Graeme I Bell

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Graeme I



Publications in SciGraph latest 50 shown

  • 2018-01-23 Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls in SCIENTIFIC DATA
  • 2017-12-19 Sequence data and association statistics from 12,940 type 2 diabetes cases and controls in SCIENTIFIC DATA
  • 2017-08 In vivo measurement and biological characterisation of the diabetes-associated mutant insulin p.R46Q (GlnB22-insulin) in DIABETOLOGIA
  • 2016-12 Beyond type 2 diabetes, obesity and hypertension: an axis including sleep apnea, left ventricular hypertrophy, endothelial dysfunction, and aortic stiffness among Mexican Americans in Starr County, Texas in CARDIOVASCULAR DIABETOLOGY
  • 2016-08 The genetic architecture of type 2 diabetes in NATURE
  • 2014-03 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility in NATURE GENETICS
  • 2013-01 In vitro scan for enhancers at the TCF7L2 locus in DIABETOLOGIA
  • 2012-03 Erratum to: Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene in REVIEWS IN ENDOCRINE AND METABOLIC DISORDERS
  • 2011-12 Neonatal Diabetes: An Expanding List of Genes Allows for Improved Diagnosis and Treatment in CURRENT DIABETES REPORTS
  • 2011-08 Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals in DIABETOLOGIA
  • 2010-09 Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene in REVIEWS IN ENDOCRINE AND METABOLIC DISORDERS
  • 2007-12 Macrosomia and neonatal hypoglycaemia in RW pedigree subjects with a mutation (Q268X) in the gene encoding hepatocyte nuclear factor 4α (HNF4A) in DIABETOLOGIA
  • 2006-07 Common polymorphisms of calpain-10 are associated with abdominal obesity in subjects at high risk of type 2 diabetes in DIABETOLOGIA
  • 2006-05 Phenotypic heterogeneity between different mutations of MODY subtypes and within MODY pedigrees in DIABETOLOGIA
  • 2005-10 The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population in DIABETOLOGIA
  • 2005-02 Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 2005-01 Imaging beta cell development in real-time using pancreatic explants from mice with green fluorescent protein-labeled pancreatic beta cells in IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY - ANIMAL
  • 2003-05 Organ alchemy: producing insulin in the liver in NATURE MEDICINE
  • 2001-04-24 Identification of three missense mutations in the peroxisome proliferator-activated receptor α gene in Japanese subjects with maturity-onset diabetes of the young in JOURNAL OF HUMAN GENETICS
  • 2000-10 Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus in NATURE GENETICS
  • 2000-08 No diabetes-associated mutations in the coding region of the hepatocyte nuclear factor-4γ gene (HNF4G) in Japanese patients with MODY in DIABETOLOGIA
  • 2000-03 Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1β1 in KIDNEY INTERNATIONAL
  • 1999-02 Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans in NATURE GENETICS
  • 1998-07 A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus in NATURE GENETICS
  • 1998-04 Hyperexcitability to sulphonylurea in MODY3 in DIABETOLOGIA
  • 1997-12 Mutation in hepatocyte nuclear factor–1β gene (TCF2) associated with MODY in NATURE GENETICS
  • 1997-10 Diabetes, dependence, asymptotics, selection and significance in NATURE GENETICS
  • 1997-03 Genetic variation in the hepatocyte nuclear factor-1a gene in Danish Caucasians with late-onset NIDDM in DIABETOLOGIA
  • 1997-01 Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families in DIABETOLOGIA
  • 1996-12 Mutations in the hepatocyte nuclear factor-4α gene in maturity-onset diabetes of the young (MODY1) in NATURE
  • 1996-09 Genetic contribution of polymorphism of the GLUT1 and GLUT4 genes to the susceptibility to type 2 (non-insulin-dependent) diabetes mellitus in different populations in ACTA DIABETOLOGICA
  • 1996-07 Increased Expression of Endothelin B Receptor mRNA Following Subarachnoid Hemorrhage in Monkeys in JOURNAL OF CEREBRAL BLOOD FLOW & METABOLISM
  • 1996-06 Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle in DIABETOLOGIA
  • 1995-12 Linkage studies in NIDDM with markers near the sulphonylurea receptor gene in DIABETOLOGIA
  • 1995-09 Candidate gene studies in pedigrees with maturity-onset diabetes of the young not linked with glucokinase in DIABETOLOGIA
  • 1995-06 Linkage and association between insulin–dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7 in NATURE GENETICS
  • 1995-03 Characterization of Japanese families with early-onset type 2 (non-insulin dependent) diabetes mellitus and screening for mutations in the glucokinase and mitochondrial tRNALeu(UUR) genes in ACTA DIABETOLOGICA
  • 1995-02 Identification of two novel amino acid polymorphisms in beta-cell/liver (GLUT2) glucose transporter in Japanese subjects in DIABETOLOGIA
  • 1994-02 Localization of somatostatin (SRIF) SSTR-1, SSTR-2 and SSTR-3 receptor mRNA in rat brain by in situ hybridization in NAUNYN-SCHMIEDEBERG'S ARCHIVES OF PHARMACOLOGY
  • 1994 Biochemical and Functional Properties of Somatostatin Receptors in GROWTH HORMONE II
  • 1993-05 Type 2 (non-insulin-dependent) diabetes mellitus associated with a mutation of the glucokinase gene in a Japanese family in DIABETOLOGIA
  • 1993-04 Human insulin receptor substrate-1 gene (IRS1): chromosomal localization to 2q35-q36.1 and identification of a simple tandem repeat DNA polymorphism in DIABETOLOGIA
  • 1993-02 Characterization of a third simple tandem repeat polymorphism in the human glucokinase gene in DIABETOLOGIA
  • 1992-10 Missense glucokinase mutation in maturity–onset diabetes of the young and mutation screening in late–onset diabetes in NATURE GENETICS
  • 1992-09 Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4 in NATURE GENETICS
  • 1992-04 Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus in NATURE
  • 1991-11 Multiple restriction fragment length polymorphisms at the GLUT2 locus: GLUT2 haplotypes for genetic analysis of Type 2 (non-insulin-dependent) diabetes mellitus in DIABETOLOGIA
  • 1991-08 Sequences of islet amyloid polypeptide precursors of an old world monkey, the pig-tailed macaque (Macaca nemestrina), and the dog (Canis familiaris) in DIABETOLOGIA
  • 1991 A Highly Informative Polymorphism of the Pepsinogen C Gene Detected by Polymerase Chain Reaction in STRUCTURE AND FUNCTION OF THE ASPARTIC PROTEINASES
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