Jürgen Neesen

3PUBLICATIONS
29CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsPredictive and prognostic markers
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Publications (3)

|Feb 24, 2024
Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria.

Alexandra Frohne, Sybille Vrabel, Franco Laccone

|Nov 29, 2022
A homozygous AP3D1 missense variant in patients with sensorineural hearing loss as the leading manifestation.

Alexandra Frohne, Martin Koenighofer, Hakan Cetin

|Oct 13, 2018
Genome amplification and cellular senescence are hallmarks of human placenta development.

Philipp Velicky, Gudrun Meinhardt, Kerstin Plessl

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