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281-OR: Type 2 Diabetes Diagnosed between 16-30 Years in South Asian and White Individuals Is Phenotypically Similar

Diabetes (New York, N.Y.), 2020-06, Vol.69 (Supplement_1)

2020

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The clinical application of non-genetic biomarkers for differential diagnosis of monogenic diabetes

Diabetes research and clinical practice, 2009-12, Vol.86, p.S15-S21

2009

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When to consider a diagnosis of MODY at the presentation of diabetes: aetiology matters for correct management

British journal of general practice, 2016-06, Vol.66 (647), p.e457-e459

2016

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The correlation between breath acetone and blood betahydroxybutyrate in individuals with type 1 diabetes

Journal of breath research, 2021-01, Vol.15 (1), p.017101-017101

2021

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The Variable Number of Tandem Repeats Upstream of the Insulin Gene Is a Susceptibility Locus for Latent Autoimmune Diabetes in Adults

Diabetes (New York, N.Y.), 2006-06, Vol.55 (6), p.1890-1894

2006

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Finding the needle in the haystack: how to identify monogenic diabetes in the paediatric clinic

Paediatrics and child health, 2022-01, Vol.32 (1), p.31-36

2022

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Fucosylated AGP glycopeptides as biomarkers of HNF1A-Maturity onset diabetes of the young

Diabetes research and clinical practice, 2022-03, Vol.185, p.109226-109226, Article 109226

2022

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A Large-Scale Association Analysis of Common Variation of the HNF1α Gene With Type 2 Diabetes in the U.K. Caucasian Population

Diabetes (New York, N.Y.), 2005-08, Vol.54 (8), p.2487-2491

2005

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Etiological Investigation of Diabetes in Young Adults Presenting With Apparent Type 2 Diabetes

Diabetes care, 2003-07, Vol.26 (7), p.2088-2093

2003

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Interlaboratory evaluation of plasma N-glycan antennary fucosylation as a clinical biomarker for HNF1A-MODY using liquid chromatography methods

Glycoconjugate journal, 2021-06, Vol.38 (3), p.375-386

2021

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Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes

Human molecular genetics, 2010-02, Vol.19 (3), p.535-544

2010

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Altered cortisol metabolism in individuals with HNF1A‐MODY

Clinical endocrinology (Oxford), 2020-09, Vol.93 (3), p.269-279

2020

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1900-P: HNF1A Deficiency Leads to Perturbed Glucagon Secretion in Humans

Diabetes (New York, N.Y.), 2020-06, Vol.69 (Supplement_1)

2020

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Genetics of type 2 diabetes

Current opinion in genetics & development, 2007-06, Vol.17 (3), p.239-244

2007

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Maturity onset diabetes of the young: clinical characteristics, diagnosis and management

Pediatric endocrinology reviews : PER, 2013, Vol.10 (2), p.234

2013

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Low frequency variants in the exons only encoding isoform A of HNF1A do not contribute to susceptibility to type 2 diabetes

PloS one, 2009-08, Vol.4 (8), p.e6615-e6615

2009

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Glucokinase MODY and Implications for Treatment Goals of Common Forms of Diabetes

Current Diabetes Reports, 2014-12, Vol.14 (12), p.559-559, Article 559

2014

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Association Studies of Insulin Receptor Substrate 1 Gene (IRS1) Variants in Type 2 Diabetes Samples Enriched for Family History and Early Age of Onset

Diabetes (New York, N.Y.), 2004-12, Vol.53 (12), p.3319-3322

2004

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Genetic Variation in the Small Heterodimer Partner Gene and Young-Onset Type 2 Diabetes, Obesity, and Birth Weight in U.K. Subjects

Diabetes (New York, N.Y.), 2003-05, Vol.52 (5), p.1276-1279

2003

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PAX6 mutation in association with ptosis, cataract, iris hypoplasia, corneal opacification and diabetes: a new variant of familial aniridia?

Clinical & experimental ophthalmology, 2013-12, Vol.41 (9), p.835-841

2013

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

Biochemia Medica, 2018-06, Vol.28 (2), p.020703-020703

2018

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Reclassification of Diabetes Etiology in a Family With Multiple Diabetes Phenotypes

The journal of clinical endocrinology and metabolism, 2014-06, Vol.99 (6), p.E1067-E1071

2014

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The use of precision diagnostics for monogenic diabetes: a systematic review and expert opinion

Communications medicine, 2023-10, Vol.3 (1), p.136-24, Article 136

2023

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Treating Hypertension in Diabetic Nephropathy

Diabetes care, 2003-06, Vol.26 (6), p.1802-1805

2003

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281-OR: Type 2 Diabetes Diagnosed between 16-30 Years in South Asian and White Individuals Is Phenotypically Similar

The clinical application of non-genetic biomarkers for differential diagnosis of monogenic diabetes

When to consider a diagnosis of MODY at the presentation of diabetes: aetiology matters for correct management

The correlation between breath acetone and blood betahydroxybutyrate in individuals with type 1 diabetes

The Variable Number of Tandem Repeats Upstream of the Insulin Gene Is a Susceptibility Locus for Latent Autoimmune Diabetes in Adults

Finding the needle in the haystack: how to identify monogenic diabetes in the paediatric clinic

Fucosylated AGP glycopeptides as biomarkers of HNF1A-Maturity onset diabetes of the young

A Large-Scale Association Analysis of Common Variation of the HNF1α Gene With Type 2 Diabetes in the U.K. Caucasian Population

Etiological Investigation of Diabetes in Young Adults Presenting With Apparent Type 2 Diabetes

Interlaboratory evaluation of plasma N-glycan antennary fucosylation as a clinical biomarker for HNF1A-MODY using liquid chromatography methods

Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes

Mutations in HNF1A Result in Marked Alterations of Plasma Glycan Profile

Altered cortisol metabolism in individuals with HNF1A‐MODY

1900-P: HNF1A Deficiency Leads to Perturbed Glucagon Secretion in Humans

Genetics of type 2 diabetes

Maturity onset diabetes of the young: clinical characteristics, diagnosis and management

Low frequency variants in the exons only encoding isoform A of HNF1A do not contribute to susceptibility to type 2 diabetes

Glucokinase MODY and Implications for Treatment Goals of Common Forms of Diabetes

Association Studies of Insulin Receptor Substrate 1 Gene (IRS1) Variants in Type 2 Diabetes Samples Enriched for Family History and Early Age of Onset

Genetic Variation in the Small Heterodimer Partner Gene and Young-Onset Type 2 Diabetes, Obesity, and Birth Weight in U.K. Subjects

PAX6 mutation in association with ptosis, cataract, iris hypoplasia, corneal opacification and diabetes: a new variant of familial aniridia?

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

Reclassification of Diabetes Etiology in a Family With Multiple Diabetes Phenotypes

The use of precision diagnostics for monogenic diabetes: a systematic review and expert opinion

Treating Hypertension in Diabetic Nephropathy

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