Mary E. Stevens
Impact in
-
- Genetic Neurodegenerative Diseases
- Genetics top 2%
- Hemoglobinopathies and Related Disorders
Papers in
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- CRISPR and Genetic Engineering 6
- Receptor Mechanisms and Signaling 4
- Cancer-related gene regulation 4
- Genetics 9
- Hemoglobinopathies and Related Disorders 6
- Animal Genetics and Reproduction 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Co-authors
- Gregory S. Barsh (6 shared papers)Edward M. Rubin (6 shared papers)Brian K. Kobilka (3 shared papers)Daniel Bernstein (2 shared papers)Kavin Desai (2 shared papers)Lutz Hein (2 shared papers)Narla Mohandas (5 shared papers)Chris Pászty (5 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (4 papers)Nature Genetics (3 papers)Development (3 papers)Developmental Biology (2 papers)Science (2 papers)
- Partner nations
- United StatesNetherlandsUnited Kingdom
In The Last Decade
Mary E. Stevens
34 papers receiving 4.0k citations
Hit Papers
Peers
Comparison fields: 5 of 118
- Cellular and Molecular Neuroscience 997
- Genetics 557
- Hematology 461
- Molecular Biology 2.5k
- Physiology 610
Countries citing papers authored by Mary E. Stevens
This map shows the geographic impact of Mary E. Stevens'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 Mary E. Stevens with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mary E. Stevens more than expected).
Fields of papers citing papers by Mary E. Stevens
This network shows the impact of papers produced by Mary E. Stevens. 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 Mary E. Stevens. The network helps show where Mary E. Stevens may publish in the future.
Co-authors
The 25 scholars most cited alongside Mary E. Stevens, 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 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A YAC Mouse Model for Huntington’s Disease with Full-Length Mutant Huntingtin, Cytoplasmic Toxicity, and Selective Striatal Neurodegeneration Hit paper breakdown → | 1999 | 669 |
| 2 | Cardiovascular Regulation in Mice Lacking α 2 -Adrenergic Receptor Subtypes b and c Hit paper breakdown → | 1996 | 385 |
| 3 | 1997 | 383 | |
| 4 | 2002 | 270 | |
| 5 | 1997 | 253 | |
| 6 | 1996 | 252 | |
| 7 | 2010 | 200 | |
| 8 | 1997 | 176 | |
| 9 | 1993 | 170 | |
| 10 | 2007 | 160 | |
| 11 | 2009 | 137 | |
| 12 | 2011 | 118 | |
| 13 | 2001 | 109 | |
| 14 | 1995 | 106 | |
| 15 | 1999 | 98 | |
| 16 | 1994 | 85 | |
| 17 | 1995 | 68 | |
| 18 | 1996 | 67 | |
| 19 | 2001 | 60 | |
| 20 | 1990 | 56 |
About Mary E. Stevens
Mary E. Stevens is a scholar working on Molecular Biology, Genetics, Genetics, Immunology and Cellular and Molecular Neuroscience, having authored 35 papers that have together received 4.1k indexed citations. Recurring topics across this work include CRISPR and Genetic Engineering (6 papers), Hemoglobinopathies and Related Disorders (6 papers), Animal Genetics and Reproduction (5 papers), Receptor Mechanisms and Signaling (4 papers), Erythrocyte Function and Pathophysiology (4 papers), Cancer-related gene regulation (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Blood properties and coagulation (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (997 citations), Genetics (557 citations), Hematology (461 citations), Molecular Biology (2.5k citations) and Physiology (610 citations). Mary E. Stevens has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include Gregory S. Barsh, Edward M. Rubin, Brian K. Kobilka, Daniel Bernstein, Kavin Desai, Lutz Hein, Narla Mohandas, Chris Pászty, Desmond Smith and Elizabeth A. Manci. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics, Development, Developmental Biology and Science.
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.