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

Ronak Y. Patel

Wyle (United States)

ORCID: 0000-0001-8111-7363

Also affiliated with AISECT University, Ministry of AYUSH, Barkatullah University

Biochemistry, 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 3%percentile
1.0Author DataRank

Indexed papers

2in 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 2 indexed papers 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.

CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase

Nucleic Acids Research(2022)10.1093/nar/gkac979
Top 19%
1.0DataRank
Top 19%46 citations

Arpad Danos, Jason Saliba, Joshua F. McMichael, Adam Coffman, Susanna Kiwala +60 more

Papers

Driven by 8 papers — median percentile 40. Top paper: “Allele-specific epigenome maps reveal sequence-dependent stochastic switching at regulatory loci”.

Allele-specific epigenome maps reveal sequence-dependent stochastic switching at regulatory loci

Science(2018)10.1126/science.aar3146
N/A
3.6DataRank · unranked
123 citations

Eugene Lurie, Ivenise Carrero, Piotr Pawliczek, Ronak Y. Patel, Joel Rozowsky +15 more

ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines

Genome Medicine(2022)10.1186/s13073-021-01004-8
N/A
2.6DataRank · unranked
85 citations

Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L Goldstein, Xi Luo +30 more

CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase

Nucleic Acids Research(2022)10.1093/nar/gkac979
Top 19%
1.0DataRank
Top 19%46 citations

Arpad Danos, Jason Saliba, Joshua F. McMichael, Adam Coffman, Susanna Kiwala +60 more

The GA4GH Variation Representation Specification (VRS): a Computational Framework for the Precise Representation and Federated Identification of Molecular Variation

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.15.426843
N/A
0DataRank · unranked
11 citations

Lawrence Babb, Gil Alterovitz, Michael Baudis, Matthew Brush, Daniel Cameron +22 more

ClinGen Variant Curation Interface: A Variant Classification Platform for the Application of Evidence Criteria from ACMG/AMP Guidelines

medRxiv(2021)10.1101/2021.02.12.21251663
N/A
0DataRank · unranked
5 citations

Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L Goldstein, Xi Luo +30 more

Evolution of the open-access CIViC knowledgebase is driven by the needs of the cancer variant interpretation community

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.13.448171
Top 100%
0DataRank
Top 100%0 citations

Arpad Danos, Susanna Kiwala, Joshua F. McMichael, Adam Coffman, Erica K. Barnell +47 more

The GA4GH Variation Representation Specification: A computational framework for variation representation and federated identification

Cell Genomics(2021)10.1016/j.xgen.2021.100027
N/A
0DataRank · unranked
56 citations

Lawrence Babb, Gil Alterovitz, Michael Baudis, Matthew Brush, Daniel Cameron +23 more

ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants

UNC Libraries(2020)10.17615/0r6z-dk65
N/A
0DataRank · unranked
0 citations

Kevin Riehle, Heidi L. Rehm, Rajarshi Ghosh, Tristan H Nelson, Aaron B. Baker +16 more