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Global microRNA expression profiles in insulin target tissues in a spontaneous rat model of type 2 diabetes

Diabetologia, 2010-06, Vol.53 (6), p.1099-1109

2010

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Cellular characterisation of the GCKR P446L variant associated with type 2 diabetes risk

Diabetologia, 2012-01, Vol.55 (1), p.114-122

2012

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Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype

Diabetologia, 2006-06, Vol.49 (6), p.1190-1197

2006

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A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes

Diabetologia, 2011-11, Vol.54 (11), p.2801-2810

2011

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Apolipoprotein M can discriminate HNF1A-MODY from Type 1 diabetes

Diabetic medicine, 2013-02, Vol.30 (2), p.246-250

2013

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Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy

Diabetic medicine, 2007-12, Vol.24 (12), p.1393-1399

2007

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RD Lawrence Lecture 2009 Old genes, new tricks: learning about blood glucose regulation from naturally occurring genetic variation in humans

Diabetic medicine, 2009-11, Vol.26 (11), p.1083-1089

Gloyn, A. L.

2009

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Association studies of variants in promoter and coding regions of beta-cell ATP-sensitive K-channel genes SUR1 and Kir6.2 with Type 2 diabetes mellitus (UKPDS 53)

Diabetic medicine, 2001-03, Vol.18 (3), p.206-212

2001

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The previously reported T342P GCK missense variant is not a pathogenic mutation causing MODY

Diabetologia, 2011-08, Vol.54 (8), p.2202-2205

2011

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Prevalence of GCK mutations in individuals screened for fasting hyperglycaemia

Diabetologia, 2009, Vol.52 (1), p.172-174

2009

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Permanent neonatal diabetes in an Asian infant

The Journal of pediatrics, 2005, Vol.146 (1), p.131-133

2005

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role for coding functional variants in HNF4A in type 2 diabetes susceptibility

Diabetologia, 2011-01, Vol.54 (1), p.111-119

2011

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Genetics: how the UKPDS contributed to determining the genetic landscape of Type 2 diabetes

Diabetic medicine, 2008-08, Vol.25 (s2), p.35-40

2008

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A tale of two glucose transporters: how GLUT2 re-emerged as a contender for glucose transport into the human beta cell

Diabetologia, 2012-09, Vol.55 (9), p.2312-2315

2012

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Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka

Diabetic medicine, 2008-03, Vol.25 (3), p.370-374

2008

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Asian MODY: are we missing an important diagnosis?

Diabetic medicine, 2006-11, Vol.23 (11), p.1257-1260

2006

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Mutations in the third gene shown to alter fasting glucose levels in the population (G6PC2) are not a common cause of monogenic forms of pancreatic B-cell dysfunction

Diabetic medicine, 2009-01, Vol.26 (1), p.113-114

2009

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Mutations in HHEX are not a common cause of monogenic forms of beta cell dysfunction

Diabetologia, 2007-09, Vol.50 (9), p.2019-2022

2007

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The genetics of type 2 diabetes

Best Practice & Research Clinical Endocrinology & Metabolism, 2001-09, Vol.15 (3), p.293-308

2001

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Complete glucokinase deficiency is not a common cause of permanent neonatal diabetes

Diabetologia, 2002-02, Vol.45 (2), p.290-290

2002

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Human calcium/calmodulin-dependent protein kinase II gamma gene (CAMK2G): cloning, genomic structure and detection of variants in subjects with Type II diabetes

Diabetologia, 2002-04, Vol.45 (4), p.580-583

2002

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Quantitative traits associated with the Type 2 diabetes susceptibility allele in Kir6.2

Diabetologia, 2003-07, Vol.46 (7), p.1021-1023

2003

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Identification of 21 novel glucokinase (GCK) mutations in UK and European Caucasians with maturity-onset diabetes of the young (MODY)

Human mutation, 2003-11, Vol.22 (5), p.417-417

2003

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

Scientific reports, 2018-11, Vol.8 (1), p.16994-16, Article 16994

2018

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Every islet matters: improving the impact of human islet research

Nature metabolism, 2022-08, Vol.4 (8), p.970

2022

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Global microRNA expression profiles in insulin target tissues in a spontaneous rat model of type 2 diabetes

Cellular characterisation of the GCKR P446L variant associated with type 2 diabetes risk

Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype

A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes

Apolipoprotein M can discriminate HNF1A-MODY from Type 1 diabetes

Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy

RD Lawrence Lecture 2009 Old genes, new tricks: learning about blood glucose regulation from naturally occurring genetic variation in humans

Association studies of variants in promoter and coding regions of beta-cell ATP-sensitive K-channel genes SUR1 and Kir6.2 with Type 2 diabetes mellitus (UKPDS 53)

The previously reported T342P GCK missense variant is not a pathogenic mutation causing MODY

Prevalence of GCK mutations in individuals screened for fasting hyperglycaemia

Permanent neonatal diabetes in an Asian infant

role for coding functional variants in HNF4A in type 2 diabetes susceptibility

Genetics: how the UKPDS contributed to determining the genetic landscape of Type 2 diabetes

A tale of two glucose transporters: how GLUT2 re-emerged as a contender for glucose transport into the human beta cell

Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka

Asian MODY: are we missing an important diagnosis?

Mutations in the third gene shown to alter fasting glucose levels in the population (G6PC2) are not a common cause of monogenic forms of pancreatic B-cell dysfunction

Mutations in HHEX are not a common cause of monogenic forms of beta cell dysfunction

The genetics of type 2 diabetes

Complete glucokinase deficiency is not a common cause of permanent neonatal diabetes

Human calcium/calmodulin-dependent protein kinase II gamma gene (CAMK2G): cloning, genomic structure and detection of variants in subjects with Type II diabetes

Quantitative traits associated with the Type 2 diabetes susceptibility allele in Kir6.2

Identification of 21 novel glucokinase (GCK) mutations in UK and European Caucasians with maturity-onset diabetes of the young (MODY)

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

Every islet matters: improving the impact of human islet research

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