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Nature|August 7, 2024
DNA-sensing inflammasomes cause recurrent atherosclerotic strokeJiayu Cao, Stefan Roth, Sijia Zhang, et al.The Journal of Clinical Endocrinology and Metabolism|December 8, 2004
Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneitySharona Tornovsky, Ana Crane, Karen E Cosgrove, et al.The Journal of Clinical Endocrinology and Metabolism|February 10, 2015
Safety and efficacy of oral octreotide in acromegaly: results of a multicenter phase III trialShlomo Melmed, Vera Popovic, Martin Bidlingmaier, et al.Nature Genetics|July 3, 2007
Common variants in WFS1 confer risk of type 2 diabetesManjinder S Sandhu, Michael N Weedon, Katherine A Fawcett, et al.Nature Medicine|June 28, 2020
Publisher Correction: Building an international consortium for tracking coronavirus health statusEran Segal, Feng Zhang, Xihong Lin, et al.Cell Metabolism|March 12, 2013
Identification of a SIRT1 mutation in a family with type 1 diabetesAnna Biason-Lauber, Marianne Böni-Schnetzler, Basil P Hubbard, et al.Biorxiv : the Preprint Server for Biology|November 19, 2025
Latent plasticity of the human pancreas across development, health, and diseaseElisabetta Mereu, Diego Balboa, Johannes Liebig, et al.Plos Genetics|May 31, 2019
Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish populationManuel A Rivas, Brandon E Avila, Jukka Koskela, et al.Plos Genetics|May 26, 2018
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish populationManuel A Rivas, Brandon E Avila, Jukka Koskela, et al.Nature Genetics|March 4, 2014
Loss-of-function mutations in SLC30A8 protect against type 2 diabetesJason Flannick, Gudmar Thorleifsson, Nicola L Beer, et al.Pageof 24