Diabetes articles within European Journal of Human Genetics

Featured

• Article | 18 February 2020

  Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 missense variant versus a 3q13.31 microdeletion including ZBTB20

  • Aurélien Juven
  • , Sophie Nambot
  •  & Laurence Faivre

• Brief Communication | 16 December 2019

  Response to multiple glucose-lowering agents in a sib-pair with a novel HNF1α (MODY3) variant

  • Clara S. H. Tan
  • , Su Fen Ang
  •  & Su Chi Lim

• Brief Communication | 19 March 2019

  Precision medicine for a man presented with diabetes at 2-month old

  • Su Fen Ang
  • , Clara Si Hua Tan
  •  & Su Chi Lim

• Article | 14 August 2018

  Linear isoforms of the long noncoding RNA CDKN2B-AS1 regulate the c-myc-enhancer binding factor RBMS1

  • Michael Hubberten
  • , Gregor Bochenek
  •  & Arne S. Schaefer

• Article | 16 April 2014

  A decade of molecular genetic testing for MODY: a retrospective study of utilization in The Netherlands

  • Stephanie S Weinreich
  • , Astrid Bosma
  •  & Martina C Cornel

• Article | 26 March 2014

  Characterization of the transcriptional machinery bound across the widely presumed type 2 diabetes causal variant, rs7903146, within TCF7L2

  • Qianghua Xia
  • , Sandra Deliard
  •  & Struan FA Grant

• Clinical Utility Gene Card | 26 February 2014

  Clinical utility gene card for: Transient Neonatal Diabetes Mellitus, 6q24-related

  • Deborah Mackay
  • , Susanne Bens
  •  & I Karen Temple

• Letter | 12 February 2014

  Redundant enhancers and causal variants in the TCF7L2 gene

  • Edward A Ruiz-Narváez

• Clinical Utility Gene Card | 12 February 2014

  Clinical utility gene card for: Maturity-onset diabetes of the young

  • Kevin Colclough
  • , Cécile Saint-Martin
  •  & Christine Bellanné-Chantelot

• Article
  22 January 2014 | Open Access

  Variation and association to diabetes in 2000 full mtDNA sequences mined from an exome study in a Danish population

  • Shengting Li
  • , Soren Besenbacher
  •  & Mikkel H Schierup

• Article | 23 January 2013

  Positive selection of protective variants for type 2 diabetes from the Neolithic onward: a case study in Central Asia

  • Laure Ségurel
  • , Frederic Austerlitz
  •  & Evelyne Heyer

• Article | 30 May 2012

  A novel missense mutation in the signal peptide of the human POMC gene: a possible additional link between early-onset type 2 diabetes and obesity

  • Monica Mencarelli
  • , Alessandra Zulian
  •  & Cecilia Invitti

• Short Report | 01 February 2012

  1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data

  • Jie Huang
  • , David Ellinghaus
  •  & Yun Li

• Article | 02 February 2011

  Heterogeneity of genetic associations of CDKAL1 and HHEX with susceptibility of type 2 diabetes mellitus by gender

  • Hyunju Ryoo
  • , Jiyoung Woo
  •  & Chaeyoung Lee