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The genetic architecture of type 2 diabetes

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Association of a Low-Frequency Variant in HNF1A With Type 2 Diabetes in a Latino Population

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Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants

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Transethnic meta‐analysis of genomewide association studies

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Multiway Admixture Deconvolution Using Phased or Unphased Ancestral Panels

inferredcites →https://doi.org/10.1002/gepi.21742openalex-snapshot

Recommended Joint and Meta‐Analysis Strategies for Case‐Control Association Testing of Single Low‐Count Variants

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RREB1, a Ras Responsive Element Binding Protein, Maps to Human Chromosome 6p25

inferredcites →https://doi.org/10.1007/978-1-60327-367-1_19openalex-snapshot

Quality Control for Genome-Wide Association Studies

inferredcites →https://doi.org/10.1007/s00125-011-2182-9openalex-snapshot

Design and cohort description of the InterAct Project: an examination of the interaction of genetic and lifestyle factors on the incidence of type 2 diabetes in the EPIC Study

inferredcites →https://doi.org/10.1007/s00125-012-2756-1openalex-snapshot

Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes

inferredcites →https://doi.org/10.1007/s00125-013-2874-4openalex-snapshot

Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4

inferredcites →https://doi.org/10.1016/j.ajhg.2008.06.005openalex-snapshot

Long-Range LD Can Confound Genome Scans in Admixed Populations

inferredcites →https://doi.org/10.1016/j.ajhg.2010.11.011openalex-snapshot

GCTA: A Tool for Genome-wide Complex Trait Analysis

inferredcites →https://doi.org/10.1016/j.ajhg.2012.09.004openalex-snapshot

Detecting and Estimating Contamination of Human DNA Samples in Sequencing and Array-Based Genotype Data

inferredcites →https://doi.org/10.1016/j.ajhg.2013.05.010openalex-snapshot

General Framework for Meta-analysis of Rare Variants in Sequencing Association Studies

inferredcites →https://doi.org/10.1016/j.ajhg.2013.11.005openalex-snapshot

Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes

inferredcites →https://doi.org/10.1016/j.ajhg.2014.03.004openalex-snapshot

Joint Analysis of Functional Genomic Data and Genome-wide Association Studies of 18 Human Traits

inferredcites →https://doi.org/10.1016/j.cell.2010.03.032openalex-snapshot

Genetic Heterogeneity in Human Disease

inferredcites →https://doi.org/10.1016/j.cell.2010.09.006openalex-snapshot

Comparative Epigenomic Analysis of Murine and Human Adipogenesis

inferredcites →https://doi.org/10.1016/j.cell.2013.10.058openalex-snapshot

Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms

inferredcites →https://doi.org/10.1016/j.jdiacomp.2012.03.025openalex-snapshot

Defective PAX4 R192H transcriptional repressor activities associated with maturity onset diabetes of the young and early onset-age of type 2 diabetes

inferredcites →https://doi.org/10.1017/thg.2015.83openalex-snapshot

The Concordance and Heritability of Type 2 Diabetes in 34,166 Twin Pairs From International Twin Registers: The Discordant Twin (DISCOTWIN) Consortium

inferredcites →https://doi.org/10.1038/embor.2012.183openalex-snapshot

Production of phosphatidylinositol 5‐phosphate via PIKfyve and MTMR3 regulates cell migration

inferredcites →https://doi.org/10.1038/nature05911openalex-snapshot

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

inferredcites →https://doi.org/10.1038/nature08494openalex-snapshot

Finding the missing heritability of complex diseases

inferredcites →https://doi.org/10.1038/nature11247openalex-snapshot

An integrated encyclopedia of DNA elements in the human genome

inferredcites →https://doi.org/10.1038/nature11632openalex-snapshot

An integrated map of genetic variation from 1,092 human genomes

inferredcites →https://doi.org/10.1038/nature12828openalex-snapshot

Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico

inferredcites →https://doi.org/10.1038/nature12975openalex-snapshot

A polygenic burden of rare disruptive mutations in schizophrenia

inferredcites →https://doi.org/10.1038/nature13425openalex-snapshot

A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes

inferredcites →https://doi.org/10.1038/nbt.1662openalex-snapshot

Discovery and characterization of chromatin states for systematic annotation of the human genome

inferredcites →https://doi.org/10.1038/nbt1295openalex-snapshot

A human phenome-interactome network of protein complexes implicated in genetic disorders

inferredcites →https://doi.org/10.1038/ncpendmet0778openalex-snapshot

Clinical implications of a molecular genetic classification of monogenic β-cell diabetes

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.1053openalex-snapshot

Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes

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.237openalex-snapshot

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

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.2507openalex-snapshot

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

inferredcites →https://doi.org/10.1038/ng.2804openalex-snapshot

Evaluating empirical bounds on complex disease genetic architecture

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.2882openalex-snapshot

Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes

inferredcites →https://doi.org/10.1038/ng.2897openalex-snapshot

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

inferredcites →https://doi.org/10.1038/ng.2901openalex-snapshot

Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease

inferredcites →https://doi.org/10.1038/ng.2915openalex-snapshot

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

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.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.608openalex-snapshot

Common SNPs explain a large proportion of the heritability for human height

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.768openalex-snapshot

Discovery and genotyping of genome structural polymorphism by sequencing on a population scale

inferredcites →https://doi.org/10.1038/ng.806openalex-snapshot

A framework for variation discovery and genotyping using next-generation DNA sequencing data

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/ng1847openalex-snapshot

Principal components analysis corrects for stratification in genome-wide association studies

inferredcites →https://doi.org/10.1038/ng2088openalex-snapshot

A new multipoint method for genome-wide association studies by imputation of genotypes

inferredcites →https://doi.org/10.1038/nmeth.1938openalex-snapshot

Detecting overlapping protein complexes in protein-protein interaction networks

inferredcites →https://doi.org/10.1038/nrg3002openalex-snapshot

New approaches to disease mapping in admixed populations

inferredcites →https://doi.org/10.1056/nejmoa0801869openalex-snapshot

Clinical Risk Factors, DNA Variants, and the Development of Type 2 Diabetes

inferredcites →https://doi.org/10.1073/pnas.0506580102openalex-snapshot

Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles

inferredcites →https://doi.org/10.1073/pnas.0903103106openalex-snapshot

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

inferredcites →https://doi.org/10.1073/pnas.0906182107openalex-snapshot

Genetic architecture of a complex trait and its implications for fitness and genome-wide association studies

inferredcites →https://doi.org/10.1073/pnas.1317023110openalex-snapshot

Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants

inferredcites →https://doi.org/10.1073/pnas.1323785111openalex-snapshot

TM6SF2 is a regulator of liver fat metabolism influencing triglyceride secretion and hepatic lipid droplet content

inferredcites →https://doi.org/10.1073/pnas.1410428111openalex-snapshot

Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes

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/10.1086/521987openalex-snapshot

Rapid and Accurate Haplotype Phasing and Missing-Data Inference for Whole-Genome Association Studies By Use of Localized Haplotype Clustering

inferredcites →https://doi.org/10.1093/bioinformatics/btn317openalex-snapshot

ForSim: a tool for exploring the genetic architecture of complex traits with controlled truth

inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot

Fast and accurate short read alignment with Burrows–Wheeler transform

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/btq615openalex-snapshot

dmGWAS: dense module searching for genome-wide association studies in protein–protein interaction networks

inferredcites →https://doi.org/10.1093/bioinformatics/btu704openalex-snapshot

minimac2: faster genotype imputation

inferredcites →https://doi.org/10.1093/biomet/80.1.27openalex-snapshot

Bias reduction of maximum likelihood estimates

inferredcites →https://doi.org/10.1093/biostatistics/kxs014openalex-snapshot

Optimal tests for rare variant effects in sequencing association studies

inferredcites →https://doi.org/10.1101/gad.269003openalex-snapshot

Opposing actions of Arx and Pax4 in endocrine pancreas development

inferredcites →https://doi.org/10.1101/gr.107524.110openalex-snapshot

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

inferredcites →https://doi.org/10.1101/gr.117259.110openalex-snapshot

Low-coverage sequencing: Implications for design of complex trait association studies

inferredcites →https://doi.org/10.1101/gr.135350.111openalex-snapshot

GENCODE: The reference human genome annotation for The ENCODE Project

inferredcites →https://doi.org/10.1111/j.0006-341x.1999.00997.xopenalex-snapshot

Genomic Control for Association Studies

inferredcites →https://doi.org/10.1111/j.1469-1809.1965.tb00500.xopenalex-snapshot

The inheritance of liability to certain diseases, estimated from the incidence among relatives

inferredcites →https://doi.org/10.1126/science.1222794openalex-snapshot

Systematic Localization of Common Disease-Associated Variation in Regulatory DNA

inferredcites →https://doi.org/10.1126/science.1246981openalex-snapshot

Genetic Screens in Human Cells Using the CRISPR-Cas9 System

inferredcites →https://doi.org/10.1371/journal.pbio.1000294openalex-snapshot

Rare Variants Create Synthetic Genome-Wide Associations

inferredcites →https://doi.org/10.1371/journal.pbio.1000579openalex-snapshot

Synthetic Associations Created by Rare Variants Do Not Explain Most GWAS Results

inferredcites →https://doi.org/10.1371/journal.pbio.1000580openalex-snapshot

Synthetic Associations Are Unlikely to Account for Many Common Disease Genome-Wide Association Signals

inferredcites →https://doi.org/10.1371/journal.pbio.1001008openalex-snapshot

The Importance of Synthetic Associations Will Only Be Resolved Empirically

inferredcites →https://doi.org/10.1371/journal.pgen.1000519openalex-snapshot

Sensitive Detection of Chromosomal Segments of Distinct Ancestry in Admixed Populations

inferredcites →https://doi.org/10.1371/journal.pgen.1001363openalex-snapshot

Transferability of Type 2 Diabetes Implicated Loci in Multi-Ethnic Cohorts from Southeast Asia

inferredcites →https://doi.org/10.2307/2531435openalex-snapshot

A Consensus Combined P-Value Test and the Family-Wide Significance of Component Tests

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Serum podocalyxin levels in patients with obesity and carbohydrates disorders

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From omics to AI —mapping the pathogenic pathways in type 2 diabetes

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Chromosome 10

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Immunogenetics

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Genetically Altered Mice as an Approach for the Investigation of Obesity and Metabolic Disease

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Other Disorders with Type 1 Diabetes and Atypical Phenotypes

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The Application of High‐Throughput Approaches in Identifying Novel Therapeutic Targets and Agents to Treat Diabetes

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Genetics’ Piece of the PI: Inferring the Origin of Complex Traits and Diseases from Proteome‐Wide Protein–Protein Interaction Dynamics

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Reagent Validation to Facilitate Experimental Reproducibility

inferred← citeshttps://doi.org/10.1002/cpt.1484openalex-snapshot

Diabetes: Is There a Future for Pharmacogenomics Guided Treatment?

inferred← citeshttps://doi.org/10.1002/cti2.1001openalex-snapshot

Genome‐wide association studies in Crohn's disease: Past, present and future

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Milk in the prevention and management of type 2 diabetes: The potential role of milk proteins

inferred← citeshttps://doi.org/10.1002/dmrr.3482openalex-snapshot

Analysis of rare coding variants in 200,000 exome‐sequenced subjects reveals novel genetic risk factors for type 2 diabetes

inferred← citeshttps://doi.org/10.1002/dmrr.3486openalex-snapshot

Screening for monogenic subtypes of gestational diabetes in a high prevalence island population – A whole exome sequencing study

inferred← citeshttps://doi.org/10.1002/edm2.179openalex-snapshot

Human and molecular genetics shed lights on fatty liver disease and diabetes conundrum

inferred← citeshttps://doi.org/10.1002/gepi.22057openalex-snapshot

Improving power for rare‐variant tests by integrating external controls

inferred← citeshttps://doi.org/10.1002/gepi.22105openalex-snapshot

Methods for meta‐analysis of multiple traits using GWAS summary statistics

inferred← citeshttps://doi.org/10.1002/gepi.22107openalex-snapshot

Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations

inferred← citeshttps://doi.org/10.1002/gepi.22123openalex-snapshot

Improved score statistics for meta‐analysis in single‐variant and gene‐level association studies

inferred← citeshttps://doi.org/10.1002/gepi.22208openalex-snapshot

Exome chip‐driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups

inferred← citeshttps://doi.org/10.1002/gepi.22261openalex-snapshot

Combining sequence data from multiple studies: Impact of analysis strategies on rare variant calling and association results

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Population genetic simulation study of power in association testing across genetic architectures and study designs

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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/hep.30403openalex-snapshot

Gallstone Disease and Type 2 Diabetes Risk: A Mendelian Randomization Study

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Body Composition and Genetic Lipodystrophy Risk Score Associate With Nonalcoholic Fatty Liver Disease and Liver Fibrosis

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Association of SIRT1 rs3758391 Polymorphism With T2DM in Bangladeshi Population: Evidence From a Case‐Control Study and Meta‐Analysis

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Polygenic Risk Score of Adolescent Idiopathic Scoliosis for Potential Clinical Use

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Rare and Common Variants in GALNT3 May Affect Bone Mass Independently of Phosphate Metabolism

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The broad pathogenetic role of TCF7L2 in human diseases beyond type 2 diabetes

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Prepregnancy Obesity Reprograms Offspring Skeletal Muscle Fibre Transition Through H3K9me3

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Functional evaluation of 16 SCHAD missense variants: Only amino acid substitutions causing congenital hyperinsulinism of infancy lead to loss‐of‐function phenotypes in vitro

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Genetic polymorphisms of diabetes‐related genes, their interaction with diabetes status, and breast cancer incidence and mortality: The Long Island Breast Cancer Study Project

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Pancreatic Islet Cell Hormones: Secretion, Function, and Diabetes Therapy

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inferred← citeshttps://doi.org/10.1002/mnfr.70346openalex-snapshot

Dual Dietary Assault: Unraveling the Synergistic Impact of High‐Fat and High‐Sucrose Intake on Type 2 Diabetes Pathogenesis

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Construction of a Plasmonic Chip for Metabolic Analysis in Cervical Cancer Screening and Evaluation

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Beta-Cell Dedifferentiation in Type 2 Diabetes: Concise Review

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Dietary SCFAs Immunotherapy: Reshaping the Gut Microbiota in Diabetes

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inferred← citeshttps://doi.org/10.1007/978-1-4939-7471-9_1openalex-snapshot

Identification of Disease Susceptibility Alleles in the Next Generation Sequencing Era

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Physiologic Interpretation of GWAS Signals for Type 2 Diabetes

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Methods and Tools in Genome-wide Association Studies

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Whole-Exome Sequencing (WES) for Illumina Short Read Sequencers Using Solution-Based Capture

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Systemic Lupus Erythematosus

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Age-Linked Non-Transmissible Diseases

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The Role of Artificial Intelligence in Diabetes Care

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Genetics of Diabetes and Diabetic Complications

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Pathogenesis of Type 2 Diabetes Mellitus

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Histone Deacetylase HDAC8 and Insulin Resistance

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Genetics of Diabetes and Diabetic Complications

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Pathogenesis of Type 2 Diabetes Mellitus

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Insulin Resistance and Mitochondrial Dysfunction

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Histone Deacetylase HDAC8 and Insulin Resistance

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Genetics of Small Vessel Disease

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Genetic Determinants and Pharmacogenetics of Osteoporosis and Osteoporotic Fracture

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Current Understanding of Genetic Factors in Idiopathic Scoliosis

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A Systems Perspective of Complex Diseases: From Reductionism to Integration

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Kidney Transplantation and Diabetic Nephropathy

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Genetik menschlicher Erkrankungen

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Genetik menschlicher Erkrankungen

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Diabetes mellitus

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Diabetes mellitus – Begutachtung

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Genetik menschlicher Erkrankungen

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Genome-Wide Association Study for Type 2 Diabetes

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The Future of and Beyond GWAS

inferred← citeshttps://doi.org/10.1007/978-981-19-4590-8_10openalex-snapshot

Nutrigenomics: Insights and Implications for Genome-Based Nutrition

inferred← citeshttps://doi.org/10.1007/978-981-97-4186-1_24openalex-snapshot

Linear Relationship Between Constructs of Physical Activity and Leisure Motivation Scale and Amount of Physical Activity Among Type 2 Diabetes Mellitus Patients: A Regression Analysis

inferred← citeshttps://doi.org/10.1007/s00018-020-03710-9openalex-snapshot

Modeling different types of diabetes using human pluripotent stem cells

inferred← citeshttps://doi.org/10.1007/s00018-021-03868-wopenalex-snapshot

Genome-wide association studies: assessing trait characteristics in model and crop plants

inferred← citeshttps://doi.org/10.1007/s00125-016-4103-4openalex-snapshot

An alternative effector gene at the type 2 diabetes-associated TCF7L2 locus?

inferred← citeshttps://doi.org/10.1007/s00125-016-4132-zopenalex-snapshot

Exome-chip association analysis reveals an Asian-specific missense variant in PAX4 associated with type 2 diabetes in Chinese individuals

inferred← citeshttps://doi.org/10.1007/s00125-017-4210-xopenalex-snapshot

Painting a new picture of personalised medicine for diabetes

inferred← citeshttps://doi.org/10.1007/s00125-017-4213-7openalex-snapshot

Towards a systematic nationwide screening strategy for MODY

inferred← citeshttps://doi.org/10.1007/s00125-017-4226-2openalex-snapshot

Precision diabetes: learning from monogenic diabetes

inferred← citeshttps://doi.org/10.1007/s00125-017-4255-xopenalex-snapshot

The case for too little melatonin signalling in increased diabetes risk

inferred← citeshttps://doi.org/10.1007/s00125-017-4270-yopenalex-snapshot

Human genetics as a model for target validation: finding new therapies for diabetes

inferred← citeshttps://doi.org/10.1007/s00125-017-4500-3openalex-snapshot

Systems biology of the IMIDIA biobank from organ donors and pancreatectomised patients defines a novel transcriptomic signature of islets from individuals with type 2 diabetes

inferred← citeshttps://doi.org/10.1007/s00125-018-4557-7openalex-snapshot

Epidemiology of diabetes and diabetic complications in China

inferred← citeshttps://doi.org/10.1007/s00125-018-4599-xopenalex-snapshot

Metabolomics insights into early type 2 diabetes pathogenesis and detection in individuals with normal fasting glucose

inferred← citeshttps://doi.org/10.1007/s00125-018-4612-4openalex-snapshot

Patterns of differential gene expression in a cellular model of human islet development, and relationship to type 2 diabetes predisposition

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/s00125-018-4690-3openalex-snapshot

Identification of a missense variant in the WFS1 gene that causes a mild form of Wolfram syndrome and is associated with risk for type 2 diabetes in Ashkenazi Jewish individuals

inferred← citeshttps://doi.org/10.1007/s00125-019-05060-zopenalex-snapshot

PAM haploinsufficiency does not accelerate the development of diet- and human IAPP-induced diabetes in mice

inferred← citeshttps://doi.org/10.1007/s00125-019-4909-yopenalex-snapshot

Type 2 diabetes: a multifaceted disease

inferred← citeshttps://doi.org/10.1007/s00125-020-05101-yopenalex-snapshot

Neurocognitive impairment in type 2 diabetes: evidence for shared genetic aetiology

inferred← citeshttps://doi.org/10.1007/s00125-020-05186-5openalex-snapshot

Beta cell dysfunction in diabetes: the islet microenvironment as an unusual suspect

inferred← citeshttps://doi.org/10.1007/s00125-021-05449-9openalex-snapshot

Multi-omics analysis identifies CpGs near G6PC2 mediating the effects of genetic variants on fasting glucose

inferred← citeshttps://doi.org/10.1007/s00125-021-05575-4openalex-snapshot

The importance of increasing population diversity in genetic studies of type 2 diabetes and related glycaemic traits

inferred← citeshttps://doi.org/10.1007/s00125-021-05618-wopenalex-snapshot

Environmental risk factors of type 2 diabetes—an exposome approach

inferred← citeshttps://doi.org/10.1007/s00125-022-05704-7openalex-snapshot

Health impact of seven herpesviruses on (pre)diabetes incidence and HbA1c: results from the KORA cohort

inferred← citeshttps://doi.org/10.1007/s00125-022-05720-7openalex-snapshot

Achievements, prospects and challenges in precision care for monogenic insulin-deficient and insulin-resistant diabetes

inferred← citeshttps://doi.org/10.1007/s00125-022-05806-2openalex-snapshot

The contribution of functional HNF1A variants and polygenic susceptibility to risk of type 2 diabetes in ancestrally diverse populations

inferred← citeshttps://doi.org/10.1007/s00125-022-05856-6openalex-snapshot

Loss of RREB1 in pancreatic beta cells reduces cellular insulin content and affects endocrine cell gene expression

inferred← citeshttps://doi.org/10.1007/s00125-023-05914-7openalex-snapshot

Investigating causality in the association between DNA methylation and type 2 diabetes using bidirectional two-sample Mendelian randomisation

inferred← citeshttps://doi.org/10.1007/s00125-023-05955-yopenalex-snapshot

Utility of genetic risk scores in type 1 diabetes

inferred← citeshttps://doi.org/10.1007/s00125-024-06163-yopenalex-snapshot

RFX6 haploinsufficiency predisposes to diabetes through impaired beta cell function

inferred← citeshttps://doi.org/10.1007/s00192-021-04917-5openalex-snapshot

The polymorphisms of extracellular matrix-remodeling genes are associated with pelvic organ prolapse

inferred← citeshttps://doi.org/10.1007/s00335-020-09839-zopenalex-snapshot

Nutrition and its role in epigenetic inheritance of obesity and diabetes across generations

inferred← citeshttps://doi.org/10.1007/s00335-021-09869-1openalex-snapshot

Alternative exon splicing and differential expression in pancreatic islets reveals candidate genes and pathways implicated in early diabetes development

inferred← citeshttps://doi.org/10.1007/s00394-024-03444-5openalex-snapshot

Healthy dietary pattern is associated with lower glycemia independently of the genetic risk of type 2 diabetes: a cross-sectional study in Finnish men

inferred← citeshttps://doi.org/10.1007/s00394-025-03791-xopenalex-snapshot

Changes in food choices and dietary patterns during the lifestyle intervention and their association with type 2 diabetes risk in participants with high or low genetic risk for type 2 diabetes

inferred← citeshttps://doi.org/10.1007/s00439-018-1894-zopenalex-snapshot

Genotype imputation for Han Chinese population using Haplotype Reference Consortium as reference

inferred← citeshttps://doi.org/10.1007/s00439-019-02034-4openalex-snapshot

Missing heritability of complex diseases: case solved?

inferred← citeshttps://doi.org/10.1007/s00592-024-02385-zopenalex-snapshot

Ultra-processed foods and type 2 diabetes mellitus incidence in RaNCD project: a prospective cohort study

inferred← citeshttps://doi.org/10.1007/s00592-025-02544-wopenalex-snapshot

Polygenic score from MODY genes is associated with type 1 diabetes and disease characteristics

inferred← citeshttps://doi.org/10.1007/s10142-022-00840-0openalex-snapshot

PAM variants were associated with type 2 diabetes mellitus risk in the Chinese population

inferred← citeshttps://doi.org/10.1007/s10528-017-9827-4openalex-snapshot

Genetic Approaches to the Study of Gene Variants and Their Impact on the Pathophysiology of Type 2 Diabetes

inferred← citeshttps://doi.org/10.1007/s10545-017-0091-xopenalex-snapshot

Metabolic pathways at the crossroads of diabetes and inborn errors

inferred← citeshttps://doi.org/10.1007/s11010-021-04114-4openalex-snapshot

Loss of Znt8 function in diabetes mellitus: risk or benefit?

inferred← citeshttps://doi.org/10.1007/s11033-020-05647-5openalex-snapshot

Genetic variants in glutamate cysteine ligase confer protection against type 2 diabetes

inferred← citeshttps://doi.org/10.1007/s11154-019-09505-zopenalex-snapshot

Genetics, adaptation to environmental changes and archaic admixture in the pathogenesis of diabetes mellitus in Indigenous Australians

inferred← citeshttps://doi.org/10.1007/s11428-019-0474-8openalex-snapshot

Genetik des Typ-2-Diabetes

inferred← citeshttps://doi.org/10.1007/s11428-020-00665-0openalex-snapshot

Diabetesclusters: Diabetessubgruppen und Folgeerkrankungen

inferred← citeshttps://doi.org/10.1007/s11428-022-00993-3openalex-snapshot

Pharmakogenetik neuer Glukosespiegelsenker: eine Chance für die Präzisionsmedizin?

inferred← citeshttps://doi.org/10.1007/s11886-017-0938-7openalex-snapshot

The Genetics of Physical Activity

inferred← citeshttps://doi.org/10.1007/s11892-017-0845-8openalex-snapshot

Arsenic Exposure and Type 2 Diabetes: MicroRNAs as Mechanistic Links?

inferred← citeshttps://doi.org/10.1007/s11892-017-0852-9openalex-snapshot

How Can Genetic Studies Help Us to Understand Links Between Birth Weight and Type 2 Diabetes?

inferred← citeshttps://doi.org/10.1007/s11892-017-0907-yopenalex-snapshot

Prioritising Causal Genes at Type 2 Diabetes Risk Loci

inferred← citeshttps://doi.org/10.1007/s11892-017-0908-xopenalex-snapshot

Mechanisms of Type 2 Diabetes Risk Loci

inferred← citeshttps://doi.org/10.1007/s11892-017-0947-3openalex-snapshot

Gene Editing and Human Pluripotent Stem Cells: Tools for Advancing Diabetes Disease Modeling and Beta-Cell Development

inferred← citeshttps://doi.org/10.1007/s11892-017-0958-0openalex-snapshot

A Decade of Genetic and Metabolomic Contributions to Type 2 Diabetes Risk Prediction

inferred← citeshttps://doi.org/10.1007/s11892-018-1025-1openalex-snapshot

Advances in the Genetics of Youth-Onset Type 2 Diabetes

inferred← citeshttps://doi.org/10.1007/s11892-018-1091-4openalex-snapshot

Epigenetics Variation and Pathogenesis in Diabetes

inferred← citeshttps://doi.org/10.1007/s11892-018-1107-0openalex-snapshot

Genetics of Obesity in Diverse Populations

inferred← citeshttps://doi.org/10.1007/s11892-019-1137-2openalex-snapshot

The Continuing Evolution of Precision Health in Type 2 Diabetes: Achievements and Challenges

inferred← citeshttps://doi.org/10.1007/s11892-019-1142-5openalex-snapshot

The Contribution of Low-Frequency and Rare Coding Variation to Susceptibility to Type 2 Diabetes

inferred← citeshttps://doi.org/10.1007/s11892-019-1168-8openalex-snapshot

Epigenetics and Type 2 Diabetes Risk

inferred← citeshttps://doi.org/10.1007/s11892-019-1169-7openalex-snapshot

Type 2 Diabetes: Multiple Genes, Multiple Diseases

inferred← citeshttps://doi.org/10.1007/s11892-019-1173-yopenalex-snapshot

The Genetic Epidemiology of Type 2 Diabetes: Opportunities for Health Translation

inferred← citeshttps://doi.org/10.1007/s11892-019-1202-xopenalex-snapshot

How Recent Advances in Genomics Improve Precision Diagnosis and Personalized Care of Maturity-Onset Diabetes of the Young

inferred← citeshttps://doi.org/10.1007/s11892-019-1230-6openalex-snapshot

Pancreatic Islet Transcriptional Enhancers and Diabetes

inferred← citeshttps://doi.org/10.1007/s11892-019-1251-1openalex-snapshot

Dietary Fat and the Genetic Risk of Type 2 Diabetes

inferred← citeshttps://doi.org/10.1007/s11892-021-01388-2openalex-snapshot

Progress in Defining the Genetic Contribution to Type 2 Diabetes in Individuals of East Asian Ancestry

inferred← citeshttps://doi.org/10.1007/s11892-024-01533-7openalex-snapshot

Lessons and Applications of Omics Research in Diabetes Epidemiology

inferred← citeshttps://doi.org/10.1007/s12020-017-1388-0openalex-snapshot

Postpartum glucose intolerance: an updated overview

inferred← citeshttps://doi.org/10.1007/s12272-018-1039-xopenalex-snapshot

Drug-induced hyperglycaemia and diabetes: pharmacogenomics perspectives

inferred← citeshttps://doi.org/10.1007/s12291-025-01334-zopenalex-snapshot

Polygenic Risk Scores for Predicting Type 2 Diabetes Using Whole-Exome Sequencing and Global Screening Array

inferred← citeshttps://doi.org/10.1007/s12529-026-10465-3openalex-snapshot

Supplementing Disease Risk Information for Type 2 Diabetes and Coronary Heart Disease with Polygenic Risk Scores: Testing a Health Action Process Approach–Inspired Path Model to Predict Health Behavior

inferred← citeshttps://doi.org/10.1007/s12561-020-09298-9openalex-snapshot

Improved Semiparametric Analysis of Polygenic Gene–Environment Interactions in Case–Control Studies

inferred← citeshttps://doi.org/10.1007/s12687-025-00790-7openalex-snapshot

The impact of supplementing traditional risk information with polygenic risk score concerning type 2 diabetes and coronary heart disease on health behavior: a randomized controlled trial

inferred← citeshttps://doi.org/10.1007/s13258-021-01214-9openalex-snapshot

Transethnic meta-analysis of exome-wide variants identifies new loci associated with male-specific metabolic syndrome

inferred← citeshttps://doi.org/10.1007/s13340-017-0324-0openalex-snapshot

Towards precision medicine for type 2 diabetes

inferred← citeshttps://doi.org/10.1007/s13410-016-0540-3openalex-snapshot

Diabetes and data in many forms

inferred← citeshttps://doi.org/10.1007/s13410-025-01527-5openalex-snapshot

Advances in genome-wide association studies of type 2 diabetes across populations: A systematic review

inferred← citeshttps://doi.org/10.1007/s15006-020-0428-5openalex-snapshot

[Diabetes and pancreatic cancer - state of the art].

inferred← citeshttps://doi.org/10.1007/s40200-020-00704-zopenalex-snapshot

Vitamin D Receptor gene polymorphisms and susceptibility to type 2 diabetes: evidence from a meta-regression and meta-analysis based on 47 studies

inferred← citeshttps://doi.org/10.1007/s40200-021-00838-8openalex-snapshot

Knowledge discovery in genetics of diabetes in Iran, a roadmap for future researches

inferred← citeshttps://doi.org/10.1007/s40200-021-00863-7openalex-snapshot

Effect of dietary fat intake and genetic risk on glucose and insulin-related traits in Brazilian young adults

inferred← citeshttps://doi.org/10.1007/s40200-022-01001-7openalex-snapshot

Role of metabolizing MTHFR gene polymorphism (rs1801133) and its mRNA expression among Type 2 Diabetes

inferred← citeshttps://doi.org/10.1007/s40200-024-01437-zopenalex-snapshot

Unraveling the understudied influence of a lead variant in the 9p21 locus on the atherogenic index among type 2 diabetes patients with coronary artery disease

inferred← citeshttps://doi.org/10.1007/s40519-020-01015-1openalex-snapshot

The obesity paradox and diabetes

inferred← citeshttps://doi.org/10.1007/s43657-022-00078-7openalex-snapshot

A Meta-Analysis of the Genome-Wide Association Studies on Two Genetically Correlated Phenotypes Suggests Four New Risk Loci for Headaches

inferred← citeshttps://doi.org/10.1016/b978-0-12-802928-2.00029-1openalex-snapshot

Genetics and Diabetes

inferred← citeshttps://doi.org/10.1016/b978-0-12-804572-5.00059-8openalex-snapshot

Nutrients and Gene Expression in Type 2 Diabetes

inferred← citeshttps://doi.org/10.1016/b978-0-12-804725-5.00001-xopenalex-snapshot

Reproducibility in Biomedical Research

inferred← citeshttps://doi.org/10.1016/b978-0-12-812536-6.00015-8openalex-snapshot

Implementation of Genomic Medicine

inferred← citeshttps://doi.org/10.1016/b978-0-12-812626-4.00009-7openalex-snapshot

The Role of Pharmacogenomics in Diabetes

inferred← citeshttps://doi.org/10.1016/b978-0-12-814841-9.00068-3openalex-snapshot

Genetic determinants of bone mass and osteoporotic fracture

inferred← citeshttps://doi.org/10.1016/b978-0-12-815876-0.00025-5openalex-snapshot

Genetics and Chronic Kidney Disease

inferred← citeshttps://doi.org/10.1016/b978-0-12-817528-6.00014-0openalex-snapshot

Molecular genetic approaches to dissect complex behaviors in zebrafish

inferred← citeshttps://doi.org/10.1016/b978-0-12-819801-8.00014-4openalex-snapshot

Epigenetic and Developmental Basis of Risk of Obesity and Metabolic Disease

inferred← citeshttps://doi.org/10.1016/b978-0-12-822229-4.00012-7openalex-snapshot

Considerations in using human pluripotent stem cell–derived pancreatic beta cells to treat type 1 diabetes

inferred← citeshttps://doi.org/10.1016/b978-0-323-91001-9.00033-5openalex-snapshot

Human population genomics approach in food metabolism

inferred← citeshttps://doi.org/10.1016/b978-0-323-95502-7.00125-1openalex-snapshot

Community Detection in Biological Networks

inferred← citeshttps://doi.org/10.1016/b978-0-443-11985-9.00015-9openalex-snapshot

Genetics of Type 2 Diabetes

inferred← citeshttps://doi.org/10.1016/b978-0-443-11985-9.00017-2openalex-snapshot

Heterogeneity of Type 2 Diabetes Mellitus

inferred← citeshttps://doi.org/10.1016/b978-0-443-13195-0.00005-3openalex-snapshot

Biochemical pathways involved in diabetes mellitus

inferred← citeshttps://doi.org/10.1016/b978-0-443-13683-2.00032-3openalex-snapshot

Genome sequencing and Big Data analysis

inferred← citeshttps://doi.org/10.1016/b978-0-443-31698-2.00013-8openalex-snapshot

Mechanistic insights of important medicinal plant compounds in managing type 2 diabetes mellitus

inferred← citeshttps://doi.org/10.1016/b978-0-443-33590-7.00011-3openalex-snapshot

Genetics and immunity: Mapping pathways in type II diabetes (T2D)

inferred← citeshttps://doi.org/10.1016/b978-0-443-45811-8.00008-8openalex-snapshot

Future perspectives: personalized medicine and senescence modulation in cardiovascular health

inferred← citeshttps://doi.org/10.1016/b978-0-444-64076-5.00031-4openalex-snapshot

Genetics of migraine

inferred← citeshttps://doi.org/10.1016/bs.apcsb.2022.02.005openalex-snapshot

Mutations in G6PC2 gene with increased risk for development of type 2 diabetes: Understanding via computational approach

inferred← citeshttps://doi.org/10.1016/bs.pmbts.2016.12.012openalex-snapshot

Therapeutic Strategies for Mitochondrial Dysfunction and Oxidative Stress in Age-Related Metabolic Disorders

inferred← citeshttps://doi.org/10.1016/j.ailsci.2021.100003openalex-snapshot

Combinatorial analytics: An essential tool for the delivery of precision medicine and precision agriculture

inferred← citeshttps://doi.org/10.1016/j.ajhg.2017.01.011openalex-snapshot

Decreased STARD10 Expression Is Associated with Defective Insulin Secretion in Humans and Mice

inferred← citeshttps://doi.org/10.1016/j.ajhg.2017.04.007openalex-snapshot

High-Resolution Genetic Maps Identify Multiple Type 2 Diabetes Loci at Regulatory Hotspots in African Americans and Europeans

inferred← citeshttps://doi.org/10.1016/j.ajhg.2017.06.005openalex-snapshot

10 Years of GWAS Discovery: Biology, Function, and Translation

inferred← citeshttps://doi.org/10.1016/j.ajhg.2018.02.020openalex-snapshot

A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression

inferred← citeshttps://doi.org/10.1016/j.ajhg.2018.03.012openalex-snapshot

Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes

inferred← citeshttps://doi.org/10.1016/j.ajhg.2019.05.001openalex-snapshot

Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland

inferred← citeshttps://doi.org/10.1016/j.ajhg.2020.08.016openalex-snapshot

Unsupervised Clustering of Missense Variants in HNF1A Using Multidimensional Functional Data Aids Clinical Interpretation

inferred← citeshttps://doi.org/10.1016/j.ajhg.2021.02.001openalex-snapshot

Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease

inferred← citeshttps://doi.org/10.1016/j.ajhg.2025.07.002openalex-snapshot

Rare-variant association studies: When are aggregation tests more powerful than single-variant tests?

inferred← citeshttps://doi.org/10.1016/j.ajhg.2025.11.013openalex-snapshot

MIRAGE: A Bayesian statistical method for gene-level rare-variant analysis incorporating functional annotations

inferred← citeshttps://doi.org/10.1016/j.annepidem.2021.07.005openalex-snapshot

Does NAFLD mediate the relationship between obesity and type 2 diabetes risk? evidence from the multi-ethnic study of atherosclerosis (MESA)

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