30 results on '"Hattersley, Andrew T."'
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2. Penetrance and expressivity of mitochondrial variants in a large clinically unselected population.
3. Hyperglycaemia is a causal risk factor for upper limb pathologies.
4. Laboratory Guidelines Are Needed for Diagnostic Genetic Testing for Monogenic Diabetes.
5. PLIN1 Haploinsufficiency Causes a Favorable Metabolic Profile.
6. Fetal alleles predisposing to metabolically favorable adiposity are associated with higher birth weight.
7. Noninvasive Fetal Genotyping by Droplet Digital PCR to Identify Maternally Inherited Monogenic Diabetes Variants.
8. A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin–creatinine ratio.
9. Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry.
10. Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic.
11. Maternal hypothyroxinaemia in pregnancy is associated with obesity and adverse maternal metabolic parameters.
12. Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations.
13. Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability.
14. Corrigendum to: A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin–creatinine ratio.
15. Low IgE Is a Useful Tool to Identify STAT3 Gain-of-Function Mutations.
16. Parental diabetes and birthweight in 236 030 individuals in the UK Biobank Study.
17. Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5–CHRNA3–CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight.
18. Amino acid properties may be useful in predicting clinical outcome in patients with Kir6.2 neonatal diabetes.
19. Genetic variation at CHRNA5-CHRNA3-CHRNB4 interacts with smoking status to influence body mass index.
20. Underlying Genetic Models of Inheritance in Established Type 2 Diabetes Associations.
21. 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.
22. Association between the T-381C polymorphism of the brain natriuretic peptide gene and risk of type 2 diabetes in human populations.
23. A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes.
24. Relapsing diabetes can result from moderately activating mutations in KCNJ11.
25. The role of genetic susceptibility in diabetic nephropathy: evidence from family studies.
26. The role of genetic susceptibility in the association of low birth weight with type 2 diabetes.
27. A distant upstream promoter of the HNF-4 α gene connects the transcription factors involved in maturity-onset diabetes of the young.
28. Adult height and proteinuria in type 2 diabetes.
29. Naturally occurring mutations in the human HNF4α gene impair the function of the transcription factor to a varying degree.
30. Kidney disease in hypomelanosis of Ito.
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