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

Natasha T. Strande

WinnMed

ORCID: 0000-0001-5148-9772
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 2%percentile
2.4Author 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.

Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients

PLoS ONE(2020)10.1371/journal.pone.0242182
Top 9%
2.4DataRank
Top 9%43 citations

Jonathan Z. Luo, Alex R. Chang, Joseph B. Leader, Dustin N. Hartzel, Bryn S. Moore +7 more

Papers

Driven by 20 papers — median percentile 46. Top paper: “Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients”.

Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients

PLoS ONE(2020)10.1371/journal.pone.0242182
Top 9%
2.4DataRank
Top 9%43 citations

Jonathan Z. Luo, Alex R. Chang, Joseph B. Leader, Dustin N. Hartzel, Bryn S. Moore +7 more

Generating Clinical-Grade Gene–Disease Validity Classifications Through the ClinGen Data Platforms

Annual Review of Biomedical Data Science(2024)10.1146/annurev-biodatasci-102423-112456
N/A
0.502DataRank · unranked
16 citations

Courtney L Thaxton, Tristan H Nelson, Marina T. DiStefano, Juliann M. Savatt, Matthew Brush +25 more

Genome-first approach of the prevalence and cancer phenotypes of pathogenic or likely pathogenic germline TP53 variants

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100242
N/A
0.449DataRank · unranked
19 citations

Natasha T. Strande, Jung Kim, Jeremy S. Haley, Jessica N. Hatton, Megan N. Frone +13 more

Genomic ascertainment for UBA1 variants and VEXAS syndrome: a population-based study

medRxiv(2022)10.1101/2022.07.27.22277962
N/A
0.241DataRank · unranked
4 citations

Dale L. Bodian, Vandan Shah, Uyenlinh L Mirshahi, Jung Kim, Yi Ding +11 more

Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis

Journal of Medical Genetics(2025)10.1136/jmg-2024-110586
N/A
0.104DataRank · unranked
1 citations

Gabe Haller, Julia Whittle, Momchil Nikolov, Addison Avery, José A. Morcuende +12 more

Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource

UNC Libraries(2020)10.17615/dtq0-px12
Top 100%
0DataRank
Top 100%0 citations

Ozge Ceyhan‐Birsoy, Bryce A. Seifert, Tam P. Sneddon, Natasha T. Strande, Erin M. Ramos +18 more

Specificity of the dRP/AP Lyase of Ku Promotes Nonhomologous End Joining (NHEJ) Fidelity at Damaged Ends

UNC Libraries(2020)10.17615/yhq0-z760
N/A
0DataRank · unranked
0 citations

Steven A. Roberts, Eric A. Hendrickson, Sehyun Oh, Dale A. Ramsden, Natasha T. Strande

Nonhomologous end joining: A good solution for bad ends

UNC Libraries(2020)10.17615/w35k-8z35
N/A
0DataRank · unranked
0 citations

David W. Wyatt, Dale A. Ramsden, Natasha T. Strande, John M. Pryor, Crystal A. Waters

Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.10.013
N/A
0DataRank · unranked
548 citations

Alicia B. Byrne, Bing Feng, Kymberleigh A. Pagel, Sean D. Mooney, Rachel Karchin +20 more

Individuals heterozygous for ALG8 protein-truncating variants are at increased risk of a mild cystic kidney disease

Kidney International(2022)10.1016/j.kint.2022.11.025
N/A
0DataRank · unranked
36 citations

Gino Sartori, Bryn S. Moore, Kiran Chintam, Gurmukteshwar Singh, Prince Mohan +5 more

Frequency of truncating FLCN variants and Birt-Hogg-Dubé–associated phenotypes in a health care system population

Genetics in Medicine(2022)10.1016/j.gim.2022.05.006
N/A
0DataRank · unranked
33 citations

Hermela Shimelis, Andrés Moreno-De-Luca, Natasha T. Strande, Matthew T. Oetjens, David H. Ledbetter +4 more

Massively parallel reporter assays discover de novo exonic splicing mutants in paralogs of Autism genes

PLoS Genetics(2022)10.1371/journal.pgen.1009884
N/A
0DataRank · unranked
36 citations

Christopher R. Neil, Jing Wang, Samantha Maguire, Luke Buerer, Mitchell Salomon +5 more

Requirements for 5′dRP/AP lyase activity in Ku

UNC Libraries(2020)10.17615/6320-z898
N/A
0DataRank · unranked
0 citations

Dale A. Ramsden, Brian Kuhlman, Ryan A. Hallett, Steven A. Roberts, Christina Strom +3 more

Frequency of FLCN Loss of Function Variants and Birt-Hogg-Dubé-Associated Phenotypes in a Healthcare System Population

medRxiv(2022)10.1101/2022.01.31.22269926
N/A
0DataRank · unranked
0 citations

Hermela Shimelis, Andrés Moreno-De-Luca, Natasha T. Strande, Matthew T. Oetjens, David H. Ledbetter +4 more

Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.002
N/A
0DataRank · unranked
315 citations

Miguel de la Hoya, George A. R. Wiggins, Amanda Lindy, Lisa M. Vincent, Michael T. Parsons +28 more

Organization and dynamics of the nonhomologous end-joining machinery during DNA double-strand break repair

UNC Libraries(2020)10.17615/z9ca-qd07
N/A
0DataRank · unranked
0 citations

Eli Rothenberg, Howard H. Chang, Michael R. Lieber, David Fenyö, Go Watanabe +6 more

Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

medRxiv(2020)10.1101/2020.02.26.20024679
N/A
0DataRank · unranked
10 citations

Stephanie B. Crowley, Myra I. Roche, Ann Katherine M. Foreman, Julianne O’Daniel, Bryce A. Seifert +22 more

Assessment of the evidence yield for the calibrated PP3/BP4 computational recommendations

Genetics in Medicine(2024)10.1016/j.gim.2024.101213
N/A
0DataRank · unranked
16 citations

Vikas Pejaver, Timothy Bergquist, Leslie G. Biesecker, Alicia B. Byrne, Emily A.W. Nadeau +21 more

Calibration of additional computational tools expands ClinGen recommendation options for variant classification with PP3/BP4 criteria

Genetics in Medicine(2025)10.1016/j.gim.2025.101402
N/A
0DataRank · unranked
45 citations

Sarah L. Stenton, Emily A.W. Nadeau, Alicia B. Byrne, Marc S. Greenblatt, Steven M. Harrison +20 more

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation

UNC Libraries(2020)10.17615/0tee-nv95
N/A
0DataRank · unranked
1 citations

Christa Lese Martin, Evans, James P., Meredith Weaver, Katrina A.B. Goddard, Margaret Piper +19 more