Kyle J Gaulton
occupation: researcher
Articles 28
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Glucocorticoid signaling in pancreatic islets modulates gene regulatory programs and genetic risk of type 2 diabetes
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Sequence logic at enhancers governs a dual mechanism of endodermal organ fate induction by FOXA pioneer factors
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An atlas of gene regulatory elements in adult mouse cerebrum
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Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
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Pancreatic islet chromatin accessibility and conformation reveals distal enhancer networks of type 2 diabetes risk
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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
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Common DNA sequence variation influences 3-dimensional conformation of the human genome
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Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
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Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.
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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
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An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
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A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk
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Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.
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Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
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Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin
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The genetic architecture of type 2 diabetes
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Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity
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Genome-wide associations for birth weight and correlations with adult disease
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Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance.
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Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation
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Multiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein Cholesterol
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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
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Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus
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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
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Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
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Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variants
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The miRNA profile of human pancreatic islets and beta-cells and relationship to type 2 diabetes pathogenesis
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A map of open chromatin in human pancreatic islets
Human - wd:Q47138686