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

Stephanie M. Ware

MACOM (United States)

ORCID: 0000-0003-4714-0142

Also affiliated with Field Museum of Natural History, Riley Hospital for Children, Indiana University Bloomington, University School, Indiana University School of Medicine, Indiana University – Purdue University Indianapolis, Indiana University

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 100%percentile
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.

Combined genome and transcriptome analysis identifies molecular signatures of aortic disease in patients with Marfan syndrome

Journal of Molecular and Cellular Cardiology Plus(2025)10.1016/j.jmccpl.2025.100467
Top 100%
0DataRank
Top 100%0 citations

Alexa V. Mederos, Ethan H Barksdale, Joel S. Corvera, Joshua L. Davis, Fang Fang +6 more

Papers

Driven by 22 papers — median percentile 0. Top paper: “The genetic architecture of pediatric cardiomyopathy”.

The genetic architecture of pediatric cardiomyopathy

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2021.12.006
N/A
0.624DataRank · unranked
63 citations

Surbhi Bhatnagar, Phillip J. Dexheimer, James D. Wilkinson, Arthi Sridhar, Xiao Fan +23 more

Preaxial polydactyly caused by Gli3 haploinsufficiency is rescued by Zic3 loss of function in mice

Human Molecular Genetics(2012)10.1093/hmg/dds002
N/A
0.584DataRank · unranked
48 citations

Allison Haaning, Stephanie M. Ware, Malgorzata E. Quinn

A Comprehensive Clinical Genetics Approach to Critical Congenital Heart Disease in Infancy

The Journal of Pediatrics(2020)10.1016/j.jpeds.2020.07.065
N/A
0.574DataRank · unranked
45 citations

Benjamin J. Landis, Ashley Parrott, Erin M. Miller, Alyxis G. Coyan, Lauren Walters‐Sen +4 more

Cardiac imaging and biomarkers for assessing myocardial fibrosis in children with hypertrophic cardiomyopathy

American Heart Journal(2023)10.1016/j.ahj.2023.06.005
N/A
0.462DataRank · unranked
10 citations

Pamela K. Woodard, Ling Shi, Taye H. Hamza, Charles E. Canter, Steven D. Colan +23 more

Genomics of pediatric cardiomyopathy

Pediatric Research(2025)10.1038/s41390-025-03819-2
N/A
0.398DataRank · unranked
11 citations

Stephanie M. Ware, Alicia M. Kamsheh, Surbhi Bhatnagar, Mohammed Absi, Elyse Miller +5 more

Loss ofZic3impairs planar cell polarity leading to abnormal left–right signaling, heart defects and neural tube defects

Human Molecular Genetics(2021)10.1093/hmg/ddab195
N/A
0DataRank · unranked
22 citations

Stephanie M. Ware, Helen M. Bellchambers

The genetic landscape of cardiovascular left–right patterning defects

Current Opinion in Genetics & Development(2022)10.1016/j.gde.2022.101937
N/A
0DataRank · unranked
29 citations

Maria B. Padua, Stephanie M. Ware, John R Wells

Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease

Journal of the American Heart Association(2022)10.1161/jaha.122.026369
N/A
0DataRank · unranked
20 citations

Benjamin M. Helm, Jeremy L. Herrmann, Madeline Hoover, Matthew D. Durbin, Lindsey Elmore +7 more

The seventh international RASopathies symposium: Pathways to a cure—expanding knowledge, enhancing research, and therapeutic discovery

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62716
N/A
0DataRank · unranked
16 citations

Amy E. Roberts, Lisa Schill, Lisa Schoyer, Beth Stronach, Grégor Andelfinger +37 more

Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability

Cell Reports Medicine(2022)10.1016/j.xcrm.2021.100501
N/A
0DataRank · unranked
11 citations

Wenjuan Zhu, Xinxiu Xu, Cullen B. Young, Tuantuan Tan, Amanda M. Smith +32 more

Congenital heart defects caused by FOXJ1

Human Molecular Genetics(2023)10.1093/hmg/ddad065
N/A
0DataRank · unranked
17 citations

Benjamin M. Helm, John R Wells, Amanda M Smith, Helen M. Bellchambers, Arthi Sridhar +2 more

A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices

Genetics in Medicine Open(2023)10.1016/j.gimo.2023.100814
N/A
0DataRank · unranked
15 citations

Lindsey R. Helvaty, Ming Li, William L. Border, Sara Fitzgerald‐Butt, Vidu Garg +11 more

Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return

European Journal of Human Genetics(2023)10.1038/s41431-023-01451-4
N/A
0DataRank · unranked
8 citations

Xiaonan Zhao, Nichole Owen, Pamela N. Luna, Ida Vogel, Inger Lily Hjuler Dorf +27 more

Single cell RNA analysis of the left–right organizer transcriptome reveals potential novel heterotaxy genes

Scientific Reports(2023)10.1038/s41598-023-36862-2
N/A
0DataRank · unranked
4 citations

Amruta R. Phatak, Mardi J. Nenni, Maria B. Padua, Hongyu Gao, Yunlong Liu +2 more

Clinical Decision Analysis of Genetic Evaluation and Testing in 1013 Intensive Care Unit Infants with Congenital Heart Defects Supports Universal Genetic Testing

Genes(2024)10.3390/genes15040505
N/A
0DataRank · unranked
12 citations

Stephanie M. Ware, Benjamin M. Helm

Genetic Testing Resources and Practice Patterns Among Pediatric Cardiomyopathy Programs

Pediatric Cardiology(2024)10.1007/s00246-024-03498-6
N/A
0DataRank · unranked
1 citations

Emily H. Kim, Melanie D. Everitt, Wendy K. Chung, Irene D. Lytrivi, Sonya Kirmani +9 more

Early ascertainment of genetic diagnoses clarifies impact on medium-term survival following neonatal congenital heart surgery

Journal of Clinical Investigation(2024)10.1172/jci180098
N/A
0DataRank · unranked
1 citations

Benjamin M. Helm, Matthew D. Durbin, Lindsey R. Helvaty, Jeremy L. Herrmann, Michael E. Johansen +3 more

A CRISPR mis-insertion in the Zic3 5′UTR inhibits in vivo translation and is predicted to result in formation of an mRNA stem-loop hairpin

Biology Open(2025)10.1242/bio.061677
N/A
0DataRank · unranked
2 citations

Maria B. Padua, Stephanie M. Ware, Helen M. Bellchambers

Combined genome and transcriptome analysis identifies molecular signatures of aortic disease in patients with Marfan syndrome

Journal of Molecular and Cellular Cardiology Plus(2025)10.1016/j.jmccpl.2025.100467
Top 100%
0DataRank
Top 100%0 citations

Alexa V. Mederos, Ethan H Barksdale, Joel S. Corvera, Joshua L. Davis, Fang Fang +6 more

Identification of a common polymorphism in COQ8B acting as a modifier of thoracic aortic aneurysm severity

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100057
N/A
0DataRank · unranked
6 citations

Dongbing Lai, Dongchuan Guo, Joel S. Corvera, Muhammad T. Idrees, Henry Stadler +7 more

SHROOM3 is downstream of the planar cell polarity pathway and loss-of-function results in congenital heart defects

Developmental Biology(2020)10.1016/j.ydbio.2020.05.013
N/A
0DataRank · unranked
37 citations

J. P. O’Kane, Samuel G Lorentz, Anthony B. Firulli, Stephanie M. Ware, Matthew D. Durbin

Pediatric cardiomyopathy and the PCM Genes study: A summary with insights on genetic testing, variant interpretation, race and ethnicity

Progress in Pediatric Cardiology(2021)10.1016/j.ppedcard.2021.101468
N/A
0DataRank · unranked
1 citations

Stephanie M. Ware