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

Federico De Marchi

Istituto Oncologico Veneto

ORCID: 0000-0002-0376-663X
Medicine

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 1 paper. Top paper: “Whole‐exome sequencing identifies functional classes of gene mutations associated with bone marrow failure in pediatric Fanconi Anemia patients”.

Whole‐exome sequencing identifies functional classes of gene mutations associated with bone marrow failure in pediatric Fanconi Anemia patients

European Journal Of Haematology(2021)10.1111/ejh.13645
N/A
0DataRank · unranked
0 citations

Natalia Zbib, Alyza Skaist, Jiang Gui, Rafael Madero‐Marroquin, Federico De Marchi +4 more