Julia Hentschel

5PUBLICATIONS
89CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsMedical biochemistry - amino acids and metabolites
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Publications (5)

|Jan 28, 2026
Who Am I? Eyebrow Follicles Minimize Donor-Derived DNA for Germline Testing After Hematopoietic Stem Cell Transplantation.

Matthias Mertens, Mona Sadlo, Jörn-Sven Kühl

|Apr 16, 2025
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

Eric N Anderson, Stephan Drukewitz, Sukhleen Kour

|Mar 19, 2025
Reclassification of ATM Missense Variants of Uncertain Significance by Integrating Results from Systematic Functional Assays into an ACMG Points-Based Framework.

Helmut Hanenberg, Fan Zhang, Nikita Malev

|Oct 03, 2022
The constitutional gain-of-function variant p.Glu1099Lys in NSD2 is associated with a novel syndrome.

Bernt Popp, Melanie Brugger, Sibylle Poschmann

|Sep 09, 2022
Ketogenic Diet Treatment of Defects in the Mitochondrial Malate Aspartate Shuttle and Pyruvate Carrier.

Bigna K Bölsterli, Eugen Boltshauser, Luigi Palmieri

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