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Diabetes Care|November 12, 2009
Clinical heterogeneity in monogenic diabetes caused by mutations in the glucokinase gene (GCK-MODY)Antonio L Cuesta-Muñoz, Tiinamaija Tuomi, Nadia Cobo-Vuilleumier, et al.
Diabetes|March 19, 2008
A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ channel activity and beta-cell glucose sensing is associated with type 2 diabetes in adultsAndrei I Tarasov, Tamara J Nicolson, Jean-Pierre Riveline, et al.
The Journal of Biological Chemistry|April 2, 2011
Endospanins regulate a postinternalization step of the leptin receptor endocytic pathwayKarin Séron, Cyril Couturier, Sandrine Belouzard, et al.
The Journal of Biological Chemistry|November 9, 2011
Human mutation within Per-Arnt-Sim (PAS) domain-containing protein kinase (PASK) causes basal insulin hypersecretionFrancesca Semplici, Martine Vaxillaire, Sarah Fogarty, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|May 18, 2012
Tryptophan metabolism activation by indoleamine 2,3-dioxygenase in adipose tissue of obese women: an attempt to maintain immune homeostasis and vascular toneIsabelle Wolowczuk, Benjamin Hennart, Audrey Leloire, et al.
Plos One|June 22, 2016
Post-Bariatric Surgery Changes in Quinolinic and Xanthurenic Acid Concentrations Are Associated with Glucose HomeostasisMarie Favennec, Benjamin Hennart, Marie Verbanck, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humansAnne-Kathrin Wermter, André Scherag, David Meyre, et al.
Diabetes|August 5, 2009
Common genetic variation near melatonin receptor MTNR1B contributes to raised plasma glucose and increased risk of type 2 diabetes among Indian Asians and European CaucasiansJohn C Chambers, Weihua Zhang, Delilah Zabaneh, et al.
Human Molecular Genetics|October 2, 2002
Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels and contribute to the genetic risk for type 2 diabetes in French CaucasiansFrancis Vasseur, Nicole Helbecque, Christian Dina, et al.
Plos One|June 30, 2015
Truncating Homozygous Mutation of Carboxypeptidase E (CPE) in a Morbidly Obese Female with Type 2 Diabetes Mellitus, Intellectual Disability and Hypogonadotrophic HypogonadismSuzanne I M Alsters, Anthony P Goldstone, Jessica L Buxton, et al.
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