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The miRNA profile of human pancreatic islets and beta-cells and relationship to type 2 diabetes pathogenesis

PloS one, 2013-01, Vol.8 (1), p.e55272-e55272

2013

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Role of KATP Channels in Glucose-Regulated Glucagon Secretion and Impaired Counterregulation in Type 2 Diabetes

Cell metabolism, 2013-12, Vol.18 (6), p.871-882

2013

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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

PLoS genetics, 2015-12, Vol.11 (12), p.e1005694-e1005694

2015

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Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia

Human mutation, 2009-11, Vol.30 (11), p.1512-1526

2009

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Understanding human fetal pancreas development using subpopulation sorting, RNA sequencing and single-cell profiling

Development (Cambridge), 2018-08, Vol.145 (16)

2018

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Systematic Functional Characterization of Candidate Causal Genes for Type 2 Diabetes Risk Variants

Diabetes (New York, N.Y.), 2016-12, Vol.65 (12), p.3805-3811

2016

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PTEN Mutations as a Cause of Constitutive Insulin Sensitivity and Obesity

The New England journal of medicine, 2012-09, Vol.367 (11), p.1002-1011

2012

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A comprehensive map of human glucokinase variant activity

Genome Biology, 2023-04, Vol.24 (1), p.97-23, Article 97

2023

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Glucokinase (GCK) mutations in hyper‐ and hypoglycemia: Maturity‐onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy

Human mutation, 2003-11, Vol.22 (5), p.353-362

Gloyn, Anna L.

2003

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Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci

eLife, 2018-02, Vol.7

2018

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Argonaute2 Mediates Compensatory Expansion of the Pancreatic β Cell

Cell metabolism, 2014-01, Vol.19 (1), p.122-134

2014

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Genetic regulation of RNA splicing in human pancreatic islets

Genome Biology, 2022-09, Vol.23 (1), p.196-28, Article 196

2022

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PAX4 loss of function increases diabetes risk by altering human pancreatic endocrine cell development

Nature communications, 2023-09, Vol.14 (1), p.6119-19, Article 6119

2023

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Monogenic diabetes: a gateway to precision medicine in diabetes

The Journal of clinical investigation, 2021-02, Vol.131 (3)

2021

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Mutations in ATP-Sensitive K+ Channel Genes Cause Transient Neonatal Diabetes and Permanent Diabetes in Childhood or Adulthood

Diabetes (New York, N.Y.), 2007-07, Vol.56 (7), p.1930-1937

2007

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Translational genomics and precision medicine: Moving from the lab to the clinic

Science (American Association for the Advancement of Science), 2019-09, Vol.365 (6460), p.1409-1413

2019

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Safe use of the ketogenic diet in an infant with microcephaly, epilepsy, and diabetes syndrome: a case report

BMC pediatrics, 2023-09, Vol.23 (1), p.1-6, Article 453

2023

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Developing a network view of type 2 diabetes risk pathways through integration of genetic, genomic and functional data

Genome medicine, 2019-03, Vol.11 (1), p.19-19, Article 19

2019

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High-Sensitivity CRP Discriminates HNF1A-MODY From Other Subtypes of Diabetes

Diabetes care, 2011-08, Vol.34 (8), p.1860-1862

2011

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Management of Neonatal Diabetes due to a KCNJ11 Mutation with Automated Insulin Delivery System and Remote Patient Monitoring

Case reports in endocrinology, 2023-08, Vol.2023, p.1-6

2023

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Species-specific differences in the expression of the HNF1A, HNF1B and HNF4A genes

PloS one, 2009-11, Vol.4 (11), p.e7855-e7855

2009

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Assessment of High-Sensitivity C-Reactive Protein Levels as Diagnostic Discriminator of Maturity-Onset Diabetes of the Young Due to HNF1A Mutations

Diabetes care, 2010-09, Vol.33 (9), p.1919-1924

2010

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Deep learning models predict regulatory variants in pancreatic islets and refine type 2 diabetes association signals

eLife, 2020-01, Vol.9

2020

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Small but mighty: microexons in glucose homeostasis

Trends in genetics, 2023-07, Vol.39 (7), p.526-527

2023

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The miRNA profile of human pancreatic islets and beta-cells and relationship to type 2 diabetes pathogenesis

Role of KATP Channels in Glucose-Regulated Glucagon Secretion and Impaired Counterregulation in Type 2 Diabetes

Human β Cell Transcriptome Analysis Uncovers lncRNAs That Are Tissue-Specific, Dynamically Regulated, and Abnormally Expressed in Type 2 Diabetes

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

Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia

Understanding human fetal pancreas development using subpopulation sorting, RNA sequencing and single-cell profiling

Systematic Functional Characterization of Candidate Causal Genes for Type 2 Diabetes Risk Variants

PTEN Mutations as a Cause of Constitutive Insulin Sensitivity and Obesity

A comprehensive map of human glucokinase variant activity

Glucokinase (GCK) mutations in hyper‐ and hypoglycemia: Maturity‐onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy

Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci

Argonaute2 Mediates Compensatory Expansion of the Pancreatic β Cell

Genetic regulation of RNA splicing in human pancreatic islets

PAX4 loss of function increases diabetes risk by altering human pancreatic endocrine cell development

Monogenic diabetes: a gateway to precision medicine in diabetes

Mutations in ATP-Sensitive K+ Channel Genes Cause Transient Neonatal Diabetes and Permanent Diabetes in Childhood or Adulthood

Translational genomics and precision medicine: Moving from the lab to the clinic

Safe use of the ketogenic diet in an infant with microcephaly, epilepsy, and diabetes syndrome: a case report

Developing a network view of type 2 diabetes risk pathways through integration of genetic, genomic and functional data

High-Sensitivity CRP Discriminates HNF1A-MODY From Other Subtypes of Diabetes

Management of Neonatal Diabetes due to a KCNJ11 Mutation with Automated Insulin Delivery System and Remote Patient Monitoring

Species-specific differences in the expression of the HNF1A, HNF1B and HNF4A genes

Assessment of High-Sensitivity C-Reactive Protein Levels as Diagnostic Discriminator of Maturity-Onset Diabetes of the Young Due to HNF1A Mutations

Deep learning models predict regulatory variants in pancreatic islets and refine type 2 diabetes association signals

Small but mighty: microexons in glucose homeostasis

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