Jörg Schmidtke
6PUBLICATIONS
15CO-AUTHORS
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Publications (6)
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|Mar 05, 2024
Diagnostic elusiveness of pathogenic variants in cases of autosomal recessive diseases.Jörg Schmidtke, Sebastian Koch, Michael Krawczak
|Sep 23, 2022
Twenty-Five Years of Contemplating Genotype-Based Hereditary Hemochromatosis Population Screening.Jörg Schmidtke
|Apr 23, 2022
PanelDesign: Integrating Epidemiological Information into the Design of Diagnostic NGS Gene Panels.Jörg Schmidtke, Peter Philipp, Kathrin Rommel
|Sep 22, 2018
Metadata Correction: Conceptualization and Implementation of the Central Information Portal on Rare Diseases: Protocol for a Qualitative Study.Svenja Litzkendorf, Tobias Hartz, Jens Göbel
|May 13, 2018
Conceptualization and Implementation of the Central Information Portal on Rare Diseases: Protocol for a Qualitative Study.Svenja Litzkendorf, Tobias Hartz, Jens Göbel
|Aug 27, 2016
Adopting Quality Criteria for Websites Providing Medical Information About Rare Diseases.Frédéric Pauer, Jens Göbel, Holger Storf
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Frequent Collaborators
3 joint publications
Frédéric Pauer
3 joint publications
Jens Göbel
3 joint publications
Holger Storf
3 joint publications
Svenja Litzkendorf
3 joint publications
Ana Babac
3 joint publications
Martin Frank
3 joint publications
Verena Lührs
3 joint publications
Franziska Schauer
3 joint publications
Tof Wagner
3 joint publications
Johann-Matthias Graf von der Schulenburg
