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Mobile Genetic Elements|October 23, 2012
Alu elements and human common diseases like obesityPeter Kuehnen, Heiko KrudeJournal of Diabetes Research|March 29, 2024
Insulin Secretion Defect in Children and Adolescents with Obesity: Clinical and Molecular Genetic CharacterizationHelena Enders-Seidlitz, Klemens Raile, Maolian Gong, et al.Endocrinology|March 24, 2011
Protein phosphatase 1 (PP-1)-dependent inhibition of insulin secretion by leptin in INS-1 pancreatic β-cells and human pancreatic isletsPeter Kuehnen, Katharina Laubner, Klemens Raile, et al.Plos Genetics|March 23, 2012
An Alu element-associated hypermethylation variant of the POMC gene is associated with childhood obesityPeter Kuehnen, Mona Mischke, Susanna Wiegand, et al.Molecular Genetics & Genomic Medicine|April 11, 2019
HDAC4 mutations cause diabetes and induce β-cell FoxO1 nuclear exclusionMaolian Gong, Yong Yu, Lei Liang, et al.Hormone Research in Paediatrics|January 19, 2026
Unmet Medical Needs in Pediatric EndocrinologyStefano Cianfarani, Sommayya Aftab, Kanetee Busiah, et al.Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Linking international registries to FHIR and Phenopackets with RareLink: a scalable REDCap-based framework for rare disease data interoperabilityAdam S L Graefe, Filip Rehburg, Samer Alkarkoukly, et al.Pageof 1