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List of works by Andrew Tym Hattersley

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Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene

scientific article
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

scientific article published on 2 December 2012
C-reactive protein and its role in metabolic syndrome: mendelian randomisation study

scientific article published in December 2005
Variation in TCF7L2 influences therapeutic response to sulfonylureas: a GoDARTs study

scientific article published on 22 May 2007
Common variants of the novel type 2 diabetes genes CDKAL1 and HHEX/IDE are associated with decreased pancreatic beta-cell function

scientific article
The fat mass- and obesity-associated locus and dietary intake in children

scientific article
Association Analysis of 6,736 U.K. Subjects Provides Replication and ConfirmsTCF7L2as a Type 2 Diabetes Susceptibility Gene With a Substantial Effect on Individual Risk

article
Genome-wide associations for birth weight and correlations with adult disease

scientific article
Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis.

scientific article
The clinical utility of C‐peptide measurement in the care of patients with diabetes

scientific article published on July 1, 2013
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

scientific article
Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus

scientific article
Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features

scientific article
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

scientific article
A common genetic variant in the 15q24 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) is associated with a reduced ability of women to quit smoking in pregnancy

scientific article published on 09 May 2009
Common variation in the DIO2 gene predicts baseline psychological well-being and response to combination thyroxine plus triiodothyronine therapy in hypothyroid patients

scientific article
Effective treatment with oral sulfonylureas in patients with diabetes due to sulfonylurea receptor 1 (SUR1) mutations

scientific article published on 19 November 2007
Evaluation of Common Variants in the Six Known Maturity-Onset Diabetes of the Young (MODY) Genes for Association With Type 2 Diabetes

article
Improved genetic testing for monogenic diabetes using targeted next-generation sequencing.

scientific article published on 15 June 2013
A genome-wide association search for type 2 diabetes genes in African Americans

scientific article published on 4 January 2012
The majority of patients with long-duration type 1 diabetes are insulin microsecretors and have functioning beta cells

scientific article published on January 2014
Maturity-onset diabetes of the young: clinical heterogeneity explained by genetic heterogeneity

scientific article published on January 1, 1998
The genetic abnormality in the beta cell determines the response to an oral glucose load

scientific article published in March 2002
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

scientific article
GATA6 haploinsufficiency causes pancreatic agenesis in humans

scientific article
Exploring the developmental overnutrition hypothesis using parental-offspring associations and FTO as an instrumental variable

scientific article
Prevalence, characteristics and clinical diagnosis of maturity onset diabetes of the young due to mutations in HNF1A, HNF4A, and glucokinase: results from the SEARCH for Diabetes in Youth

scientific article published on 14 June 2013
Definition, epidemiology and classification of diabetes in children and adolescents

scientific article published on September 2009
Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes

scientific article published on 18 November 2009
Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients

scientific article published in October 2004
A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes

scientific article
Renal cysts and diabetes syndrome resulting from mutations in hepatocyte nuclear factor-1beta

scientific article
Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects

scientific article
Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight

scientific article published on March 2016
Meta-analysis and a large association study confirm a role for calpain-10 variation in type 2 diabetes susceptibility

scientific article published on November 2003
Reduced-function SLC22A1 polymorphisms encoding organic cation transporter 1 and glycemic response to metformin: a GoDARTS study

scientific article published on 31 March 2009
A common haplotype of the glucokinase gene alters fasting glucose and birth weight: association in six studies and population-genetics analyses

scientific article published on 6 October 2006
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes.

scientific article published on 19 November 2012
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

scientific article published on 22 December 2017
Prevalence of vascular complications among patients with glucokinase mutations and prolonged, mild hyperglycemia

scientific article
The effect of early, comprehensive genomic testing on clinical care in neonatal diabetes: an international cohort study.

scientific article published on 28 July 2015
Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis

scientific article
Genetic variation at CHRNA5-CHRNA3-CHRNB4 interacts with smoking status to influence body mass index

scientific article published on 18 May 2011
Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data

scientific article
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

scientific article
Common variants at 12q15 and 12q24 are associated with infant head circumference

scientific article published on 15 April 2012
KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes

scientific article published in January 2005
The diagnosis and management of monogenic diabetes in children and adolescents

scientific article published on September 2009
Type 2 diabetes risk alleles are associated with reduced size at birth

scientific article published on 19 February 2009
Ethnic subgroup differences in hypertension in Pakistan

scientific article published on May 2003

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