Eric Wenzel

3PUBLICATIONS
9CO-AUTHORS
Child and adolescent developmentCrystallographyGene expression (incl. microarray and other genome-wide approaches)
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Publications (3)

|Jul 29, 2025
Uniparental disomy leads to a novel cause of MC2R-related familial glucocorticoid deficiency type 1.

Amica Corda Müller-Nedebock, Eric Wenzel, Roland Pfäffle

|Jun 16, 2025
Detecting monogenic obesity: a systematic exome-wide workup of over 500 individuals.

Robert Künzel, Helene Faust, Linnaeus Bundalian

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