Simone Zittel

Also affiliated with University Medical Center Hamburg-Eppendorf

MedicineNeuroscience

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 8 papers. Top paper: “The R1441C-LRRK2 mutation induces myeloid immune cell exhaustion in an age- and sex-dependent manner”.

The R1441C-LRRK2 mutation induces myeloid immune cell exhaustion in an age- and sex-dependent manner

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.12.562063

N/A

0.165DataRank · unranked

2 citations

Karen N. McFarland, Hannah A. Staley, Noelle Neighbarger, Susen Schaake, Norbert Brüggemann +6 more

RAB32 -linked Parkinson’s disease: Deep phenotyping, MDSGene literature review, and application of SynNeurGe criteria

medRxiv(2025)10.1101/2025.06.03.25328628

N/A

0.104DataRank · unranked

1 citations

Francesco Cavallieri, Max Borsche, Giulia Toschi, Franco Valzania, Valentina Fioravanti +22 more

Genetic Risk Factors in Isolated Dystonia Escape Genome‐Wide Association Studies

Movement Disorders(2024)10.1002/mds.29968

N/A

0DataRank · unranked

4 citations

Katja Lohmann, Eva‐Juliane Vollstedt, Tobias Reinberger, Lisa‐Marie Nuxoll, Gamze Kilic‐Berkmen +53 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

Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large‐Scale Exome Sequencing

Annals of Clinical and Translational Neurology(2025)10.1002/acn3.70100

N/A

0DataRank · unranked

13 citations

Fabian Ott, Sebastian Loens, Gamze Kilic‐Berkmen, Ai Huey Tan, Shen‐Yang Lim +43 more

RAB32 ‐Linked Parkinson's Disease: Deep Phenotyping, MDSGene Literature Review, and Application of SynNeurGe Criteria

Movement Disorders(2025)10.1002/mds.70037

N/A

0DataRank · unranked

5 citations

Francesco Cavallieri, Max Borsche, Giulia Toschi, Franco Valzania, Valentina Fioravanti +23 more

Genetic Diversity and Expanded Phenotypes in Dystonia: Insights from Large-Scale Exome Sequencing

medRxiv(2024)10.1101/2024.12.02.24316741

N/A

0DataRank · unranked

5 citations

Fabian Ott, Sebastian Loens, Gamze Kilic‐Berkmen, Ai Huey Tan, Shen‐Yang Lim +42 more

The R1441C-Lrrk2 mutation induces myeloid immune cell exhaustion in an age- and sex-dependent manner in mice

Science Translational Medicine(2024)10.1126/scitranslmed.adl1535

N/A

0DataRank · unranked

14 citations

Karen N. McFarland, Hannah A. Staley, Noelle Neighbarger, Susen Schaake, Norbert Brüggemann +6 more