Martine Vaxillaire


Ontology type: schema:Person     


Person Info

NAME

Martine

SURNAME

Vaxillaire

Publications in SciGraph latest 50 shown

  • 2014-08 Type 2 diabetes-related genetic risk scores associated with variations in fasting plasma glucose and development of impaired glucose homeostasis in the prospective DESIR study in DIABETOLOGIA
  • 2013-03 Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetes in DIABETOLOGIA
  • 2012-10 GATA6 inactivating mutations are associated with heart defects and, inconsistently, with pancreatic agenesis and diabetes in DIABETOLOGIA
  • 2012-03 Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes in NATURE GENETICS
  • 2011-11 A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes in DIABETOLOGIA
  • 2009-12 Contribution of type 2 diabetes associated loci in the Arabic population from Tunisia: a case-control study in BMC MEDICAL GENETICS
  • 2009-12 Functional and genetic analysis in type 2 diabetes of Liver X receptor alleles – a cohort study in BMC MEDICAL GENETICS
  • 2009-10 Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia in NATURE GENETICS
  • 2009-05 Mutations in G6PC2 do not contribute to monogenic forms of early infancy diabetes and beta cell dysfunction in DIABETOLOGIA
  • 2008-03 Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study in JOURNAL OF MOLECULAR MEDICINE
  • 2007-01 No major contribution of TCF7L2 sequence variants to maturity onset of diabetes of the young (MODY) or neonatal diabetes mellitus in French white subjects in DIABETOLOGIA
  • 2006-12 Analysis of common PTPN1gene variants in type 2 diabetes, obesity and associated phenotypes in the French population in BMC MEDICAL GENETICS
  • 2005-12 Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1 in HUMAN GENETICS
  • 2005-03 Effect of common polymorphisms in the HNF4α promoter on susceptibility to type 2 diabetes in the French Caucasian population in DIABETOLOGIA
  • 2004-12 The EIF2AK3 gene region and type I diabetes in subjects from South India in GENES & IMMUNITY
  • 2003-03 Does the −11377 promoter variant of APM1 gene contribute to the genetic risk for Type 2 diabetes mellitus in Japanese families? in DIABETOLOGIA
  • 2002-09 Rare variants identified in the HNF-4α β-cell-specific promoter and alternative exon 1 lack biological significance in maturity onset diabetes of the young and young onset Type II diabetes in DIABETOLOGIA
  • 2002-03 The genetic abnormality in the beta cell determines the response to an oral glucose load in DIABETOLOGIA
  • 2002-03 Glucokinase gene mutations are not a common cause of permanent neonatal diabetes in France in DIABETOLOGIA
  • 1998-08 Mutation screening in 18 Caucasian families suggest the existence of other MODY genes in DIABETOLOGIA
  • 1997-01 Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families in DIABETOLOGIA
  • 1996-01 Assessment of insulin sensitivity in glucokinase-deficient subjects in DIABETOLOGIA
  • 1995-04 A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q in NATURE GENETICS
  • 1992-06 Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus in NATURE
  • 1992-03 Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus in NATURE
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