Stephanie E Wallace
Impact in
- Genetics top 10%
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Rheumatology top 10%
- Moyamoya disease diagnosis and treatment
Papers in
- Genetics 12
- Connective tissue disorders research 6
- Dermatological and Skeletal Disorders 2
- BRCA gene mutations in cancer 2
- Genomic variations and chromosomal abnormalities 2
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- Advanced biosensing and bioanalysis techniques 2
- Co-authors
- Dušan Pavčnik (1 shared paper)K C Wright (1 shared paper)Dianna M. Milewicz (7 shared papers)Ellen S. Regalado (6 shared papers)William R. Wilcox (2 shared papers)Dongchuan Guo (5 shared papers)Pertchoui B. Mekikian (1 shared paper)Ralph S. Lachman (1 shared paper)
- Journals
- Genetics in Medicine (3 papers)Clinical Genetics (2 papers)Pharmaceuticals (1 paper)The American Journal of Human Genetics (1 paper)Radiology (1 paper)
- Partner nations
- United StatesUnited KingdomFrance
In The Last Decade
Stephanie E Wallace
35 papers receiving 742 citations
Peers
Comparison fields: 5 of 98
- Genetics 323
- Rheumatology 71
- Pulmonary and Respiratory Medicine 132
- Cardiology and Cardiovascular Medicine 90
- Pediatrics, Perinatology and Child Health 60
Countries citing papers authored by Stephanie E Wallace
This map shows the geographic impact of Stephanie E Wallace'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 E Wallace with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie E Wallace more than expected).
Fields of papers citing papers by Stephanie E Wallace
This network shows the impact of papers produced by Stephanie E Wallace. 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 E Wallace. The network helps show where Stephanie E Wallace may publish in the future.
Co-authors
The 25 scholars most cited alongside Stephanie E Wallace, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 160 | |
| 2 | 2016 | 61 | |
| 3 | 1992 | 57 | |
| 4 | 2004 | 51 | |
| 5 | 2013 | 49 | |
| 6 | 2018 | 42 | |
| 7 | 2019 | 37 | |
| 8 | 2018 | 35 | |
| 9 | 2019 | 35 | |
| 10 | 2013 | 34 | |
| 11 | 1985 | 25 | |
| 12 | Precision medical and surgical management for thoracic aortic aneurysms and acute aortic dissections based on the causative mutant gene. | 2016 | 23 |
| 13 | 2015 | 20 | |
| 14 | 2018 | 16 | |
| 15 | 2019 | 14 | |
| 16 | 2023 | 13 | |
| 17 | 2022 | 12 | |
| 18 | 2014 | 12 | |
| 19 | 2016 | 10 | |
| 20 | 2017 | 10 |
About Stephanie E Wallace
Stephanie E Wallace is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Cardiology and Cardiovascular Medicine and Epidemiology, having authored 37 papers that have together received 774 indexed citations. Recurring topics across this work include Connective tissue disorders research (6 papers), Aortic Disease and Treatment Approaches (5 papers), Moyamoya disease diagnosis and treatment (2 papers), Dermatological and Skeletal Disorders (2 papers), Advanced biosensing and bioanalysis techniques (2 papers), BRCA gene mutations in cancer (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Cardiac Valve Diseases and Treatments (2 papers). The work is most often cited by research in Genetics (323 citations), Rheumatology (71 citations), Pulmonary and Respiratory Medicine (132 citations), Cardiology and Cardiovascular Medicine (90 citations) and Pediatrics, Perinatology and Child Health (60 citations). Stephanie E Wallace has collaborated with scholars based in United States, United Kingdom and France. Frequent co-authors include Dušan Pavčnik, K C Wright, Dianna M. Milewicz, Ellen S. Regalado, William R. Wilcox, Dongchuan Guo, Pertchoui B. Mekikian, Ralph S. Lachman, Jill A. Rosenfeld and David W. Stockton. Their work appears in journals such as Genetics in Medicine, Clinical Genetics, Pharmaceuticals, The American Journal of Human Genetics and Radiology.
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.