John Neidhardt

10PUBLICATIONS
85CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Optical technologyNeurology and neuromuscular diseasesFood sustainabilityDevelopmental genetics (incl. sex determination)
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Publications (10)

|Aug 27, 2026
Genetic Findings in Seven Cochlear Implanted Patients with Severe-to-Profound Hearing Loss.

|Mar 13, 2026
CACNB3 defects are associated with infantile idiopathic nystagmus.

Christoph Jüschke, Kira Linsel, Marta Owczarek-Lipska

|Oct 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function.

Reza Asadollahi, Aisha Ahmad, Paranchai Boonsawat

|Mar 11, 2024
Rich microbial and depolymerising diversity in Antarctic krill gut.

Lars Möller, Yevhen Vainshtein, Bettina Meyer

|Aug 04, 2023
Skewed X-inactivation is associated with retinal dystrophy in female carriers of RPGR mutations.

Muhammad Usman, Christoph Jüschke, Fei Song

|Mar 29, 2023
In Vivo Efficacy and Safety Evaluations of Therapeutic Splicing Correction Using U1 snRNA in the Mouse Retina.

Sebastian Swirski, Oliver May, Malte Ahlers

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Frequent Collaborators

3 joint publications

Christoph Jüschke

2 joint publications

Anja U Bräuer

1 joint publications

Vesna Jakšić

1 joint publications

Isabel Gross