Peter Kühnen

12PUBLICATIONS
78CO-AUTHORS
Gene and molecular therapyRecommender systemsCancer geneticsNutrigenomics and personalised nutritionAdolescent health
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Publications (12)

|Aug 14, 2026
Precision Medicine in patients with rare forms of genetic obesity: Necessity for coordinated and structured care.

|Nov 18, 2025
RareLink: scalable REDCap-based framework for rare disease interoperability linking international registries to FHIR and Phenopackets.

Adam S L Graefe, Filip Rehburg, Samer Alkarkoukly

|Jun 25, 2025
Hyperphagia in rare melanocortin-4 receptor pathway diseases: therapeutic options and assessing treatment response.

Jesús Argente, Karine Clément, Jessica Duis

|May 19, 2025
Linking international registries to FHIR and Phenopackets with RareLink: a scalable REDCap-based framework for rare disease data interoperability.

Adam S L Graefe, Filip Rehburg, Samer Alkarkoukly

|Jan 24, 2025
Defining Hyperphagia for Improved Diagnosis and Management of MC4R Pathway-Associated Disease: A Roundtable Summary.

Steven B Heymsfield, Karine Clément, Beatrice Dubern

|Mar 29, 2024
Insulin Secretion Defect in Children and Adolescents with Obesity: Clinical and Molecular Genetic Characterization.

Helena Enders-Seidlitz, Klemens Raile, Maolian Gong

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Frequent Collaborators

4 joint publications

Susanna Wiegand

2 joint publications

Sophie A I Klopfenstein

2 joint publications

Thomas Debertshäuser

2 joint publications

Alexander Bartschke