Olaf Rieß

Bernstein Center for Computational Neuroscience Tübingen

Also affiliated with University of Tübingen

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 5%percentile

0.345Author DataRank

Indexed papers

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Progression of biological markers in spinocerebellar ataxia type 3: longitudinal analysis of prospective data from the ESMI cohort

The Lancet Regional Health - Europe(2025)10.1016/j.lanepe.2025.101339

Top 51%

0.345DataRank

Top 51%9 citations

Héctor García‐Moreno, Mónica Ferreira, Jeannette Hübener‐Schmid, Tamara Schaprian, Philipp Wegner +47 more

Papers

Driven by 14 papers — median percentile 49. Top paper: “The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases”.

The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases

Human Mutation(2022)10.1002/humu.24353

N/A

1.3DataRank · unranked

63 citations

Davide Piscia, Leslie Matalonga, Alberto Corvò, Carles García, Marcos Fernández-Callejo +46 more

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.015

N/A

0.604DataRank · unranked

55 citations

Mona Grimmel, Matias Wagner, J. Christopher Hennings, Christian Marx, René G. Feichtinger +41 more

Genomes in clinical care

npj Genomic Medicine(2024)10.1038/s41525-024-00402-2

N/A

0.510DataRank · unranked

29 citations

Marc Sturm, Benita Menden, Alexandra Liebmann, German Demidov, Dennis Witt +10 more

Stage‐Dependent Biomarker Changes in Spinocerebellar Ataxia Type 3

Annals of Neurology(2023)10.1002/ana.26824

N/A

0.505DataRank · unranked

28 citations

Moritz Berger, Carlo Wilke, Jeannette Hübener‐Schmid, Tamara Schaprian, Magda M. Santana +34 more

Brain malformations and seizures by impaired chaperonin function of TRiC

Science(2024)10.1126/science.adp8721

N/A

0.489DataRank · unranked

25 citations

Piere Rodriguez-Aliaga, Weimin Yuan, Lena Franken, Kamil K. Zajt, Dimah Hasan +82 more

Progression of biological markers in spinocerebellar ataxia type 3: longitudinal analysis of prospective data from the ESMI cohort

The Lancet Regional Health - Europe(2025)10.1016/j.lanepe.2025.101339

Top 51%

0.345DataRank

Top 51%9 citations

Héctor García‐Moreno, Mónica Ferreira, Jeannette Hübener‐Schmid, Tamara Schaprian, Philipp Wegner +47 more

Bi-allelic KICS2 mutations impair KICSTOR complex-mediated mTORC1 regulation, causing intellectual disability and epilepsy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.019

N/A

0.269DataRank · unranked

5 citations

Martin D. Burkhalter, Chrisovalantou Huridou, Linda Sofan, Timo Roser, Kirsten Cremer +29 more

Blood and cerebellar abundance of ATXN3 splice variants in spinocerebellar ataxia type 3/Machado-Joseph disease

Neurobiology of Disease(2024)10.1016/j.nbd.2024.106456

N/A

0DataRank · unranked

8 citations

Jeannette Hübener‐Schmid, Rebecca Tagett, Ana F. Ferreira, Ana Rosa Vieira Melo, João Vasconcelos +18 more

A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutations

Blood(2024)10.1182/blood.2023022576

N/A

0DataRank · unranked

6 citations

Е. А. Деордиева, Larissa Doll, Mohammad ElGamacy, Benjamin Dannenmann, Joana Azevedo +24 more

Alpha-synuclein research: defining strategic moves in the battle against Parkinson’s disease

npj Parkinson s Disease(2021)10.1038/s41531-021-00203-9

N/A

0DataRank · unranked

178 citations

Thomas Gasser, Robert H. Edwards, Markus Zweckstetter, Ronald Melki, Leonidas Stefanis +15 more

Calpain-1 ablation partially rescues disease-associated hallmarks in models of Machado-Joseph disease

Human Molecular Genetics(2020)10.1093/hmg/ddaa010

N/A

0DataRank · unranked

19 citations

Eva Haas, Yacine Maringer, Stefan Hauser, Nicolas Casadei, Athar H. Chishti +3 more

Stage-dependent biomarker changes in spinocerebellar ataxia type 3

medRxiv(2023)10.1101/2023.04.21.23287817

N/A

0DataRank · unranked

10 citations

Moritz Berger, Carlo Wilke, Jeannette Hübener‐Schmid, Tamara Schaprian, Magda M. Santana +34 more

GGC expansion in ZFHX3 causes SCA4 and impairs autophagy

medRxiv(2023)10.1101/2023.10.26.23297560

N/A

0DataRank · unranked

3 citations

Caspar Groß, Elena Buena Atienza, Sharan Paul, Mandi Gandelman, Tobias B. Haack +25 more

Blood and cerebellar abundance of ATXN3 splice variants in spinocerebellar ataxia type 3/Machado-Joseph disease

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.22.537936

N/A

0DataRank · unranked

1 citations

Jeannette Hübener‐Schmid, Rebecca Tagett, Ana F. Ferreira, Ana Rosa Vieira Melo, João Vasconcelos +19 more

Olaf Rieß

Indexed papers

Top data-sharing exemplar

Papers