🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Dorota Hoffman‐Zacharska

Instytut Matki i Dziecka

ORCID: 0000-0001-7367-512X

Also affiliated with University of Warsaw

NeuroscienceMedicineBiochemistry, 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 6%percentile
0.332Author DataRank

Indexed papers

1in 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 1 indexed paper 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 →

Top data-sharing exemplar

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

Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Project

PLoS ONE(2023)10.1371/journal.pone.0292180
Top 52%
0.332DataRank
Top 52%7 citations

Harutyun Madoev, Anna Aasly, Azlina Ahmad‐Annuar, Bashayer Al‐Mubarak, Roy N. Alcalay +78 more

Papers

Driven by 6 papers — median percentile 48. Top paper: “Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications”.

Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications

Brain(2021)10.1093/brain/awab321
N/A
2.9DataRank · unranked
149 citations

Yuanyuan Liu, Mahmoud Koko, Cathrine E. Gjerulfsen, Lukas Sonnenberg, Julian Schubert +95 more

Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Project

PLoS ONE(2023)10.1371/journal.pone.0292180
Top 52%
0.332DataRank
Top 52%7 citations

Harutyun Madoev, Anna Aasly, Azlina Ahmad‐Annuar, Bashayer Al‐Mubarak, Roy N. Alcalay +78 more

De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies

Brain(2021)10.1093/brain/awab409
N/A
0DataRank · unranked
17 citations

Jolien Roovers, Noor Smal, Candace T. Myers, Dilşad Türkdoğan, Filip Roelens +29 more

Frequency of mutations in PRKN, PINK1, and DJ1 in Patients With Early-Onset Parkinson Disease from neighboring countries in Central Europe

Parkinsonism & Related Disorders(2021)10.1016/j.parkreldis.2021.03.026
N/A
0DataRank · unranked
15 citations

Jennifer A. Lindemann, Dorota Hoffman‐Zacharska, Alexandra I. Soto‐Beasley, Maria Barcikowska, Magdalena Boczarska‐Jedynak +25 more

Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications

medRxiv(2021)10.1101/2021.03.22.21253711
N/A
0DataRank · unranked
5 citations

Yuanyuan Liu, Cathrine E. Gjerulfsen, Mahmoud Koko, Lukas Sonnenberg, Julian Schubert +95 more

Cathepsin B p.Gly284Val Variant in Parkinson’s Disease Pathogenesis

International Journal of Molecular Sciences(2022)10.3390/ijms23137086
N/A
0DataRank · unranked
16 citations

Xu Hou, Jenny M. Bredenberg, Fabienne C. Fiesel, Liam T. Cocker, Alexandra I. Soto‐Beasley +33 more