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

John Garcia

MACOM (United States)

ORCID: 0000-0001-6631-4174

Also affiliated with Invitae (United States)

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 5%percentile
0.481Author 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.

Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM)

Journal of Molecular Diagnostics(2021)10.1016/j.jmoldx.2021.01.014
Top 40%
0.481DataRank
Top 40%8 citations

Alexander Ing, Christian Antolik, Christina Austin‐Tse, Linnea M. Baudhuin, Lucas Bronicki +25 more

Papers

Driven by 8 papers — median percentile 60. Top paper: “Using an integrated knowledge translation approach to build a public health research agenda”.

Using an integrated knowledge translation approach to build a public health research agenda

Health Research Policy and Systems(2014)10.1186/1478-4505-12-6
N/A
0.489DataRank · unranked
25 citations

Sandra Regan, Dana Gore, Ruta Valaitis, John Garcia, Heather Manson +2 more

Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM)

Journal of Molecular Diagnostics(2021)10.1016/j.jmoldx.2021.01.014
Top 40%
0.481DataRank
Top 40%8 citations

Alexander Ing, Christian Antolik, Christina Austin‐Tse, Linnea M. Baudhuin, Lucas Bronicki +25 more

Decreased heart dose with deep inspiration breath hold for the treatment of gastric lymphoma with IMRT

Clinical and Translational Radiation Oncology(2020)10.1016/j.ctro.2020.05.013
N/A
0DataRank · unranked
18 citations

Jillian R. Gunther, Penny Fang, Stacy L. Peterson, Karen Roach, Pei-Fong Wong +9 more

Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death

European Heart Journal(2021)10.1093/eurheartj/ehab687
N/A
0DataRank · unranked
145 citations

Arnon Adler, Ahmad S. Amin, Emanuela Abiusi, Melanie Care, Hennie Bikker +15 more

An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome

Circulation(2020)10.1161/circulationaha.119.043132
N/A
0DataRank · unranked
402 citations

Valeria Novelli, Ahmad S. Amin, Emanuela Abiusi, Melanie Care, Eline A. Nannenberg +14 more

Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group

Genetics in Medicine(2023)10.1016/j.gim.2023.101036
N/A
0DataRank · unranked
70 citations

Marcie Steeves, Pınar Bayrak‐Toydemir, Katherine A. Benson, Bradley P. Coe, Laura K. Conlin +42 more

The genetic architecture of Plakophilin 2 cardiomyopathy

Genetics in Medicine(2021)10.1038/s41436-021-01233-7
N/A
0DataRank · unranked
36 citations

Anna Kirillova, Chloe Reuter, John Garcia, Hana Zouk, Megan Hawley +28 more

An assessment of the role of vinculin loss of function variants in inherited cardiomyopathy

Human Mutation(2020)10.1002/humu.24061
N/A
0DataRank · unranked
19 citations

Naif A. M. Almontashiri, Leslie G. Biesecker, Natalie Berger, Wendy K. Chung, John Garcia +17 more