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Olaf Riess

23PUBLICATIONS

287CO-AUTHORS

Gene mappingMajor global burdens of diseaseGenomicsNeurogeneticsMolecular evolution

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Publications (23)

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|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

|May 09, 2025

sc-MULTI-omics approach in nano-rare diseases: understanding the pathophysiological mechanism of Mulvihill-Smith Syndrome.

Angelika Riess, Cristiana Roggia, Antje Schulze Selting

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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

5 joint publications

Jonasz Jeremiasz Weber

4 joint publications

Nicolas Casadei

4 joint publications

German Demidov

4 joint publications

Rana Dilara Incebacak Eltemur

4 joint publications

Huu Phuc Nguyen

4 joint publications

Jakob Admard

Frequent Collaborators

8 joint publications

Marc Sturm

7 joint publications

Tobias Haack

6 joint publications

Jeannette Huebener-Schmid

5 joint publications

Priscila Pereira Sena

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