Andrew T. Hattersley
Exeter, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 417 publications
Bi-allelic variants in the non-protein-coding minor spliceosome components RNU6ATAC and RNU4ATAC cause syndromic monogenic autoimmune diabetes.
Journal: American journal of human genetics
Published: July 14, 2026
Genetic and maternal environmental contributions to estimated fetal weight at 20 weeks gestation compared with birthweight.
Journal: medRxiv : the preprint server for health sciences
Published: July 03, 2026
Clinical Utility of a Type 1 Diabetes Genetic Risk Score Measured as Part of MODY Genetic Testing.
Journal: Diabetes care
Published: May 14, 2026
Kidney outcomes with GLP-1 receptor agonists in people with type 2 diabetes already receiving SGLT2 inhibitors: a target trial emulation study using UK primary care data.
Journal: The Lancet. Primary care
Published: May 11, 2026
Trends in Second-Line Initiations and Treatment Outcomes Across Age and Frailty Groups in People With Type 2 Diabetes: UK Population-Based Study, 2019-2024.
Journal: Diabetes, obesity & metabolism
Published: March 30, 2026
Age-related reference intervals for thyroid function tests are beneficial in adults over 60 years.
Journal: Annals of clinical biochemistry
Published: February 09, 2026
Age-related reference intervals for thyroid function tests are beneficial in adults over 60 years.
Journal: Annals of clinical biochemistry
Published: February 09, 2026
To Cluster or Not to Cluster? A Comparison of Approaches to Targeting Type 2 Diabetes Glucose-Lowering Therapy in the TriMaster Crossover Trial.
Journal: Diabetes care
Published: January 16, 2026
Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects.
Journal: Nature communications
Published: December 14, 2025
Precision Prescribing of SGLT2 Inhibitors in Individuals With Type 2 Diabetes for Primary Prevention of Heart Failure: Model Development and Validation Study.
Journal: Diabetes care
Published: December 09, 2025
Bi-allelic variants in the non-protein-coding minor spliceosome components RNU6ATAC and RNU4ATAC cause syndromic monogenic autoimmune diabetes.
Journal: American journal of human genetics
Published: December 01, 2025
Last Updated: 09/26/2026