Stephanie J. DeWard
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders 3
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- Renal Diseases and Glomerulopathies 2
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- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- Genetic and Kidney Cyst Diseases 2
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- Renal and related cancers 2
- RNA modifications and cancer 1
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- Alcoholism and Thiamine Deficiency 1
- Co-authors
- Jerry VockleyDeborah MarsdenElizabeth McCrackenEmil KakkisSuneeta Madan‐KhetarpalAmy GoldsteinJie HuLakshmi Mehta
- Journals
- The American Journal of Human Genetics (1 paper)European Journal of Human Genetics (1 paper)Molecular Genetics and Metabolism (1 paper)
- Partner nations
- United StatesCanadaChile
In The Last Decade
Stephanie J. DeWard
11 papers receiving 361 citations
Peers
Comparison fields: 5 of 57
- Clinical Biochemistry 152
- Nephrology 37
- Physiology 98
- Genetics 102
- Molecular Biology 210
Countries citing papers authored by Stephanie J. DeWard
This map shows the geographic impact of Stephanie J. DeWard'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 J. DeWard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie J. DeWard more than expected).
Fields of papers citing papers by Stephanie J. DeWard
This network shows the impact of papers produced by Stephanie J. DeWard. 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 J. DeWard. The network helps show where Stephanie J. DeWard may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Stephanie J. DeWard, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 6 | |
| 2 | 2017 | 83 | |
| 3 | 2016 | 36 | |
| 4 | 2015 | 81 | |
| 5 | 2014 | 59 | |
| 6 | 2013 | 29 | |
| 7 | 2013 | 17 | |
| 8 | 2013 | 18 | |
| 9 | 2012 | 2 | |
| 10 | 2011 | 38 | |
| 11 | 2011 | 3 |
About Stephanie J. DeWard
Stephanie J. DeWard is a scholar working on Clinical Biochemistry, Nephrology and Genetics, having authored 11 papers that have together received 372 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic and Kidney Cyst Diseases (2 papers), Renal and related cancers (2 papers), Renal Diseases and Glomerulopathies (2 papers), Alcoholism and Thiamine Deficiency (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Clinical Biochemistry (152 citations), Nephrology (37 citations) and Physiology (98 citations). Stephanie J. DeWard has collaborated with scholars based in United States, Canada and Chile. Frequent co-authors include Jerry Vockley, Deborah Marsden, Elizabeth McCracken, Emil Kakkis, Suneeta Madan‐Khetarpal, Amy Goldstein, Jie Hu, Lakshmi Mehta, Urvashi Surti and Anne Slavotinek. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics and Molecular Genetics and Metabolism.
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.