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

Vicente Vicente

Instituto de Salud Carlos III

ORCID: 0000-0002-4278-3264

Also affiliated with Centre for Biomedical Network Research on Rare Diseases, Centro Regional de Hemodonación, Universidad de Murcia

MedicineBiochemistry, 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 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 3 papers. Top paper: “A novel genetic variant in PTGS1 affects N‐glycosylation of cyclooxygenase‐1 causing a dominant‐negative effect on platelet function and bleeding diathesis”.

A novel genetic variant in PTGS1 affects N‐glycosylation of cyclooxygenase‐1 causing a dominant‐negative effect on platelet function and bleeding diathesis

American Journal of Hematology(2020)10.1002/ajh.26076
N/A
0DataRank · unranked
4 citations

Marilena Crescente, María Eugenia de la Morena‐Barrio, Melissa V. Chan, Elena Almarza, Nuria Revilla +24 more

Expanding the genetic spectrum of TUBB1-related thrombocytopenia

Blood Advances(2021)10.1182/bloodadvances.2020004057
N/A
0DataRank · unranked
37 citations

Loredana Bury, Shinji Kunishima, Marı́a Luisa Lozano, Agustín Rodríguez‐Alén, Nuria Revilla +15 more

Full-length antithrombin frameshift variant with aberrant C-terminus causes endoplasmic reticulum retention with a dominant-negative effect

JCI Insight(2022)10.1172/jci.insight.161430
N/A
0DataRank · unranked
13 citations

Mara Toderici, Joseph E. Chambers, José A. Martínez‐Menárguez, Pedro Garrido, Horacio Pérez‐Sánchez +10 more