Publications — Radcliffe Department of Medicine

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Homozygous hypomorphic HNF1A alleles are a novel cause of young-onset diabetes and result in sulphonylurea sensitive diabetes

GLOYN A. et al, (2020), Diabetes Care

Loss of ZnT8 function protects against diabetes by enhanced insulin secretion.

Dwivedi OP. et al, (2019), Nat Genet

A CRISPR/Cas9 genome editing pipeline in the EndoC-βH1 cell line to study genes implicated in beta cell function

Grotz A. et al, (2019)

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

Wesolowska-Andersen A. et al, (2019)

Exocrine or endocrine? A circulating pancreatic elastase that regulates glucose homeostasis

Gloyn AL., (2019), Nature Metabolism, 1, 853 - 855

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

Zeggini E. et al, (2019), Science (New York, N.Y.), 365, 1409 - 1413

Investigating a Candidate Causal Allele in Type 2 Diabetes Susceptibility Gene PAM as a Cause of Neonatal Diabetes Mellitus

Sengupta S. et al, (2019), DIABETES, 68

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

Fernández-Tajes J. et al, (2019), Genome Med, 11

Fostering improved human islet research: a European perspective

Marchetti P. et al, (2019), Diabetologia

Plasma Fucosylated Glycans and C-Reactive Protein as Biomarkers of HNF1A-MODY in Young Adult-Onset Nonautoimmune Diabetes.

Juszczak A. et al, (2019), Diabetes Care, 42, 17 - 26

Electrophysiological properties of human beta-cell lines EndoC-βH1 and -βH2 conform with human beta-cells.

Hastoy B. et al, (2018), Sci Rep, 8

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.

Mahajan A. et al, (2018), Nat Genet, 50, 1505 - 1513

Precision medicine in the management of type 2 diabetes.

Gloyn AL. and Drucker DJ., (2018), Lancet Diabetes Endocrinol, 6, 891 - 900

Loss of ZnT8 function protects against diabetes by enhanced insulin secretion

Dwivedi OP. et al, (2018)

Author Correction: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition.

Small KS. et al, (2018), Nat Genet, 50

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

Ramond C. et al, (2018), Development, 145

Type 2 diabetes risk alleles in PAM impact insulin release from human pancreatic β-cells.

Thomsen SK. et al, (2018), Nat Genet, 50, 1122 - 1131

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

Perez-Alcantara M. et al, (2018), Diabetologia, 61, 1614 - 1622

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

Fernéndez-Tajes J. et al, (2018)

Maturity onset diabetes of the young due to HNF1A variants in Croatia.

Pavić T. et al, (2018), Biochem Med (Zagreb), 28

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