Olaf H. Riess
Hoppe Seyler Str. 3
Tuebingen, BW 72076, Germany
Tuebingen, BW 72076, Germany
Last Updated: 09/26/2026
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Found 252 publications
Prenatal Phenotypic Features of Five Fetal Cases With RNU4ATAC-Associated Microcephalic Osteodysplastic Primordial Dwarfism Type I.
Journal: Prenatal diagnosis
Published: May 07, 2026
Implementation of a medical genomics program for rare diseases in Uruguay.
Journal: Orphanet journal of rare diseases
Published: February 26, 2026
Prevention of ubiquitination at K6 and K9 in mutant huntingtin exacerbates disease pathology in a knock-in mouse model.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: January 08, 2026
Association of rare apolipoprotein E ε4 homozygosity with an earlier age at onset in spinocerebellar ataxia type 3.
Journal: Human molecular genetics
Published: December 23, 2025
Genetic contribution to severe COVID-19 in adults under 60 years without major comorbidities in the German National Pandemic Cohort Network (NAPKON).
Journal: Human genomics
Published: November 07, 2025
Altered light-dark phase-dependent behavioral responses and suprachiasmatic nucleus pathology in an α-synuclein rat model of Parkinson's disease.
Journal: NPJ Parkinson's disease
Published: October 09, 2025
Dysregulated NK-cell gene expression defines the enduring symptoms of long COVID-19.
Journal: Frontiers in immunology
Published: October 08, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Journal: Nature genetics
Published: June 24, 2025
Influence of ATXN2 intermediate CAG repeats, 9bp duplication and alternative splicing on SCA3 pathogenesis.
Journal: Acta neuropathologica communications
Published: June 24, 2025
Last Updated: 09/26/2026