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Olaf Rieß

Observed names: O Rieß, O. Rieß, Olaf Riess, Riess, Olaf
OpenAlex ID: A5113544213
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
2016 · Suzanne Lesage, Valérie Drouet, et al. · The American Journal of Human Genetics · 459
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Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
2017 · Laurie A Robak, Iris E Jansen, et al. · Brain · 438
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Solving patients with rare diseases through programmatic reanalysis of genome-phenome data
2021 · Leslie Matalonga, Carles Hernández-Ferrer, et al. · European Journal of Human Genetics · 69
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Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses
2025 · Steven Laurie, Wouter Steyaert, et al. · Nature Medicine · 63
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Solving unsolved rare neurological diseases—a Solve-RD viewpoint
2021 · Rebecca Schüle, Dagmar Timmann, et al. · European Journal of Human Genetics · 19
The genetic landscape of sporadic adult-onset degenerative ataxia: a multi-modal genetic study of 377 consecutive patients from the longitudinal multi-centre SPORTAX cohort
2025 · Danique Beijer, David Mengel, et al. · EBioMedicine · 16
An interconnected data infrastructure to support large-scale rare disease research
2024 · Lennart F Johansson, Steve Laurie, et al. · GigaScience · 10
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Konsensusempfehlung des Deutschen Konsortiums Familiärer Brust- und Eierstockkrebs zum Umgang mit Ergebnissen der Multigenanalyse
2018 · Anke Waha, Beatrix Versmold, et al. · TumorDiagnostik & Therapie · 6
Medizinische Genetik für die Praxis
2014 · Ute Moog, Olaf Rieß, et al. · Thieme eBooks · 5
Behandlungs- und Forschungszentrum für Seltene Erkrankungen Tübingen
2010 · O. Rieß, H. Graessner · Medizinische Genetik · 4
Publisher Correction: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses
2025 · Steven Laurie, Wouter Steyaert, et al. · Nature Medicine · 1
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Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data
2021 · Leslie Matalonga, Carles Hernández-Ferrer, et al. · European Journal of Human Genetics · 1
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Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
2021 · Birte Zurek, Kornelia Ellwanger, et al. · European Journal of Human Genetics · 1
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Gentherapie neurologischer Erkrankungen
1998 · O. Rieß · Springer eBooks · 1
Genomic correlates of metastatic competence and progression in human melanoma
2026 · Eftychia Chatziioannou, Karan Luthria, et al. · bioRxiv (Cold Spring Harbor Laboratory)
Additional file 5 of Brain region-resolved pharmacodynamics of an antisense oligonucleotide targeting human SNCA 3′UTR in BAC-hSNCA rats
2026 · Marianna Naki, Fedon-Giasin Kattan, et al. · Figshare
Implementation of a medical genomics program for rare diseases in Uruguay
2026 · Camila Simoes, María Fernanda Domínguez, et al. · Orphanet Journal of Rare Diseases
Additional file 1 of Implementation of a medical genomics program for rare diseases in Uruguay
2026 · Camila Simoes, María Fernanda Domínguez, et al. · Figshare
Additional file 2 of Implementation of a medical genomics program for rare diseases in Uruguay
2026 · Camila Simoes, María Fernanda Domínguez, et al. · Figshare
Additional file 3 of Implementation of a medical genomics program for rare diseases in Uruguay
2026 · Camila Simoes, María Fernanda Domínguez, et al. · Figshare
Additional file 4 of Implementation of a medical genomics program for rare diseases in Uruguay
2026 · Camila Simoes, María Fernanda Domínguez, et al. · Figshare
Correction to: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses (Nature Medicine, (2025), 31, 2, (478-489), 10.1038/s41591-024-03420-w)
2025 · Steven Laurie, Wouter Steyaert, et al. · Newcastle University ePrints (Newcastle Univesity)
Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 10.1038/s41431-021-00901-1)
2021 · Rebecca Schüle, Dagmar Timmann, et al. · Newcastle University ePrints (Newcastle Univesity)
The Treatabolome Database and Platform: enhancing Rare Diseases’ treatment visibility.
2021 · Hernandez-Ferrer, Carles, Matalonga, Leslie, et al. · HAL
Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint
2021 · Rebecca Schüle, Dagmar Timmann, et al. · European Journal of Human Genetics
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Works count: 30
Citation count: 1,095
H-index: 7
I10-index: 7
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