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

John E. Gorzynski

Stanford Medicine

ORCID: 0000-0002-9034-9016

Also affiliated with Stanford 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 4%percentile
0.801Author 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.

High-throughput SARS-CoV-2 and host genome sequencing from single nasopharyngeal swabs

medRxiv(2020)10.1101/2020.07.27.20163147
Top 25%
0.801DataRank
Top 25%9 citations

Hannah N. De Jong, David Amar, Craig D. Hughes, Alexander G. Ioannidis, Rob Bierman +37 more

Papers

Driven by 13 papers — median percentile 75. Top paper: “Beyond the exome: What’s next in diagnostic testing for Mendelian conditions”.

Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.009
N/A
2.2DataRank · unranked
123 citations

Chloe Reuter, Shruti Marwaha, Medhat Mahmoud, Michael Duyzend, Hayk Barseghyan +91 more

High-throughput SARS-CoV-2 and host genome sequencing from single nasopharyngeal swabs

medRxiv(2020)10.1101/2020.07.27.20163147
Top 25%
0.801DataRank
Top 25%9 citations

Hannah N. De Jong, David Amar, Craig D. Hughes, Alexander G. Ioannidis, Rob Bierman +37 more

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

Genome Research(2025)10.1101/gr.279323.124
N/A
0.425DataRank · unranked
11 citations

Bohan Ni, Chloe Reuter, John E. Gorzynski, Sarah Fazal, Devon Bonner +13 more

Deconvoluting complex correlates of COVID-19 severity with a multi-omic pandemic tracking strategy

Nature Communications(2022)10.1038/s41467-022-32397-8
N/A
0DataRank · unranked
9 citations

Alexander G. Ioannidis, David Jimenez‐Morales, John E. Gorzynski, Hannah N. De Jong, Xiran Liu +65 more

A 3’UTR Insertion Is a Candidate Causal Variant at the TMEM106B Locus Associated with Increased Risk for FTLD-TDP

medRxiv(2023)10.1101/2023.07.06.23292312
N/A
0DataRank · unranked
11 citations

Yann Le Guen, Yi Zeng, John E. Gorzynski, Tanner Jensen, Chengran Yang +13 more

APOE loss-of-function variants: Compatible with longevity and associated with resistance to Alzheimer’s Disease pathology

medRxiv(2023)10.1101/2023.07.20.23292771
N/A
0DataRank · unranked
5 citations

Yann Le Guen, Sunny Chen, Eun-Gyung Lee, Lesley Leong, John E. Gorzynski +18 more

Local read haplotagging enables accurate long-read small variant calling

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.07.556731
N/A
0DataRank · unranked
4 citations

Daniel E. Cook, Maria Nattestad, Brandy McNulty, John E. Gorzynski, Sneha D. Goenka +8 more

APOE loss-of-function variants: Compatible with longevity and associated with resistance to Alzheimer’s disease pathology

Neuron(2024)10.1016/j.neuron.2024.01.008
N/A
0DataRank · unranked
41 citations

Yann Le Guen, Sunny Chen, Eun-Gyung Lee, Lesley Leong, John E. Gorzynski +23 more

Local read haplotagging enables accurate long-read small variant calling

Nature Communications(2024)10.1038/s41467-024-50079-5
N/A
0DataRank · unranked
20 citations

Daniel E. Cook, Maria Nattestad, Lucas Brambrink, Brandy McNulty, John E. Gorzynski +9 more

Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

Genetics in Medicine(2024)10.1016/j.gim.2024.101199
N/A
0DataRank · unranked
14 citations

Seth Berger, Samantha Baxter, Erica D. Smith, Changrui Xiao, Daniel G. Calame +89 more

A 3′UTR Insertion Is a Candidate Causal Variant at the TMEM106B Locus Associated With Increased Risk for FTLD-TDP

Neurology Genetics(2024)10.1212/nxg.0000000000200124
N/A
0DataRank · unranked
12 citations

Yann Le Guen, Yi Zeng, John E. Gorzynski, Tanner Jensen, Chengran Yang +13 more

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

medRxiv(2024)10.1101/2024.03.22.24304565
N/A
0DataRank · unranked
5 citations

Bohan Ni, Chloe Reuter, John E. Gorzynski, Sarah Fazal, Devon Bonner +13 more

Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing

Nature Biotechnology(2022)10.1038/s41587-022-01221-5
N/A
0DataRank · unranked
121 citations

John E. Gorzynski, Kishwar Shafin, Dianna G. Fisk, Trevor Pesout, Tanner Jensen +24 more