Axel Schmidt

13PUBLICATIONS
229CO-AUTHORS
Cell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)Host-parasite interactionsGene mappingNeurogenetics
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Publications (13)

|Aug 20, 2026
A homozygous lamin B receptor variant resulting in Pelger-Huët anomaly without skeletal dysplasia.

|Jul 08, 2026
Polygenic scores as modifiers in Mendelian diseases.

|Feb 19, 2026
Host control of persistent Epstein-Barr virus infection.

Axel Schmidt, T Madhusankha Alawathurage, Friederike S David

|Feb 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Benita Menden, Rana D Incebacak Eltemur, German Demidov

|Jun 24, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Axel Schmidt, Magdalena Danyel, Kathrin Grundmann

|May 21, 2025
Genome-wide association study of long COVID.

Vilma Lammi, Tomoko Nakanishi, Samuel E Jones

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Frequent Collaborators

5 joint publications

Tobias Haack

5 joint publications

Hannah Klinkhammer

5 joint publications

Peter M Krawitz

5 joint publications

Markus Nöthen