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

Sanja Rogić

University of British Columbia

ORCID: 0000-0002-9988-3661

Also affiliated with Canada's Michael Smith Genome Sciences Centre

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

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 3 papers. Top paper: “ModelMatcher: A scientist‐centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research”.

ModelMatcher: A scientist‐centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research

Human Mutation(2022)10.1002/humu.24364

N/A

0.425DataRank · unranked

16 citations

Lucian Li, Sanja Rogić, Guillaume Poirier‐Morency, Seon-Young Kim, Undiagnosed Diseases Network +8 more

ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.30.462504

N/A

0DataRank · unranked

3 citations

Lucian Li, Sanja Rogić, Guillaume Poirier‐Morency, Seon-Young Kim, Undiagnosed Diseases Network +8 more

Revealing function-altering MECP2 mutations in individuals with autism spectrum disorder using yeast and Drosophila

Genetics(2025)10.1093/genetics/iyaf121

N/A

0DataRank · unranked

3 citations

Jessica Schmitt, Graeme H. McIntosh, Barry P. Young, Tianshun Lian, Jie Liu +14 more