Olaf Riess

24PUBLICATIONS
293CO-AUTHORS
NeonatologyGene mappingMajor global burdens of diseaseGenomicsNeurogenetics
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Publications (24)

|Aug 14, 2026
Prenatal Phenotypic Features of Five Fetal Cases With RNU4ATAC-Associated Microcephalic Osteodysplastic Primordial Dwarfism Type I.

|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

|Jan 08, 2026
Prevention of ubiquitination at K6 and K9 in mutant huntingtin exacerbates disease pathology in a knock-in mouse model.

Pengfei Qi, Libo Yu-Taeger, Hezhou Han

|Oct 15, 2025
Germany's national genomDE strategy.

Andreas Till, Roman A Siddiqui, Christian Altbürger

|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

|Jun 13, 2025
Long-Read Sequencing Identifies Mosaic Sequence Variations in Friedreich's Ataxia-GAA Repeats.

Joohyun Park, Claudia Dufke, Zofia Fleszar

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Frequent Collaborators

8 joint publications

Marc Sturm

7 joint publications

Tobias Haack

6 joint publications

Jeannette Huebener-Schmid

5 joint publications

Priscila Pereira Sena