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The genetic architecture of type 2 diabetes
scientific article (publication date: 11 July 2016)
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scholarly article
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title
The genetic architecture of type 2 diabetes
(English)
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main subject
type 2 diabetes
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genetics
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author
Oluf Borbye Pedersen
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Niels Grarup
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Tõnu Esko
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language of work or name
English
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publication date
11 July 2016
0 references
published in
Nature
0 references
volume
536
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page(s)
41-47
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issue
7614
0 references
cites work
TM6SF2 is a regulator of liver fat metabolism influencing triglyceride secretion and hepatic lipid droplet content
1 reference
stated in
PubMed Central
reference URL
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1 May 2017
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1 May 2017
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1 May 2017
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1 May 2017
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1 May 2017
GENCODE: the reference human genome annotation for The ENCODE Project
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1 May 2017
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1 May 2017
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1 May 2017
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
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1 May 2017
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
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1 May 2017
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
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1 May 2017
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
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1 May 2017
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1 May 2017
Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia
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1 May 2017
A framework for variation discovery and genotyping using next-generation DNA sequencing data
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1 May 2017
GCTA: a tool for genome-wide complex trait analysis
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1 May 2017
Discovery and characterization of chromatin states for systematic annotation of the human genome
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1 May 2017
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
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1 May 2017
METAL: fast and efficient meta-analysis of genomewide association scans
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1 May 2017
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
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1 May 2017
Common SNPs explain a large proportion of the heritability for human height
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1 May 2017
Genetic heterogeneity in human disease
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1 May 2017
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1 May 2017
Finding the missing heritability of complex diseases
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1 May 2017
Sensitive detection of chromosomal segments of distinct ancestry in admixed populations
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1 May 2017
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
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1 May 2017
Fast and accurate short read alignment with Burrows-Wheeler transform
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1 May 2017
Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering
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1 May 2017
A Bayesian measure of the probability of false discovery in genetic epidemiology studies
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1 May 2017
A new multipoint method for genome-wide association studies by imputation of genotypes
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1 May 2017
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
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1 May 2017
A human phenome-interactome network of protein complexes implicated in genetic disorders
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1 May 2017
Principal components analysis corrects for stratification in genome-wide association studies
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1 May 2017
Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles
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1 May 2017
Genomic control for association studies
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1 May 2017
The Concordance and Heritability of Type 2 Diabetes in 34,166 Twin Pairs From International Twin Registers: The Discordant Twin (DISCOTWIN) Consortium
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3 June 2018
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
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3 June 2018
minimac2: faster genotype imputation
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3 June 2018
Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes
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3 June 2018
A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes
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3 June 2018
Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population
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3 June 2018
Joint analysis of functional genomic data and genome-wide association studies of 18 human traits
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3 June 2018
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
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3 June 2018
Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease
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3 June 2018
A polygenic burden of rare disruptive mutations in schizophrenia
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3 June 2018
Leveraging cross-species transcription factor binding site patterns: from diabetes risk loci to disease mechanisms
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3 June 2018
Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variants
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3 June 2018
Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes
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3 June 2018
Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants
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3 June 2018
Recommended joint and meta-analysis strategies for case-control association testing of single low-count variants
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3 June 2018
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Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4.
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3 June 2018
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion
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3 June 2018
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes.
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3 June 2018
Production of phosphatidylinositol 5-phosphate via PIKfyve and MTMR3 regulates cell migration
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3 June 2018
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3 June 2018
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3 June 2018
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3 June 2018
Defective PAX4 R192H transcriptional repressor activities associated with maturity onset diabetes of the young and early onset-age of type 2 diabetes
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3 June 2018
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3 June 2018
Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits
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3 June 2018
Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes
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3 June 2018
Low-coverage sequencing: implications for design of complex trait association studies
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3 June 2018
Discovery and genotyping of genome structural polymorphism by sequencing on a population scale
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3 June 2018
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3 June 2018
Synthetic associations are unlikely to account for many common disease genome-wide association signals
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3 June 2018
Synthetic associations created by rare variants do not explain most GWAS results
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3 June 2018
dmGWAS: dense module searching for genome-wide association studies in protein-protein interaction networks
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3 June 2018
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3 June 2018
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3 June 2018
Evolution in health and medicine Sackler colloquium: Genetic architecture of a complex trait and its implications for fitness and genome-wide association studies
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3 June 2018
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3 June 2018
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3 June 2018
Clinical implications of a molecular genetic classification of monogenic beta-cell diabetes
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3 June 2018
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5034897
retrieved
26 November 2018
Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5034897
retrieved
26 November 2018
Long-range LD can confound genome scans in admixed populations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5034897
retrieved
26 November 2018
Identifiers
DOI
10.1038/NATURE18642
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4596160
Dimensions Publication ID
1036558635
0 references
OpenCitations bibliographic resource ID
4596160
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4596160
PMCID
5034897
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4596160
PubMed ID
27398621
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4596160
Springer Nature article ID
10.1038/nature18642
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