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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Meta‐analysis of sex‐specific genome‐wide association studies
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Resetting the bar: Statistical significance in whole‐genome sequencing‐based association studies of global populations
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Joint Analysis of Functional Genomic Data and Genome-wide Association Studies of 18 Human Traits
inferredcites →https://doi.org/10.1016/j.cmet.2013.01.011openalex-snapshot
TCF7L2 and Diabetes: A Tale of Two Tissues, and of Two Species
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A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor 1
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Guidance for the utility of linear models in meta-analysis of genetic association studies of binary phenotypes
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A second generation human haplotype map of over 3.1 million SNPs
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Biological, clinical and population relevance of 95 loci for blood lipids
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New genetic loci link adipose and insulin biology to body fat distribution
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Genetic studies of body mass index yield new insights for obesity biology
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A global reference for human genetic variation
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The genetic architecture of type 2 diabetes
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Analysis of protein-coding genetic variation in 60,706 humans
inferredcites →https://doi.org/10.1038/ncomms11764openalex-snapshot
The genetic regulatory signature of type 2 diabetes in human skeletal muscle
inferredcites →https://doi.org/10.1038/ng.1019openalex-snapshot
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
inferredcites →https://doi.org/10.1038/ng.2213openalex-snapshot
Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits
inferredcites →https://doi.org/10.1038/ng.2383openalex-snapshot
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
inferredcites →https://doi.org/10.1038/ng.2435openalex-snapshot
Bayesian refinement of association signals for 14 loci in 3 common diseases
inferredcites →https://doi.org/10.1038/ng.2870openalex-snapshot
Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variants
inferredcites →https://doi.org/10.1038/ng.3190openalex-snapshot
Efficient Bayesian mixed-model analysis increases association power in large cohorts
inferredcites →https://doi.org/10.1038/ng.3406openalex-snapshot
An atlas of genetic correlations across human diseases and traits
inferredcites →https://doi.org/10.1038/ng.3437openalex-snapshot
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
inferredcites →https://doi.org/10.1038/ng.3643openalex-snapshot
A reference panel of 64,976 haplotypes for genotype imputation
inferredcites →https://doi.org/10.1038/ng.3714openalex-snapshot
Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance
inferredcites →https://doi.org/10.1038/ng.3943openalex-snapshot
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
inferredcites →https://doi.org/10.1038/ng.530openalex-snapshot
A map of open chromatin in human pancreatic islets
inferredcites →https://doi.org/10.1038/ng.548openalex-snapshot
Variance component model to account for sample structure in genome-wide association studies
inferredcites →https://doi.org/10.1038/ng.609openalex-snapshot
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
inferredcites →https://doi.org/10.1038/ng.921openalex-snapshot
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
inferredcites →https://doi.org/10.1038/nm1187openalex-snapshot
Deletion of Cdkn1b ameliorates hyperglycemia by maintaining compensatory hyperinsulinemia in diabetic mice
inferredcites →https://doi.org/10.1038/nrg.2016.56openalex-snapshot
Type 2 diabetes: genetic data sharing to advance complex disease research
inferredcites →https://doi.org/10.1038/s41588-018-0084-1openalex-snapshot
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
inferredcites →https://doi.org/10.1038/s41588-018-0088-xopenalex-snapshot
Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition
inferredcites →https://doi.org/10.1038/s41588-018-0180-2openalex-snapshot
Author Correction: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition
inferredcites →https://doi.org/10.1038/sdata.2017.115openalex-snapshot
Whole genome characterization of sequence diversity of 15,220 Icelanders
inferredcites →https://doi.org/10.1056/nejmoa032922openalex-snapshot
Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes
inferredcites →https://doi.org/10.1056/nejmoa055068openalex-snapshot
Activating Mutations in theABCC8Gene in Neonatal Diabetes Mellitus
inferredcites →https://doi.org/10.1056/nejmoa0804742openalex-snapshot
Genotype Score in Addition to Common Risk Factors for Prediction of Type 2 Diabetes
inferredcites →https://doi.org/10.1073/pnas.1621192114openalex-snapshot
Genetic regulatory signatures underlying islet gene expression and type 2 diabetes
inferredcites →https://doi.org/10.1073/pnas.97.4.1607openalex-snapshot
neurogenin3 is required for the development of the four endocrine cell lineages of the pancreas
inferredcites →https://doi.org/10.1074/jbc.m116.747667openalex-snapshot
The Inhibitory Role of α2,6-Sialylation in Adipogenesis
inferredcites →https://doi.org/10.1086/519024openalex-snapshot
A Bayesian Measure of the Probability of False Discovery in Genetic Epidemiology Studies
inferredcites →https://doi.org/10.1093/bioinformatics/btq126openalex-snapshot
PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associations
inferredcites →https://doi.org/10.1093/bioinformatics/btq340openalex-snapshot
METAL: fast and efficient meta-analysis of genomewide association scans
inferredcites →https://doi.org/10.1093/bioinformatics/btu848openalex-snapshot
PRSice: Polygenic Risk Score software
inferredcites →https://doi.org/10.1093/bioinformatics/btw613openalex-snapshot
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis
inferredcites →https://doi.org/10.1093/hmg/5.11.1809openalex-snapshot
Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy
inferredcites →https://doi.org/10.1111/j.0006-341x.1999.00997.xopenalex-snapshot
Genomic Control for Association Studies
inferredcites →https://doi.org/10.1126/science.1262110openalex-snapshot
The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
inferredcites →https://doi.org/10.1126/science.7716547openalex-snapshot
Cloning of the β Cell High-Affinity Sulfonylurea Receptor: a Regulator of Insulin Secretion
inferredcites →https://doi.org/10.1210/edrv.20.2.0361openalex-snapshot
Molecular Biology of Adenosine Triphosphate-Sensitive Potassium Channels
inferredcites →https://doi.org/10.1371/journal.pgen.1004235openalex-snapshot
A Central Role for GRB10 in Regulation of Islet Function in Man
inferredcites →https://doi.org/10.1371/journal.pgen.1004633openalex-snapshot
Identification of a Regulatory Variant That Binds FOXA1 and FOXA2 at the CDC123/CAMK1D Type 2 Diabetes GWAS Locus
inferredcites →https://doi.org/10.1371/journal.pgen.1005694openalex-snapshot
Transcript Expression Data from Human Islets Links Regulatory Signals from Genome-Wide Association Studies for Type 2 Diabetes and Glycemic Traits to Their Downstream Effectors
inferredcites →https://doi.org/10.1371/journal.pgen.1006711openalex-snapshot
Phenome-wide heritability analysis of the UK Biobank
inferredcites →https://doi.org/10.1371/journal.pmed.0030374openalex-snapshot
Combining Information from Common Type 2 Diabetes Risk Polymorphisms Improves Disease Prediction
inferredcites →https://doi.org/10.1371/journal.pone.0000841openalex-snapshot
Heterogeneity in Meta-Analyses of Genome-Wide Association Investigations
inferredcites →https://doi.org/10.2337/db10-1008openalex-snapshot
Permanent Neonatal Diabetes and Enteric Anendocrinosis Associated With Biallelic Mutations in NEUROG3
inferredcites →https://doi.org/10.2337/db13-0949openalex-snapshot
Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity
inferredcites →https://doi.org/10.2337/db16-1253openalex-snapshot
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
inferredcites →https://doi.org/10.2337/db16-1452openalex-snapshot
A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants
inferredcites →https://doi.org/10.2337/diabetes.49.12.2201openalex-snapshot
Parental transmission of type 2 diabetes: the Framingham Offspring Study.
inferredcites →https://doi.org/10.3389/fgene.2015.00331openalex-snapshot
Mapping Mammalian Cell-type-specific Transcriptional Regulatory Networks Using KD-CAGE and ChIP-seq Data in the TC-YIK Cell Line
inferredcites →https://doi.org/10.7554/elife.31977openalex-snapshot
Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Sequencing and imputation in GWAS: Cost‐effective strategies to increase power and genomic coverage across diverse populations
inferred← citeshttps://doi.org/10.1002/gepi.22327openalex-snapshot
Validating the doubly weighted genetic risk score for the prediction of type 2 diabetes in the Lifelines and Estonian Biobank cohorts
inferred← citeshttps://doi.org/10.1007/s00125-018-4659-2openalex-snapshot
Identification of novel high-impact recessively inherited type 2 diabetes risk variants in the Greenlandic population
inferred← citeshttps://doi.org/10.1007/s00125-019-4823-3openalex-snapshot
Genomic annotation of disease-associated variants reveals shared functional contexts
inferred← citeshttps://doi.org/10.1007/s00125-020-05350-xopenalex-snapshot
Sexually dimorphic roles for the type 2 diabetes-associated C2cd4b gene in murine glucose homeostasis
inferred← citeshttps://doi.org/10.1007/s11892-018-1009-1openalex-snapshot
Prioritising Risk Factors for Type 2 Diabetes: Causal Inference through Genetic Approaches
inferred← citeshttps://doi.org/10.1007/s11892-018-1021-5openalex-snapshot
Shared Genetic Contribution of Type 2 Diabetes and Cardiovascular Disease: Implications for Prognosis and Treatment
inferred← citeshttps://doi.org/10.1007/s11892-018-1085-2openalex-snapshot
The Impact of Pancreatic Beta Cell Heterogeneity on Type 1 Diabetes Pathogenesis
inferred← citeshttps://doi.org/10.1016/j.cell.2018.05.051openalex-snapshot
Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model
inferred← citeshttps://doi.org/10.1016/j.coph.2018.08.002openalex-snapshot
Inflammatory stress in islet β-cells: therapeutic implications for type 2 diabetes?
inferred← citeshttps://doi.org/10.1016/j.gde.2018.02.005openalex-snapshot
Pharmacogenetics and target identification in diabetes
inferred← citeshttps://doi.org/10.1016/j.gde.2018.02.010openalex-snapshot
Genetic architecture of obesity and related metabolic traits — recent insights from isolated populations
inferred← citeshttps://doi.org/10.1016/s0140-6736(18)31132-2openalex-snapshot
Genomic insights into the causes of type 2 diabetes
inferred← citeshttps://doi.org/10.1038/s41467-019-08492-8openalex-snapshot
Genome-wide gene-based analyses of weight loss interventions identify a potential role for NKX6.3 in metabolism
inferred← citeshttps://doi.org/10.1038/s41467-021-25614-3openalex-snapshot
A functional genomics pipeline identifies pleiotropy and cross-tissue effects within obesity-associated GWAS loci
inferred← citeshttps://doi.org/10.1038/s41467-022-29551-7openalex-snapshot
Multidimensional chromatin profiling of zebrafish pancreas to uncover and investigate disease-relevant enhancers
inferred← citeshttps://doi.org/10.1038/s41588-018-0113-0openalex-snapshot
Sizing up whole-genome sequencing studies of common diseases
inferred← citeshttps://doi.org/10.1038/s41588-019-0457-0openalex-snapshot
Human pancreatic islet three-dimensional chromatin architecture provides insights into the genetics of type 2 diabetes
inferred← citeshttps://doi.org/10.1038/s41588-022-01261-2openalex-snapshot
A genome-wide CRISPR screen identifies CALCOCO2 as a regulator of beta cell function influencing type 2 diabetes risk
inferred← citeshttps://doi.org/10.1038/s41590-018-0129-8openalex-snapshot
Approaches and advances in the genetic causes of autoimmune disease and their implications
inferred← citeshttps://doi.org/10.1038/s41598-018-34743-7openalex-snapshot
Electrophysiological properties of human beta-cell lines EndoC-βH1 and -βH2 conform with human beta-cells
inferred← citeshttps://doi.org/10.1038/s41598-020-69363-7openalex-snapshot
PPARG (Pro12Ala) genetic variant and risk of T2DM: a systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1101/2020.02.12.939348openalex-snapshot
Functional characterization of thousands of type 2 diabetes-associated and chromatin-modulating variants under steady state and endoplasmic reticulum stress
inferred← citeshttps://doi.org/10.1101/308296openalex-snapshot
BGEN: a binary file format for imputed genotype and haplotype data
inferred← citeshttps://doi.org/10.1101/371450openalex-snapshot
Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries
inferred← citeshttps://doi.org/10.1101/399139openalex-snapshot
EndoC-βH1 multi-genomic profiling defines gene regulatory programs governing human pancreatic β cell identity and function
inferred← citeshttps://doi.org/10.1101/435743openalex-snapshot
Islet Gene View - a tool to facilitate islet research
inferred← citeshttps://doi.org/10.1101/445874openalex-snapshot
Comparative genetic architectures of schizophrenia in East Asian and European populations
inferred← citeshttps://doi.org/10.1146/annurev-genom-083117-021602openalex-snapshot
Genotype Imputation from Large Reference Panels
inferred← citeshttps://doi.org/10.1161/circgen.118.002090openalex-snapshot
Human Genetics of Obesity and Type 2 Diabetes Mellitus
inferred← citeshttps://doi.org/10.1371/journal.pmed.1002654openalex-snapshot
Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: A soft clustering analysis
inferred← citeshttps://doi.org/10.18388/pb.2018_126openalex-snapshot
Epigenetyczna regulacja ekspresji genów â nowy mechanizm łączący otyłość z rozwojem cukrzycy typu 2
inferred← citeshttps://doi.org/10.2337/dbi17-0045openalex-snapshot
A Global Overview of Precision Medicine in Type 2 Diabetes
inferred← citeshttps://doi.org/10.33612/diss.230450750openalex-snapshot
Improving the personalized prediction of complex traits and diseases: application to type 2 diabetes
inferred← citeshttps://doi.org/10.3390/genes9080374openalex-snapshot
High-Throughput Approaches onto Uncover (Epi)Genomic Architecture of Type 2 Diabetes
inferred← citeshttps://doi.org/10.47672/ajhmn.1592openalex-snapshot
Biomarkers for Prediabetes, Type 2 Diabetes, and Associated Complications
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