Stephanie M. Ware

8.4k total citations · 1 hit paper
141 papers, 4.9k citations indexed

About

Stephanie M. Ware is a scholar working on Molecular Biology, Epidemiology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Stephanie M. Ware has authored 141 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 94 papers in Molecular Biology, 52 papers in Epidemiology and 50 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Stephanie M. Ware's work include Congenital heart defects research (69 papers), Congenital Heart Disease Studies (50 papers) and Cardiomyopathy and Myosin Studies (35 papers). Stephanie M. Ware is often cited by papers focused on Congenital heart defects research (69 papers), Congenital Heart Disease Studies (50 papers) and Cardiomyopathy and Myosin Studies (35 papers). Stephanie M. Ware collaborates with scholars based in United States, Canada and Germany. Stephanie M. Ware's co-authors include John W. Belmont, Jeffrey A. Towbin, Robert B. Hinton, Susan Fernbach, John L. Jefferies, Jason Cowan, Erin M. Miller, William J. Craigen, Lirong Zhu and Martina Brueckner and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Circulation and Journal of Clinical Investigation.

In The Last Decade

Stephanie M. Ware

131 papers receiving 4.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association

2018 370 citations Vidu Garg, Seema Mital et al. profile →

Peers

Stephanie M. Ware

EPIDE

CCM

GENET

SURGE

Mary Ella Pierpont United States

Amy E. Roberts United States

Kim L. McBride United States

M. Cristina Digilio Italy

Barbara R. Pober United States

Colin K. L. Phoon United States

Elizabeth Goldmuntz United States

Cecilia Camacho‐Hübner United Kingdom

Edward Blair United Kingdom

Yukihiro Hasegawa Japan

Mary Ella Pierpont United States

Stephanie M. Ware

3.9k ×1.3

1.6k ×1.1

EPIDE

726 ×0.5

CCM

1.6k ×1.4

GENET

1.2k ×1.4

SURGE

Citations per year, relative to Stephanie M. Ware Stephanie M. Ware (= 1×) peers Mary Ella Pierpont

Countries citing papers authored by Stephanie M. Ware

Since Specialization

Citations

This map shows the geographic impact of Stephanie M. Ware's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Stephanie M. Ware with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie M. Ware more than expected).

Fields of papers citing papers by Stephanie M. Ware

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephanie M. Ware. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Stephanie M. Ware. The network helps show where Stephanie M. Ware may publish in the future.

Co-authorship network of co-authors of Stephanie M. Ware

This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie M. Ware. A scholar is included among the top collaborators of Stephanie M. Ware based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Stephanie M. Ware. Stephanie M. Ware is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Lee, Teresa M., Stephanie M. Ware, Surbhi Bhatnagar, et al.. (2025). Genomics of pediatric cardiomyopathy. Pediatric Research. 97(4). 1381–1392. 1 indexed citations

Yatsenko, Svetlana A., Cecilia Lo, Xinxiu Xu, et al.. (2024). Case Report: An association of left ventricular outflow tract obstruction with 5p deletions. Frontiers in Genetics. 15. 1451746–1451746. 1 indexed citations

Geddes, Gabrielle C., et al.. (2023). Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects. The Journal of Pediatrics. 260. 113495–113495. 8 indexed citations

Padua, Maria B., et al.. (2023). Single cell RNA analysis of the left–right organizer transcriptome reveals potential novel heterotaxy genes. Scientific Reports. 13(1). 10688–10688. 2 indexed citations

Li, Ming, William L. Border, Sara Fitzgerald‐Butt, et al.. (2023). A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices. SHILAP Revista de lepidopterología. 1(1). 100814–100814. 9 indexed citations

Landis, Benjamin J., Benjamin M. Helm, Jeremy L. Herrmann, et al.. (2022). Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease. Journal of the American Heart Association. 11(19). e026369–e026369. 12 indexed citations

Fleming, Emily, et al.. (2020). Adolescents with congenital heart defects: a patient and parental perspective of genetic information and genetic risk. Cardiology in the Young. 30(2). 219–226. 6 indexed citations

Burkhalter, Martin D., Arthi Sridhar, Cornelia Donow, et al.. (2019). Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis. Journal of Clinical Investigation. 129(7). 2841–2855. 42 indexed citations

Schubert, Jeffrey, Muhammad Tariq, Gabrielle C. Geddes, et al.. (2018). Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathy. Human Mutation. 39(12). 2083–2096. 18 indexed citations

10.

Mital, Seema, Kiran Musunuru, Vidu Garg, et al.. (2016). Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart Association. Circulation Cardiovascular Genetics. 9(5). 448–467. 57 indexed citations

11.

Landis, Benjamin J., et al.. (2016). Bicuspid Aortic Valve: a Review with Recommendations for Genetic Counseling. PMC. 1 indexed citations

12.

Azhar, Mohamad & Stephanie M. Ware. (2016). Genetic and Developmental Basis of Cardiovascular Malformations. PMC.

13.

Tandon, Animesh, John L. Jefferies, Chet Villa, et al.. (2015). Dystrophin Genotype–Cardiac Phenotype Correlations in Duchenne and Becker Muscular Dystrophies Using Cardiac Magnetic Resonance Imaging. The American Journal of Cardiology. 115(7). 967–971. 21 indexed citations

14.

Hinton, Robert B., Kim L. McBride, Steven B. Bleyl, et al.. (2015). Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach. PMC. 2 indexed citations

15.

Tariq, Muhammad & Stephanie M. Ware. (2014). Importance of genetic evaluation and testing in pediatric cardiomyopathy. PMC. 3 indexed citations

16.

James, Jeanne, Paula Goldenberg, Robert B. Hinton, et al.. (2014). Aortopathy in the 7q11.23 microduplication syndrome. American Journal of Medical Genetics Part A. 167(2). 363–370. 25 indexed citations

17.

Cast, Ashley, Chunlei Gao, Jeffrey D. Amack, & Stephanie M. Ware. (2012). An essential and highly conserved role for Zic3 in left–right patterning, gastrulation and convergent extension morphogenesis. Developmental Biology. 364(1). 22–31. 26 indexed citations

18.

Tariq, Muhammad, John W. Belmont, Seema R. Lalani, Teresa A. Smolarek, & Stephanie M. Ware. (2011). SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing. Genome biology. 12(9). R91–R91. 47 indexed citations

19.

Ware, Stephanie M., et al.. (2011). Spectrum of Clinical Diseases Caused By Disorders of Primary Cilia. Proceedings of the American Thoracic Society. 8(5). 444–450. 79 indexed citations

20.

Ware, Stephanie M., Akira Sato, Raymond Habas, et al.. (2005). The Vg1 - related protein Gdf3 acts in a Nodal signaling pathway in the pre-gastrulation mouse embryo. Development. 133(2). 319–329. 125 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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