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

Raúl Tonda

Centro Nacional de Análisis Genómico

ORCID: 0000-0001-7893-2404

Also affiliated with Universitat de Barcelona

Biochemistry, Genetics and Molecular BiologyMedicine

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 2%percentile
2.0Author 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.

precisionFDA Truth Challenge V2: Calling variants from short- and long-reads in difficult-to-map regions

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.13.380741
Top 11%
2.0DataRank
Top 11%67 citations

Justin Wagner, Jennifer McDaniel, Sarah H. Stephens, Samuel T. Westreich, Anish G. Prasanna +68 more

Papers

Driven by 5 papers — median percentile 89. Top paper: “precisionFDA Truth Challenge V2: Calling variants from short- and long-reads in difficult-to-map regions”.

precisionFDA Truth Challenge V2: Calling variants from short- and long-reads in difficult-to-map regions

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.13.380741
Top 11%
2.0DataRank
Top 11%67 citations

Justin Wagner, Jennifer McDaniel, Sarah H. Stephens, Samuel T. Westreich, Anish G. Prasanna +68 more

The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases

Human Mutation(2022)10.1002/humu.24353
N/A
1.3DataRank · unranked
63 citations

Davide Piscia, Leslie Matalonga, Alberto Corvò, Carles García, Marcos Fernández-Callejo +46 more

Host genetic and immune factors drive evasion of HIV-1 pathogenesis in viremic non-progressors

Med(2024)10.1016/j.medj.2024.09.007
N/A
0.487DataRank · unranked
11 citations

Inmaculada Hernández, Judith Dalmau, Juan C. Nieto, Víctor Urrea, Lidia Garrido-Sanz +19 more

Exome-wide rare variant analysis in familial essential tremor

Parkinsonism & Related Disorders(2020)10.1016/j.parkreldis.2020.11.021
N/A
0DataRank · unranked
15 citations

Gabrielle Houle, Sara Ortega‐Cubero, Sara Bandrés‐Ciga, Ignacio Álvarez, María Cárcel +28 more

IDENTIFICATION OF MODIFIER GENE VARIANTS OVERREPRESENTED IN FAMILIAL HYPOMAGNESEMIA WITH HYPERCALCIURIA AND NEPHROCALCINOSIS PATIENTS WITH A MORE AGGRESSIVE RENAL PHENOTYPE

medRxiv(2023)10.1101/2023.11.08.23298254
N/A
0DataRank · unranked
3 citations

Jordi Morata, M. Durán, Joseph Torchia, Raúl Tonda, M Ferrer +6 more