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)Chris Pászty (5 shared papers)Narla Mohandas (5 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (4 papers)Development (3 papers)Nature Genetics (3 papers)Genetics (2 papers)Developmental Biology (2 papers)
- Partner nations
- United StatesNetherlandsCanada
In The Last Decade
Mary E. Stevens
34 papers receiving 4.0k citations
Mary E. Stevens's Hit Papers
Peers
Comparison fields: 5 of 120
- Cellular and Molecular Neuroscience 968
- Genetics 513
- Hematology 435
- Molecular Biology 2.4k
- Physiology 552
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 | 668 |
| 2 | Cardiovascular Regulation in Mice Lacking α 2 -Adrenergic Receptor Subtypes b and c Hit paper breakdown → | 1996 | 388 |
| 3 | 1997 | 387 | |
| 4 | 2002 | 273 | |
| 5 | 1997 | 253 | |
| 6 | 1996 | 252 | |
| 7 | 2010 | 201 | |
| 8 | 1997 | 176 | |
| 9 | 1993 | 170 | |
| 10 | 2007 | 161 | |
| 11 | 2009 | 137 | |
| 12 | 2011 | 119 | |
| 13 | 2001 | 110 | |
| 14 | 1995 | 106 | |
| 15 | 1999 | 97 | |
| 16 | 1994 | 85 | |
| 17 | 1995 | 68 | |
| 18 | 1996 | 67 | |
| 19 | 2001 | 60 | |
| 20 | 1999 | 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 Hemoglobinopathies and Related Disorders (6 papers), CRISPR and Genetic Engineering (6 papers), Animal Genetics and Reproduction (5 papers), Receptor Mechanisms and Signaling (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Erythrocyte Function and Pathophysiology (4 papers), Cancer-related gene regulation (4 papers) and Pharmacological Effects and Assays (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (968 citations), Genetics (513 citations), Hematology (435 citations), Molecular Biology (2.4k citations) and Physiology (552 citations). Mary E. Stevens has collaborated with scholars based in United States, Netherlands and Canada. Frequent co-authors include Gregory S. Barsh, Edward M. Rubin, Brian K. Kobilka, Daniel Bernstein, Kavin Desai, Lutz Hein, Chris Pászty, Narla Mohandas, Desmond Smith and Elizabeth A. Manci. Their work appears in journals such as Proceedings of the National Academy of Sciences, Development, Nature Genetics, Genetics and Developmental Biology.
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.