Andrew T Hattersley


Ontology type: schema:Person     


Person Info

NAME

Andrew T

SURNAME

Hattersley

Publications in SciGraph latest 50 shown

  • 2019-04 Homozygosity mapping provides supporting evidence of pathogenicity in recessive Mendelian disease in GENETICS IN MEDICINE
  • 2019-03 Correction: Homozygosity mapping provides supporting evidence of pathogenicity in recessive Mendelian disease in GENETICS IN MEDICINE
  • 2019-01-07 Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci in MOLECULAR PSYCHIATRY
  • 2018-12 A UK nationwide prospective study of treatment change in MODY: genetic subtype and clinical characteristics predict optimal glycaemic control after discontinuing insulin and metformin in DIABETOLOGIA
  • 2018-12 Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion in CLINICAL EPIGENETICS
  • 2018-11 Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps in NATURE GENETICS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-05 Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome in DIABETOLOGIA
  • 2018-04 Maternal and fetal genetic contribution to gestational weight gain in INTERNATIONAL JOURNAL OF OBESITY
  • 2018-04 A type 1 diabetes genetic risk score can discriminate monogenic autoimmunity with diabetes from early-onset clustering of polygenic autoimmunity with diabetes in DIABETOLOGIA
  • 2018-04 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes in NATURE GENETICS
  • 2018-01 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2017-12-19 Sequence data and association statistics from 12,940 type 2 diabetes cases and controls in SCIENTIFIC DATA
  • 2017-12 Pancreas and gallbladder agenesis in a newborn with semilobar holoprosencephaly, a case report in BMC MEDICAL GENETICS
  • 2017-12 Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance in NATURE COMMUNICATIONS
  • 2017-12 Erratum to: Methods for evaluating medical tests and biomarkers in DIAGNOSTIC AND PROGNOSTIC RESEARCH
  • 2017-11 Screening for neonatal diabetes at day 5 of life using dried blood spot glucose measurement in DIABETOLOGIA
  • 2017-10 Costs and Treatment Pathways for Type 2 Diabetes in the UK: A Mastermind Cohort Study in DIABETES THERAPY
  • 2017-05 Precision diabetes: learning from monogenic diabetes in DIABETOLOGIA
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2017-02 Methods for Evaluating Medical Tests and Biomarkers in DIAGNOSTIC AND PROGNOSTIC RESEARCH
  • 2016-12 Beta cell function and ongoing autoimmunity in long-standing, childhood onset type 1 diabetes in DIABETOLOGIA
  • 2016-11-23 A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape in NATURE COMMUNICATIONS
  • 2016-10 South Asian individuals with diabetes who are referred for MODY testing in the UK have a lower mutation pick-up rate than white European people in DIABETOLOGIA
  • 2016-10 Genome-wide associations for birth weight and correlations with adult disease in NATURE
  • 2016-10 A reference panel of 64,976 haplotypes for genotype imputation in NATURE GENETICS
  • 2016-08 The genetic architecture of type 2 diabetes in NATURE
  • 2016-07 Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors in DIABETOLOGIA
  • 2016-07 Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk in DIABETOLOGIA
  • 2016-06 Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes in DIABETOLOGIA
  • 2015-12 Neonatal diabetes as an isolated manifestation of ipex: an expanding spectrum of disease phenotype with FOXP3 mutation in INTERNATIONAL JOURNAL OF PEDIATRIC ENDOCRINOLOGY
  • 2015-12 Biallelic RFX6 mutations can cause childhood as well as neonatal onset diabetes mellitus in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-12 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-12 Biallelic RFX6 mutations can cause childhood as well as neonatal onset diabetes mellitus in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-12 Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility in NATURE COMMUNICATIONS
  • 2015-09 3. A Novel, Inexpensive Test Can Discriminate between Type 1 and Type 2 Diabetes (1745-P) in NEDERLANDS TIJDSCHRIFT VOOR DIABETOLOGIE
  • 2015-02 Genetic studies of body mass index yield new insights for obesity biology in NATURE
  • 2015-02 HNF1B-associated renal and extra-renal disease—an expanding clinical spectrum in NATURE REVIEWS NEPHROLOGY
  • 2015-02 New genetic loci link adipose and insulin biology to body fat distribution in NATURE
  • 2014-12 A diagnostic approach for defining idiopathic remitting diabetes: a retrospective cohort study in BMC ENDOCRINE DISORDERS
  • 2014-11 Defining the role of common variation in the genomic and biological architecture of adult human height in NATURE GENETICS
  • 2014-11 Neurogenin 3 is important but not essential for pancreatic islet development in humans in DIABETOLOGIA
  • 2014-08 Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease in NATURE GENETICS
  • 2014-06 Discovery of biomarkers for glycaemic deterioration before and after the onset of type 2 diabetes: rationale and design of the epidemiological studies within the IMI DIRECT Consortium in DIABETOLOGIA
  • 2014-03 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility in NATURE GENETICS
  • 2014-01 Cross-sectional and longitudinal studies suggest pharmacological treatment used in patients with glucokinase mutations does not alter glycaemia in DIABETOLOGIA
  • 2014-01 Erratum to: The majority of patients with long-duration type 1 diabetes are insulin microsecretors and have functioning beta cells in DIABETOLOGIA
  • 2014-01 Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis in NATURE GENETICS
  • 2014-01 The majority of patients with long-duration type 1 diabetes are insulin microsecretors and have functioning beta cells in DIABETOLOGIA
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