Nature, 2020, 586, 769-775
37.9145Citations (PDF)
68Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Nature Genetics, 2020, 52, 1314-1332
25.2167Citations (PDF)
69Physical Activity, Genetic Susceptibility, and the Risk of Latent Autoimmune Diabetes in Adults and Type 2 Diabetes
Journal of Clinical Endocrinology and Metabolism, 2020, 105, e4112-e4123
4.119Citations (PDF)
70The role of polygenic risk and susceptibility genes in breast cancer over the course of life
Nature Communications, 2020, 11,
13.7155Citations (PDF)
71Human Physiology of Genetic Defects Causing Beta-cell Dysfunction
Journal of Molecular Biology, 2020, 432, 1579-1598
4.115Citations (PDF)
72Glucose-dependent insulinotropic peptide and risk of cardiovascular events and mortality: a prospective study
Diabetologia, 2020, 63, 1043-1054
7.627Citations (PDF)
73An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease
European Journal of Human Genetics, 2020, 29, 309-324
3.025Citations (PDF)
74Consumption of red meat, genetic susceptibility, and risk of LADA and type 2 diabetes
European Journal of Nutrition, 2020, 60, 769-779
3.413Citations (PDF)
75Associations of autozygosity with a broad range of human phenotypes
Nature Communications, 2019, 10,
13.7117Citations (PDF)
76Loss of ZnT8 function protects against diabetes by enhanced insulin secretion
Nature Genetics, 2019, 51, 1596-1606
25.2133Citations (PDF)
77Genetic architecture of human plasma lipidome and its link to cardiovascular disease
Nature Communications, 2019, 10,
13.7168Citations (PDF)
78Interaction Between Overweight and Genotypes of HLA, TCF7L2, and FTO in Relation to the Risk of Latent Autoimmune Diabetes in Adults and Type 2 Diabetes
Journal of Clinical Endocrinology and Metabolism, 2019, 104, 4815-4826
4.124Citations (PDF)
79Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Nature, 2019, 570, 71-76
37.9303Citations (PDF)
801-Hour Post-OGTT Glucose Improves the Early Prediction of Type 2 Diabetes by Clinical and Metabolic Markers
Journal of Clinical Endocrinology and Metabolism, 2019, 104, 1131-1140
4.166Citations (PDF)
81The associations of daylight and melatonin receptor 1B gene rs10830963 variant with glycemic traits: the prospective PPP-Botnia study
Annals of Medicine, 2019, 51, 58-67
3.810Citations (PDF)
82Genotypes of HLA, TCF7L2, and FTO as potential modifiers of the association between sweetened beverage consumption and risk of LADA and type 2 diabetes
European Journal of Nutrition, 2019, 59, 127-135
3.48Citations (PDF)
83Novel subgroups of adult-onset diabetes and their association with outcomes: a data-driven cluster analysis of six variables
Lancet Diabetes and Endocrinology,the, 2018, 6, 361-369
21.81,954Citations (PDF)
84Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Nature Genetics, 2018, 50, 559-571
25.2429Citations (PDF)
85A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
Diabetes, 2018, 67, 1414-1427
4.2171Citations (PDF)
86Overweight, obesity and the risk of LADA: results from a Swedish case–control study and the Norwegian HUNT Study
Diabetologia, 2018, 61, 1333-1343
7.680Citations (PDF)
87Glycaemic variability-based classification of impaired glucose tolerance vs. type 2 diabetes using continuous glucose monitoring data
Computers in Biology and Medicine, 2018, 96, 141-146
6.317Citations (PDF)
88Diabetes and Prediabetes Classification Using Glycemic Variability Indices From Continuous Glucose Monitoring Data
Journal of Diabetes Science and Technology, 2018, 12, 105-113
2.943Citations (PDF)
89First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes
Diabetes Care, 2018, 41, 2396-2403
6.2119Citations (PDF)
90Obstructive sleep apnoea and the risk for coronary heart disease and type 2 diabetes: a longitudinal population-based study in Finland
BMJ Open, 2018, 8, e022752
1.982Citations (PDF)
91Melatonin receptor 1B gene rs10830963 polymorphism, depressive symptoms and glycaemic traits
Annals of Medicine, 2018, 50, 704-712
3.87Citations (PDF)
92Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study
Lancet Diabetes and Endocrinology,the, 2018, 6, 637-646
21.8156Citations (PDF)
93Genetic evidence of assortative mating in humans
Nature Human Behaviour, 2017, 1,
9.1308Citations (PDF)
94Early metabolic markers identify potential targets for the prevention of type 2 diabetes
Diabetologia, 2017, 60, 1740-1750
7.6120Citations (PDF)
95An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Diabetes, 2017, 66, 2888-2902
4.2717Citations (PDF)
96A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk
Diabetes, 2017, 66, 2019-2032
4.251Citations (PDF)
97Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance
Nature Communications, 2017, 8,
13.7128Citations (PDF)
98New Blood Pressure–Associated Loci Identified in Meta-Analyses of 475 000 Individuals
Circulation: Cardiovascular Genetics, 2017, 10,
3.852Citations (PDF)
99Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
Scientific Data, 2017, 4,
5.736Citations (PDF)
100Biliary Anomalies in Patients With HNF1B Diabetes
Journal of Clinical Endocrinology and Metabolism, 2017, 102, 2075-2082
4.125Citations (PDF)
101Genetic determinants of circulating GIP and GLP-1 concentrations
JCI Insight, 2017, 2,
5.451Citations (PDF)
102The genetic architecture of type 2 diabetes
Nature, 2016, 536, 41-47
37.91,051Citations (PDF)
103Increased Melatonin Signaling Is a Risk Factor for Type 2 Diabetes
Cell Metabolism, 2016, 23, 1067-1077
25.2235Citations (PDF)
104Smoking and the Risk of LADA: Results From a Swedish Population-Based Case-Control Study
Diabetes Care, 2016, 39, 794-800
6.229Citations (PDF)
105Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes
Diabetologia, 2016, 59, 1702-1713
7.621Citations (PDF)
106DNA methylation of loci within ABCG1 and PHOSPHO1 in blood DNA is associated with future type 2 diabetes risk
Epigenetics, 2016, 11, 482-488
3.0180Citations (PDF)
107Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Nature Genetics, 2016, 48, 1151-1161
25.2298Citations (PDF)
108Blood-based biomarkers of age-associated epigenetic changes in human islets associate with insulin secretion and diabetes
Nature Communications, 2016, 7,
13.7225Citations (PDF)
109Influence of Familial Renal Glycosuria Due to Mutations in the SLC5A2 Gene on Changes in Glucose Tolerance over Time
PLoS ONE, 2016, 11, e0146114
2.328Citations (PDF)
110Modelling of OGTT curve identifies 1 h plasma glucose level as a strong predictor of incident type 2 diabetes: results from two prospective cohorts
Diabetologia, 2015, 58, 87-97
7.6135Citations (PDF)
111Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus
PLoS Genetics, 2015, 11, e1004876
3.2108Citations (PDF)
112Low birthweight is associated with an increased risk of LADA and type 2 diabetes: results from a Swedish case–control study
Diabetologia, 2015, 58, 2525-2532
7.621Citations (PDF)
113Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
Nature Genetics, 2015, 47, 1415-1425
25.2408Citations (PDF)
114A Central Role for GRB10 in Regulation of Islet Function in Man
PLoS Genetics, 2014, 10, e1004235
3.2173Citations (PDF)
115The many faces of diabetes: a disease with increasing heterogeneity
Lancet, The, 2014, 383, 1084-1094
62.3579Citations (PDF)
116Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms
Cell, 2014, 156, 343-358
33.7122Citations (PDF)
117Type 2 diabetes susceptibility gene variants predispose to adult-onset autoimmune diabetes
Diabetologia, 2014, 57, 1859-1868
7.662Citations (PDF)
118Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Nature Genetics, 2014, 46, 234-244
25.21,030Citations (PDF)
119Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
Nature Genetics, 2014, 46, 357-363
25.2480Citations (PDF)
120Zinc transporter type 8 autoantibodies (ZnT8A): prevalence and phenotypic associations in latent autoimmune diabetes patients and patients with adult onset type 1 diabetes
Autoimmunity, 2013, 46, 251-258
3.124Citations (PDF)
121Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes
Nature Genetics, 2013, 45, 1380-1385
25.2138Citations (PDF)
122Metabolite Profiling Reveals Normal Metabolic Control in Carriers of Mutations in the Glucokinase Gene (MODY2)
Diabetes, 2013, 62, 653-661
4.243Citations (PDF)
123Link Between GIP and Osteopontin in Adipose Tissue and Insulin Resistance
Diabetes, 2013, 62, 2088-2094
4.284Citations (PDF)
124Early Metabolic Markers of the Development of Dysglycemia and Type 2 Diabetes and Their Physiological Significance
Diabetes, 2013, 62, 1730-1737
4.2340Citations (PDF)
125The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis
PLoS Medicine, 2013, 10, e1001474
8.1192Citations (PDF)
126Effects of Common Genetic Variants Associated With Type 2 Diabetes and Glycemic Traits on α- and β-Cell Function and Insulin Action in Humans
Diabetes, 2013, 62, 2978-2983
4.297Citations (PDF)
127Novel 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, 2012, 8, e1002607
3.2453Citations (PDF)
128Association of variants in HLA-DQA1-DQB1, PTPN22, INS, and CTLA4 with GAD autoantibodies and insulin secretion in nondiabetic adults of the Botnia Prospective Study
European Journal of Endocrinology, 2012, 167, 27-33
4.09Citations (PDF)
129Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Nature Genetics, 2012, 44, 981-990
25.21,863Citations (PDF)
130A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans
PLoS ONE, 2012, 7, e29202
2.3204Citations (PDF)
131Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes
Diabetes, 2011, 60, 2624-2634
4.2352Citations (PDF)
132Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants
Genetic Epidemiology, 2011, 35, 236-246
3.1104Citations (PDF)
133Pleiotropic Effects of GIP on Islet Function Involve Osteopontin
Diabetes, 2011, 60, 2424-2433
4.289Citations (PDF)
134Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge
Nature Genetics, 2010, 42, 142-148
25.2617Citations (PDF)
135Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Nature Genetics, 2010, 42, 579-589
25.21,700Citations (PDF)
136Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
Nature Genetics, 2010, 42, 949-960
25.2899Citations (PDF)
137Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Nature Genetics, 2010, 42, 937-948
25.22,774Citations (PDF)
138Minimal Contribution of Fasting Hyperglycemia to the Incidence of Type 2 Diabetes in Subjects With Normal 2-h Plasma Glucose
Diabetes Care, 2010, 33, 557-561
6.251Citations (PDF)
139Latent Autoimmune Diabetes in Adults Differs Genetically From Classical Type 1 Diabetes Diagnosed After the Age of 35 Years
Diabetes Care, 2010, 33, 2062-2064
6.275Citations (PDF)
140Detailed Physiologic Characterization Reveals Diverse Mechanisms for Novel Genetic Loci Regulating Glucose and Insulin Metabolism in Humans
Diabetes, 2010, 59, 1266-1275
4.2249Citations (PDF)
141GAD Antibody Positivity Predicts Type 2 Diabetes in an Adult Population
Diabetes, 2010, 59, 416-422
4.252Citations (PDF)
142New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Nature Genetics, 2010, 42, 105-116
25.22,098Citations (PDF)
143Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution
PLoS Genetics, 2009, 5, e1000508
3.2466Citations (PDF)
144Fasting Versus Postload Plasma Glucose Concentration and the Risk for Future Type 2 Diabetes
Diabetes Care, 2009, 32, 281-286
6.2233Citations (PDF)
145A Variant in the KCNQ1 Gene Predicts Future Type 2 Diabetes and Mediates Impaired Insulin Secretion
Diabetes, 2009, 58, 2409-2413
4.293Citations (PDF)
146Genetic Variation in ATP5O Is Associated with Skeletal Muscle ATP50 mRNA Expression and Glucose Uptake in Young Twins
PLoS ONE, 2009, 4, e4793
2.327Citations (PDF)
147Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus
Nature Genetics, 2008, 40, 1092-1097
25.2730Citations (PDF)
148Clinical Risk Factors, DNA Variants, and the Development of Type 2 Diabetes
New England Journal of Medicine, 2008, 359, 2220-2232
34.6841Citations (PDF)
149Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
Nature Genetics, 2008, 40, 638-645
25.21,736Citations (PDF)
150Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Nature Genetics, 2008, 41, 25-34
25.21,628Citations (PDF)
151Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion
Nature Genetics, 2008, 41, 82-88
25.2689Citations (PDF)
152Variants in MTNR1B influence fasting glucose levels
Nature Genetics, 2008, 41, 77-81
25.2697Citations (PDF)
153The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts
PLoS Genetics, 2007, 3, e61
3.2135Citations (PDF)
154Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes
Journal of Clinical Investigation, 2007, 117, 2155-2163
10.6725Citations (PDF)
155Common Variants in the ENPP1 Gene Are Not Reproducibly Associated With Diabetes or Obesity
Diabetes, 2006, 55, 3180-3184
4.276Citations (PDF)
156Genetic Prediction of Future Type 2 Diabetes
PLoS Medicine, 2005, 2, e345
8.1125Citations (PDF)
157Association Testing of the Protein Tyrosine Phosphatase 1B Gene (PTPN1) With Type 2 Diabetes in 7,883 People
Diabetes, 2005, 54, 1884-1891
4.253Citations (PDF)
158A 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
Human Molecular Genetics, 2003, 12, 1865-1873
2.970Citations (PDF)
159A Combination of Human Leukocyte Antigen DQB1*02 and the Tumor Necrosis Factor α Promoter G308A Polymorphism Predisposes to an Insulin-Deficient Phenotype in Patients with Type 2 Diabetes
Journal of Clinical Endocrinology and Metabolism, 2003, 88, 2767-2774
4.133Citations (PDF)
160Glutamic Acid Decarboxylase Antibody Positivity Is Associated with an Impaired Insulin Response to Glucose and Arginine in Nondiabetic Patients with Autoimmune Thyroiditis
Journal of Clinical Endocrinology and Metabolism, 2002, 87, 1177-1183
4.120Citations (PDF)
161Autoimmunity to CD38 and GAD in Type I and Type II diabetes: CD38 and HLA genotypes and clinical phenotypes
Diabetologia, 2002, 45, 1298-1306
7.654Citations (PDF)
162Glutamic Acid Decarboxylase Antibody Positivity Is Associated with an Impaired Insulin Response to Glucose and Arginine in Nondiabetic Patients with Autoimmune Thyroiditis
Journal of Clinical Endocrinology and Metabolism, 2002, 87, 1177-1183
4.18Citations (PDF)
163Prediction of silent celiac disease at diagnosis of childhood type 1 diabetes by tissue transglutaminase autoantibodies and HLA
Pediatric Diabetes, 2001, 2, 58-65
5.533Citations (PDF)
164Possible Human Leukocyte Antigen-Mediated Genetic Interaction between Type 1 and Type 2 Diabetes 1
Journal of Clinical Endocrinology and Metabolism, 2001, 86, 574-582
4.143Citations (PDF)
165The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
Nature Genetics, 2000, 26, 76-80
25.21,707Citations (PDF)
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170Title is missing!
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